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Comparing Paclitaxel–Carboplatin with Paclitaxel–Cisplatin as the Front-Line Chemotherapy for Patients with Figo IIIC Serous-Type Tubo-Ovarian Cancer

Bibliographic Data

ID15484137
AuthorsChen-Yu Huang (0000-0003-3527-2789, National Yang Ming Chiao Tung University), Min Cheng (0000-0002-7419-3867, National Yang Ming Chiao Tung University), Na-Rong Lee (Taipei Veterans General Hospital), Hsin‐Yi Huang (0000-0002-8466-9865, Taipei Veterans General Hospital), Hsin-Yi Huang (0000-0002-4765-1869, Biostatics Task Force, Taipei Veterans General Hospital, Taipei 112, Taiwan), Wen-Ling Lee (0000-0003-4956-896X, Oriental Institute of Technology), Wen-Hsun Chang (National Yang Ming Chiao Tung University, corresponding author), Peng‐Hui Wang (0000-0002-6048-8541, National Yang Ming Chiao Tung University, corresponding author)
Year2020
Volume17
Issue7
Pages2213-2213
Publication date2020-03-26
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph17072213
PMID32224896
OpenAlexW3013843155
LanguageEN
Citations received1
References cited141

The use of weekly chemotherapy for the treatment of patients with advanced-stage serous-type epithelial Tubo-ovarian cancer (ETOC), and primary peritoneal serous carcinoma (PPSC) is acceptable as the front-line postoperative chemotherapy after primary cytoreductive surgery (PCS). The main component of dose-dense chemotherapy is weekly paclitaxel (80 mg/m 2 ), but it would be interesting to know what is the difference between combination of triweekly cisplatin (20 mg/m 2 ) or triweekly carboplatin (carboplatin area under the curve 5-7 mg/mL per min [AUC 5-7]) in the dose-dense paclitaxel regimen. Therefore, we compared the outcomes of women with Gynecology and Obstetrics (FIGO) stage IIIC ETOC and PPSC treated with PCS and a subsequent combination of dose-dense weekly paclitaxel and triweekly cisplatin (paclitaxel-cisplatin) or triweekly carboplatin using AUC 5 (paclitaxel-carboplatin). Between January 2010 and December 2016, 40 women with International Federation of Gynecology and Obstetrics (FIGO) stage IIIC EOC, FTC, or PPSC were enrolled, including 18 treated with paclitaxel-cisplatin and the remaining 22 treated with paclitaxel-carboplatin. There were no statistically significant differences in disease characteristics of patients between two groups. Outcomes in paclitaxel-cisplatin group seemed to be little better than those in paclitaxel-carboplatin (median progression-free survival [PFS] 30 versus 25 months as well as median overall survival [OS] 58.5 versus 55.0 months); however, neither reached a statistically significant difference. In terms of adverse events (AEs), patients in paclitaxel-carboplatin group had more AEs, with a higher risk of neutropenia and grade 3/4 neutropenia, and the need for a longer period to complete the front-line chemotherapy, and the latter was associated with worse outcome for patients. We found that a period between the first-time chemotherapy to the last dose (6 cycles) of chemotherapy >21 weeks was associated with a worse prognosis in patients compared to that ≤21 weeks, with hazard ratio (HR) of 81.24 for PFS and 9.57 for OS. As predicted, suboptimal debulking surgery (>1 cm) also contributed to a worse outcome than optimal debulking surgery (≤1 cm) with HR of 14.38 for PFS and 11.83 for OS. Based on the aforementioned findings, both regimens were feasible and effective, but maximal efforts should be made to achieve optimal debulking surgery and following the on-schedule administration of dose-dense weekly paclitaxel plus triweekly platinum compounds. Randomized trials validating the findings are warranted

Cancer · Carboplatin · Chemotherapy · Cisplatin · Ovarian cancer · Paclitaxel · Regimen · Serous fluid · Endometrial and Cervical Cancer Treatments · Intraperitoneal and Appendiceal Malignancies · Medicine · Ovarian cancer diagnosis and treatment · Internal Medicine · Oncology

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Citations per year0.17
Citation span2020 - 2020 (1)
Highly citedNo

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