评估成人急性淋巴细胞白血病治疗方案的长期随访的重要性。

B Clarkson, J Gaynor, C Little, E Berman, S Kempin, M Andreeff, S Gulati, I Cunningham, T Gee
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引用次数: 29

摘要

在过去的20年里,我们治疗了250例未经治疗的急性淋巴细胞白血病(ALL)成人(大于15岁),采用了5种连续的多药方案:L2、L10、L10M、L17/17M和L20。与L2和较近的协议(24%-32%)相比,L10和L10M协议具有最高的长期(大于5年)缓解百分比(分别为52%和40%);部分原因是后一种方案中不良风险因素的发生率更高。前199例患者至少3年随访后的总体长期生存率为31%,163例患者中35%达到完全缓解(CR), 5年以上无复发。163例患者的无病生存率在6年后达到33%的平台期。连续CR维持1.5年、3年和5年后患者复发的比例分别为42%、28%和6%;该系列6年后尚未出现复发。随着首次缓解持续时间的延长,复发后生存率逐渐提高。化疗或骨髓移植(BMT)在第二次或以后缓解的治疗结果不令人满意,只有少数长期幸存者。最近,我们尝试选择首次缓解期早期复发风险最高的患者进行BMT治疗,但由于各种原因,包括早期死亡、未能达到CR、早期复发、患者拒绝或医疗禁忌症,实际接受BMT治疗的符合条件的患者数量一直很低。(摘要删节250字)
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Importance of long-term follow-up in evaluating treatment regimens for adults with acute lymphoblastic leukemia.

During the past 20 years, we have treated 250 previously untreated adults (greater than age 15 years) with acute lymphoblastic leukemia (ALL) with five successive multidrug protocols: L2, L10, L10M, L17/17M, and L20. The L10 and L10M protocols had the highest percentage of long-term (greater than 5 years) remissions (52% and 40% respectively) compared with the L2 and more recent protocols (24%-32%); this is partly attributable to a greater prevalence of adverse risk factors among the latter protocols. The overall long-term survival of the first 199 patients with minimum 3 years follow-up is now 31%, with 35% of the 163 patients achieving complete remission (CR) remaining free of relapse for greater than 5 years. The disease-free survival of the 163 patients reaches a plateau of 33% after 6 years. The percentages of patients subsequently relapsing after remaining in continuous CR for 1.5, 3, and 5 years are 42%, 28%, and 6%, respectively; no relapses have yet occurred after 6 years in this series. Postrelapse survival improved progressively with longer duration of first remission. The results of treatment in second or later remission with either chemotherapy or bone marrow transplantation (BMT) were unsatisfactory and there were only a few long-term survivors. Recently we have attempted to select patients at highest risk of early relapse for BMT in first remission, but the number of eligible patients actually having BMTs has been low for a variety of reasons, including early death, failure to reach CR, early relapse, patient refusal, or medical contraindications.(ABSTRACT TRUNCATED AT 250 WORDS)

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