黄慧强, 彭玉龙, 潘战和, 蔡清清, 林旭滨, 蔡绮纯. CTOP与CHOP方案治疗外周T细胞淋巴瘤的疗效比较[J]. 中国肿瘤临床, 2006, 33(11): 638-640.
引用本文: 黄慧强, 彭玉龙, 潘战和, 蔡清清, 林旭滨, 蔡绮纯. CTOP与CHOP方案治疗外周T细胞淋巴瘤的疗效比较[J]. 中国肿瘤临床, 2006, 33(11): 638-640.
Huang Huiqiang, Peng Yulong, Pan Zhanhe, Cai Qingqing, Lin Xubin, Cai Qichun. Comparison of Therapeutic Effects of CTOP and CHOP Regimen on Unspecified Peripheral T-cell Lymphoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(11): 638-640.
Citation: Huang Huiqiang, Peng Yulong, Pan Zhanhe, Cai Qingqing, Lin Xubin, Cai Qichun. Comparison of Therapeutic Effects of CTOP and CHOP Regimen on Unspecified Peripheral T-cell Lymphoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(11): 638-640.

CTOP与CHOP方案治疗外周T细胞淋巴瘤的疗效比较

Comparison of Therapeutic Effects of CTOP and CHOP Regimen on Unspecified Peripheral T-cell Lymphoma

  • 摘要: 目的 :比较含吡喃阿霉素(THP)的CTOP方案与含阿霉素(ADM)的CHOP方案治疗外周T细胞性非霍奇金氏淋巴瘤-非特异性(PTCL-U)的疗效和不良反应。 方法 :采用两种方案治疗PTCL-U患者共130例,THP组49例,ADM组81例。 结果 :两组患者临床特征指标相似(P>0.05)。可评价疗效129例,两组有效率分别为71.6%和72.8%,CR率分别为43.2%和39.5%(P>0.05)。骨髓抑制、胃肠道反应、脱发为主要不良反应。Ⅲ~Ⅳ度白细胞降低、血小板和血红蛋白降低发生率两组无明显差异;脱发ADM组高于THP组(31.1%:14.0%,P<0.001);ADM组心脏毒性稍高于THP组(11.1%%:6.1%,P=0.522)。中位随访24个月(1~88个月),两组预计5年生存率分别为22.0%和42.2%(P<0.01)。 结论 :采用含THP的CTOP方案治疗PTCL-U疗效较好,毒性较低,远期生存率较高,值得临床进一步研究。

     

    Abstract: Objective :To compare the efficacy and toxicity of CTOP (with THP) and CHOP in thetreatment of unspecified peripheral T-cell lymphoma (PTCL- U). Methods :One hundred and thirty pa-tients with PTCL- U were treated with combined chemotherapy, including CTOP and CHOP, from Jan-uary 1997 to December 2003 in the Cancer Center, among which 49 were treated by CTOP and 81 byCHOP regimen. The rate of response, toxicity and long- term survival for the two regimens were ana-lyzed retrospectively. Results :The clinical characteristics of the two groups were similar (P>0.05). Atotal of 129 patients were eligible. The response rate for CHOP and CTOP was 71.6% and 72.8%, re-spectively (P>0.05) and the CR rate was 43.2% and 39.5%, respectively (P>0.05). Major toxicity wasmyelosuppression, GI toxicity and alopecia. There was no difference between the two groups in gradeⅢ~Ⅳ toxicity in neutropenia, thrombocytopenia and anemia. Incidence of alopecia was higher in theCHOP group (31.1% vs. 14.0%, P=0.000). Although cardiotoxicity was high in CHOP group (11.1% vs.6.1%), no statistical difference between the two groups was confirmed (P=0.522).Median follow-up was24 months (ranged from 1 to 88 months). The 5- year overall survival rate for CHOP and CTOP groupwas 22.0% and 44.2%, respectively (P<0.01). Conclusions :THP in the CTOP regimen may be moreeffective on PTCL- U with lower toxicity and better long term survival. Randomized clinical trial is war-ranted.

     

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