Literature DB >> 18952557

Carboplatin plus gemcitabine repeating doublet therapy in recurrent breast cancer.

Robert A Nagourney1, Marshall Flam, John Link, Steven Hager, Jonathan Blitzer, William Lyons, Barbara L Sommers, Steven Evans.   

Abstract

PURPOSE: The combination of cisplatin plus gemcitabine is active in metastatic breast cancer. Carboplatin plus gemcitabine, widely used in ovarian and non-small-cell lung cancers, has also been used in breast cancer. This trial examined the efficacy and toxicity of split-dose carboplatin plus gemcitabine in advanced breast cancer. PATIENTS AND METHODS: Patients with measurable disease, recurrent after adjuvant and < or = 1 previous treatment for systemic disease, received carboplatin area under the curve = 2.0 (Calvert) plus gemcitabine 800 mg/m2, both drugs administered days 1 and 8 every 21 days. Of 15 patients accrued, 13 are fully evaluable.
RESULTS: There were 2 complete (13.3%) and 6 partial (40%) responses, for an overall response rate by intention to treat of 53.3% (95% CI, 28%-82%). The median time to progression was 4.5 months (95% CI, 2.03-6.97 months), and median overall survival was 28.8 months (95% CI, 9.4-48.2 months). There were 2 patients with grade 3 (13.3%) anemia, 7 patients with grade 3 (46.6%) and 4 patients (26.6%) with grade 4 neutropenia, 4 patients with grade 3 (26.6%) and 3 patients (20%) with grade 4 thrombocytopenia.
CONCLUSION: The repeating doublet of split-dose carboplatin plus gemcitabine reveals activity comparable to that of cisplatin plus gemcitabine, is well tolerated, and warrants evaluation in patients with recurrent breast cancer.

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Year:  2008        PMID: 18952557     DOI: 10.3816/CBC.2008.n.052

Source DB:  PubMed          Journal:  Clin Breast Cancer        ISSN: 1526-8209            Impact factor:   3.225


  6 in total

1.  Toxicity Assessment of a Phase III Study Evaluating FEC-Doc and FEC-Doc Combined with Gemcitabine as an Adjuvant Treatment for High-Risk Early Breast Cancer: the SUCCESS-A Trial.

Authors:  L Schröder; B Rack; H Sommer; J G Koch; T Weissenbacher; W Janni; A Schneeweiss; M Rezai; R Lorenz; B Jäger; A Schramm; L Häberle; P A Fasching; T W P Friedl; M W Beckmann; C Scholz
Journal:  Geburtshilfe Frauenheilkd       Date:  2016-05       Impact factor: 2.915

2.  Combination of gemcitabine and cisplatin is highly active in women with endometrial carcinoma: results of a prospective phase 2 trial.

Authors:  Jubilee Brown; Judith A Smith; Lois M Ramondetta; Anil K Sood; Pedro T Ramirez; Robert L Coleman; Charles F Levenback; Mark F Munsell; Maria Jung; Judith K Wolf
Journal:  Cancer       Date:  2010-11-01       Impact factor: 6.860

3.  Randomised phase II trial of gemcitabine plus vinorelbine vs gemcitabine plus cisplatin vs gemcitabine plus capecitabine in patients with pretreated metastatic breast cancer.

Authors:  H J Stemmler; D diGioia; W Freier; H W Tessen; G Gitsch; W Jonat; W Brugger; E Kettner; W Abenhardt; H Tesch; H J Hurtz; S Rösel; O Brudler; V Heinemann
Journal:  Br J Cancer       Date:  2011-03-15       Impact factor: 7.640

4.  Combination of gemcitabine-containing magnetoliposome and oxaliplatin-containing magnetoliposome in breast cancer treatment: A possible mechanism with potential for clinical application.

Authors:  Hui Ye; Jiansong Tong; Jiangyi Liu; Wenman Lin; Chengshou Zhang; Kai Chen; Jie Zhao; Wenjing Zhu
Journal:  Oncotarget       Date:  2016-07-12

Review 5.  Overcoming tumor cell chemoresistance using nanoparticles: lysosomes are beneficial for (stearoyl) gemcitabine-incorporated solid lipid nanoparticles.

Authors:  Zhe Chen; Yuanqiang Zheng; Yanchun Shi; Zhengrong Cui
Journal:  Int J Nanomedicine       Date:  2018-01-09

Review 6.  Promising molecular mechanisms responsible for gemcitabine resistance in cancer.

Authors:  Yanfei Jia; Jingwu Xie
Journal:  Genes Dis       Date:  2015-07-30
  6 in total

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