Please use this identifier to cite or link to this item: https://doi.org/10.3802/jgo.2018.29.e96
Title: Weekly versus 3-weekly paclitaxel in combination with carboplatin in advanced ovarian cancer: which is the optimal adjuvant chemotherapy regimen?
Authors: Lee, Matilda X
Tan, David SP
Keywords: Science & Technology
Life Sciences & Biomedicine
Oncology
Obstetrics & Gynecology
Epithelial Ovarian Cancer
Paclitaxel
Chemotherapy
Pharmacogenetics
PHASE-III TRIAL
GYNECOLOGIC-ONCOLOGY-GROUP
PRIMARY PERITONEAL CANCER
EPITHELIAL OVARIAN
MOLECULAR SUBTYPES
BRCA2 MUTATIONS
FALLOPIAN-TUBE
OPEN-LABEL
CONVENTIONAL PACLITAXEL
STAGE-III
Issue Date: 1-Nov-2018
Publisher: KOREAN SOC GYNECOLOGY ONCOLOGY & COLPOSCOPY
Citation: Lee, Matilda X, Tan, David SP (2018-11-01). Weekly versus 3-weekly paclitaxel in combination with carboplatin in advanced ovarian cancer: which is the optimal adjuvant chemotherapy regimen?. JOURNAL OF GYNECOLOGIC ONCOLOGY 29 (6). ScholarBank@NUS Repository. https://doi.org/10.3802/jgo.2018.29.e96
Abstract: The 3-weekly regimen of carboplatin and paclitaxel is the backbone of first line adjuvant chemotherapy for advanced ovarian cancer. The landmark Japanese Gynaecologic Oncology Group (JGOG) 3016 study demonstrated significant improvements in progression-free survival and overall survival with dose dense weekly administration of paclitaxel in combination with 3-weekly carboplatin. However, efforts to replicate these benefits have failed in subsequent phase III trials. Weekly paclitaxel is purported to have enhanced antitumor activity, with stronger anti-angiogenic effects, and yet is better tolerated. In this review, we explore the rationale for dose dense weekly paclitaxel, and compare the relevant trials as well as quality of life considerations. Possible reasons for the difference in outcomes between the JGOG 3016 and other studies are reviewed, with a focus on how the addition of bevacizumab, the variations between histological and molecular subtypes of epithelial ovarian cancers, and ethnic pharmacogenetic differences may potentially affect the efficacy of dose dense paclitaxel.
Source Title: JOURNAL OF GYNECOLOGIC ONCOLOGY
URI: https://scholarbank.nus.edu.sg/handle/10635/206511
ISSN: 20050380
20050399
DOI: 10.3802/jgo.2018.29.e96
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