Recomendaciones para el diagnóstico, seguimiento y tratamiento cáncer del pulmón de células no pequeñas temprano en Colombia

Autores/as

  • Diego Hernando Pardo Asociación Colombiana de Cirugía de Tórax
  • Lucia Viola Centro de Tratamiento e Investigación sobre Cáncer (CTIC)
  • Jairo Zuluaga Centro de Tratamiento e Investigación sobre Cáncer (CTIC)
  • Leonardo Rojas Centro de Tratamiento e Investigación sobre Cáncer (CTIC)
  • Iván Andrés Bobadilla Centro de Tratamiento e Investigación sobre Cáncer (CTIC)
  • Stella Martínez Centro de Tratamiento e Investigación sobre Cáncer (CTIC)
  • Iván José Bustillo Clínica Portoazul, Barranquilla
  • Luis Gerardo Garcia-Herreros Fundación Santa Fe de Bogotá
  • Ricardo Adolfo Zapata Clínica CardioVID
  • Adriana Serna Hospital Santa Clara, Bogotá
  • Ana Margarita Baldión Fundación Santa Fe de Bogotá
  • Darwin José Padilla Clínica General del Norte, Barranquilla
  • Willfredy Castaño Hospital Pablo Tobón Uribe
  • Liliana Arias Hospital Universitario San Ignacio
  • Alejandro Ruíz Centro de Tratamiento e Investigación sobre Cáncer (CTIC)
  • Oscar Arrieta Instituto Nacional de Cancerología – INCaN, México
  • Andrés Felipe Cardona Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

DOI:

https://doi.org/10.56050/01205498.2316

Resumen

Introducción: El cáncer de pulmón de células no pequeñas (CPCNP) de- rivado o no de la exposición crónica al humo por combustión del tabaco representa un problema sanitario global y local dada su alta letalidad, por la rápida progresión de la medicina de precisión y el impacto presupues- tal de las nuevas intervenciones. Dada la notable evolución de los métodos diagnósticos y terapéuticos para el CPCNP, se decidió realizar un consenso orientado a priorizar las necesidades del entorno colombiano, adaptando las recomendaciones de múltiples esfuerzos integrativos previos. Objetivo: Generar recomendaciones para optimizar el manejo integral de los pacientes con CPCNP en Colombia a partir de la discusión estructurada en un grupo focal de expertos incluyendo cirujanos de tórax, oncólogos clínicos, radiólogos, patólogos, neumólogos y genetistas. Dada la transición epidemiológica de la enfermedad se hizo énfasis en las etapas tempranas de la enfermedad. Métodos: Usando una herramienta digital (AGREE II Tool) para la caracterización de información relevante se elaboraron y discutieron las preguntas orientadoras para cada sesión sincrónica. En paralelo se hizo una revisión sistemática de la literatura usando la plataforma SCOPUS con énfasis en la extracción de guías de práctica clínica (GPC), metaanálisis, estudios clínicos y documentos de consenso. Además, se evaluaron y sintetizaron las principales recomendaciones de la International Agency for the Study of Lung Cancer (IASLC), de la American Asociation of Clinical Oncology (ASCO), de la European Society of Medical Oncology (ESMO), la National Comprehensive Cancer Network (NCCN), y del National Institute for Health and Care Excellence (NICE). A partir de las discusiones se seleccionaron 15 ejes primarios para la discusión considerando el tamizaje para poblaciones en riesgo, la estadificación, el tratamiento y el seguimiento. Después de cada discusión virtual se realizaron votaciones y se estimó el nivel de acuerdo para cada una. Resultados: En 5 sesiones grupales se discutieron 15 preguntas orientadoras que derivaron en 82 recomendaciones (8 tamizaje, 11 estadificación, 4 diagnóstico y 59 tratamiento). Setenta y siete obtuvieron un alto nivel de acuerdo (>80 %), 5 un nivel intermedio (30-79 %), y ninguna obtuvo nivel bajo. Finalmente, 67 cumplieron con los dos criterios de aceptación (tamizaje 8, estadificación 11, diagnóstico 3, tratamiento 48). Conclusión: A partir de la revisión sistemática de la literatura y la discusión multidisciplinaria se realizaron recomendaciones orientadas a mejorar el manejo del paciente con CPCNP en el contexto colombiano.

Biografía del autor/a

Diego Hernando Pardo, Asociación Colombiana de Cirugía de Tórax

Asociación Colombiana de Cirugía de Tórax (ASOCOLTORAX), Bogotá, Colombia.

Lucia Viola, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Clínica de Oncología Torácica, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.
Unidad Oncología Torácica, Fundación Neumológica Colombiana - FNC, Bogotá Colombia.

Jairo Zuluaga, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Clínica de Oncología Torácica, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.

Leonardo Rojas, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Clínica de Oncología Torácica, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.

Iván Andrés Bobadilla, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Asistencial Radioterapia, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.

Stella Martínez, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Clínica de Oncología Torácica, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.

Iván José Bustillo, Clínica Portoazul, Barranquilla

Departamento Oncología Clínica, Clínica Portoazul, Barranquilla, Colombia.

Luis Gerardo Garcia-Herreros, Fundación Santa Fe de Bogotá

Departamento de Cirugía, Unidad Cirugía de Tórax, Fundación Santa Fe de Bogotá, Bogotá, Colombia.

Ricardo Adolfo Zapata, Clínica CardioVID

Clínica CardioVID. Obra de la Congregación Mariana, Medellín Colombia.

Adriana Serna, Hospital Santa Clara, Bogotá

Unidad Cirugía de Tórax, Hospital Santa Clara, Bogotá, Colombia.

Ana Margarita Baldión, Fundación Santa Fe de Bogotá

Departamento de Patología, Fundación Santa Fe de Bogotá, Bogotá, Colombia.

Darwin José Padilla, Clínica General del Norte, Barranquilla

Organización Clínica General del Norte, Barranquilla, Colombia.

Willfredy Castaño, Hospital Pablo Tobón Uribe

Hospital Pablo Tobón Uribe, Medellín Colombia.

Liliana Arias, Hospital Universitario San Ignacio

Hospital Universitario San Ignacio, Bogotá, Colombia.

Alejandro Ruíz, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Clínica de Oncología Torácica, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.
Fundación para la Investigación Clínica y Molecular Aplicada del Cáncer – FICMAC, Bogotá, Colombia.

Oscar Arrieta, Instituto Nacional de Cancerología – INCaN, México

Unidad Oncología Torácica, Instituto Nacional de Cancerología – INCaN, Ciudad de México, México.

Andrés Felipe Cardona, Centro de Tratamiento e Investigación sobre Cáncer (CTIC)

Unidad Funcional Clínica de Oncología Torácica, Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo (CTIC), Bogotá, Colombia.

Referencias bibliográficas

Gerstung M, Jolly C, Leshchiner I, Dentro SC, Gonzalez S, Rosebrock D, et al.; PCAWG Consortium. The evolutionary history of 2,658 cancers. Nature. 2020;578(7793):122-128. doi: 10.1038/s41586- 019-1907-7.

Martincorena I, Campbell PJ. Somatic mutation in cancer and normal cells. Science. 2015;349(6255):1483- 9. doi: 10.1126/science.aab4082.

ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium. Pan-cancer analysis of whole genomes. Nature. 2020;578(7793):82-93. doi: 10.1038/s41586-020-1969-6.

Jolly C, Van Loo P. Timing somatic events in the evolution of cancer. Genome Biol. 2018;19(1):95. doi: 10.1186/s13059-018-1476-3.

ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium. Pan-cancer analysis of whole genomes. Nature. 2020;578(7793):82-93. doi: 10.1038/s41586-020-1969-6.

Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71(3):209-249. doi: 10.3322/caac.21660.

WHO. [Internet]. WHO press release 263: Latest global cancer data. [Consultado 24 de octubre 2023]. Disponible en: https://www.who.int/cancer/PRGlobocanFinal.pdf

Cronin KA, Scott S, Firth AU, Sung H, Henley SJ, Sherman RL, et al. Annual report to the nation on the status of cancer, part 1: National cancer statistics. Cancer. 2022;128(24):4251-4284. doi: 10.1002/ cncr.34479.

GBD 2017 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018;392(10159):1789-1858. doi: 10.1016/S0140- 6736(18)32279-7.

Pan American Health Organization. Health in the Americas+, 2017 Edition. Summary: Regional Outlook and Country Profiles. Washington, D.C.: PAHO; 2017.

World Health Organization.[Internet] Cancer Today. Global Cancer Observatory. Published 2020. Accessed February 15, 2021. [Consultado 24 de octubre 2023]. Disponible en: https://gco.iarc.fr/

Pardo C, De Vries E, Buitrago L, Gamboa Ó. Altas de Mortalidad Por Cáncer En Colombia. Cuarta Edición. Vol 1.; 2017. https://www.cancer.gov.co/ATLAS_de_Mortalidad_por_cancer_en_Colombia.pdf

Piñeros M, Sierra MS, Forman D. Descriptive epidemiology of lung cancer and current status of tobacco control measures in Central and South America. Cancer Epidemiol. 2016;44:S90-S99. doi:10.1016/j.canep.2016.03.002

Sierra MS, Soerjomataram I, Forman D. Etiology of lung cancer (C33-34) in Central and South America. In: Cancer in Central and South America. Int Agency Res Cancer. 2016;7:1-9.

Hernández Vargas JA, Ramírez Barbosa PX, Valbuena-Garcia AM, Acuña-Merchán LA, González-Diaz JA, Lopes G. National Cancer Information System Within the Framework of Health Insurance in Colombia: A Real-World Data Approach to Evaluate Access to Cancer Care. JCO Glob Oncol. 2021;(7):1329-1340. doi:10.1200/go.21.00155

Cuenta de Alto Costo - Fondo Colombiano de Enfermedades de Alto. Situación del cáncer en la población adulta atendida en el SGSSS de Colombia 2020. [internet] 2020. [Consultado 24 de octubre 2023]. Disponible en: https://cuentadealtocosto.org/site/publicaciones/situacion-del-cancer-en-la-poblacion-adulta-atendida-en-el-sgsss-de-colombia-2020/

Ministerio de Justicia y del Derecho – Observatorio de Drogas de Colombia. Estudio Nacional de Consumo de Sustancias Psicoactivas Colombia 2019. [Internet] 2019. [Consultado 24 de octubre 2023]. Disponible en: https://www.unodc.org/documents/colombia/2013/septiembre/Estudio_Nacional_Consumo_1996.pdf

Rivera D esperanza, Niño AB. ABC de la ley antitabaco (ley 1335 de 2009). Hechos & Acciones. 2009;2(2):1-8.

Alarcón M, Bruges R, Carvajal C, Vallejo C, Beltrán R. Características de los pacientes con cáncer de pulmón de célula no pequeña en el Instituto Nacional de Cancerología de Colombia. Rev Colomb Cancerol. 2011;17(2):642-647.

Cardona AF, Mejía SA, Viola L, Chamorro DF, Rojas L, Ruíz-Patiño A, et al. Lung Cancer In Colombia. J Thor Oncol. 2022;17(8):953-960. doi: 10.1016/j. jtho.2022.02.015.

Passiglia F, Bertolaccini L, Del Re M, Facchinetti F, Ferrara R, Franchina T, et al. Diagnosis and treatment of early and locally advanced non-small-cell lung cancer: The 2019 AIOM (Italian Association of Medical Oncology) clinical practice guidelines. Crit Rev Oncol Hematol. 2020;148:102862.

NSCLC Meta-analysis Collaborative Group. Preoperative chemotherapy for non-small-cell lung cancer: a systematic review and meta-analysis of individual participant data. Lancet. 2014;383(9928):1561-71.

Li F, Chen Y, Wu J, Li C, Chen S, Zhu Z, Qin W, Liu M, Hu B, Liu S, Zhong W. The earlier, the better? A review of neoadjuvant immunotherapy in resectable non-small-cell lung cancer. Chronic Dis Transl Med. 2022;8(2):100-111.

NSCLC Meta-analysis Collaborative Group. Preoperative chemotherapy for non-small-cell lung cancer: a systematic review and meta-analysis of individual participant data. Lancet. 2014;383(9928):1561-71.

Li F, Chen Y, Wu J, Li C, Chen S, Zhu Z, Qin W, Liu M, Hu B, Liu S, Zhong W. The earlier, the better? A review of neoadjuvant immunotherapy in resectable non-small-cell lung cancer. Chronic Dis Transl Med. 2022;8(2):100-111.

Felip E, Rosell R, Maestre JA, Rodríguez-Paniagua JM, Morán T, Astudillo J, et al.; Spanish Lung Cancer Group. Preoperative chemotherapy plus surgery versus surgery plus adjuvant chemotherapy versus surgery alone in early-stage non-small-cell lung cancer. J Clin Oncol. 2010;28(19):3138-45.

Sugarbaker DJ, Herndon J, Kohman LJ, Krasna MJ, Green MR. Results of cancer and leukemia group B protocol 8935. A multiinstitutional phase II trimodality trial for stage IIIA (N2) non-small-cell lung cancer. Cancer and Leukemia Group B Thoracic Surgery Group. J Thorac Cardiovasc Surg. 1995;109(3):473-83.

Kirn DH, Lynch TJ, Mentzer SJ, Lee TH, Strauss GM, Elias AD, Skarin AT, Sugarbaker DJ. Multimodality therapy of patients with stage IIIA, N2 non-small-cell lung cancer. Impact of preoperative chemotherapy on resectability and downstaging. J Thorac Cardiovasc Surg. 1993;106(4):696-702.

Andre F, Grunenwald D, Pignon JP, Dujon A, Pujol JL, Brichon PY, Brouchet L, Quoix E, Westeel V, Le Chevalier T. Survival of patients with resected N2 non-small-cell lung cancer: evidence for a subclassification and implications. J Clin Oncol. 2000;18(16):2981-9. doi: 10.1200/ JCO.2000.18.16.2981.

Martini N, Kris MG, Flehinger BJ, Gralla RJ, Bains MS, Burt ME, et al. Preoperative chemotherapy for stage IIIa (N2) lung cancer: the SloanKettering experience with 136 patients. Ann Thorc Surg. 1993;55:1365-1374.

Blumenthal GM, Bunn PA Jr, Chaft JE, McCoach CE, Perez EA, Scagliotti GV, et al. Current Status and Future Perspectives on Neoadjuvant Therapy in Lung Cancer. J Thorac Oncol. 2018;13(12):1818- 1831.

Zhang X, Xu Q, Yu X, Huang M, Li S, Sheng L, et al. What Is Long-Term Survival and Which First-Line Immunotherapy Brings Long-Term Survival for Advanced Wild-Type Non-Small Cell Lung Cancer: A Network Meta-Analysis Based on Integrated Analysis. Front Immunol. 2022;13:764643.

Shen Z, Lu Y, Sui Y, Feng S, Feng J, Zhou J. Therapeutic Strategies for Resectable Stage-IIIA N2 Non-Small Cell Lung Cancer Patients: A Network Meta-Analysis. Clin Med Insights Oncol. 2022;16:11795549221109487.

Spigel DR, Faivre-Finn C, Gray JE, Vicente D, Planchard D, Paz-Ares L, et al. Five-Year Survival Outcomes From the PACIFIC Trial: Durvalumab After Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer. J Clin Oncol. 2022;40(12):1301-1311.

Liu J, Blake SJ, Yong MC, Harjunpää H, Ngiow SF, Takeda K, et al. Improved Efficacy of Neoadjuvant Compared to Adjuvant Immunotherapy to Eradicate Metastatic Disease. Cancer Discov. 2016;6(12):1382-1399.

Yi JS, Ready N, Healy P, Dumbauld C, Osborne R, Berry M, et al. Immune Activation in Early-Stage Non-Small Cell Lung Cancer Patients Receiving Neoadjuvant Chemotherapy Plus Ipilimumab. Clin Cancer Res. 2017;23(24):7474-7482.

Hwang M, Canzoniero JV, Rosner S, Zhang G, White JR, Belcaid Z, et al. Peripheral blood immune cell dynamics reflect antitumor immune responses and predict clinical response to immunotherapy. J Immunother Cancer. 2022;10(6):e004688. doi: 10.1136/jitc-2022-004688.

Forde PM, Chaft JE, Pardoll DM. Neoadjuvant PD-1 Blockade in Resectable Lung Cancer. N Engl J Med. 2018;379(9):e14.

Eberhardt WEE, De Ruysscher D, Weder W, Le Péchoux C, De Leyn P, Hoffmann H, et al. 2nd ESMO Consensus Conference in Lung Cancer: locally advanced stage III non-small-cell lung cancer. Ann Oncol 2015;26:1573–88. https://doi.org/10.1093/annonc/mdv187.

National Comprehensive Cancer Network. [Internet]. Development and Update of Guidelines 2023. [Consultado 30 de Julio 2023]Disponible en: https://www.nccn.org/guidelines/guidelines-process/development-and-update-of-guidelines.

ESMO Guidelines Committee (GLC). [Internet]. ESMO Standard Operating Procedures (SOPs) for Consensus Conference (CC) recommendations. ESMO CC SOP Version 1.0.. [Consultado 20 de Julio 2023]. Disponible en: https://www.esmo.org/content/download/77792/1426729/1/ESMO-ConsensusConference-SOPs.pdf.

National Lung Screening Trial Research Team; Aberle DR, Adams AM, Berg CD, Black WC, Clapp JD, Fagerstrom RM, et al. Reduced lung-cancer mortality with low-dose computed tomographic screening. N Engl J Med. 2011;365(5):395-409. doi: 10.1056/NEJMoa1102873.

Osarogiagbon RU, Yang PC, Sequist LV. Expanding the Reach and Grasp of Lung Cancer Screening. Am Soc Clin Oncol Educ Book. 2023;43:e389958. doi: 10.1200/EDBK_389958.

Sands J, Tammemägi MC, Couraud S, Baldwin DR, Borondy-Kitts A, Yankelevitz D, et al. Lung Screening Benefits and Challenges: A Review of The Data and Outline for Implementation. J Thorac Oncol. 2021;16(1):37-53. doi: 10.1016/j.jtho.2020.10.127.

de Koning HJ, van der Aalst CM, de Jong PA, Scholten ET, Nackaerts K, Heuvelmans MA, et al. Reduced Lung-Cancer Mortality with Volume CT Screening in a Randomized Trial. N Engl J Med. 2020;382(6):503-513. doi: 10.1056/NEJ- Moa1911793.

Romero D. NELSON updated. Nat Rev Clin Oncol. 2020;17(4):197. doi: 10.1038/s41571-020- 0342-x.

Ettinger DS, Wood DE, Aisner DL, Akerley W, Bauman JR, Bharat A, et al. NCCN Guidelines® Insights: Non-Small Cell Lung Cancer, Version 2.2023. J Natl Compr Canc Netw. 2023;21(4):340- 350. doi: 10.6004/jnccn.2023.0020.

Wood DE, Kazerooni EA, Aberle D, Berman A, Brown LM, et al. NCCN Guidelines® Insights: Lung Cancer Screening, Version 1.2022. J Natl Compr Canc Netw. 2022;20(7):754-764. doi: 10.6004/ jnccn.2022.0036.

Jonas DE, Reuland DS, Reddy SM. Screening for Lung Cancer With Low-Dose Computed Tomography: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force. JAMA. 2021;325(10):971–987. doi:10.1001/ jama.2021.0377

Field JK, Vulkan D, Davies MPA, Baldwin DR, Brain KE, Devaraj A, et al. Lung cancer mortality reduction by LDCT screening: UKLS randomised trial results and international meta-analysis. Lancet Reg Health Eur. 2021;10:100179. doi: 10.1016/j. lanepe.2021.100179.

Pastorino U, Silva M, Sestini S, Sabia F, Boeri M, Cantarutti A, et al. Prolonged lung cancer screening reduced 10-year mortality in the MILD trial: new confirmation of lung cancer screening efficacy. Ann Oncol. 2019;30(10):1672. doi: 10.1093/annonc/ mdz169. Erratum for: Ann Oncol. 2019;30(7):1162- 1169.

National Lung Screening Trial Research Team. Lung Cancer Incidence and Mortality with Extended Follow-up in the National Lung Screening Trial. J Thorac Oncol. 2019;14(10):1732-1742. doi: 10.1016/j. jtho.2019.05.044.

US Preventive Services Task Force. [Internet] Lung Cancer: Screening. Final Evidence Review [Consultado 25 de marzo 2023]. Disponible en:. https://www.uspreventiveservicestaskforce.org/uspstf/recommendation/lung-cancer-screening.

Tammemägi MC, Church TR, Hocking WG, Silvestri GA, Kvale PA, Riley TL, et al. Evaluation of the lung cancer risks at which to screen everand never-smokers: screening rules applied to the PLCO and NLST cohorts. PLoS Med. 2014;11(12):e1001764. doi: 10.1371/journal.pmed.1001764.

Hoffman RM, Atallah RP, Struble RD, Badgett RG. Lung Cancer Screening with Low-Dose CT: a Meta-Analysis. J Gen Intern Med. 2020;35(10):3015- 3025. doi: 10.1007/s11606-020-05951-7.

Hunger T, Wanka-Pail E, Brix G, Griebel J. Lung Cancer Screening with Low-Dose CT in Smokers: A Systematic Review and Meta-Analysis. Diagnostics (Basel). 2021;11(6):1040. doi: 10.3390/diagnostics11061040.

Bonney A, Malouf R, Marchal C, Manners D, Fong KM, Marshall HM, et al. Impact of low-dose computed tomography (LDCT) screening on lung cancer-related mortality. Cochrane Database Syst Rev. 2022;8(8):CD013829. doi: 10.1002/14651858. CD013829.pub2.

Armstrong C. Lung Cancer Screening Recommendations from the ACCP. Am Fam Physician. 2018;98(11):688-689.

Mazzone PJ, White CS, Kazerooni EA, Smith RA, Thomson CC. Proposed Quality Metrics for Lung Cancer Screening Programs: A National Lung Cancer Roundtable Project. Chest. 2021;160(1):368- 378. doi: 10.1016/j.chest.2021.01.063.

Mazzone PJ, Silvestri GA, Souter LH, Caverly TJ, Kanne JP, Katki HA, Wiener RS, Detterbeck FC. Executive Summary: Screening for Lung Cancer: Chest Guideline and Expert Panel Report. Chest. 2021;160(5):1959-1980. doi: 10.1016/j. chest.2021.07.003.

Nicholson AG, Tsao MS, Beasley MB, Borczuk AC, Brambilla E, Cooper WA, et al. The 2021 WHO Classification of Lung Tumors: Impact of Advances Since 2015. J Thorac Oncol. 2022;17(3):362-387. doi: 10.1016/j.jtho.2021.11.003.

Lindeman NI, Cagle PT, Aisner DL, Arcila ME, Beasley MB, Bernicker EH, et al. Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors: Guideline From the College of American Pathologists, the International Association for the Study of Lung Cancer, and the Association for Molecular Pathology. J Thorac Oncol. 2018;13(3):323- 358. doi: 10.1016/j.jtho.2017.12.001.

Hirsch FR, Wynes MW, Gandara DR, Bunn PA Jr. The tissue is the issue: personalized medicine for non-small cell lung cancer. Clin Cancer Res. 2010;16(20):4909-11. doi: 10.1158/1078-0432. CCR-10-2005.

Mata DA, Harries L, Williams EA, Hiemenz MC, Decker B, Tse JY, et al. Method of Tissue Acquisition Affects Success of Comprehensive Genomic Profiling in Lung Cancer. Arch Pathol Lab Med. 2023;147(3):338-347. doi: 10.5858/arpa.2021- 0313-OA.

Penault-Llorca F, Kerr KM, Garrido P, Thunnissen E, Dequeker E, Normanno N, Patton SJ, et al. Expert opinion on NSCLC small specimen biomarker testing - Part 2: Analysis, reporting, and quality assessment. Virchows Arch. 2022;481(3):351-366. doi: 10.1007/s00428-022-03344-1.

Penault-Llorca F, Kerr KM, Garrido P, Thunnissen E, Dequeker E, Normanno N, et al. Expert opinion on NSCLC small specimen biomarker testing - Part 1: Tissue collection and management. Virchows Arch. 2022;481(3):335-350. doi: 10.1007/s00428- 022-03343-2.

Dietel M, Bubendorf L, Dingemans AM, Dooms C, Elmberger G, García RC, et al. Diagnostic procedures for non-small-cell lung cancer (NSCLC): recommendations of the European Expert Group. Thorax. 2016;71(2):177-84. doi: 10.1136/thoraxjnl-2014-206677.

Gan Q, Roy-Chowdhuri S. Small but powerful: the promising role of small specimens for biomarker testing. J Am Soc Cytopathol. 2020;9(5):450-460. doi: 10.1016/j.jasc.2020.05.001.

Rivera MP, Mehta AC, Wahidi MM. Establishing the diagnosis of lung cancer: Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest. 2013;143(5 Suppl):e142S-e165S. doi: 10.1378/chest.12-2353.

Wang Memoli JS, Nietert PJ, Silvestri GA. Meta-analysis of guided bronchoscopy for the evaluation of the pulmonary nodule. Chest. 2012;142(2):385- 393. doi: 10.1378/chest.11-1764

Fielding DI, Chia C, Nguyen P, Bashirzadeh F, Hundloe J, Brown IG, et al. Prospective randomised trial of endobronchial ultrasound-guide sheath versus computed tomography-guided percutaneous core biopsies for peripheral lung lesions. Intern Med J. 2012;42(8):894-900. doi: 10.1111/j.1445- 5994.2011.02707.x.

Shinagawa N. A review of existing and new methods of bronchoscopic diagnosis of lung cancer. Respir Investig. 2019;57(1):3-8. doi: 10.1016/j.resinv.2018.08.004.

Fielding D, Kurimoto N. Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration for Diagnosis and Staging of Lung Cancer. Clin Chest Med. 2018;39(1):111-123. doi: 10.1016/j. ccm.2017.11.012.

Sung S, Heymann JJ, Crapanzano JP, Moreira AL, Shu C, Bulman WA, et al. Lung cancer cytology and small biopsy specimens: diagnosis, predictive biomarker testing, acquisition, triage, and management. J Am Soc Cytopathol. 2020;9(5):332-345. doi: 10.1016/j.jasc.2020.04.014. Epub 2020 May 28.

Gilbert CR, Wahidi MM, Yarmus LB, Roy-Chowdhuri S, Pastis NJ 2nd. Key Highlights for the College of American Pathology Statement on Collection and Handling of Thoracic Small Biopsy and Cytology Specimens for Ancillary Studies. Chest. 2020;158(6):2282-2284. doi: 10.1016/j. chest.2020.07.053.

Roy-Chowdhuri S, Dacic S, Ghofrani M, Illei PB, Layfield LJ, Lee C, et al. Collection and Handling of Thoracic Small Biopsy and Cytology Specimens for Ancillary Studies: Guideline From the College of American Pathologists in Collaboration With the American College of Chest Physicians, Association for Molecular Pathology, American Society of Cytopathology, American Thoracic Society, Pulmonary Pathology Society, Papanicolaou Society of Cytopathology, Society of Interventional Radiology, and Society of Thoracic Radiology. Arch Pathol Lab Med. 2020;. doi: 10.5858/arpa.2020-0119-CP.

Zhang HF, Zeng XT, Xing F, Fan N, Liao MY. The diagnostic accuracy of CT-guided percutaneous core needle biopsy and fine needle aspiration in pulmonary lesions: a meta-analysis. Clin Radiol. 2016;71(1):e1-10. doi: 10.1016/j.crad.2015.09.009.

Kim L, Tsao MS. Tumour tissue sampling for lung cancer management in the era of personalised therapy: what is good enough for molecular testing? Eur Respir J. 2014;44(4):1011-22. doi: 10.1183/09031936.00197013.

Schneider F, Smith MA, Lane MC, Pantanowitz L, Dacic S, Ohori NP. Adequacy of core needle biopsy specimens and fine-needle aspirates for molecular testing of lung adenocarcinomas. Am J Clin Pathol. 2015;143(2):193-200. doi: 10.1309/AJCPMY8UI- 7WSFSYY.

Travis WD, Dacic S, Wistuba I, Sholl L, Adusumilli P, Bubendorf L, et al. IASLC Multidisciplinary Recommendations for Pathologic Assessment of Lung Cancer Resection Specimens After Neoadjuvant Therapy. J Thorac Oncol. 2020;15(5):709-740. doi: 10.1016/j.jtho.2020.01.005.

Evison M, Crosbie P, Navani N, Callister M, Rintoul RC, Baldwin D, et al. How should performance in EBUS mediastinal staging in lung cancer be measured? Br J Cancer. 2016;115(8):e9. doi: 10.1038/ bjc.2016.253.

Um SW, Kim HK, Jung SH, Han J, Lee KJ, Park HY, et al. Endobronchial ultrasound versus mediastinoscopy for mediastinal nodal staging of non-small-cell lung cancer. J Thorac Oncol. 2015;10(2):331-7. doi: 10.1097/JTO.0000000000000388.

Nardecchia E, Cattoni M, Dominioni L. Endobronchial ultrasound-transbronchial needle aspiration for mediastinal staging of non-small cell lung cancer: variability of results and perspectives. J Thorac Dis. 2017;9(Suppl 5):S418-S424. doi: 10.21037/ jtd.2017.04.12.

Liu X, Yang K, Guo W, Ye M, Liu S. Mediastinal Nodal Staging Performance of Combined Endobronchial and Esophageal Endosonography in Lung Cancer Cases: A Systematic Review and Meta-Analysis. Front Surg. 2022;9:890993. doi: 10.3389/fsurg.2022.890993.

Sanz-Santos J, Almagro P, Malik K, Martinez-Camblor P, Caro C, Rami-Porta R. Confirmatory Mediastinoscopy after Negative Endobronchial Ultrasound-guided Transbronchial Needle Aspiration for Mediastinal Staging of Lung Cancer: Systematic Review and Meta-analysis. Ann Am Thorac Soc. 2022;19(9):1581-1590. doi: 10.1513/AnnalsATS.202111-1302OC.

Gunawan A, Manuel L, Fong LS, Bassin L. In patients with lung cancer is combined endobronchial ultrasound and endoscopic ultrasound superior to conventional mediastinoscopy in staging the mediastinum? Ann Med Surg (Lond). 2021;71:102953. doi: 10.1016/j.amsu.2021.102953.

Yu Lee-Mateus A, Garcia-Saucedo JC, Abia-Trujillo D, Labarca G, Patel NM, Pascual JM, et al. Comparing diagnostic sensitivity of different needle sizes for lymph nodes suspected of lung cancer in endobronchial ultrasound transbronchial needle aspiration: Systematic review and meta-analysis. Clin Respir J. 2021;15(12):1328-1336. doi: 10.1111/ crj.13436.

Eapen GA, Shah AM, Lei X, Jimenez CA, Morice RC, Yarmus L, et al.; American College of Chest Physicians Quality Improvement Registry, Education, and Evaluation (AQuIRE) Participants. Complications, consequences, and practice patterns of endobronchial ultrasound-guided transbronchial needle aspiration: Results of the AQuIRE registry. Chest. 2013;143(4):1044-1053. doi: 10.1378/ chest.12-0350.

Leong P, Deshpande S, Irving LB, Bardin PG, Farmer MW, Jennings BR, et al. Endoscopic ultrasound fine-needle aspiration by experienced pulmonologists: a cusum analysis. Eur Respir J. 2017;50(5):1701102. doi: 10.1183/13993003.01102-2017.

Steinfort DP, Siva S, Leong TL, Rose M, Herath D, Antippa P, et al. Systematic Endobronchial Ultrasound-guided Mediastinal Staging Versus Positron Emission Tomography for Comprehensive Mediastinal Staging in NSCLC Before Radical Radiotherapy of Non-small Cell Lung Cancer: A Pilot Study. Medicine (Baltimore). 2016;95(8):e2488. doi: 10.1097/ MD.0000000000002488.

Cole AJ, Hardcastle N, Turgeon GA, Thomas R, Irving LB, Jennings BR, et al. Systematic endobronchial ultrasound-guided transbronchial needle aspiration improves radiotherapy planning in non-small cell lung cancer. ERJ Open Res. 2019;5(3):00004- 2019. doi: 10.1183/23120541.00004-2019.

Ost DE, Niu J, Zhao H, Grosu HB, Giordano SH. Quality Gaps and Comparative Effectiveness in Lung Cancer Staging and Diagnosis. Chest. 2020;157(5):1322-1345. doi: 10.1016/j. chest.2019.09.025.

Evison M, Crosbie P, Martin J, Shah R, Doran H, Borrill Z, et al. EBUS-guided mediastinal lung cancer staging: monitoring of quality standards improves performance. Thorax. 2016;71(8):762-3. doi: 10.1136/thoraxjnl-2015-206985.

Steinfort DP, Evison M, Witt A, Tsaknis G, Kheir F, Manners D, et al.; WABIP Taskforce on Quality Indicators in EBUS Bronchoscopy. Proposed quality indicators and recommended standard reporting items in performance of EBUS bronchoscopy: An official World Association for Bronchology and Interventional Pulmonology Expert Panel consensus statement. Respirology. 2023;28(8):722-743. doi: 10.1111/resp.14549.

Silvestri GA, Gonzalez AV, Jantz MA, Margolis ML, Gould MK,Tanoue LT, et al. Methods for staging non-small cell lung cancer:diagnosis and management of lung cancer, 3rd ed: American Collegeof Chest Physicians evidence-based clinical practice guidelines. Chest. 2013;143(Suppl 5):e211S–e250S.

Lung Cancer Clinical Expert Group. Endobronchial ultrasoundservice specifications.https://www.roycastle.org/app/uploads/2020/12/Appendices-1-4-EBUS-service-specification-final-to-NHSE. pdf 116.

De Leyn P, Dooms C, Kuzdzal J, Lardinois D, Passlick B, Rami-Porta R, et al. Revised ESTS guidelines for preoperative mediastinal lymph node staging for non-small-cell lung cancer. Eur J Cardiothorac Surg. 2014;45(5):787-98. doi: 10.1093/ejcts/ ezu028.

Turna A, Melek H, Kara HV, Kılıç B, Erşen E, Kaynak K. Validity of the updated European Society of Thoracic Surgeons staging guideline in lung cancer patients. J Thorac Cardiovasc Surg. 2018;155(2):789- 795. doi: 10.1016/j.jtcvs.2017.09.090.

Dooms C, Vansteenkiste J. Prognostic value of fluorodeoxyglucose uptake in non-small cell lung cancer: time for standardization and validation. J Thorac Oncol. 2010;5(5):583-4. doi: 10.1097/ JTO.0b013e3181d95cc8.

De Leyn P, Stroobants S, De Wever W, Lerut T, Coosemans W, Decker G, et al. Prospective comparative study of integrated positron emission tomography-computed tomography scan compared with remediastinoscopy in the assessment of residual mediastinal lymph node disease after induction chemotherapy for mediastinoscopy-proven stage IIIA-N2 Non-small-cell lung cancer: a Leuven Lung Cancer Group Study. J Clin Oncol. 2006;24(21):3333-9. doi: 10.1200/JCO.2006.05.6341.

Cerfolio RJ, Bryant AS, Ojha B. Restaging patients with N2 (stage IIIa) non-small cell lung cancer after neoadjuvant chemoradiotherapy: a prospective study. J Thorac Cardiovasc Surg. 2006;131(6):1229- 35. doi: 10.1016/j.jtcvs.2005.08.070.

Jiang L, Huang W, Liu J, Harris K, Yarmus L, Shao W, et al.; AME Lung Cancer Collaborative Group. Endosonography with lymph node sampling for restaging the mediastinum in lung cancer: A systematic review and pooled data analysis. J Thorac Cardiovasc Surg. 2020;159(3):1099-1108.e5. doi: 10.1016/j.jtcvs.2019.07.095.

Chang YL, Wu CT, Lin SC, Hsiao CF, Jou YS, Lee YC. Clonality and prognostic implications of p53 and epidermal growth factor receptor somatic aberrations in multiple primary lung cancers. Clin Cancer Res. 2007;13(1):52-8. doi: 10.1158/1078-0432. CCR-06-1743.

Dijkman BG, Schuurbiers OC, Vriens D, Looijen-Salamon M, Bussink J, Timmer-Bonte JN, et al. The role of (18)F-FDG PET in the differentiation between lung metastases and synchronous second primary lung tumours. Eur J Nucl Med Mol Imaging. 2010;37(11):2037-47. doi: 10.1007/s00259- 010-1505-2.

Arai J, Tsuchiya T, Oikawa M, Mochinaga K, Hayashi T, Yoshiura K, et al. Clinical and molecular analysis of synchronous double lung cancers. Lung Cancer. 2012 Aug;77(2):281-7. doi: 10.1016/j.lungcan.2012.04.003.

Detterbeck FC, Franklin WA, Nicholson AG, Girard N, Arenberg DA, Travis WD, et al.; IASLC Staging and Prognostic Factors Committee; Advisory Boards; Multiple Pulmonary Sites Workgroup. The IASLC Lung Cancer Staging Project: Background Data and Proposed Criteria to Distinguish Separate Primary Lung Cancers from Metastatic Foci in Patients with Two Lung Tumors in the Forthcoming Eighth Edition of the TNM Classification for Lung Cancer. J Thorac Oncol. 2016 ;11(5):651-665. doi: 10.1016/j.jtho.2016.01.025.

Wu C, Zhao C, Yang Y, He Y, Hou L, Li X, et al. High Discrepancy of Driver Mutations in Patients with NSCLC and Synchronous Multiple Lung Ground- Glass Nodules. J Thorac Oncol. 2015 ;10(5):778- 783. doi: 10.1097/JTO.0000000000000487.

Detterbeck FC, Marom EM, Arenberg DA, Franklin WA, Nicholson AG, Travis WD, et al.; IASLC Staging and Prognostic Factors Committee; Advisory Boards; Multiple Pulmonary Sites Workgroup. The IASLC Lung Cancer Staging Project: Background Data and Proposals for the Application of TNM Staging Rules to Lung Cancer Presenting as Multiple Nodules with Ground Glass or Lepidic Features or a Pneumonic Type of Involvement in the Forthcoming Eighth Edition of the TNM Classification. J Thorac Oncol. 2016;11(5):666- 680. doi: 10.1016/j.jtho.2015.12.113.

Marinelli D, Gallina FT, Pannunzio S, Di Civita MA, Torchia A, Giusti R, et al. Surgical and survival outcomes with perioperative or neoadjuvant immune-checkpoint inhibitors combined with platinum-based chemotherapy in resectable NSCLC: A systematic review and meta-analysis of randomised clinical trials. Crit Rev Oncol Hematol. 2023;192:104190. doi: 10.1016/j.critrevonc.2023.104190.

Chen Y, Qin J, Wu Y, Lin Q, Wang J, Zhang W, et al. Does major pathological response after neoadjuvant Immunotherapy in resectable nonsmall-cell lung cancers predict prognosis? A systematic review and meta-analysis. Int J Surg. 2023;109(9):2794- 2807. doi: 10.1097/JS9.0000000000000496.

Wu Y, Verma V, Gay CM, Chen Y, Liang F, et al. Neoadjuvant immunotherapy for advanced, resectable non-small cell lung cancer: A systematic review and meta-analysis. Cancer. 2023;129(13):1969-1985. doi: 10.1002/cncr.34755.

Jiang J, Wang Y, Gao Y, Sugimura H, Minervini F, Uchino J, et al. Neoadjuvant immunotherapy or chemoimmunotherapy in non-small cell lung cancer: a systematic review and meta-analysis. Transl Lung Cancer Res. 2022;11(2):277-294. doi: 10.21037/tlcr-22-75.

Travis WD, Dacic S, Sholl LM, Wistuba II. Pathologic Assessment of Lung Squamous Cell Carcinoma After Neoadjuvant Immunotherapy. J Thorac Oncol. 2021;16(1):e9-e10. doi: 10.1016/j.jtho.2020.11.009.

Weissferdt A, Pataer A, Swisher SG, Heymach JV, Gibbons DL, Cascone T, et al. Controversies and challenges in the pathologic examination of lung resection specimens after neoadjuvant treatment. Lung Cancer. 2021;154:76-83. doi: 10.1016/j.lungcan.2021.02.014.

Pataer A, Weissferdt A, Vaporciyan AA, Correa AM, Sepesi B, Wistuba II, et al. Evaluation of Pathologic Response in Lymph Nodes of Patients With Lung Cancer Receiving Neoadjuvant Chemotherapy. J Thorac Oncol. 2021;16(8):1289-1297. doi: 10.1016/j.jtho.2021.03.029.

Weissferdt A, Pataer A, Vaporciyan AA, Correa AM, Sepesi B, Moran CA, et al. Agreement on Major Pathological Response in NSCLC Patients Receiving Neoadjuvant Chemotherapy. Clin Lung Cancer. 2020;21(4):341-348. doi: 10.1016/j. cllc.2019.11.003.

Predina JD, Keating J, Patel N, Nims S, Singhal S. Clinical implications of positive margins following non-small cell lung cancer surgery. J Surg Oncol. 2016;113(3):264-9. doi: 10.1002/jso.24130.

Owen RM, Force SD, Gal AA, Feingold PL, Pickens A, Miller DL, et al. Routine intraoperative frozen section analysis of bronchial margins is of limited utility in lung cancer resection. Ann Thorac Surg. 2013;95(6):1859-65; discussion 1865-6. doi: 10.1016/j.athoracsur.2012.12.016.

Hancock JG, Rosen JE, Antonicelli A, Moreno A, Kim AW, Detterbeck FC, et al. Impact of adjuvant treatment for microscopic residual disease after non-small cell lung cancer surgery. Ann Thorac Surg. 2015;99(2):406-13. doi: 10.1016/j.athoracsur.2014.09.033.

Feizi I, Sokouti M, Golzari SE, Gojazede M, Farahnak MR, Hashemzadeh S, et al. Determination of safe margin in the surgical pathologic specimens of non-small cell carcinoma of the lung. Pneumologia. 2013;62(1):16-8.

Cavalheri V, Granger C. Preoperative exercise training for patients with non-small cell lung cancer. Cochrane Database Syst Rev. 2017;6(6):CD012020. doi: 10.1002/14651858.CD012020.pub2.

Athanassiadi K, Magouliotis D, Chatzimichali E, Liverakou E, Katsandri A, Kalomenidis I, et al. Prehabilitation in lung cancer surgery: A review and meta-analysis of RCT studies. Eur Resp J. 2023;62: PA3773; DOI: 10.1183/13993003.congress-2023. PA3773

Voorn MJJ, Driessen EJM, Reinders RJEF, van Kampen-van den Boogaart VEM, Bongers BC, Janssen-Heijnen MLG. Effects of exercise prehabilitation and/or rehabilitation on health-related quality of life and fatigue in patients with non-small cell lung cancer undergoing surgery: A systematic review. Eur J Surg Oncol. 2023;49(10):106909. doi: 10.1016/j.ejso.2023.04.008.

Goldsmith I, Chesterfield-Thomas G, Toghill H. Pre-treatment optimization with pulmonary rehabilitation in lung cancer: Making the inoperable patients operable. EClinicalMedicine. 2020;31:100663. doi: 10.1016/j.eclinm.2020.100663.

Burnett C, Bestall JC, Burke S, Morgan E, Murray RL, Greenwood-Wilson S, et al. Prehabilitation and Rehabilitation for Patients with Lung Cancer: A Review of Where we are Today. Clin Oncol (R Coll Radiol). 2022;34(11):724-732. doi: 10.1016/j. clon.2022.08.028.

Stout NL, Santa Mina D, Lyons KD, Robb K, Silver JK. A systematic review of rehabilitation and exercise recommendations in oncology guidelines. CA Cancer J Clin. 2021;71(2):149-175. doi: 10.3322/ caac.21639.

Videtic GMM, Donington J, Giuliani M, Heinzerling J, Karas TZ, Kelsey CR, et al. Stereotactic body radiation therapy for early-stage non-small cell lung cancer: Executive Summary of an ASTRO Evidence-Based Guideline. Pract Radiat Oncol. 2017;7(5):295-301. doi: 10.1016/j. prro.2017.04.014.

Schneider BJ, Daly ME, Kennedy EB, Antonoff MB, Broderick S, Feldman J, et al. Stereotactic Body Radiotherapy for Early-Stage Non-Small- Cell Lung Cancer: American Society of Clinical Oncology Endorsement of the American Society for Radiation Oncology Evidence-Based Guideline. J Clin Oncol. 2018;36(7):710-719. doi: 10.1200/ JCO.2017.74.9671.

Howington JA, Blum MG, Chang AC, Balekian AA, Murthy SC. Treatment of stage I and II non-small cell lung cancer: Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest. 2013;143(5 Suppl):e278S-e313S. doi: 10.1378/chest.12-2359.

Guckenberger M, Andratschke N, Dieckmann K, Hoogeman MS, Hoyer M, Hurkmans C, et al. ESTRO ACROP consensus guideline on implementation and practice of stereotactic body radiotherapy for peripherally located early stage non-small cell lung cancer. Radiother Oncol. 2017;124(1):11-17. doi: 10.1016/j.radonc.2017.05.012.

Tandberg DJ, Tong BC, Ackerson BG, Kelsey CR. Surgery versus stereotactic body radiation therapy for stage I non-small cell lung cancer: A comprehensive review. Cancer. 2018;124(4):667-678. doi: 10.1002/cncr.31196.

Levy A, Mercier O, Le Péchoux C. Indications and Parameters Around Postoperative Radiation Therapy for Lung Cancer. J Clin Oncol. 2022;40(6):556- 566. doi: 10.1200/JCO.21.01774.

NSCLC Meta-analysis Collaborative Group. Preoperative chemotherapy for non-small-cell lung cancer: a systematic review and meta-analysis of individual participant data. Lancet. 2014;383(9928):1561-71. doi: 10.1016/S0140-6736(13)62159-5.

Le Péchoux C, Mercier O, Belemsagha D. Role of adjuvant radiotherapy in completely resected non- small-cell lung cancer. EJC. 2013;Suppl 11:123- 130.

Postoperative radiotherapy in non-small-cell lung cancer: systematic review and meta-analysis of individual patient data from nine randomised controlled trials. PORT Meta-analysis Trialists Group. Lancet. 1998;352(9124):257-63.

Burdett S, Rydzewska L, Tierney J, Fisher D, Parmar MK, Arriagada R, Pignon JP, Le Pechoux C; PORT Meta-analysis Trialists Group. Postoperative radiotherapy for non-small cell lung cancer. Cochrane Database Syst Rev. 2016;10(10):CD002142. doi: 10.1002/14651858.CD002142.pub4.

Chien JC, Hu YC, Tsai YJ, Chien YT, Feng IJ, Shiue YL. Predictive Value of Clinicopathological Factors to Guide Post-Operative Radiotherapy in Completely Resected pN2-Stage III Non-Small Cell Lung Cancer. Diagnostics (Basel). 2023;13(19):3095. doi: 10.3390/diagnostics13193095.

Kim BH, Kim JS, Kim HJ. Exploring the past, present, and future of postoperative radiotherapy for N2 stage non-small cell lung cancer. Radiat Oncol J. 2023;41(3):144-153. doi: 10.3857/roj.2023.00430.

Robinson CG, Patel AP, Bradley JD, DeWees T, Waqar SN, Morgensztern D, et al. Postoperative radiotherapy for pathologic N2 non-small-cell lung cancer treated with adjuvant chemotherapy: a review of the National Cancer Data Base. J Clin Oncol. 2015;33(8):870-6. doi: 10.1200/JCO.2014.58.5380.

Mikell JL, Gillespie TW, Hall WA, Nickleach DC, Liu Y, Lipscomb J, et al. Postoperative radiotherapy is associated with better survival in non-small cell lung cancer with involved N2 lymph nodes: results of an analysis of the National Cancer Data Base. J Thorac Oncol. 2015;10(3):462-71. doi: 10.1097/ JTO.0000000000000411.

Hui Z, Men Y, Hu C, Kang J, Sun X, Bi N, et al. Effect of Postoperative Radiotherapy for Patients With pIIIA-N2 Non-Small Cell Lung Cancer After Complete Resection and Adjuvant Chemotherapy: The Phase 3 PORT-C Randomized Clinical Trial. JAMA Oncol. 2021;7(8):1178-1185. doi: 10.1001/ jamaoncol.2021.

Le Pechoux C, Pourel N, Barlesi F, Lerouge D, Antoni D, Lamezec B, et al. Postoperative radiotherapy versus no postoperative radiotherapy in patients with completely resected non-small-cell lung cancer and proven mediastinal N2 involvement (Lung ART): an open-label, randomised, phase 3 trial. Lancet Oncol. 2022 Jan;23(1):104-114. doi: 10.1016/S1470-2045(21)00606-9. . Erratum in: Lancet Oncol. 2022;23(7):e319.

Pignon JP, Tribodet H, Scagliotti GV, Douillard JY, Shepherd FA, Stephens RJ, et al. Lung adjuvant cisplatin evaluation: a pooled analysis by the LACE Collaborative Group. J Clin Oncol. 2008;26(21):3552. doi: 10.1200/JCO.2007.13.9030.

Kenmotsu H, Yamamoto N, Misumi T, Yoh K, Saito H, Sugawara S, et al. Five-Year Overall Survival Analysis of the JIPANG Study: Pemetrexed or Vinorelbine Plus Cisplatin for Resected Stage II-II- IA Nonsquamous Non-Small-Cell Lung Cancer. J Clin Oncol. 2023;41(34):5242. doi: 10.1200/ JCO.23.00179.

Ohe Y, Ohashi Y, Kubota K, Tamura T, Nakagawa K, Negoro S, et al. Randomized phase III study of cisplatin plus irinotecan versus carboplatin plus paclitaxel, cisplatin plus gemcitabine, and cisplatin plus vinorelbine for advanced non-small-cell lung cancer: Four-Arm Cooperative Study in Japan. Ann Oncol. 2007;18(2):317. doi: 10.1093/annonc/ mdl377.

Belani CP, Ramilingam S, Perry MC, LaRocca RV, Rinaldi D, Gable PS, et al. Randomized, phase III study of weekly paclitaxel in combination with carboplatin versus standard every-3-weeks administration of carboplatin and paclitaxel for patients with previously untreated advanced non-small-cell lung cancer. J Clin Oncol. 2008;26(3):468. doi: 10.1200/ JCO.2007.13.1912.

Wu YL, Tsuboi M, He J, John T, Grohe C, Majem K, et al. Osimertinib in Resected EGFR-Mutated Non-Small-Cell Lung Cancer. N Engl J Med. 2020;383(18):1711. doi: 10.1056/NEJMoa2027071.

Tsuboi M, Herbst RS, John T, Kato T, Majem M, GrohéC, et al. Overall Survival with Osimertinib in Resected EGFR-Mutated NSCLC. N Engl J Med. 2023;389(2):137. doi: 10.1056/NEJMoa2304594.

Solomon B, Ahn JS, Dziadziuszko R, Barlesi F, Nishio M, Lee DH, et al. Alina: efficacy and safety of adjuvant alectinib versus chemotherapy in patients with early-stage ALK+ NSCLC. LBA2. ESMO Congress. 2023.

Felip E, Altorki N, Zhou C, Vallières E, Martínez-MartíA, Rittmeyer A, et al. Overall survival with adjuvant atezolizumab after chemotherapy in resected stage II-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase III trial.. Ann Oncol. 2023;34(10):907. doi: 10.1016/j.annonc.2023.07.001.

O’Brien M, Paz-Ares L, Marreaud S, Dafni U, Oselin K, Havel L, et al. Pembrolizumab versus placebo as adjuvant therapy for completely resected stage IB-IIIA non-small-cell lung cancer (PEARLS/KEYNOTE-091): an interim analysis of a randomised, triple-blind, phase 3 trial. Lancet Oncol. 2022;23(10):1274. doi: 10.1016/S1470- 2045(22)00518-6.

Wakelee H, Liberman M, Kato T, Tsuboi M, Lee SH, Gao S, et al. Perioperative Pembrolizumab for Early-Stage Non-Small-Cell Lung Cancer. N Engl J Med. 2023;389(6):491. doi: 10.1056/NEJ- Moa2302983.

Spicer JD, Gao S, Liberman M, Kato T, Tsuboi M, Lee SH, et al. Overall Survival in the KEYNOTE-671 Study of Perioperative Pembrolizumab for Early-Stage NSCLC. LBA56. ESMO Congress. 2023.

Yasuhiro Tsutani, Kentaro Imai, Hiroyuki Ito, Takahiro Mimae, Yoshihiro Miyata, Norihiko Ikeda, et al. Adjuvant chemotherapy for pathological stage I non-small cell lung cancer with high-risk factors for recurrence: A multicenter study. Abstract 8500. ASCO Annual Meeting. 2019.

Cómo citar

[1]
Pardo, D.H. et al. 2023. Recomendaciones para el diagnóstico, seguimiento y tratamiento cáncer del pulmón de células no pequeñas temprano en Colombia. Medicina. 45, 4 (dic. 2023), 767–804. DOI:https://doi.org/10.56050/01205498.2316.

Descargas

Los datos de descargas todavía no están disponibles.

Descargas

Publicado

2023-12-31

Número

Sección

Artículos Especiales
Crossref Cited-by logo