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首页> 外文期刊>Current HIV research >Oxaliplatin based chemotherapy and concomitant highly active antiretroviral therapy in the treatment of 24 patients with colorectal cancer and HIV infection.
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Oxaliplatin based chemotherapy and concomitant highly active antiretroviral therapy in the treatment of 24 patients with colorectal cancer and HIV infection.

机译:以奥沙利铂为基础的化疗及伴随的高活性抗逆转录病毒疗法治疗24例结直肠癌和HIV感染患者。

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BACKGROUND: Although FOLFOX4 is considered the standard chemotherapy regimen for colorectal cancer (CRC), few data are available on its results in human immunodeficiency (HIV)-related CRC. The results were analyzed to evaluate feasibility and activity of FOLFOX4 plus highly active antiretroviral therapy (HAART) in metastatic CRC (mCRC) HIV-seropositive patients. PATIENTS AND METHODS: From January 2002 to March 2007, 24 patients were selected among the CRC HIV-seropositive patients treated with FOLFOX4 and concomitant HAART within the Italian Cooperative Group on AIDS and Tumors (GICAT). RESULTS: Four median cycles of chemotherapy were administered; the most common severe toxicity was neutropenia (37.5%). An overall response rate of 50% was observed; 4.2% of patients achieved complete response and 45.8% partial response. No opportunistic infections occurred during or immediately after chemotherapy. The median CD4+ count was 380 (range 220-570) at diagnosis. CONCLUSIONS: To our knowledge, this is the largest study describing activity and tolerability of FOLFOX4 and HAART, in this setting. FOLFOX4 plus concomitant HAART resulted feasible and active also in HIV-seropositive patients. Moreover, the concomitant use of HAART did not to seem to increase the FOLFOX4 toxicity. This study suggests the good tolerability of the FOLFOX4, making it a reasonable option for combination with HAART.
机译:背景:尽管FOLFOX4被认为是结直肠癌(CRC)的标准化疗方案,但关于其与人类免疫缺陷(HIV)相关的CRC结果的数据很少。分析结果以评估FOLFOX4加上高活性抗逆转录病毒疗法(HAART)在转移性CRC(mCRC)HIV血清阳性患者中的可行性和活性。患者与方法:从2002年1月至2007年3月,在意大利艾滋病与肿瘤合作组织(GICAT)中,从接受FOLFOX4和伴随HAART治疗的CRC HIV阳性患者中选择24例。结果:进行了四个中位化疗周期。最常见的严重毒性反应是中性粒细胞减少(37.5%)。总体响应率为50%; 4.2%的患者获得了完全缓解,部分缓解了45.8%。在化疗期间或之后均未发生机会性感染。诊断时CD4 +的中位数为380(范围为220-570)。结论:据我们所知,这是描述FOLFOX4和HAART在这种情况下的活性和耐受性的最大研究。 FOLFOX4加伴随的HAART在HIV血清阳性患者中也可行且有效。此外,同时使用HAART似乎并没有增加FOLFOX4的毒性。这项研究表明FOLFOX4具有良好的耐受性,使其成为与HAART组合的合理选择。

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