Indirect treatment comparison of olaparib and talazoparib in germline BRCA-mutated HER2-negative metastatic breast cancer

被引:8
作者
McCrea, Charles [1 ]
Hettle, Robert [1 ]
Gulati, Poonam [1 ]
Taneja, Ankush [2 ]
Rajora, Preety [2 ]
机构
[1] AstraZeneca, 136 Hills Rd,Acad House, Cambridge CB2 8PA, England
[2] BresMed, 906-912,JMD Megapolis,Sohna Rd, Gurugram 122018, Haryana, India
关键词
BRCA; breast cancer; breast cancer gene; HER2-negative; HER2; metastatic breast cancer; Olaparib; OPEN-LABEL; CHEMOTHERAPY; MULTICENTER; VELIPARIB; OVARIAN;
D O I
10.2217/cer-2021-0097
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Aim: Two poly(ADP-ribose) polymerase (PARP) inhibitors olaparib and talazoparib are approved for patients with germline BRCA-mutated (gBRCAm) HER2-negative metastatic breast cancer. Methods: A Bayesian fixed-effects indirect treatment comparison (ITC) analysis was performed to simulate the comparative efficacy (primary outcome of progression-free survival [PFS]) and safety of PARP inhibitor monotherapy. Results: ITC of data from the OlympiAD (olaparib) and EMBRACA (talazoparib) studies suggested no significant difference in efficacy (PFS) between olaparib and talazoparib. However, there were differences in specific adverse events; patients receiving olaparib had a higher rate of nausea and vomiting, while those receiving talazoparib had a higher rate of alopecia and anemia. Discussion: These data support the benefit of the PARP inhibitor class in gBRCAm HER2-negative metastatic breast cancer.
引用
收藏
页码:1021 / 1030
页数:10
相关论文
共 27 条
[1]  
[Anonymous], 2018, Breast Cancer Facts and Figures
[2]  
Deeks J.J., 2023, Cochrane handbook for systematic reviews of interventions
[3]   Parp-2 is required to maintain hematopoiesis following sublethal γ-irradiation in mice [J].
Farres, Jordi ;
Martin-Caballero, Juan ;
Martinez, Carlos ;
Lozano, Juan J. ;
Llacuna, Laura ;
Ampurdanes, Coral ;
Ruiz-Herguido, Cristina ;
Dantzer, Francoise ;
Schreiber, Valerie ;
Villunger, Andreas ;
Bigas, Anna ;
Yelamos, Jose .
BLOOD, 2013, 122 (01) :44-54
[4]  
FDA, 2018, TALZEENA TAL PRESCR
[5]  
FDA, 2014, LYNPARZA OLAP PRESCR
[6]   Olaparib in patients with recurrent high-grade serous or poorly differentiated ovarian carcinoma or triple-negative breast cancer: a phase 2, multicentre, open-label, non-randomised study [J].
Gelmon, Karen A. ;
Tischkowitz, Marc ;
Mackay, Helen ;
Swenerton, Kenneth ;
Robidoux, Andre ;
Tonkin, Katia ;
Hirte, Hal ;
Huntsman, David ;
Clemons, Mark ;
Gilks, Blake ;
Yerushalmi, Rinat ;
Macpherson, Euan ;
Carmichael, James ;
Oza, Amit .
LANCET ONCOLOGY, 2011, 12 (09) :852-861
[7]   Veliparib with temozolomide or carboplatin/paclitaxel versus placebo with carboplatin/paclitaxel in patients with BRCA1/2 locally recurrent/metastatic breast cancer: randomized phase II study [J].
Han, H. S. ;
Dieras, V. ;
Robson, M. ;
Palacova, M. ;
Marcom, P. K. ;
Jager, A. ;
Bondarenko, I. ;
Citrin, D. ;
Campone, M. ;
Telli, M. L. ;
Domchek, S. M. ;
Friedlander, M. ;
Kaufman, B. ;
Garber, J. E. ;
Shparyk, Y. ;
Chmielowska, E. ;
Jakobsen, E. H. ;
Kaklamani, V. ;
Gradishar, W. ;
Ratajczak, C. K. ;
Nickner, C. ;
Qin, Q. ;
Qian, J. ;
Shepherd, S. P. ;
Isakoff, S. J. ;
Puhalla, S. .
ANNALS OF ONCOLOGY, 2018, 29 (01) :154-161
[8]  
Harbeck N, 2019, NAT REV DIS PRIMERS, V5, DOI [10.1038/s41572-019-0111-2, 10.1038/s41572-019-0122-z]
[9]   Cisplatin plus gemcitabine versus paclitaxel plus gemcitabine as first-line therapy for metastatic triple-negative breast cancer (CBCSG006): a randomised, open-label, multicentre, phase 3 trial [J].
Hu, Xi-Chun ;
Zhang, Jian ;
Xu, Bing-He ;
Cai, Li ;
Ragaz, Joseph ;
Wang, Zhong-Hua ;
Wang, Bi-Yun ;
Teng, Yue-E ;
Tong, Zhong-Sheng ;
Pan, Yue-Yin ;
Yin, Yong-Mei ;
Wu, Chang-Ping ;
Jiang, Ze-Fei ;
Wang, Xiao-Jia ;
Lou, Gu-Yin ;
Liu, Dong-Geng ;
Feng, Ji-Feng ;
Luo, Jian-Feng ;
Sun, Kang ;
Gu, Ya-Jia ;
Wu, Jiong ;
Shao, Zhi-Min .
LANCET ONCOLOGY, 2015, 16 (04) :436-446
[10]   Talazoparib in Patients with a Germline BRCA-Mutated Advanced Breast Cancer: Detailed Safety Analyses from the Phase III EMBRACA Trial [J].
Hurvitz, Sara A. ;
Gocalves, Anthony ;
Rugo, Hope S. ;
Lee, Yung-Hun ;
Fehrenbacher, Louis ;
Mina, Lida A. ;
Diab, Sami ;
Blum, Joanne L. ;
Chakrabarti, Jayeta ;
Elmeliegy, Mohamed ;
DeAnnuntis, Liza ;
Gauthier, Eric ;
Czibere, Akos ;
Tudor, Iulia Cristina ;
Quek, Ruben G. W. ;
Litton, Jennifer K. ;
Ettl, Johannes .
ONCOLOGIST, 2020, 25 (03) :E439-E450