Incidence risk of PD-1/PD-L1 related diarrhea in non-small cell lung cancer (NSCLC) patients: a systematic review and meta-analysis

被引:7
作者
Zhang, Caiqing [1 ]
Zhang, Shuisheng [2 ]
Xu, Deguo [3 ]
Liu, Rujun [4 ]
Zhu, Qingshan [5 ]
Zhao, Yi [6 ]
Mao, Yantao [7 ]
Tian, Yuan [3 ]
机构
[1] Shandong Univ, Dept Resp, Shandong Prov Qianfoshan Hosp, Jinan 250014, Shandong, Peoples R China
[2] Peking Univ, Dept Gen Surg, Hosp 3, Beijing 100191, Peoples R China
[3] Shandong Univ, Dept Radiotherapy Oncol, Shandong Prov Qianfoshan Hosp, Jinan 250014, Shandong, Peoples R China
[4] LongKou Peoples Hosp, Dept Oncol, Yantai 265701, Shandong, Peoples R China
[5] Anyang Canc Hosp Henan Prov, Dept Radiotherapy Oncol, Anyang 455000, Henan, Peoples R China
[6] Dalian Med Univ, Dept Oncol, Affiliated Hosp 1, Dalian 116000, Liaoning, Peoples R China
[7] Yantaishan Hosp Shandong Prov, Dept Oncol, Yantai 264000, Peoples R China
关键词
diarrhea; PD-1/PD-L1; NSCLC; meta-analysis; PHASE-III TRIAL; OPEN-LABEL; DOCETAXEL; NIVOLUMAB; ATEZOLIZUMAB; MULTICENTER; PEMBROLIZUMAB; RESPONSES; SAFETY;
D O I
10.2147/CMAR.S202756
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We designed the study to illustrate the OR of programmed cell death-1 (PD-1) or ligand 1 (PD-L1) inhibitor-related diarrhea in patients with non-small cell lung cancer. Method: This systematic review and meta-analysis were put into practice according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. Incidence of all grades for PD-1/PD-L1 inhibitor-related diarrhea in NSCLC was taken into account. Results: After screening and eligibility assessment of 57 articles, a total of 12 clinical trials involving 6,659 participants were collected for the final meta-analysis. The incidence risk of diarrhea for all grades was lower in PD-1 inhibitor monotherapy compared to monochemotherapy of docetaxel (OR=0.31, 95% CI [0.24, 0.41]; I-2=0%, Z=8.23 (p<0.00001)), while a similar result could also be seen in PD-L1 inhibitor monotherapy group (OR=0.41, 95% CI [0.27, 0.64]; I-2=59%, Z=3.92 [p<0.00001]). The opposite result can be seen when PD-1/PD-L1 inhibitor combined chemotherapy was compared to chemotherapy alone (OR=1.51, 95% CI [1.22, 1.87]; I-2=0%, Z=3.77 [p<0.00001]). Similar incidence trend could also be seen in the meta-analysis of diarrhea for grade 1-2 and grade 3-5. Conclusion: The incidence risk of diarrhea associated with PD-1/-PD-L1 inhibitor monotherapy was significantly lower than that of docetaxel monotherapy group. However it was higher in PD-1/PD-L1 inhibitor combined with chemotherapy group compared with the chemotherapy alone group.
引用
收藏
页码:3957 / 3969
页数:13
相关论文
共 39 条
[1]  
[Anonymous], NEWCASTLE OTTAWA SCA
[2]  
[Anonymous], 2011, BMJ, V343, pd5928, DOI [DOI 10.1136/BMJ.D5928, 10.1136/bmj.d5928]
[3]  
[Anonymous], SCIENCE
[4]  
[Anonymous], 2015, LANCET ONCOL, DOI DOI 10.1016/S1470-2045(15)70054-9
[5]   Overall Survival with Durvalumab after Chemoradiotherapy in Stage III NSCLC [J].
Antonia, S. J. ;
Villegas, A. ;
Daniel, D. ;
Vicente, D. ;
Murakami, S. ;
Hui, R. ;
Kurata, T. ;
Chiappori, A. ;
Lee, K. H. ;
de Wit, M. ;
Cho, B. C. ;
Bourhaba, M. ;
Quantin, X. ;
Tokito, T. ;
Mekhail, T. ;
Planchard, D. ;
Kim, Y. -C. ;
Karapetis, C. S. ;
Hiret, S. ;
Ostoros, G. ;
Kubota, K. ;
Gray, J. E. ;
Paz-Ares, L. ;
Carpeno, J. de Castro ;
Faivre-Finn, C. ;
Reck, M. ;
Vansteenkiste, J. ;
Spigel, D. R. ;
Wadsworth, C. ;
Melillo, G. ;
Taboada, M. ;
Dennis, P. A. ;
Ozguroglu, M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (24) :2342-2350
[6]   Avelumab versus docetaxel in patients with platinum-treated advanced non-small-cell lung cancer (JAVELIN Lung 200): an open-label, randomised, phase 3 study [J].
Barlesi, Fabrice ;
Vansteenkiste, Johan ;
Spigel, David ;
Ishii, Hidenobu ;
Garassino, Marina ;
de Marinis, Filippo ;
Ozguroglu, Mustafa ;
Szczesna, Aleksandra ;
Polychronis, Andreas ;
Uslu, Ruchan ;
Krzakowski, Maciej ;
Lee, Jong-Seok ;
Calabro, Luana ;
Frontera, Osvaldo Aren ;
Ellers-Lenz, Barbara ;
Bajars, Marcis ;
Ruisi, Mary ;
Park, Keunchil .
LANCET ONCOLOGY, 2018, 19 (11) :1468-1479
[7]   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
[8]   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
[9]   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
[10]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188