Outcomes of metastatic urothelial carcinoma following discontinuation of enfortumab-vedotin

被引:6
作者
Curran, Catherine [1 ]
Adib, Elio [1 ]
Kazakova, Vera [2 ]
Grivas, Petros [3 ]
Diamantopoulos, Leonidas Nikolaos [3 ,4 ]
Alva, Ajjai Shivaram [5 ]
Su, Christopher [5 ]
Jain, Rohit K. [6 ]
Tandon, Ankita [6 ]
Necchi, Andrea [7 ,10 ,11 ]
Marandino, Laura [8 ]
Plastini, Trisha M. [9 ]
Merchan, Jaime R. [9 ]
Sonpavde, Guru [1 ]
机构
[1] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] St Elizabeths Med Ctr, Brighton, MA USA
[3] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle Canc Care Alliance, Seattle, WA 98195 USA
[4] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[5] Univ Michigan, Rogel Canc Ctr, Ann Arbor, MI 48109 USA
[6] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[7] Fdn IRCCS Ist Nazl Tumori, Milan, Italy
[8] Univ Turin, Candiolo Canc Inst FPO IRCCS, Dept Oncol, Candiolo, Italy
[9] Univ Miami, Miami, FL USA
[10] Univ Vita Salute San Raffaele, Milan, Italy
[11] IRCCS San Raffaele Hosp, Milan, Italy
关键词
Bladder cancer; Urinary tract neoplasms; Discontinuation; Clinical outcomes; Enfortumab vedotin; RETROSPECTIVE ANALYSIS; CANCER; CHEMOTHERAPY; CISPLATIN; THERAPY;
D O I
10.1016/j.clgc.2021.08.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This retrospective study demonstrates poor outcomes of metastatic urothelial carcinoma patients following discontinuation of Enfortumab Vedotin (EV). Only 51% received therapy after discontinuation of EV. Benchmarks for the interpretation of activity of new agents following EV were identified. The duration of EV was identified as a potential prognostic factor following discontinuation of EV. Background: Enfortumab vedotin (EV) is approved to treat metastatic urothelial carcinoma (mUC) following platinum and PD1/L1 inhibitors. Since the outcomes and patterns of therapy of patients following discontinuation of EV are unknown, we conducted a retrospective study to assess this issue. Methods: Data were retrospectively obtained from patients with mUC following discontinuation of EV after prior platinum-based chemotherapy and PD1/L1 inhibitors. Objective response rate (ORR) was evaluated in those who received therapy post-EV. Statistical analyses were performed to describe the overall survival (OS) and compare patient characteristics and outcomes of those who did or did not receive treatment post-EV. Results: Data were available for 63 patients from 6 institutions: 46 (73%) were male and median age was 68 years (range 43-83). The median OS was 32 weeks. Thirty-two patients (51%) received therapy after EV. The OS of those who did vs. did not receive post-EV therapy was significantly different (median 43.1 vs. 16.9 weeks, P = .015). Longer duration of prior EV therapy was associated with receipt of post-EV therapy (P = .0437) as well as OS in both the treated (P = .045) and untreated groups (P = .012). Objective response was observed in 3 of 32 patients (9.4%) who received therapy post-EV. Conclusion: Outcomes of patients with mUC following discontinuation of EV are dismal and only 51% received therapy after discontinuation of EV. This study identifies benchmarks for the interpretation of activity of new agents following EV and raises the hypothesis for duration of EV as a potential prognostic factor following discontinuation of EV. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:11 / 16
页数:6
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