Post-progression survival after cessation of treatment with nivolumab for advanced non-small cell lung cancer: A retrospective study

被引:7
作者
Yano, Yukihiro [1 ]
Kurebe, Hiroyuki [1 ]
Edahiro, Ryuya [1 ]
Hosono, Yuki [1 ]
Nakatsubo, Saeko [1 ]
Nishida, Kohei [1 ]
Sawa, Nobuyuki [1 ]
Ishijima, Mikako [1 ]
Uenami, Takeshi [1 ]
Kanazu, Masaki [1 ]
Akazawa, Yuki [1 ]
Yamaguchi, Toshihiko [1 ]
Mori, Masahide [1 ]
机构
[1] Natl Hosp Org, Toneyama Natl Hosp, Dept Thorac Oncol, Toyonaka, Osaka, Japan
关键词
RESPONSE RATES; CHEMOTHERAPY; PEMBROLIZUMAB; INHIBITORS; DOCETAXEL;
D O I
10.1371/journal.pone.0203070
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objectives The effectiveness of treatment after cessation of nivolumab in patients with advanced non-small cell lung cancer (NSCLC) has not been well investigated. The aim of the present study was to clarify the clinical benefit of post-nivolumab treatment in such patients. Materials and methods A retrospective review was conducted on patients who received treatment after cessation of nivolumab due to disease progression or adverse events at the Toneyama National Hospital between January 2016 and April 2017. Results Among 64 patients treated with nivolumab, 26 patients received treatment after cessation of nivolumab due to disease progression (n = 21) or adverse events (n = 5). The median age of the patients was 68 years and 19 patients were male. Nineteen patients had performance status (PS) 1 or less at initiation of post-nivolumab treatment. Four, 20, and 2 patients were treated with platinum doublets, a single agent, and molecular targeting agents, respectively. Response rate, disease control rate, and median progression-free survival of first-line post-nivolumab treatment were 34.6% (9 patients), 73.1% (19 patients), and 2.8 months (95% confidence interval [CI]: 1.7-5.2), respectively. Adverse events (>= grade 3) and treatment cessation were observed in 57.7% (15 patients) and 19.2% (5 patients), respectively. There were no statistically significant differences for the majority of patient characteristics between the groups with (n = 26) and without post-nivolumab treatment. However, PS at cessation of nivolumab and post-progression survival (PPS) after cessation of nivolumab (median PPS: 12.6 vs. 1.4 months, 95% CI: 3.8-14.7 vs. 0.4-2.2) were significantly different between the groups. A multivariate Cox regression analysis showed significant correlation of PS at cessation of nivolumab (hazard ratio [HR]: 0.34, 95% CI: 0.13-0.87) and post-nivolumab treatment (HR: 0.19, 95% CI: 0.08-0.43) with prolonged PPS after nivolumab. Conclusion Median post-progression survival in patients with advanced NSCLC who received post-nivolumab treatment was approximately 1 year.
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共 17 条
[1]   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
[2]   Nivolumab versus Docetaxel in Advanced Squamous-Cell Non-Small-Cell Lung Cancer [J].
Brahmer, Julie ;
Reckamp, Karen L. ;
Baas, Paul ;
Crino, Lucio ;
Eberhardt, Wilfried E. E. ;
Poddubskaya, Elena ;
Antonia, Scott ;
Pluzanski, Adam ;
Vokes, Everett E. ;
Holgado, Esther ;
Waterhouse, David ;
Ready, Neal ;
Gainor, Justin ;
Aren Frontera, Osvaldo ;
Havel, Libor ;
Steins, Martin ;
Garassino, Marina C. ;
Aerts, Joachim G. ;
Domine, Manuel ;
Paz-Ares, Luis ;
Reck, Martin ;
Baudelet, Christine ;
Harbison, Christopher T. ;
Lestini, Brian ;
Spigel, David R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (02) :123-135
[3]   Phase I Study of Single-Agent Anti-Programmed Death-1 (MDX-1106) in Refractory Solid Tumors: Safety, Clinical Activity, Pharmacodynamics, and Immunologic Correlates [J].
Brahmer, Julie R. ;
Drake, Charles G. ;
Wollner, Ira ;
Powderly, John D. ;
Picus, Joel ;
Sharfman, William H. ;
Stankevich, Elizabeth ;
Pons, Alice ;
Salay, Theresa M. ;
McMiller, Tracee L. ;
Gilson, Marta M. ;
Wang, Changyu ;
Selby, Mark ;
Taube, Janis M. ;
Anders, Robert ;
Chen, Lieping ;
Korman, Alan J. ;
Pardoll, Drew M. ;
Lowy, Israel ;
Topalian, Suzanne L. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (19) :3167-3175
[4]   Immunological Effects of Conventional Chemotherapy and Targeted Anticancer Agents [J].
Galluzzi, Lorenzo ;
Buque, Aitziber ;
Kepp, Oliver ;
Zitvogel, Laurence ;
Kroemer, Guido .
CANCER CELL, 2015, 28 (06) :690-714
[5]   Clinical outcomes of patients with non-small cell lung cancer (NSCLC) receiving chemotherapy after immune checkpoint blockade. [J].
Grigg, Claud ;
Reuland, Brian D. ;
Sacher, Adrian G. ;
Yeh, Randy ;
Rizvi, Naiyer A. ;
Shu, Catherine A. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
[6]   Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial [J].
Herbst, Roy S. ;
Baas, Paul ;
Kim, Dong-Wan ;
Felip, Enriqueta ;
Perez-Gracia, Jose L. ;
Han, Ji-Youn ;
Molina, Julian ;
Kim, Joo-Hang ;
Arvis, Catherine Dubos ;
Ahn, Myung-Ju ;
Majem, Margarita ;
Fidler, Mary J. ;
de Castro, Gilberto, Jr. ;
Garrido, Marcelo ;
Lubiniecki, Gregory M. ;
Shentu, Yue ;
Im, Ellie ;
Dolled-Filhart, Marisa ;
Garon, Edward B. .
LANCET, 2016, 387 (10027) :1540-1550
[7]   Post-Progression Survival after EGFR-TKI for Advanced Non-Small Cell Lung Cancer Harboring EGFR Mutations [J].
Kogure, Yoshihito ;
Saka, Hideo ;
Oki, Masahide ;
Saito, Toshiki I. ;
Ahmed, Shimaa Nour Moursi ;
Kitagawa, Chiyoe ;
Imaizumi, Kazuyoshi .
PLOS ONE, 2015, 10 (08)
[8]   Carboplatin and pemetrexed with or without pembrolizumab for advanced, non-squamous non-small-cell lung cancer: a randomised, phase 2 cohort of the open-label KEYNOTE-021 study [J].
Langer, Corey J. ;
Gadgeel, Shirish M. ;
Borghaei, Hossein ;
Papadimitrakopoulou, Vassiliki A. ;
Patnaik, Amita ;
Powell, Steven F. ;
Gentzler, Ryan D. ;
Martins, Renato G. ;
Stevenson, James P. ;
Jalal, Shadia I. ;
Panwalkar, Amit ;
Yang, James Chih-Hsin ;
Gubens, Matthew ;
Sequist, Lecia V. ;
Awad, Mark M. ;
Fiore, Joseph ;
Ge, Yang ;
Raftopoulos, Harry ;
Gandhi, Leena .
LANCET ONCOLOGY, 2016, 17 (11) :1497-1508
[9]   Response to salvage chemotherapy following exposure to immune checkpoint inhibitors in patients with non-small cell lung cancer. [J].
Leger, Paul Denis ;
Rothschild, Sasha ;
Castellanos, Emily ;
Pillai, Rathi Narayana ;
York, Sally Jane ;
Horn, Leora .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
[10]   Platinum-based drugs disrupt STAT6-mediated suppression of immune responses against cancer in humans and mice [J].
Lesterhuis, W. Joost ;
Punt, Cornelis J. A. ;
Hato, Stanleyson V. ;
Eleveld-Trancikova, Dagmar ;
Jansen, Bastiaan J. H. ;
Nierkens, Stefan ;
Schreibelt, Gerty ;
de Boer, Annemiek ;
Van Herpen, Carla M. L. ;
Kaanders, Johannes H. ;
van Krieken, Johan H. J. M. ;
Adema, Gosse J. ;
Figdor, Carl G. ;
de Vries, I. Jolanda M. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (08) :3100-3108