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高危急性淋巴细胞白血病儿童患者的骨髓复发:不同方案治疗患者的复发时间和初始临床特征比较。儿童癌症与白血病研究组(CCLSG)

[Bone marrow relapse in high-risk pediatric patients with acute lymphoblastic leukemia: a comparison of relapse times and initial clinical features of patients on different protocols. Children's Cancer and Leukemia Study group (CCLSG)].

作者信息

Tsurusawa M, Katano N, Hirota T, Koizumi S, Asami K, Chin M, Ota S, Kawakami T, Hatae Y, Sekine I, Iwai A, Anami K, Nishi K, Miyake M, Watanabe A, Yatabe M, Kawakami K, Gushi K, Yokota S, Gusiken T, Kikuta A, Mimaya J, Okada N, Iga M, Fujimoto T

出版信息

Rinsho Ketsueki. 1998 Aug;39(8):565-73.

PMID:9785974
Abstract

To clarify the efficacy of modern intensive chemotherapy for ALL patients with unfavorable features, we compared the time to failure and initial clinical features of children who relapsed in the bone marrow or combined sites, as documented by early CCLSG studies (H811 and H851; 1981-1987) and later studies (H874 and H/HH911; 1987-1993) concerning high-risk ALL patients. In the later studies patients outcomes with new intensive regimens employing early intensification and reinduction therapy were apparently better than those of patients in the early studies with conventional regimens. When we compared the number of relapsed patients based on duration of first remission, we found that the improved outcomes for patients in the later studies were due to a decrease in the number who relapsed 7-36 months after the start of treatment (intermediate relapse), and that the percentage of those who relapsed within the first 6 months of therapy (early relapse) was higher. Patients with high initial WBC counts tended to relapse much earlier than those with low initial WBC counts. However, in the later studies, patients with high WBC counts often relapsed after the termination of therapy (late relapse). These results suggest that the intensive chemotherapy regimens used in the later studies can prevent the development of drug resistant leukemic clones, except in extremely high-risk patients likely to relapse within the first 6 months of therapy.

摘要

为了阐明现代强化化疗对所有具有不良特征的急性淋巴细胞白血病(ALL)患者的疗效,我们比较了早期儿童癌症研究组(CCLSG)研究(H811和H851;1981 - 1987年)以及后来关于高危ALL患者的研究(H874和H/HH911;1987 - 1993年)中记录的骨髓或联合部位复发儿童的失败时间和初始临床特征。在后来的研究中,采用早期强化和再诱导治疗的新强化方案的患者结局明显优于早期采用传统方案的患者。当我们根据首次缓解持续时间比较复发患者数量时,发现后来研究中患者结局的改善是由于治疗开始后7 - 36个月复发(中期复发)的患者数量减少,而治疗前6个月内复发(早期复发)的患者比例更高。初始白细胞计数高的患者往往比初始白细胞计数低的患者复发早得多。然而,在后来的研究中,白细胞计数高的患者常在治疗结束后复发(晚期复发)。这些结果表明,后来研究中使用的强化化疗方案可以预防耐药白血病克隆的出现,但极有可能在治疗前6个月内复发的极高危患者除外。

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