Literature DB >> 33562736

Safety and Efficacy of Weekly Paclitaxel and Cisplatin Chemotherapy for Ovarian Cancer Patients with Hypersensitivity to Carboplatin.

Shinichi Tate1, Kyoko Nishikimi1, Ayumu Matsuoka1, Satoyo Otsuka1, Makio Shozu1.   

Abstract

BACKGROUND: This study aimed to evaluate the safety and efficacy of weekly paclitaxel and cisplatin chemotherapy (wTP) in patients with ovarian cancer who developed carboplatin hypersensitivity reaction (HSR).
METHODS: We retrospectively investigated 86 patients with ovarian, fallopian tube, and peritoneal carcinoma who developed carboplatin HSR during previous chemotherapy (carboplatin and paclitaxel) at our institution between 2011 and 2019. After premedication was administered, paclitaxel was administered over 1 h, followed by cisplatin over 1 h (paclitaxel 80 mg/m2; cisplatin 25 mg/m2; 1, 8, 15 day/4 weeks). We investigated the incidence of patients who successfully received wTP for at least one cycle, treatments compliance, progression-free survival (PFS), and overall survival (OS).
RESULTS: The median number of wTP administration cycles was 4 (Interquartile Range IQR, 3-7), 71 patients (83%) successfully received wTP, and 15 patients (17%) developed cisplatin HSR. The efficacy of treatment was as follows: 55 (64%) patients completed the scheduled wTP, 9 (10%) patients discontinued due to HSR to cisplatin within 6 cycles, 1 (1%) patient discontinued due to renal toxicity (grade 2) at the 6th cycle, and 21 (24%) patients discontinued due to progressive disease within 6 cycles. The median PFS and OS after administration of wTP were 10.9 months (95% CI: 7.7-17.7) and 25.9 months (95% CI: 19.0-50.2), respectively.
CONCLUSIONS: wTP was safe and well-tolerated in patients who developed carboplatin HSR.

Entities:  

Keywords:  carboplatin; cisplatin; hypersensitivity reaction; ovarian cancer; platinum-sensitive disease; recurrence

Year:  2021        PMID: 33562736      PMCID: PMC7915680          DOI: 10.3390/cancers13040640

Source DB:  PubMed          Journal:  Cancers (Basel)        ISSN: 2072-6694            Impact factor:   6.639


  29 in total

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10.  Weekly dose-dense chemotherapy in first-line epithelial ovarian, fallopian tube, or primary peritoneal carcinoma treatment (ICON8): primary progression free survival analysis results from a GCIG phase 3 randomised controlled trial.

Authors:  Andrew R Clamp; Elizabeth C James; Iain A McNeish; Andrew Dean; Jae-Weon Kim; Dearbhaile M O'Donnell; Jane Hook; Christopher Coyle; Sarah Blagden; James D Brenton; Raj Naik; Tim Perren; Sudha Sundar; Adrian D Cook; Gosala S Gopalakrishnan; Hani Gabra; Rosemary Lord; Graham Dark; Helena M Earl; Marcia Hall; Susana Banerjee; Rosalind M Glasspool; Rachel Jones; Sarah Williams; Ann Marie Swart; Sally Stenning; Mahesh Parmar; Richard Kaplan; Jonathan A Ledermann
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