Atezolizumab in Platinum-treated Locally Advanced or Metastatic Urothelial Carcinoma: Clinical Experience from an Expanded Access Study in the United States

被引:22
作者
Pal, Sumanta Kumar [1 ]
Hoffman-Censits, Jean [2 ]
Zheng, Hanzhe [3 ]
Kaiser, Constanze [3 ]
Tayama, Darren [3 ]
Bellmunt, Joaquim [4 ]
机构
[1] City Hope Comprehens Canc Ctr, Duarte, CA USA
[2] Sidney Kimmel Canc Ctr Jefferson, Philadelphia, PA USA
[3] Genentech Inc, San Francisco, CA 94080 USA
[4] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA USA
关键词
Atezolizumab; Expanded access program; Immunotherapy; Urothelial carcinoma; PHASE-II TRIAL; RANDOMIZED-TRIAL; SINGLE-ARM; OPEN-LABEL; CANCER; CISPLATIN; MULTICENTER; DOCETAXEL; PLUS; PEMBROLIZUMAB;
D O I
10.1016/j.eururo.2018.02.010
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Atezolizumab (anti-programmed death-ligand 1) was approved in the USA, Europe, and elsewhere for treatment-naive and platinum-treated locally advanced/metastatic urothelial carcinoma (mUC). Objective: To report efficacy and safety from an atezolizumab expanded access study. Design, setting, and participants: This single-arm, open-label study enrolled 218 patients at 36 US sites. Key eligibility criteria included progression during/following >= 1 platinum-based chemotherapy for mUC or in perioperative setting (progression within 12 mo) and Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2. Intervention: Patients received atezolizumab1200 mg intravenously every 3 wk until loss of clinical benefit, unacceptable toxicity, consent withdrawal, decision to discontinue, death, atezolizumab commercial availability, or study closure. Outcome measurements and statistical analysis: Key end points reported herein included Response Evaluation Criteria in Solid Tumors v1.1 objective response rate and duration, disease control rate (DCR; response or stable disease), and safety. Results and limitations: All patients received prior systemic therapy (68% mUC; 27% adjuvant; and 26% neoadjuvant). At baseline, 57% of 214 treated patients had ECOG PS >= 1, 19% had hemoglobin <10 g/dl, and 25% had liver metastases. Median treatment duration was 9 wk (interquartile range [IQR], 6-12 wk). Median follow-up duration was 2.3 mo (IQR, 1.6-3.4 mo) overall and 2.7 mo (IQR, 2.0-3.5 mo) in patients not known to have died. Seventeen of 114 evaluable patients (15%) had objective responses (16 ongoing at study termination). DCR was 49%. Treatment-related adverse events (mostly fatigue) occurred in 98 of 214 treated patients. Conclusions: The benefit/risk profile of atezolizumab was consistent with that observed in previous studies, despite pretreatment and poor prognostic factors. These results suggest a potential role for atezolizumab in a broader patient range than typically eligible for phase 1-3 studies. Patient summary: In this expanded access study, atezolizumab was active and tolerable in a range of patients with platinum-treated metastatic urothelial carcinoma. (C) 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:800 / 806
页数:7
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