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Published in: International Journal of Clinical Oncology 1/2019

01-01-2019 | Review Article

Significance of re-biopsy of histological tumor samples in advanced non-small-cell lung cancer in clinical practice

Authors: Katsuyuki Hotta, Kiichiro Ninomiya, Eiki Ichihara, Katsuyuki Kiura

Published in: International Journal of Clinical Oncology | Issue 1/2019

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Abstract

The significance of evaluating oncogenes, including EGFR mutations, ALK abnormalities, and PD-L1 expression has become broadly recognized with recent advances in molecular biology. It is now extremely important to investigate tumor oncogene status in each patient at the initial diagnosis. By contrast, the significance of conducting a re-biopsy in the salvage setting has not been systematically reviewed. This review reports that the significance of a re-biopsy varies depending on the clinical situation.
Literature
1.
go back to reference Hotta K, Matsuo K, Ueoka H et al (2004) Meta-analysis of randomized clinical trials comparing cisplatin to carboplatin in patients with advanced non-small-cell lung cancer. J Clin Oncol 22:3852–3859CrossRefPubMed Hotta K, Matsuo K, Ueoka H et al (2004) Meta-analysis of randomized clinical trials comparing cisplatin to carboplatin in patients with advanced non-small-cell lung cancer. J Clin Oncol 22:3852–3859CrossRefPubMed
2.
go back to reference Hotta K, Matsuo K, Ueoka H et al (2004) Addition of platinum compounds to a new agent in patients with advanced non-small-cell lung cancer: a literature based meta-analysis of randomised trials. Ann Oncol 15:1782–1789CrossRefPubMed Hotta K, Matsuo K, Ueoka H et al (2004) Addition of platinum compounds to a new agent in patients with advanced non-small-cell lung cancer: a literature based meta-analysis of randomised trials. Ann Oncol 15:1782–1789CrossRefPubMed
3.
go back to reference Hotta K, Matsuo K (2007) Long-standing debate on cisplatin- versus carboplatin-based chemotherapy in the treatment of advanced non-small-cell lung cancer. J Thorac Oncol 2:96CrossRefPubMed Hotta K, Matsuo K (2007) Long-standing debate on cisplatin- versus carboplatin-based chemotherapy in the treatment of advanced non-small-cell lung cancer. J Thorac Oncol 2:96CrossRefPubMed
4.
go back to reference Hotta K, Fujiwara Y, Matsuo K et al (2007) Recent improvement in the survival of patients with advanced non small cell lung cancer enrolled in phase III trials of first-line, systemic chemotherapy. Cancer 109:939–948CrossRefPubMed Hotta K, Fujiwara Y, Matsuo K et al (2007) Recent improvement in the survival of patients with advanced non small cell lung cancer enrolled in phase III trials of first-line, systemic chemotherapy. Cancer 109:939–948CrossRefPubMed
5.
go back to reference Hotta K, Takigawa N, Hisamoto-Sato A et al (2013) Reappraisal of short-term low-volume hydration in cisplatin-based chemotherapy: results of a prospective feasibility study in advanced lung cancer in the Okayama Lung Cancer Study Group Trial 1002. Jpn J Clin Oncol 43:1115–1123CrossRefPubMed Hotta K, Takigawa N, Hisamoto-Sato A et al (2013) Reappraisal of short-term low-volume hydration in cisplatin-based chemotherapy: results of a prospective feasibility study in advanced lung cancer in the Okayama Lung Cancer Study Group Trial 1002. Jpn J Clin Oncol 43:1115–1123CrossRefPubMed
6.
go back to reference Ninomiya K, Hotta K, Hisamoto-Sato A et al (2016) Short-term low-volume hydration in cisplatin-based chemotherapy for patients with lung cancer: the second prospective feasibility study in the Okayama Lung Cancer Study Group Trial 1201. Int J Clin Oncol 21:81–87CrossRefPubMed Ninomiya K, Hotta K, Hisamoto-Sato A et al (2016) Short-term low-volume hydration in cisplatin-based chemotherapy for patients with lung cancer: the second prospective feasibility study in the Okayama Lung Cancer Study Group Trial 1201. Int J Clin Oncol 21:81–87CrossRefPubMed
7.
go back to reference Hotta K, Ninomiya K, Takigawa N et al (2015) Reappraisal of short-term low-volume hydration in cisplatin-based chemotherapy; hoping for it as a public domain. Jpn J Clin Oncol 45:603–604PubMed Hotta K, Ninomiya K, Takigawa N et al (2015) Reappraisal of short-term low-volume hydration in cisplatin-based chemotherapy; hoping for it as a public domain. Jpn J Clin Oncol 45:603–604PubMed
8.
go back to reference Lynch TJ, Bell DW, Sordella R et al (2004) Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib. N Engl J Med 350:2129–2139CrossRefPubMed Lynch TJ, Bell DW, Sordella R et al (2004) Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib. N Engl J Med 350:2129–2139CrossRefPubMed
9.
go back to reference Kris MG, Johnson BE, Berry LD et al (2014) Using multiplexed assays of oncogenic drivers in lung cancers to select targeted drugs. JAMA 311:1998–2006CrossRefPubMedPubMedCentral Kris MG, Johnson BE, Berry LD et al (2014) Using multiplexed assays of oncogenic drivers in lung cancers to select targeted drugs. JAMA 311:1998–2006CrossRefPubMedPubMedCentral
10.
go back to reference Hotta K, Kiura K, Toyooka S et al (2007) Clinical significance of epidermal growth factor receptor gene mutations on treatment outcome after first-line cytotoxic chemotherapy in Japanese patients with non-small-cell lung cancer. J Thorac Oncol 2:632–637CrossRefPubMed Hotta K, Kiura K, Toyooka S et al (2007) Clinical significance of epidermal growth factor receptor gene mutations on treatment outcome after first-line cytotoxic chemotherapy in Japanese patients with non-small-cell lung cancer. J Thorac Oncol 2:632–637CrossRefPubMed
11.
go back to reference Mok TS, Wu Y-L, Ahn M-J et al (2017) AURA3 Investigators. Osimertinib or platinum-pemetrexed in EGFR T790M-positive lung cancer. N Engl J Med 376:629–640CrossRefPubMed Mok TS, Wu Y-L, Ahn M-J et al (2017) AURA3 Investigators. Osimertinib or platinum-pemetrexed in EGFR T790M-positive lung cancer. N Engl J Med 376:629–640CrossRefPubMed
12.
go back to reference Jänne PA, Yang JC, Kim DW et al (2015) AZD9291 in EGFR inhibitor-resistant non-small-cell lung cancer. N Engl J Med 372:1689–1699CrossRefPubMed Jänne PA, Yang JC, Kim DW et al (2015) AZD9291 in EGFR inhibitor-resistant non-small-cell lung cancer. N Engl J Med 372:1689–1699CrossRefPubMed
13.
go back to reference Hata A, Katakami N, Yoshioka H et al (2015) Spatiotemporal T790M Heterogeneity in individual patients with EGFR-mutant non-small-cell lung cancer after acquired resistance to EGFR-TKI. J Thorac Oncol 10:1553–1559CrossRefPubMed Hata A, Katakami N, Yoshioka H et al (2015) Spatiotemporal T790M Heterogeneity in individual patients with EGFR-mutant non-small-cell lung cancer after acquired resistance to EGFR-TKI. J Thorac Oncol 10:1553–1559CrossRefPubMed
14.
go back to reference Ichihara E, Hotta K, Kubo T et al (2018) Clinical significance of repeat rebiopsy in detecting the EGFR T790M secondary mutation in patients with non-small cell lung cancer. Oncotarget 9(50):29525–29531CrossRefPubMedPubMedCentral Ichihara E, Hotta K, Kubo T et al (2018) Clinical significance of repeat rebiopsy in detecting the EGFR T790M secondary mutation in patients with non-small cell lung cancer. Oncotarget 9(50):29525–29531CrossRefPubMedPubMedCentral
15.
go back to reference Hata A, Masago K, Katakami N et al (2014) Spatiotemporal T790M heterogeneity in a patient with EGFR-mutant non-small-cell lung cancer. J Thorac Oncol 9:e64–e65CrossRefPubMed Hata A, Masago K, Katakami N et al (2014) Spatiotemporal T790M heterogeneity in a patient with EGFR-mutant non-small-cell lung cancer. J Thorac Oncol 9:e64–e65CrossRefPubMed
16.
go back to reference Soria JC, Ohe Y, Vansteenkiste J, Reungwetwattana T et al (2018) FLAURA Investigators. Osimertinib in untreated EGFR-mutated advanced non-small-cell lung cancer. N Engl J Med 378:113–125CrossRefPubMed Soria JC, Ohe Y, Vansteenkiste J, Reungwetwattana T et al (2018) FLAURA Investigators. Osimertinib in untreated EGFR-mutated advanced non-small-cell lung cancer. N Engl J Med 378:113–125CrossRefPubMed
18.
19.
go back to reference Tokaca N, Wotherspoon A, Nicholson AG et al (2017) Lack of response to nivolumab in a patient with EGFR-mutant non-small cell lung cancer adenocarcinoma sub-type transformed to small cell lung cancer. Lung Cancer 111:65–68CrossRefPubMed Tokaca N, Wotherspoon A, Nicholson AG et al (2017) Lack of response to nivolumab in a patient with EGFR-mutant non-small cell lung cancer adenocarcinoma sub-type transformed to small cell lung cancer. Lung Cancer 111:65–68CrossRefPubMed
20.
go back to reference Peters S, Camidge DR, Shaw AT et al (2017) ALEX Trial Investigators. Alectinib versus crizotinib in untreated ALK-positive non-small-cell lung cancer. N Engl J Med 377:829–838CrossRefPubMed Peters S, Camidge DR, Shaw AT et al (2017) ALEX Trial Investigators. Alectinib versus crizotinib in untreated ALK-positive non-small-cell lung cancer. N Engl J Med 377:829–838CrossRefPubMed
21.
go back to reference Hida T, Nokihara H, Kondo M et al (2017) Alectinib versus crizotinib in patients with ALK-positive non-small-cell lung cancer (J-ALEX): an open-label, randomised phase 3 trial. Lancet 390:29–39CrossRefPubMed Hida T, Nokihara H, Kondo M et al (2017) Alectinib versus crizotinib in patients with ALK-positive non-small-cell lung cancer (J-ALEX): an open-label, randomised phase 3 trial. Lancet 390:29–39CrossRefPubMed
22.
go back to reference Horinouchi H, Maemondo M, Hida T et al (2017) Phase 2 study of ceritinib in patients with ALK + NSCLC with prior alectinib treatment in Japan: ASCEND-9. J Thorac Oncol 12(Supple 2):S1952–S1953CrossRef Horinouchi H, Maemondo M, Hida T et al (2017) Phase 2 study of ceritinib in patients with ALK + NSCLC with prior alectinib treatment in Japan: ASCEND-9. J Thorac Oncol 12(Supple 2):S1952–S1953CrossRef
23.
go back to reference Isozaki H, Hotta K, Ichihara E et al (2016) Protocol design for the bench to bed trial in alectinib-refractory non-small-cell lung cancer patients harboring the EML4-ALK fusion gene (ALRIGHT/OLCSG1405). Clin Lung Cancer 17:602–605CrossRefPubMed Isozaki H, Hotta K, Ichihara E et al (2016) Protocol design for the bench to bed trial in alectinib-refractory non-small-cell lung cancer patients harboring the EML4-ALK fusion gene (ALRIGHT/OLCSG1405). Clin Lung Cancer 17:602–605CrossRefPubMed
24.
go back to reference Gainor JF, Dardaei L, Yoda S et al (2016) Molecular mechanisms of resistance to first- and second-Generation ALK inhibitors in ALK-rearranged lung cancer. Cancer Discov 6:1118–1133CrossRefPubMedPubMedCentral Gainor JF, Dardaei L, Yoda S et al (2016) Molecular mechanisms of resistance to first- and second-Generation ALK inhibitors in ALK-rearranged lung cancer. Cancer Discov 6:1118–1133CrossRefPubMedPubMedCentral
25.
go back to reference Reck M, Rodríguez-Abreu D, Robinson AG et al (2016) KEYNOTE-024 Investigators. Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer. N Engl J Med 375:1823–1833CrossRefPubMed Reck M, Rodríguez-Abreu D, Robinson AG et al (2016) KEYNOTE-024 Investigators. Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer. N Engl J Med 375:1823–1833CrossRefPubMed
26.
go back to reference Sheng J, Fang W, Yu J et al (2016) Expression of programmed death ligand-1 on tumor cells varies pre and post chemotherapy in non-small cell lung cancer. Sci Rep 6:20090CrossRefPubMedPubMedCentral Sheng J, Fang W, Yu J et al (2016) Expression of programmed death ligand-1 on tumor cells varies pre and post chemotherapy in non-small cell lung cancer. Sci Rep 6:20090CrossRefPubMedPubMedCentral
27.
go back to reference Song Z, Yu X, Zhang Y (2016) Altered expression of programmed death-ligand 1 after neo-adjuvant chemotherapy in patients with lung squamous cell carcinoma. Lung Cancer 99:166–171CrossRefPubMed Song Z, Yu X, Zhang Y (2016) Altered expression of programmed death-ligand 1 after neo-adjuvant chemotherapy in patients with lung squamous cell carcinoma. Lung Cancer 99:166–171CrossRefPubMed
28.
go back to reference Rittmeyer A, Barlesi F, Waterkamp D et al (2017) Atezolizumab versus docetaxel in patients with previously treated non-small-cell lung cancer (OAK): a phase 3, open-label, multicentre randomised controlled trial. Lancet 389:255–265CrossRefPubMed Rittmeyer A, Barlesi F, Waterkamp D et al (2017) Atezolizumab versus docetaxel in patients with previously treated non-small-cell lung cancer (OAK): a phase 3, open-label, multicentre randomised controlled trial. Lancet 389:255–265CrossRefPubMed
29.
go back to reference Gadgeel S, Kowanetz F, Zou W et al Clinical efficacy of atezolizumab (Atezo) in PD-L1 subgroups defined by SP142 and 22C3 IHC assays in 2L + NSCLC: Results from the randomized OAK study. ESMO 2017 (Abs 1296O) Gadgeel S, Kowanetz F, Zou W et al Clinical efficacy of atezolizumab (Atezo) in PD-L1 subgroups defined by SP142 and 22C3 IHC assays in 2L + NSCLC: Results from the randomized OAK study. ESMO 2017 (Abs 1296O)
30.
go back to reference Herbst RS, Baas P, Kim DW et al (2016) Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial. Lancet 387:1540–1550CrossRefPubMed Herbst RS, Baas P, Kim DW et al (2016) Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial. Lancet 387:1540–1550CrossRefPubMed
31.
go back to reference Gandhi L, Rodriguez-Abreu D, Gadgeel S et al (2018) Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer. N Engl J Med 378(22):2078–2092CrossRefPubMed Gandhi L, Rodriguez-Abreu D, Gadgeel S et al (2018) Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer. N Engl J Med 378(22):2078–2092CrossRefPubMed
32.
go back to reference Kato Y, Hotta K, Takigawa N et al (2014) Factor associated with failure to administer subsequent treatment after progression in the first-line chemotherapy in EGFR-mutant non-small cell lung cancer: Okayama Lung Cancer Study Group experience. Cancer Chemother Pharmacol 73:943–950CrossRefPubMed Kato Y, Hotta K, Takigawa N et al (2014) Factor associated with failure to administer subsequent treatment after progression in the first-line chemotherapy in EGFR-mutant non-small cell lung cancer: Okayama Lung Cancer Study Group experience. Cancer Chemother Pharmacol 73:943–950CrossRefPubMed
33.
go back to reference Hotta K, Kiura K, Tabata M et al (2014) A Survey of Japanese thoracic oncologists’perception of diagnostic and treatment strategies for EGFR-mutant or EML4-ALK-fusion non-small cell lung cancer. Chest 146:e222–e225CrossRefPubMed Hotta K, Kiura K, Tabata M et al (2014) A Survey of Japanese thoracic oncologists’perception of diagnostic and treatment strategies for EGFR-mutant or EML4-ALK-fusion non-small cell lung cancer. Chest 146:e222–e225CrossRefPubMed
34.
go back to reference Hotta K, Tabata M, Kiura K et al (2007) Gefitinib induces premature senescence in non-small-cell lung cancer cells with or without EGFR gene mutation. Oncol Rep 17:313–317PubMed Hotta K, Tabata M, Kiura K et al (2007) Gefitinib induces premature senescence in non-small-cell lung cancer cells with or without EGFR gene mutation. Oncol Rep 17:313–317PubMed
35.
go back to reference Gainor JF, Shaw AT, Sequist LV et al (2016) EGFR Mutations and ALK rearrangements are associated with low response rates to PD-1 pathway blockade in non-small cell lung cancer: a retrospective analysis. Clin Cancer Res 22:4585–4593CrossRefPubMedPubMedCentral Gainor JF, Shaw AT, Sequist LV et al (2016) EGFR Mutations and ALK rearrangements are associated with low response rates to PD-1 pathway blockade in non-small cell lung cancer: a retrospective analysis. Clin Cancer Res 22:4585–4593CrossRefPubMedPubMedCentral
36.
go back to reference Kim TJ, Hong SA, Kim O et al (2017) Changes in PD-L1 expression according to tumor infiltrating lymphocytes of acquired EGFR-TKI resistant EGFR-mutant non-small-cell lung cancer. Oncotarget 8:107630–107639PubMedPubMedCentral Kim TJ, Hong SA, Kim O et al (2017) Changes in PD-L1 expression according to tumor infiltrating lymphocytes of acquired EGFR-TKI resistant EGFR-mutant non-small-cell lung cancer. Oncotarget 8:107630–107639PubMedPubMedCentral
37.
go back to reference Kowanetz M, Socinski MA, Zou W et al (2018) IMpower150: Efficacy of atezolizumab plus bevacizumab and chemotherapy in 1L metastatic nonsquamous NSCLC across key subgroups. Presented at: 2018 AACR Annual Meeting, 2018; Chicago, Illinois. Abstract CT076 Kowanetz M, Socinski MA, Zou W et al (2018) IMpower150: Efficacy of atezolizumab plus bevacizumab and chemotherapy in 1L metastatic nonsquamous NSCLC across key subgroups. Presented at: 2018 AACR Annual Meeting, 2018; Chicago, Illinois. Abstract CT076
38.
go back to reference Haratani K, Hayashi H, Tanaka T et al (2017) Tumor immune microenvironment and nivolumab efficacy in EGFR mutation-positive non-small-cell lung cancer based on T790M status after disease progression during EGFR-TKI treatment. Ann Oncol 28:1532–1539CrossRefPubMed Haratani K, Hayashi H, Tanaka T et al (2017) Tumor immune microenvironment and nivolumab efficacy in EGFR mutation-positive non-small-cell lung cancer based on T790M status after disease progression during EGFR-TKI treatment. Ann Oncol 28:1532–1539CrossRefPubMed
Metadata
Title
Significance of re-biopsy of histological tumor samples in advanced non-small-cell lung cancer in clinical practice
Authors
Katsuyuki Hotta
Kiichiro Ninomiya
Eiki Ichihara
Katsuyuki Kiura
Publication date
01-01-2019
Publisher
Springer Japan
Published in
International Journal of Clinical Oncology / Issue 1/2019
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-018-1344-x

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