Limited role of KRAS mutation in guiding immunotherapy in advanced non-small-cell lung cancer

被引:2
作者
Li, Hong-Shuai [1 ]
Liu, Cheng-Ming [2 ]
Wang, Yan [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Canc, Canc Hosp, Natl Canc Ctr,Dept Med Oncol, Beijing 100021, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Canc, Natl Canc Ctr, Dept Thorac Surg,Canc Hosp, Beijing 100021, Peoples R China
基金
中国国家自然科学基金;
关键词
co-mutation status; immunotherapy; KRAS; mutation subtypes; non-small-cell lung cancer; COOCCURRING GENOMIC ALTERATIONS; CLINICOPATHOLOGICAL CHARACTERISTICS; PD-L1; EXPRESSION; OPEN-LABEL; OUTCOMES; IMMUNE; NSCLC; ADENOCARCINOMA; DOCETAXEL; ATEZOLIZUMAB;
D O I
10.2217/fon-2021-1488
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The success of sotorasib (AMG-510) and adagrasib (MRTX-849) has resolved the problem of non-availability of drugs for patients with KRAS(G12C)-mutated non-small-cell lung cancer. However, more research is required before these drugs can be introduced as a first-line treatment for those patients, and there are no available drugs for other non-G12C-mutated patients so far; therefore, immunotherapy remains the optimal first-line treatment in this situation. The role of KRAS in affecting the response to immunotherapy in non-small-cell lung cancer has not been fully elucidated. The purpose of this review was to summarize the impact of KRAS mutations, a highly heterogeneous group, on immunotherapy to provide clinicians and researchers with relevant information that can help guide decision-making. Plain language summary Sotorasib (AMG-510) and adagrasib (MRTX-849) have changed the problem of non-availability of targeted drugs for patients with KRAS-mutated lung cancer. However, thus far, immunotherapy remains the optimal treatment for lung cancer patients with KRAS mutations who have not received previous treatment. The role of KRAS in affecting the response to immunotherapy in non-small-cell lung cancer has not been fully elucidated. The purpose of this review was to summarize the impact of KRAS mutations, a highly heterogeneous group, on immunotherapy to provide clinicians and researchers with relevant information that can help guide decision-making.
引用
收藏
页码:2433 / 2443
页数:11
相关论文
共 55 条
[1]   SMARCA4 and Other SWItch/Sucrose NonFermentable Family Genomic Alterations in NSCLC: Clinicopathologic Characteristics and Outcomes to Immune Checkpoint Inhibition [J].
Alessi, Joao V. ;
Ricciuti, Biagio ;
Spurr, Liam F. ;
Gupta, Hersh ;
Li, Yvonne Y. ;
Glass, Carolyn ;
Nishino, Mizuki ;
Cherniack, Andrew D. ;
Lindsay, James ;
Sharma, Bijaya ;
Felt, Kristen D. ;
Rodig, Scott J. ;
Cheng, Michael L. ;
Sholl, Lynette M. ;
Awad, Mark M. .
JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (07) :1176-1187
[2]  
Alessi JVM, 2020, J CLIN ONCOL, V38
[3]  
[Anonymous], 2022, NCCN Guidelines Version 1.2022 Breast Cancer Risk Reduction
[4]   Treatment Outcomes and Clinical Characteristics of Patients with KRAS-G12C-Mutant Non-Small Cell Lung Cancer [J].
Arbour, Kathryn C. ;
Rizvi, Hira ;
Plodkowski, Andrew J. ;
Hellmann, Matthew D. ;
Knezevic, Andrea ;
Heller, Glenn ;
Yu, Helena A. ;
Ladanyi, Marc ;
Kris, Mark G. ;
Arcila, Maria E. ;
Rudin, Charles M. ;
Lito, Piro ;
Riely, Gregory J. .
CLINICAL CANCER RESEARCH, 2021, 27 (08) :2209-2215
[5]   Effects of Co-occurring Genomic Alterations on Outcomes in Patients with KRAS-Mutant Non-Small Cell Lung Cancer [J].
Arbour, Kathryn C. ;
Jordan, Emmett ;
Kim, Hyunjae Ryan ;
Dienstag, Jordan ;
Yu, Helena A. ;
Sanchez-Vega, Francisco ;
Lito, Piro ;
Berger, Michael ;
Solit, David B. ;
Hellmann, Matthew ;
Kris, Mark G. ;
Rudin, Charles M. ;
Ni, Ai ;
Arcila, Maria ;
Ladanyi, Marc ;
Riely, Gregory J. .
CLINICAL CANCER RESEARCH, 2018, 24 (02) :334-340
[6]   Distinct initiating events underpin the immune and metabolic heterogeneity of KRAS-mutant lung adenocarcinoma [J].
Best, Sarah A. ;
Ding, Sheryl ;
Kersbergen, Ariena ;
Dong, Xueyi ;
Song, Ji-Ying ;
Xie, Yi ;
Reljic, Boris ;
Li, Kaiming ;
Vince, James E. ;
Rathi, Vivek ;
Wright, Gavin M. ;
Ritchie, Matthew E. ;
Sutherland, Kate D. .
NATURE COMMUNICATIONS, 2019, 10 (1)
[7]   Synergy between the KEAP1/NRF2 and PI3K Pathways Drives Non-Small-Cell Lung Cancer with an Altered Immune Microenvironment [J].
Best, Sarah A. ;
De Souza, David P. ;
Kersbergen, Ariena ;
Policheni, Antonia N. ;
Dayalan, Saravanan ;
Tull, Dedreia ;
Rathi, Vivek ;
Gray, Daniel H. ;
Ritchie, Matthew E. ;
McConville, Malcolm J. ;
Sutherland, Kate D. .
CELL METABOLISM, 2018, 27 (04) :935-+
[8]   Sotorasib: First Approval [J].
Blair, Hannah A. .
DRUGS, 2021, 81 (13) :1573-1579
[9]   Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer [J].
Borghaei, H. ;
Paz-Ares, L. ;
Horn, L. ;
Spigel, D. R. ;
Steins, M. ;
Ready, N. E. ;
Chow, L. Q. ;
Vokes, E. E. ;
Felip, E. ;
Holgado, E. ;
Barlesi, F. ;
Kohlhaeufl, M. ;
Arrieta, O. ;
Burgio, M. A. ;
Fayette, J. ;
Lena, H. ;
Poddubskaya, E. ;
Gerber, D. E. ;
Gettinger, S. N. ;
Rudin, C. M. ;
Rizvi, N. ;
Crino, L. ;
Blumenschein, G. R. ;
Antonia, S. J. ;
Dorange, C. ;
Harbison, C. T. ;
Finckenstein, F. Graf ;
Brahmer, J. R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (17) :1627-1639
[10]  
Cancer Genome Atlas Research Network, 2018, Nature, V559, pE12, DOI [10.1038/nature13385, 10.1038/s41586-018-0228-6]