Mapisal versus urea cream as prophylaxis for capecitabine-associated hand-foot syndrome

• Verfasst von: Hofheinz, Ralf-Dieter [VerfasserIn]
• Verfasst von: Gencer, Deniz [VerfasserIn]
• Verfasst von: Schneeweiss, Andreas [VerfasserIn]
• Titel: Mapisal versus urea cream as prophylaxis for capecitabine-associated hand-foot syndrome
• Titelzusatz: a randomized phase III trial of the AIO Quality of Life Working Group
• Verf.angabe: Ralf-Dieter Hofheinz, Deniz Gencer, Holger Schulz, Michael Stahl, Susanna Hegewisch-Becker, Luisa Mantovani Loeffler, Ursula Kronawitter, Georg Bolz, Jochem Potenberg, Felix Tauchert, Salah-Eddin Al-Batran, and Andreas Schneeweiss
• E-Jahr: 2015
• Jahr: August 1 2015
• Umfang: 6 S.
• Fussnoten: Gesehen am 15.02.2018
• Titel Quelle: Enthalten in: Journal of clinical oncology
• Ort Quelle: Alexandria, Va. : American Society of Clinical Oncology, 1983
• Jahr Quelle: 2015
• Band/Heft Quelle: 33(2015), 22, Seite 2444-2449
• ISSN Quelle: 1527-7755
• DOI: doi:10.1200/JCO.2014.60.4587
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1569897549

Abstract

Purpose: Hand-foot syndrome (HFS) is a frequently occurring adverse event associated with anticancer drugs. This study compares a newly introduced ointment containing several antioxidants and exhibiting high radical protection factor, which has been available on the German market since 2011, with urea cream for prevention of HFS in patients treated with capecitabine. Patients and Methods: Patients with GI tumors or breast cancer treated with capecitabine were included in this randomized phase III study. The primary end point was prevention of HFS of any grade within 6 weeks of treatment as indicated by a standardized patient diary. The study had 80% power to show a 20% reduction of the incidence of HFS with the new ointment. Secondary end points included time to development of HFS greater than grade 1, evaluation of capecitabine dose intensity, and quality of life analyses. Results: A total of 152 patients were evaluable. In total, 47 of 152 patients experienced HFS (30.9%), 39.5% with the new ointment and 22.4% in the urea arm (stratified odds ratio, 2.37; P = .02). Time to HFS greater than grade 1 was comparable, but time to any-grade HFS was significantly longer in the urea group (P = .03). Capecitabine dose intensity, time under study, and percentage of days with correct administration of study medication were identical, as were adverse events except for HFS. Skin-related quality of life was significantly worse in the group treated with the new ointment at the end of study treatment. Conclusion: This trial demonstrated that 10% urea cream was superior to the new ointment at preventing HFS over the first 6 weeks of treatment with capecitabine.