ATTLAS, IMpower151 and ORIENT-31: Dusting off IMpower150 for Post-Osimertinib in EGFR-Mutated NSCLC?

被引:4
作者
Lee, Jii Bum
Ou, Sai-Hong Ignatius [1 ,2 ,3 ,4 ]
机构
[1] Yonsei Univ, Yonsei Canc Ctr, Dept Internal Med, Div Med Oncol,Coll Med, Seoul, South Korea
[2] Univ Calif Orange, Chao Family Comprehens Canc Ctr, Dept Med, Div Hematol Oncol,Irvine Sch Med, Orange, CA USA
[3] Chao Family Comprehens Canc Ctr, Orange, CA USA
[4] Univ Calif Orange, Chao Family Comprehens Canc Ctr, Dept Med, Div Hematol Oncol,Irvine Sch Med, 200 South Manchester Ave,Suite 400, Orange, CA 92868 USA
关键词
atezolizumab; bevacizumab; chemotherapy; EGFR-mutant; NSCLC; FLAURA-2;
D O I
10.2147/LCTT.S460870
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Treatment strategies for post-epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) therapy in EGFRmutant non-small cell lung cancer (NSCLC) is an ongoing challenge. Previously, the IMPRESS trial comparing platinum doublet chemotherapy with or without EGFR-TKI did not demonstrate any progression-free survival (PFS) benefit. The retrospective subgroup analysis of IMpower150 indicated that the quad regimen (carboplatin, paclitaxel, bevacizumab, atezolizumab) improved PFS and overall survival (OS) in patients with EGFR-mutant NSCLC who progressed on first-generation EGFR-TKIs. Given the retrospective nature of the analysis, the IMpower150 regimen is not approved in the US for post-EGFR-TKI treatment. Currently, osimertinib or other third-generation (3G) EGFR-TKIs is the first-line standard of care for advanced EGFR-mutant NSCLC. MARIPOSA-2 provided the first randomized trial post-osimertinib in EGFR-mutant NSCLC patients with another quad regimen (platinum, pemetrexed, lazertinib, amivantamab). The IMpower150 and MARIPOSA-2 quad regimens differ in the principle of whether to continue or even "double-down" on EGFR inhibition. Recently, three prospective randomized trials conducted in Asia offered promising results, showing that a quad regimen of doublet platinum chemotherapy plus anti-angiogenesis agent and ICI may be as efficacious as MARIPOSA-2 with a lower rate of toxicities and accounting for the PFS difference if 1L chemotherapy plus osimertinib instead of osimertinib monotherapy. In particular, the median PFS achieved by the quad regimens of ATTLAS and IMpower151 is 8.5 months. However, only 8.2% and 17.9% of the EGFR-mutant NSCLC patients who received the quad regimens progressed on 3G EGFR-TKI, respectively. Here, we discuss how the results of IMpower151 and ATTLAS may rejuvenate interest in a non-EGFR containing quad regimen as a potential post-osimertinib monotherapy treatment. Randomized trials comparing the results of these studies, including the quad regimen of MARIPOSA-2 versus the quad regimen of IMpower151/Impower150/ATTLAS in post-osimertinib (or other 3G EGFR-TKI) progression, are urgently needed.
引用
收藏
页码:81 / 85
页数:5
相关论文
共 18 条
[1]   The Additional Exclusions of ROS1 Fusions (In Addition to EGFR Mutation and ALK Fusions) in the Cemiplimab NSCLC FDA Indication (EMPOWER-Lung 1and-Lung 3) . Catching Up with Current Scientific View of Immunotherapy in Never-Smoker Predominant Actionable Driver Mutation Positive NSCLC? [J].
Brazel, Danielle ;
Ou, Saihong Ignatius .
LUNG CANCER-TARGETS AND THERAPY, 2023, 14 :63-69
[2]   POSing the question: MARIPOSA-2, do the ends justify the means? [J].
Chen, M. F. ;
Piotrowska, Z. ;
Yu, H. A. .
ANNALS OF ONCOLOGY, 2024, 35 (01) :4-6
[3]  
Cho BC, 2023, ESMO C, V1, pLBA14
[4]   Impact of EGFR-TKI Treatment on the Tumor Immune Microenvironment in EGFR Mutation-Positive Non-Small Cell Lung Cancer [J].
Isomoto, Kohsuke ;
Haratani, Koji ;
Hayashi, Hidetoshi ;
Shimizu, Shigeki ;
Tomida, Shuta ;
Niwa, Takashi ;
Yokoyama, Toshihide ;
Fukuda, Yasushi ;
Chiba, Yasutaka ;
Kato, Ryoji ;
Tanizaki, Junko ;
Tanaka, Kaoru ;
Takeda, Masayuki ;
Ogura, Takashi ;
Ishida, Tadashi ;
Ito, Akihiko ;
Nakagawa, Kazuhiko .
CLINICAL CANCER RESEARCH, 2020, 26 (08) :2037-2046
[5]  
Kim TM, 2023, J Clin Oncol, V1
[6]   And Still They Come Over Troubled Waters: Can Asia's Third-Generation EGFR Tyrosine Kinase Inhibitors (Furmonertinib, Aumolertinib, Rezivertinib, Limertinib, Befotertinib, SH-1028, and Lazertinib) Affect Global Treatment of EGFR plus NSCLC [J].
Lau, Sally C. M. ;
Ou, Sai-Hong Ignatius .
JOURNAL OF THORACIC ONCOLOGY, 2022, 17 (10) :1144-1154
[7]   A Phase II Study of Pembrolizumab in EGFR-Mutant, PD-L1+, Tyrosine Kinase Inhibitor Naive Patients With Advanced NSCLC [J].
Lisberg, A. ;
Cummings, A. ;
Goldman, J. W. ;
Bornazyan, K. ;
Reese, N. ;
Wang, T. ;
Coluzzi, P. ;
Ledezma, B. ;
Mendenhall, M. ;
Hunt, J. ;
Wolf, B. ;
Jones, B. ;
Madrigal, J. ;
Horton, J. ;
Spiegel, M. ;
Carroll, J. ;
Gukasyan, J. ;
Williams, T. ;
Sauer, L. ;
Wells, C. ;
Hardy, A. ;
Linares, P. ;
Lim, C. ;
Ma, L. ;
Adame, C. ;
Garon, Edward B. .
JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (08) :1138-1145
[8]   Amivantamab plus lazertinib vs osimertinib as first-line treatment among Asian patients with EGFR-mutated, advanced non-small cell lung cancer (NSCLC): MARIPOSA subgroup analysis [J].
Lu, S. ;
Cho, B. C. ;
Lee, J-S. ;
Lee, S-H. ;
Danchaivijitr, P. ;
Liu, B. ;
Alip, A. ;
Xiong, H. ;
How, S. H. ;
Chang, G-C. ;
Yang, J. C-H. ;
Yoshioka, H. ;
Xia, K. ;
Martinez, M. ;
Bauml, J. M. ;
Sethi, S. ;
Hayashi, H. .
ANNALS OF ONCOLOGY, 2023, 34 :S1661-S1661
[9]   Sintilimab plus bevacizumab biosimilar IBI305 and chemotherapy for patients with EGFR-mutated non-squamous non-small-cell lung cancer who progressed on EGFR tyrosine-kinase inhibitor therapy (ORIENT-31): first interim results from a randomised, double-blind, multicentre, phase 3trial [J].
Lu, Shun ;
Wu, Lin ;
Jian, Hong ;
Chen, Ying ;
Wang, Qiming ;
Fang, Jian ;
Wang, Ziping ;
Hu, Yanping ;
Sun, Meili ;
Han, Liang ;
Miao, Liyun ;
Ding, Cuimin ;
Cui, Jiuwei ;
Li, Baolan ;
Pan, Yueyin ;
Li, Xingya ;
Ye, Feng ;
Liu, Anwen ;
Wang, Ke ;
Cang, Shundong ;
Zhou, Hui ;
Sun, Xing ;
Ferry, David ;
Lin, Yong ;
Wang, Shuyan ;
Zhang, Wen ;
Zhang, Chengli .
LANCET ONCOLOGY, 2022, 23 (09) :1167-1179
[10]   Nivolumab (NIVO) plus chemotherapy (chemo) vs chemo in patients (pts) with EGFR-mutated metastatic non-small cell lung cancer (mNSCLC) with disease progression after EGFR tyrosine kinase inhibitors (TKIs) in CheckMate 722 [J].
Mok, T. S. K. ;
Nakagawa, K. ;
Park, K. ;
Ohe, Y. ;
Girard, N. ;
Kim, H. R. ;
Wu, Y-L. ;
Gainor, J. ;
Lee, S-H. ;
Chiu, C-H. ;
Sang-We, K. ;
Cheng-Ta, Y. ;
Liang, W. ;
Wu, L. ;
Lin, M-C. ;
Samol, J. ;
Zhang, X. ;
Sylvester, J. ;
Li, S. ;
Yang, J. C-H. .
ANNALS OF ONCOLOGY, 2022, 33 :S1561-S1562