Li Qun-hua, DU Xin, Huang Zi-lun, Luo Cheng-wei, Zhong Li-ye, Lin Wei
Department of Hematology, Guangdong Provincial People's Hospital, Guangzhou 510080, China.
Zhonghua Yi Xue Za Zhi. 2005 May 11;85(17):1195-7.
To evaluate the therapeutic effects of chemotherapeutic regimen containing pirarubicin (THP) on the treatment of high-risk or refractory and relapsed acute leukemia (AL) in adults.
Forty patients with high-risk or refractory and relapsed AL, 26 males and 14 females, aged 33 (14-63) received treatment regimens with THP: TA regimen [THP + cytosine-arabinoside (Ara-C)] for acute myeloid leukemia (AML) and TAOP regimen [THP + Ara-C + vincristine (VCR) + prednisone (Pred)] for acute lymphocytic leukemia (ALL) or biphenotype-AL. Forty matched patients received mitoxantron (MIT) + Ara-C for AML or MIT + Ara-C + VCR + Pred for ALL and biphenotype AL as controls. The therapeutic effects were observed.
The complete remission (CR) rate was 47.5% vs 45% (P > 0.05), partial response (PR) rate was 25% vs 20% (P > 0.05), and overall response (OR) rate was 72.5% vs 65% (P > 0.05) in the treatment group and control group. The continuous CR time was 528 days in the treatment group, significantly longer than in the control group (463 days, P < 0.05). Marrow suppression was more serious in the treatment group. The patients in the treatment group had higher incidence of infections (P < 0.05). The time with sustained recovery of platelet number was 13.9 days in the treatment group, significantly longer than in the control group (P < 0.05).
Regimens with THP are more effective on treatment of high-risk or refractory and relapsed AL in adults, however, with more serious marrow suppression and higher incidence of infection.
评估含吡柔比星(THP)的化疗方案治疗成人高危或难治复发急性白血病(AL)的疗效。
40例高危或难治复发AL患者,男26例,女14例,年龄33(14 - 63)岁,接受含THP的治疗方案:急性髓系白血病(AML)采用TA方案[THP + 阿糖胞苷(Ara - C)],急性淋巴细胞白血病(ALL)或双表型AL采用TAOP方案[THP + Ara - C + 长春新碱(VCR)+ 泼尼松(Pred)]。40例匹配患者接受米托蒽醌(MIT)+ Ara - C治疗AML,或MIT + Ara - C + VCR + Pred治疗ALL和双表型AL作为对照。观察疗效。
治疗组与对照组的完全缓解(CR)率分别为47.5%和45%(P > 0.05),部分缓解(PR)率分别为25%和20%(P > 0.05),总缓解(OR)率分别为72.5%和65%(P > 0.05)。治疗组持续CR时间为528天,显著长于对照组(463天,P < 0.05)。治疗组骨髓抑制更严重。治疗组患者感染发生率更高(P < 0.05)。治疗组血小板计数持续恢复时间为13.9天,显著长于对照组(P < 0.05)。
含THP的方案治疗成人高危或难治复发AL更有效,但骨髓抑制更严重,感染发生率更高。