PMID- 32693975 OWN - NLM STAT- MEDLINE DCOM- 20210805 LR - 20210805 IS - 1873-2496 (Electronic) IS - 1078-1439 (Linking) VI - 38 IP - 12 DP - 2020 Dec TI - Discontinuation of first-line molecular-targeted therapy and prognosis in patients with metastatic renal cell carcinoma: Impact of disease progression vs. adverse events. PG - 937.e19-937.e25 LID - S1078-1439(20)30293-3 [pii] LID - 10.1016/j.urolonc.2020.06.023 [doi] AB - OBJECTIVES: We evaluated the impact of discontinuation of first-line (1L) molecular-targeted therapy on prognostic outcomes among patients with metastatic renal cell carcinoma (mRCC). METHODS: Study patients with mRCC were treated with 1L molecular-targeted agents at 4 separate institutions. Prognostic outcomes in this patient cohort were analyzed retrospectively based on whether discontinuation of 1L therapy was related to adverse events (AEs) or progression of disease (PD). RESULTS: Of the 201 patients enrolled, 117 patients (58%) and 84 patients (42%) discontinued 1L targeted therapy due to PD and AEs, respectively. Second-line therapy was subsequently provided to 101 (86%) and 66 (79%) of the patients who discontinued 1L therapy secondary to PD or AEs, respectively. Patients who discontinued 1L therapy due to AEs were significantly older than those with PD. The progression-free survival and overall survival from the initiation of 1L targeted therapy were significantly longer in patients who discontinued 1L therapy due to AE than in those who discontinued 1L therapy due to PD. The OS from the initiation of second-line targeted therapy was significantly longer in patients who discontinued 1L therapy due to AE than those with PD. Furthermore, AE as a reason for discontinuation of 1L targeted therapy as opposed to PD was independently associated with longer progression-free survival and OS as determined by multivariate analysis. CONCLUSIONS: Our findings suggest that mRCC patients who discontinue 1L therapy due to AEs have a more favorable prognosis than those who discontinue therapy due to PD. CI - Copyright (c) 2020 Elsevier Inc. All rights reserved. FAU - Ando, Ryosuke AU - Ando R AD - Department of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. Electronic address: ryo@med.nagoya-cu.ac.jp. FAU - Takahara, Kiyoshi AU - Takahara K AD - Department of Urology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan. FAU - Ito, Toshiki AU - Ito T AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan. FAU - Kanao, Kent AU - Kanao K AD - Department of Urology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Uro-Oncology, Saitama Medical University International Medical Center, Hidaka, Saitama, Japan. FAU - Kobayashi, Ikuo AU - Kobayashi I AD - Department of Urology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan. FAU - Shiroki, Ryoichi AU - Shiroki R AD - Department of Urology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan. FAU - Sumitomo, Makoto AU - Sumitomo M AD - Department of Urology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan. FAU - Miyake, Hideaki AU - Miyake H AD - Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan. FAU - Yasui, Takahiro AU - Yasui T AD - Department of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. LA - eng PT - Journal Article PT - Multicenter Study DEP - 20200718 PL - United States TA - Urol Oncol JT - Urologic oncology JID - 9805460 SB - IM MH - Aged MH - Carcinoma, Renal Cell/*drug therapy/secondary MH - Disease Progression MH - Female MH - Humans MH - Kidney Neoplasms/*drug therapy/pathology MH - Male MH - Middle Aged MH - Molecular Targeted Therapy/*adverse effects MH - Prognosis MH - Retrospective Studies MH - *Withholding Treatment OTO - NOTNLM OT - Discontinuation therapy OT - Metastatic renal cell carcinoma OT - Molecular-targeted therapy COIS- Conflicts of interest The authors have no conflicts of interest to declare. EDAT- 2020/07/23 06:00 MHDA- 2021/08/06 06:00 CRDT- 2020/07/23 06:00 PHST- 2020/03/31 00:00 [received] PHST- 2020/06/03 00:00 [revised] PHST- 2020/06/20 00:00 [accepted] PHST- 2020/07/23 06:00 [pubmed] PHST- 2021/08/06 06:00 [medline] PHST- 2020/07/23 06:00 [entrez] AID - S1078-1439(20)30293-3 [pii] AID - 10.1016/j.urolonc.2020.06.023 [doi] PST - ppublish SO - Urol Oncol. 2020 Dec;38(12):937.e19-937.e25. doi: 10.1016/j.urolonc.2020.06.023. Epub 2020 Jul 18.