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How clinical practice is changing the rules: the sunitinib 2/1 schedule in metastatic renal cell carcinoma

Articolo
Data di Pubblicazione:
2017
Abstract:
Introduction: Currently, sunitinib is a standard of care in first-line treatment for metastatic renal cell carcinoma (mRCC). However, with the standard 4/2 schedule (sunitinib 50 mg/day; 4 consecutive weeks on treatment; 2 weeks' rest), 50% of patients require dose reductions to mitigate toxicity, highlighting the need to investigate alternative dosing schedules that improve tolerability without compromising efficacy. Areas covered: We present a concise critical review of published studies comparing the efficacy and safety of the 4/2 and 2/1 schedule (2 weeks on treatment; 1 week rest) for sunitinib. While all studies evaluating the 2/1 schedule have a low level of evidence, the results indicate that the 2/1 schedule improves tolerability compared with the 4/2 schedule, including significant reductions in the incidence of specific adverse events. It was not possible to make any definitive conclusions regarding efficacy due to methodologic limitations of these studies. Expert commentary: In the absence of strong evidence supporting the safety and efficacy of the 2/1 schedule, we recommend that patients should be initiated on sunitinib therapy with the standard 4/2 schedule and only be switched to the 2/1 schedule after the development of dose-limiting toxicities from weeks 3-4 (cycle 1) of the 4/2 schedule cycle.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Angiogenesis inhibitors; dose schedule; renal cell carcinoma; standard of care; sunitinib; Antineoplastic Agents; Carcinoma, Renal Cell; Dose-Response Relationship, Drug; Drug Administration Schedule; Humans; Indoles; Kidney Neoplasms; Neoplasm Metastasis; Pyrroles; Research Design; Sunitinib
Elenco autori:
Bracarda, S.; Negrier, S.; Casper, J.; Porta, C.; Schmidinger, M.; Larkin, J.; Gross Goupil, M.; Escudier, B.
Autori di Ateneo:
PORTA CAMILLO
Link alla scheda completa:
https://iris.unipv.it/handle/11571/1301806
Pubblicato in:
EXPERT REVIEW OF ANTICANCER THERAPY
Journal
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http://www.tandfonline.com/loi/iery20#.VhIiC7fouDY
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