Prognostic Impact of Histologic Subtype and Divergent Differentiation in Patients with Metastatic Urothelial Carcinoma Treated with Enfortumab Vedotin: A Multicenter Retrospective Study

Author:

Minato Akinori1,Furubayashi Nobuki2,Nagata Yujiro1,Tomoda Toshihisa3,Masaoka Hiroyuki4,Song Yoohyun4,Hori Yoshifumi5,Kiyoshima Keijiro6,Negishi Takahito2,Kuroiwa Kentaro5,Seki Narihito4,Tomisaki Ikko1,Harada Kenichi1,Nakamura Motonobu2,Fujimoto Naohiro1

Affiliation:

1. Department of Urology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan

2. Department of Urology, National Hospital Organization Kyushu Cancer Center, Fukuoka 811-1395, Japan

3. Department of Urology, Oita Prefectural Hospital, Oita 870-8511, Japan

4. Department of Urology, Kyushu Central Hospital of the Mutual Aid Association of Public School Teachers, Fukuoka 815-8588, Japan

5. Department of Urology, Miyazaki Prefectural Miyazaki Hospital, Miyazaki 880-8510, Japan

6. Department of Urology, Japanese Red Cross Fukuoka Hospital, Fukuoka 815-8555, Japan

Abstract

Subtype of urothelial carcinoma (SUC), defined here as urothelial carcinoma with any histologic subtype or divergent differentiation, is a clinically aggressive disease. However, the efficacy of enfortumab vedotin (EV) against SUC remains unclear. Hence, this study aimed to assess the oncological outcomes of patients with SUC treated with EV for metastatic disease. We retrospectively evaluated consecutive patients with advanced lower and upper urinary tract cancer who received EV after platinum-based chemotherapy and immune checkpoint blockade therapy at six institutions. The objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) were compared between patients with pure urothelial carcinoma (PUC) and those with SUC. We identified 44 and 18 patients with PUC and SUC, respectively. Squamous differentiation was the most common subtype element, followed by glandular differentiation and sarcomatoid subtype. Although patients with SUC had a comparable ORR to those with PUC, the duration of response for SUC was short. Patients with SUC had poorer PFS than those with PUC; however, no significant difference was observed in OS. Multivariate analysis revealed that SUC was significantly associated with shorter PFS. Although the response of metastatic SUC to EV was similar to that of PUC, SUC showed faster progression than PUC.

Funder

JSPS KAKENHI

Publisher

MDPI AG

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