Avelumab (anti-PD-L1) in platinum-resistant/refractory ovarian cancer: JAVELIN Ovarian 200 Phase III study design

被引:64
作者
Pujade-Lauraine, Eric [1 ]
Fujiwara, Keiichi [2 ]
Dychter, Samuel S. [3 ]
Devgan, Geeta [4 ]
Monk, Bradley J. [5 ,6 ]
机构
[1] Univ Paris 05, Hop Hotel Dieu, AP HP, Ctr Canc Femme & Rech Clin, Paris, France
[2] Saitama Med Univ Int Med Ctr, Saitama, Japan
[3] Pfizer Oncol, La Jolla, CA 92121 USA
[4] Pfizer Oncol, New York, NY 10017 USA
[5] Univ Arizona, Arizona Oncol US Oncol Network, Phoenix, AZ 85016 USA
[6] Creighton Univ, Phoenix, AZ 85016 USA
关键词
avelumab; ovarian cancer; PD-L1; PEGYLATED LIPOSOMAL DOXORUBICIN; RECURRENT EPITHELIAL OVARIAN; INFILTRATING T-CELLS; QUALITY-OF-LIFE; OPEN-LABEL; PD-L1; EXPRESSION; LUNG-CANCER; SOLID TUMOR; CHEMOTHERAPY; CARCINOMA;
D O I
10.2217/fon-2018-0070
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Avelumab is a human anti-PD-L1 checkpoint inhibitor with clinical activity in multiple solid tumors. Here, we describe the rationale and design for JAVELIN Ovarian 200 (NCT02580058), the first randomized Phase III trial to evaluate the role of checkpoint inhibition in women with ovarian cancer. This three-arm trial is comparing avelumab administered alone or in combination with pegylated liposomal doxorubicin versus pegylated liposomal doxorubicin alone in patients with platinum-resistant/refractory recurrent ovarian, fallopian tube or peritoneal cancer. Eligible patients are not preselected based on PD-L1 expression and may have received up to three prior lines of chemotherapy for platinum-sensitive disease, but none for resistant disease. Overall survival and progression-free survival are primary end points, and secondary end points include biomarker evaluations and pharmacokinetics.
引用
收藏
页码:2103 / 2113
页数:11
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