The efficacy of molecular targeted therapy and nivolumab therapy for metastatic non‐clear cell renal cell carcinoma: A retrospective analysis using the Michinoku Japan urological cancer study group database

Author:

Koguchi Tomoyuki1ORCID,Naito Sei2ORCID,Hatakeyama Shingo3ORCID,Numakura Kazuyuki4,Muto Yumina4,Kato Renpei5ORCID,Kojima Takahiro6,Kawasaki Yoshihide7,Morozumi Kento7,Kandori Shuya6ORCID,Kawamura Sadafumi8,Nishiyama Hiroyuki6,Ito Akihiro7,Habuchi Tomonori4,Obara Wataru5,Ohyama Chikara3,Tsuchiya Norihiko2,Kojima Yoshiyuki1

Affiliation:

1. Department of Urology Fukushima Medical University School of Medicine Fukushima Japan

2. Department of Urology Yamagata University Faculty of Medicine Yamagata Japan

3. Department of Urology and Advanced Blood Purification Therapy Hirosaki University Graduate of Medicine Hirosaki Japan

4. Department of Urology Akita University Graduate School of Medicine Akita Japan

5. Department of Urology Iwate Medical University School of Medicine Iwate Japan

6. Department of Urology University of Tsukuba, Graduate School of Comprehensive Human Sciences Tsukuba Japan

7. Department of Urology Tohoku University School of Medicine Sendai Japan

8. Department of Urology Miyagi Cancer Center Natori Japan

Abstract

AbstractObjectivesTo investigate the efficacy of pharmacotherapy for metastatic non‐clear cell renal cell carcinoma (nccRCC) in Japanese population.MethodsIn this retrospective analysis, we compared the time to treatment failure (TTF) for molecular‐targeted agents as first‐line therapy, or nivolumab therapy as sequential therapy between ccRCC and nccRCC using the data of Japanese metastatic RCC patients registered in the Michinoku Japan Urological Cancer Study Group database.ResultsIn total, 511 cases of ccRCC and 77 cases of nccRCC were treated with pharmacotherapy. After excluding the patients who received cytokine therapy, chemotherapy, or others, there were 391 ccRCC patients and 60 nccRCC patients who were treated with tyrosine kinase inhibitors (TKIs), and 7 ccRCC patients and 7 nccRCC patients who were treated with mammalian‐target of rapamycin inhibitors (mTORIs). In addition, 132 ccRCC patients and 16 nccRCC patients received nivolumab. There was no significant difference in IMDC risk classification before first‐line therapy between ccRCC and nccRCC groups, or in each subgroup within the nccRCC group. TTF for TKIs (161 days, 95% CI: 75‐212 days) and mTORIs (21 days, 95% CI: 9‐31 days) didn’t differ significantly between nccRCC and ccRCC groups (205 days, 95% CI: 174‐243 days and 33 days, 95% CI: 8‐113 days, respectively). TTF for TKIs was significantly longer than that for mTORIs in nccRCC group (p<0.01). There was no significant difference in TTF between the different TKIs in nccRCC group. In addition, no significant difference in TTF for nivolumab was seen between ccRCC and nccRCC groups.ConclusionsThe results showed that the efficacy of molecular‐targeted agents as first‐line therapy was similar oncological outcomes between metastatic nccRCC and ccRCC in Japanese patients. TKIs may be more effective than mTORIs in metastatic nccRCC patients. Nivolumab administration might also be as effective in nccRCC patients as in ccRCC patients in Japanese population.

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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