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
Charité Campus Virchow Klinium, Berlin, Germany.
J Clin Oncol. 2003 Jul 15;21(14):2747-53. doi: 10.1200/JCO.2003.12.011.
To study whether hematopoietic stem-cell transplantation (HSCT) after reduced-intensity conditioning is effective and tolerable in patients with advanced chronic lymphocytic leukemia (CLL).
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.
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.
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.
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。
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)。
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%)。
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。