Cancer Res Treat.  2019 Oct;51(4):1578-1588. 10.4143/crt.2018.671.

Temsirolimus in Asian Metastatic/Recurrent Non-clear Cell Renal Carcinoma

Affiliations
  • 1Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea. rha7655@yuhs.ac
  • 2Song-Dang Institute for Cancer Research, Yonsei University College of Medicine, Seoul, Korea.
  • 3Division of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea.
  • 4Department of Biostatistics, Yonsei University College of Medicine, Seoul, Korea.
  • 5Department of Internal Medicine, Chungnam National University, Daejeon, Korea.
  • 6Division of Hematology-Oncology, Department of Internal Medicine, Dongnam Institute of Radiological and Medical Sciences, Busan, Korea.
  • 7Division of Hematology-Oncology, Pusan National University, Busan, Korea.
  • 8Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
  • 9Department of Preventive Medicine and Institute of Health Services Research, Yonsei University College of Medicine, Seoul, Korea.
  • 10Division of Pathology, Yonsei University College of Medicine, Seoul, Korea.
  • 11Brain Korea 21 Project for Medical Sciences, Yonsei University College of Medicine, Seoul, Korea.

Abstract

PURPOSE
Temsirolimus is effective in the treatment for metastatic non-clear cell renal cell carcinoma (nccRCC) with poor prognosis. We aim to investigate the efficacy and tolerability of temsirolimus in treatment of naïve Asian patients with metastatic/recurrent nccRCC.
MATERIALS AND METHODS
From January 2008 to July 2017, data of treatment-naïve, metastatic/recurrent nccRCC patients, who were treated with temsirolimus according to the standard protocol, were collected. The primary end-point was progression-free survival (PFS). Secondary end points were overall survival (OS), objective response rate (ORR), and tolerability of temsirolimus.
RESULTS
Forty-four metastatic/recurrent nccRCC patients, 10 from prospective and 34 from retrospective groups, were enrolled; 24 patients (54%) were papillary type, and other histology subtypes included 11 chromophobes (25%), two collecting ducts (5%), one Xp11.2 translocation (2%), and six others (14%). The median PFS and OS were 7.6 months and 17.6 months, res-pectively. ORR was 11% and disease control rate was 83%. Patients with prior nephrectomy had longer PFS (hazard ratio [HR], 0.16; 95% confidence interval [CI], 0.06 to 0.42; p < 0.001) and OS (HR, 0.15; 95% CI, 0.05 to 0.45; p < 0.001). Compared to favorable/intermediate prognosis group, poor prognosis group had shorter median PFS (4.7 months vs. 7.6 months [HR, 2.91; 95% CI, 1.39 to 6.12; p=0.005]) and median OS (9.2 months vs. 17.6 months [HR, 2.84; 95% CI, 1.23 to 6.56; p=0.015]).
CONCLUSION
Temsirolimus not only benefits poor-risk nccRCC patients, but it is also effective in favorable or intermediate-risk group in Asians. Temsirolimus was well-tolerated with manageable adverse events.

Keyword

Temsirolimus; First-line; Asian; Renal cell carcinoma; Efficacy; Tolerability

MeSH Terms

Asian Continental Ancestry Group*
Carcinoma, Renal Cell
Disease-Free Survival
Humans
Nephrectomy
Prognosis
Prospective Studies
Retrospective Studies

Figure

  • Fig. 1. Efficacy of temsirolimus in non-clear cell renal cell carcinoma. (A) Progression-free survival (PFS). (B) Overall survival (OS). CI, confidence interval.

  • Fig. 2. Kaplan-Meier curves of progression-free survival (PFS) according to subgroups. (A) With or without sarcomatoid features. (B) Papillary, chromophobe, others. (C) Prognostic group by Advanced Renal Cell Cancer criteria. HR, hazard ratio; CI, confidence interval.

  • Fig. 3. Kaplan-Meier curves of overall survival (OS) according to subgroups. (A) With or without sarcomatoid features. (B) Papillary, chromophobe, others. (C) Prognostic group by Advanced Renal Cell Cancer criteria. HR, hazard ratio; CI, confidence interval.


Reference

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