2008
DOI: 10.3816/cbc.2008.n.052
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Carboplatin plus Gemcitabine Repeating Doublet Therapy in Recurrent Breast Cancer

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Cited by 19 publications
(15 citation statements)
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“…Observed toxicities were similar to those seen in the previous study [94]. In a third smaller study on 13 patients, an RR of 53.3%, a median TTP of 4.5 months and a median OS of 28.8 months were observed [95]. More recently, Chan et al [96] evaluated this combination in 41 anthracycline- and taxane-resistant MBC patients and documented an RR of 39% (CR 2%, PR 37%).…”
Section: Experience With Combination Chemotherapysupporting
confidence: 70%
“…Observed toxicities were similar to those seen in the previous study [94]. In a third smaller study on 13 patients, an RR of 53.3%, a median TTP of 4.5 months and a median OS of 28.8 months were observed [95]. More recently, Chan et al [96] evaluated this combination in 41 anthracycline- and taxane-resistant MBC patients and documented an RR of 39% (CR 2%, PR 37%).…”
Section: Experience With Combination Chemotherapysupporting
confidence: 70%
“…Two randomized controlled trials have demonstrated the efficacy of gemcitabine/taxane combinations as first-line and/or second-line treatment for metastatic breast cancer [9,10]. Many other studies have examined the efficacy and safety of gemcitabine in combination with paclitaxel, carboplatin, or cisplatin in patients with advanced metastatic breast cancer [11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30]. However, most of these studies have involved small numbers of patients, and it is difficult to compare the results because of differences in the treatment regimens and the clinically diverse study populations.…”
Section: Introductionmentioning
confidence: 99%
“…25,26 For example, gemcitabine is a deoxycytidine analog and is widely used in the treatment of solid tumors. [27][28][29] However, tumor resistance of gemcitabine often seriously limits its effect. 30 These drugs may interact with DNA in two ways: by acting as structural analogs of the precursors and intermediates for the synthetic pathway, and therefore interfering with the synthesis of purines and pyrimidines, or by acting as false bases in the assembly of the DNA double helix during replication and transcription.…”
Section: Antimetabolitesmentioning
confidence: 99%
“…10 Gemcitabine (2′,2′-difluorodeoxycytidine, dFdC) is a deoxycytidine analog with antitumor activity against a wide variety of solid tumors such as pancreatic, non-small-cell lung cancer (NSCLC), breast cancer, and ovarian cancer, alone or in combination with other chemotherapeutic agents. [27][28][29]96 Moreover, gemcitabine is indicated in several hematological disorders such as acute leukemia. 97 Furthermore, gemcitabine enhances the cytotoxicity of cisplatin by increasing the formation of cytotoxic platinum-DNA adducts and is also a potent radiosensitizer used in radiation therapy.…”
Section: Nucleoside Analogs and Gemcitabinementioning
confidence: 99%