Immunotherapy Following Anaplastic Lymphoma Kinase Inhibitor Therapy for Patients with Anaplastic Lymphoma Kinase-Positive Non-small Cell Lung Cancer in Japan

被引:0
作者
Shimomura, Yuki [1 ]
Mizutani, Megumi [2 ]
Yoshida, Hisako [1 ]
Ihara, Yasutaka [1 ,3 ]
Shintani, Ayumi [1 ]
机构
[1] Osaka Metropolitan Univ, Grad Sch Med, Dept Med Stat, 1-4-3 Asahi Machi,Abeno Ku, Osaka 5458585, Japan
[2] Osaka Metropolitan Univ, Grad Sch Med, Dept Resp Med, Osaka, Japan
[3] Daiichi Sankyo Co Ltd, Global DX, Digital Transformat Management Div, Data Intelligence Dept, Tokyo, Japan
关键词
CHEMOTHERAPY; CRIZOTINIB; GENE;
D O I
10.1007/s11523-024-01116-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAlthough anaplastic lymphoma kinase inhibitors (ALKis) are the effective initial treatment for patients with anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC), most patients experience resistance to ALKis, leading to the need for alternative therapies. Immune checkpoint inhibitors (ICIs) are a standard NSCLC treatment. On the other hand, their efficacy remains unclear for ALK-positive NSCLC.ObjectiveWe aim to describe the treatment patterns and treatment outcomes for patients with ALK-positive NSCLC receiving later-line ICI treatment.MethodsThis retrospective cohort study used claims data from Japanese acute care hospitals and included patients with lung cancer (International Classification of Diseases, 10th version (ICD-10), code: C34) diagnosed between 1 December 2015 and 31 January 2023. We extracted patients who received ALKis as first-line therapy and subsequent lines of treatment. Patient characteristics and treatment patterns and durations were descriptively summarized. Time to treatment discontinuation (TTD) for ICIs was examined using Kaplan-Meier estimates.ResultsOf 478 patients who received ALKi as first-line treatment, 30 received ICIs, 249 ALKis, and 154 non-ICI/ALKi therapy as second-line treatment. Most patient characteristics showed no differences among the groups. ICIs were more likely to be administered to patients who underwent shorter durations of ALKi treatment. The median TTD for ICIs was 66 days, with a 1 year TTD rate of 13%.ConclusionsGiven the rarity of ALK-positive NSCLC, this study contributes to add evidence through an expanded database and increased sample size, supporting previous suggestions that ICIs have limited effectiveness in patients positive for ALK.
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收藏
页码:171 / 180
页数:10
相关论文
共 41 条
[1]  
[Anonymous], 2016, Cancer Discov, V6, pOF7, DOI [10.1158/2159-8290.CD-NB2016-076, 10.1158/2159-8290.CD-NB2016-044]
[3]   Complete and prolonged response to anti-PD1 therapy in an ALK rearranged lung adenocarcinoma [J].
Baldacci, Simon ;
Gregoire, Valerie ;
Patrucco, Enrico ;
Chiarle, Roberto ;
Jamme, Philippe ;
Wasielewski, Eric ;
Descarpentries, Clotilde ;
Copin, Marie-Christine ;
Awad, Mark M. ;
Cortot, Alexis B. .
LUNG CANCER, 2020, 146 :366-369
[4]   Analysis of time-to-treatment discontinuation of targeted therapy, immunotherapy, and chemotherapy in clinical trials of patients with non-small-cell lung cancer [J].
Blumenthal, G. M. ;
Gong, Y. ;
Kehl, K. ;
Mishra-Kalyani, P. ;
Goldberg, K. B. ;
Khozin, S. ;
Kluetz, P. G. ;
Oxnard, G. R. ;
Pazdur, R. .
ANNALS OF ONCOLOGY, 2019, 30 (05) :830-838
[5]   Real-world progression-free survival (rwPFS) and the impact of PD-L1 and smoking in driver-mutated non-small cell lung cancer (NSCLC) treated with immunotherapy [J].
Bodor, J. Nicholas ;
Bauman, Jessica R. ;
Handorf, Elizabeth A. ;
Ross, Eric A. ;
Clapper, Margie L. ;
Treat, Joseph .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2023, 149 (05) :1755-1763
[6]  
Cancer Statistics in Japan, 2023, FDN PROMOTION CANC R
[7]   Association of Tumor Mutational Burden With DNA Repair Mutations and Response to Anti-PD-1/PD-L1 Therapy in Non-Small-Cell Lung Cancer [J].
Chae, Young Kwang ;
Davis, Andrew A. ;
Raparia, Kirtee ;
Agte, Sarita ;
Pan, Alan ;
Mohindra, Nisha ;
Villaflor, Victoria ;
Giles, Francis .
CLINICAL LUNG CANCER, 2019, 20 (02) :88-+
[8]   Current and Evolving Methods to Visualize Biological Data in Cancer Research [J].
Chia, Puey Ling ;
Gedye, Craig ;
Boutros, Paul C. ;
Wheatley-Price, Paul ;
John, Thomas .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2016, 108 (08)
[9]   Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer [J].
Gandhi, L. ;
Rodriguez-Abreu, D. ;
Gadgeel, S. ;
Esteban, E. ;
Felip, E. ;
De Angelis, F. ;
Domine, M. ;
Clingan, P. ;
Hochmair, M. J. ;
Powell, S. F. ;
Cheng, S. Y. -S. ;
Bischoff, H. G. ;
Peled, N. ;
Grossi, F. ;
Jennens, R. R. ;
Reck, M. ;
Hui, R. ;
Garon, E. B. ;
Boyer, M. ;
Rubio-Viqueira, B. ;
Novello, S. ;
Kurata, T. ;
Gray, J. E. ;
Vida, J. ;
Wei, Z. ;
Yang, J. ;
Raftopoulos, H. ;
Pietanza, M. C. ;
Garassino, M. C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (22) :2078-2092
[10]   Nivolumab plus Ipilimumab in Advanced Non-Small-Cell Lung Cancer [J].
Hellmann, M. D. ;
Paz-Ares, L. ;
Bernabe Caro, R. ;
Zurawski, B. ;
Kim, S. -W. ;
Carcereny Costa, E. ;
Park, K. ;
Alexandru, A. ;
Lupinacci, L. ;
de la Mora Jimenez, E. ;
Sakai, H. ;
Albert, I. ;
Vergnenegre, A. ;
Peters, S. ;
Syrigos, K. ;
Barlesi, F. ;
Reck, M. ;
Borghaei, H. ;
Brahmer, J. R. ;
O'Byrne, K. J. ;
Geese, W. J. ;
Bhagavatheeswaran, P. ;
Rabindran, S. K. ;
Kasinathan, R. S. ;
Nathan, F. E. ;
Ramalingam, S. S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 381 (21) :2020-2031