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A Retrospective Study of Gemcitabine and Carboplatin With or Without Intravenous Vitamin C on Patients With Advanced Triple-Negative Breast Cancer

机译:吉西他滨和卡铂联合或不联合静脉使用维生素C对晚期三阴性乳腺癌患者的回顾性研究

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摘要

This is a retrospective study to examine the effect of chemotherapy with or without intravenous vitamin C (IVC) on women with advanced triple-negative breast cancer (TNBC). From 2008 to 2016, a total of 113 patients with pathologically confirmed TNBC at Clifford Hospital were evaluated, and 70 patients were matched and divided into IVC (treatment group) and non-IVC groups (control group). The match was according to age, menopausal status, and metastatic sites. In the control group, 35 patients received gemcitabine and carboplatin. In the treatment group, 35 patients received the same chemotherapy plus IVC. Baseline characteristics were not significantly different between the 2 groups. According to the criteria of RECIST 1.1 (Response Evaluation Criteria in Solid Tumors), enhanced computed tomography scan was compared after 2 cycles of chemotherapy. In the treatment group, 2/35 cases had a complete remission (CR), 15/35 cases had partial remission (PR), and 13/35 cases had stable disease (SD). The response rate was 48.6%. In the control group, there were no CR cases, 14/35 cases had PR, 14/35 cases had SD, and the response rate was 40.0% ( > .05). The median progression-free survival time and median overall survival time was 7 months (95% confidence interval [CI] =1.5-28.5 months) and 27 months (95% CI = 4-40 months) in the treatment group compared with 4.5 months (95% CI = 1.5-8 months) and 18 months (95% CI = 3-26 months) in the control group ( < .05). All patients experienced diverse reactions in the gastrointestinal tract and myelosuppression. The incidence of adverse reactions in the treatment group was significantly lower than that of the control group ( < .05). IVC may have an effect on improving the prognosis of patients with advanced TNBC.
机译:这是一项回顾性研究,旨在检查有或没有静脉注射维生素C(IVC)的化疗对晚期三阴性乳腺癌(TNBC)妇女的影响。从2008年到2016年,对Clifford医院的113例经病理证实的TNBC患者进行了评估,将70例患者进行了匹配,分为IVC(治疗组)和非IVC组(对照组)。根据年龄,更年期状态和转移部位进行匹配。在对照组中,有35名患者接受了吉西他滨和卡铂治疗。在治疗组中,有35例患者接受了相同的化疗加IVC。两组之间的基线特征无显着差异。根据RECIST 1.1的标准(实体瘤反应评估标准),在2个化疗周期后比较了增强型计算机断层扫描。在治疗组中,完全缓解(CR)的患者占2/35,部分缓解(PR)的患者占15/35,疾病稳定(SD)的患者占13/35。回应率为48.6%。对照组中无CR病例,PR为14/35例,SD为14/35例,缓解率为40.0%(> 0.05)。治疗组的中位无进展生存时间和中位总生存时间分别为7个月(95%置信区间[CI] = 1.5-28.5个月)和27个月(95%CI = 4-40个月),而对照组为4.5个月对照组(95%CI = 1.5-8个月)和18个月(95%CI = 3-26个月)(<.05)。所有患者在胃肠道和骨髓抑制中经历了多种反应。治疗组不良反应的发生率明显低于对照组(<0.05)。 IVC可能会改善晚期TNBC患者的预后。

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