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减低强度预处理和异基因干细胞移植后慢性淋巴细胞白血病移植物抗白血病效应的证据:德国移植协作研究组

Evidence of a graft-versus-leukemia effect in chronic lymphocytic leukemia after reduced-intensity conditioning and allogeneic stem-cell transplantation: the Cooperative German Transplant Study Group.

作者信息

Schetelig J, Thiede C, Bornhauser M, Schwerdtfeger R, Kiehl M, Beyer J, Sayer H G, Kroger N, Hensel M, Scheffold C, Held T K, Hoffken K, Ho A D, Kienast J, Neubauer A, Zander A R, Fauser A A, Ehninger G, Siegert W

机构信息

Charité Campus Virchow Klinium, Berlin, Germany.

出版信息

J Clin Oncol. 2003 Jul 15;21(14):2747-53. doi: 10.1200/JCO.2003.12.011.

Abstract

PURPOSE

To study whether hematopoietic stem-cell transplantation (HSCT) after reduced-intensity conditioning is effective and tolerable in patients with advanced chronic lymphocytic leukemia (CLL).

PATIENTS AND METHODS

Thirty patients with advanced B-cell CLL were included into the study. After reduced-intensity conditioning with fludarabine, busulfan, and antithymocyte globulin, patients received a transplant from related (n = 15) or unrelated donors (n = 15). Minimal residual disease (MRD) was monitored with a clone-specific polymerase chain reaction.

RESULTS

After a median follow-up of 2 years, 23 patients are alive (to date). Neutrophil and platelet engraftment occurred after a median of 17.5 and 15 days, respectively. Acute graft-versus-host disease (GVHD) grade 2 to 4 was observed in 17 patients (56%), and chronic GVHD was observed in 21 patients (75%). Twelve patients (40%) achieved a complete remission (CR), and 16 patients (53%) achieved a partial remission. Late CR occurred up to 2 years after transplantation. MRD was monitored in eight patients with CR. All patients achieved a molecular CR. At last follow-up, six patients were in ongoing molecular CR. Causes of death were treatment-related complications in four patients and progressive disease in three patients. The probability of overall survival, progression-free survival, and nonrelapse mortality at 2 years was 72% (95% confidence interval [CI], 54% to 90%), 67% (95% CI, 49% to 85%), and 15% (95% CI, 1% to 29%), respectively.

CONCLUSION

Treatment-related mortality after reduced-intensity conditioning followed by allogeneic HSCT was low. The procedure induced molecular remissions in patients with advanced CLL. The observation of late remissions provided evidence of a graft-versus-leukemia effect.

摘要

目的

研究减低剂量预处理后的造血干细胞移植(HSCT)对晚期慢性淋巴细胞白血病(CLL)患者是否有效且耐受。

患者与方法

30例晚期B细胞CLL患者纳入本研究。采用氟达拉滨、白消安和抗胸腺细胞球蛋白进行减低剂量预处理后,患者接受来自相关供者(n = 15)或无关供者(n = 15)的移植。采用克隆特异性聚合酶链反应监测微小残留病(MRD)。

结果

中位随访2年后,23例患者存活(截至目前)。中性粒细胞和血小板植入分别发生在中位时间17.5天和15天后。17例患者(56%)观察到2至4级急性移植物抗宿主病(GVHD),21例患者(75%)观察到慢性GVHD。12例患者(40%)达到完全缓解(CR),16例患者(53%)达到部分缓解。移植后2年仍有患者出现晚期CR。对8例CR患者进行了MRD监测。所有患者均达到分子学CR。在最后一次随访时,6例患者处于持续分子学CR状态。死亡原因包括4例与治疗相关的并发症和3例疾病进展。2年时的总生存率、无进展生存率和非复发死亡率分别为72%(95%置信区间[CI],54%至90%)、67%(95%CI,49%至85%)和15%(95%CI,1%至29%)。

结论

减低剂量预处理后进行异基因HSCT的治疗相关死亡率较低。该方法可诱导晚期CLL患者出现分子学缓解。晚期缓解的观察提供了移植物抗白血病效应的证据。

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