Literature DB >> 31279483

The Alternative 2/1 Schedule of Sunitinib is Superior to the Traditional 4/2 Schedule in Patients With Metastatic Renal Cell Carcinoma: A Meta-analysis.

Yi Sun1, Jiejing Li1, Xiangcai Yang1, Guiqian Zhang1, Xin Fan2.   

Abstract

Alternate sunitinib schedules attracted the interest of oncologists recently owing to their superior safety profile. This meta-analysis compared the tolerability and efficacy of a new alternative dosing schedule (2 weeks on/1 week off) of sunitinib with the traditional 4/2 schedule in patients with metastatic renal cell carcinoma (mRCC). Studies were retrieved from Medline, Cochrane Central, Scopus, Embase, and Web of Science databases. Data were extracted and pooled as hazard ratio (HR: survival data) or odds ratio (OR: dichotomous data) using Comprehensive Meta-analysis software. Based on data of 1173 patients, the progression-free survival (HR, 0.52; 95% confidence interval [CI], 0.39-0.95; P < .0001), overall survival (HR, 0.6; 95% CI, 0.43-0.85; P < .0001), and stable disease rates (OR, 0.38; 95% CI, 0.19-0.76; P = .006) were significantly improved on the alternative 2/1 schedule, compared with the traditional 4/2 schedule. However, the complete response (OR, 1.32; 95% CI, 0.34-5.22; P = .69) and partial response (OR, 1.34; 95% CI, 0.44-4.14; P = .61) rates were comparable between the 2 regimens. The tolerability of the alternative 2/1 schedule was superior to the traditional one as investigated adverse events like fatigue (OR, 2.91; 95% CI, 1.89-4.46; P < .0001), hypertension (OR, 2.08; 95% CI, 1.56-2.75; P < .0001), and diarrhea (OR, 2.18; 95% CI, 1.19-3.98; P = .012) were significantly less common. In conclusion, the alternative 2/1 sunitinib schedule provides improved tolerability and survival in patients with mRCC. Large randomized trials with long follow-up periods are required to validate and confirm these findings.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alternative schedule; Sunitinib; Targeted therapy; Traditional schedule; mRCC

Mesh:

Substances:

Year:  2019        PMID: 31279483     DOI: 10.1016/j.clgc.2019.05.003

Source DB:  PubMed          Journal:  Clin Genitourin Cancer        ISSN: 1558-7673            Impact factor:   2.872


  5 in total

Review 1.  Does an Alternative Sunitinib Dosing Schedule Really Improve Survival Outcomes over a Conventional Dosing Schedule in Patients with Metastatic Renal Cell Carcinoma? An Updated Systematic Review and Meta-Analysis.

Authors:  Doo Yong Chung; Dong Hyuk Kang; Jong Won Kim; Do Kyung Kim; Joo Yong Lee; Chang Hee Hong; Kang Su Cho
Journal:  Cancers (Basel)       Date:  2019-11-21       Impact factor: 6.639

Review 2.  Targeting the Deterministic Evolutionary Trajectories of Clear Cell Renal Cell Carcinoma.

Authors:  Adam Kowalewski; Marek Zdrenka; Dariusz Grzanka; Łukasz Szylberg
Journal:  Cancers (Basel)       Date:  2020-11-09       Impact factor: 6.639

Review 3.  Individualized Management of Blood Concentration in Patients with Gastrointestinal Stromal Tumors.

Authors:  Hao Xu; Qi Liu
Journal:  Onco Targets Ther       Date:  2021-01-05       Impact factor: 4.147

Review 4.  Imatinib, sunitinib and pazopanib: From flat-fixed dosing towards a pharmacokinetically guided personalized dose.

Authors:  Kim Westerdijk; Ingrid M E Desar; Neeltje Steeghs; Winette T A van der Graaf; Nielka P van Erp
Journal:  Br J Clin Pharmacol       Date:  2020-01-21       Impact factor: 4.335

5.  The relationship between sunitinib exposure and both efficacy and toxicity in real-world patients with renal cell carcinoma and gastrointestinal stromal tumour.

Authors:  Kim Westerdijk; Stefanie D Krens; Winette T A van der Graaf; Sasja F Mulder; Carla M L van Herpen; Tineke Smilde; Nielka P van Erp; Ingrid M E Desar
Journal:  Br J Clin Pharmacol       Date:  2020-05-26       Impact factor: 3.716

  5 in total

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