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Efficacy and Safety of Vinorelbine Plus Cisplatin vs. Gemcitabine Plus Cisplatin for Treatment of Metastatic Triple-Negative Breast Cancer After Failure with Anthracyclines and Taxanes.
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- Author(s): Wang J;Wang J; Zheng R; Zheng R; Wang Z; Wang Z; Yang Y; Yang Y; Wang M; Wang M; Zou W; Zou W
- Source:
Medical science monitor : international medical journal of experimental and clinical research [Med Sci Monit] 2017 Sep 28; Vol. 23, pp. 4657-4664. Date of Electronic Publication: 2017 Sep 28.
- Publication Type:
Comparative Study; Journal Article
- Language:
English
- Additional Information
- Source:
Publisher: International Scientific Information, Inc Country of Publication: United States NLM ID: 9609063 Publication Model: Electronic Cited Medium: Internet ISSN: 1643-3750 (Electronic) Linking ISSN: 12341010 NLM ISO Abbreviation: Med Sci Monit Subsets: MEDLINE
- Publication Information:
Publication: 2014- : Smithtown, NY : International Scientific Information, Inc.
Original Publication: Warsaw, Poland : Medical Science International
- Subject Terms:
- Abstract:
BACKGROUND This study aimed to compare the efficacy and safety of vinorelbine plus cisplatin (NP regimen) vs. gemcitabine plus cisplatin (GP regimen) for treatment of metastatic TNBC after failure with anthracyclines and taxanes. MATERIAL AND METHODS A total of 48 patients with metastatic TNBC that failed in anthracyclines and taxanes treatment were enrolled and randomly grouped. Patients in the NP group (n=22) were given 25 mg/m² vinorelbine on days 1 and 8 and 25 mg/m² cisplatin on days 2-4 of each 21-day cycle, while subjects in the GP group (n=26) were administered 1000 mg/m² gemcitabine on days 1 and 8 and 25 mg/m² cisplatin on days 2-4 of each 21-day cycle. The treatment response and adverse events were compared between the 2 groups every 2 cycles. RESULTS The ORR, DCR, and median TTP were 45.5%, 77.3%, and 5 months in the NP group, and 46.2%, 80.8%, and 5.2 months in the GP group, and no significant differences were observed in ORR, DCR, and median TTP between the 2 groups (P>0.05). The major adverse events included grade I-II bone marrow inhibition, gastrointestinal reactions, and phlebitis, and a lower incidence of thrombocytopenia and rash and a higher incidence of phlebitis was found in the NP group than in the GP group (P<0.05). CONCLUSIONS Either NP or GP regimen is active and tolerated in treatment of metastatic TNBC with anthracyclines and/or taxanes resistance, which may be used as a salvage treatment for metastatic TNBC.
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- Accession Number:
0 (Anthracyclines)
0 (Taxoids)
0W860991D6 (Deoxycytidine)
5V9KLZ54CY (Vinblastine)
Q20Q21Q62J (Cisplatin)
Q6C979R91Y (Vinorelbine)
0 (Gemcitabine)
- Publication Date:
Date Created: 20170929 Date Completed: 20180528 Latest Revision: 20221207
- Publication Date:
20231215
- Accession Number:
PMC5629993
- Accession Number:
10.12659/msm.905300
- Accession Number:
28957036
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