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140例异基因骨髓移植后复发恶性肿瘤患者的供体白细胞输注

Donor leukocyte infusions in 140 patients with relapsed malignancy after allogeneic bone marrow transplantation.

作者信息

Collins R H, Shpilberg O, Drobyski W R, Porter D L, Giralt S, Champlin R, Goodman S A, Wolff S N, Hu W, Verfaillie C, List A, Dalton W, Ognoskie N, Chetrit A, Antin J H, Nemunaitis J

机构信息

Texas Oncology, PA, Dallas, USA.

出版信息

J Clin Oncol. 1997 Feb;15(2):433-44. doi: 10.1200/JCO.1997.15.2.433.

Abstract

PURPOSE

Recipients of allogeneic bone marrow transplants (BMTs) who have relapsed may attain complete remissions when treated with transfusions of leukocytes obtained from the original bone marrow donor. We performed a retrospective study to characterize better this new treatment modality.

PATIENTS AND METHODS

We surveyed 25 North American BMT programs regarding their use of donor leukocyte infusions (DLI). Detailed forms were used to gather data regarding the original BMT, relapse, DLI, response to DLI, complications of DLI, and long-term follow-up evaluation. Reports of 140 patients were thus available for analysis.

RESULTS

Complete responses were observed in 60% (95% confidence interval [CI], 51.9% to 68.1%) of chronic myelogenous leukemia (CML) patients who received DLI and did not receive pre-DLI chemotherapy; response rates were higher in patients with cytogenetic and chronic-phase relapse (75.7%; 95% CI, 68.2% to 83.2%) than in patients with accelerated-phase (33.3%; 95% CI, 19.7% to 46.9%) or blastic-phase (16.7%; 95% CI, 1.9% to 31.9%) relapse. The actuarial probability of remaining in complete remission at 2 years was 89.6%. Complete remission rates in acute myelogenous leukemia (AML) (n = 39) and acute lymphocytic leukemia (ALL) (n = 11) patients who had not received pre-DLI chemotherapy were 15.4% (95% CI, 9.6% to 21.2%) and 18.2% (95% CI, 6.6% to 29.8%), respectively. Complete remissions were also observed in two of four assessable myeloma patients and two of five assessable myelodysplasia patients. Complications of DLI included acute graft-versus-host disease (GVHD) (60%; 95% CI, 51.4% to 68.6%), chronic GVHD (60.7%; 95% CI, 50.3% to 71.1%), and pancytopenia (18.6%; 95% CI, 12.2% to 25.0%). Pre-DLI characteristics predictive of complete response in CML patients were post-BMT chronic GVHD, pre-DLI disease status of chronic phase, and time interval between BMT to DLI less than 2 years. Acute and chronic GVHD post-DLI were highly correlated with disease response (P < .00001).

CONCLUSION

DLI results in complete remissions in a high percentage of patients with relapsed chronic-phase CML. Complete remissions are observed less frequently in patients with advanced CML and acute leukemia. GVHD and pancytopenia occur commonly; GVHD is highly correlated with response.

摘要

目的

接受异基因骨髓移植(BMT)后复发的患者,接受来自原骨髓供体的白细胞输注治疗时,可能会实现完全缓解。我们进行了一项回顾性研究,以更好地描述这种新的治疗方式。

患者与方法

我们就北美25个BMT项目使用供体白细胞输注(DLI)的情况进行了调查。使用详细表格收集有关原始BMT、复发、DLI、对DLI的反应、DLI的并发症以及长期随访评估的数据。由此获得了140例患者的报告用于分析。

结果

接受DLI且未接受DLI前化疗的慢性粒细胞白血病(CML)患者中,60%(95%置信区间[CI],51.9%至68.1%)观察到完全缓解;细胞遗传学和慢性期复发的患者缓解率(75.7%;95%CI,68.2%至83.2%)高于加速期(33.3%;95%CI,19.7%至46.9%)或急变期(16.7%;95%CI,1.9%至31.9%)复发的患者。2年时持续完全缓解的精算概率为89.6%。未接受DLI前化疗的急性髓细胞白血病(AML)(n = 39)和急性淋巴细胞白血病(ALL)(n = 11)患者的完全缓解率分别为15.4%(95%CI,9.6%至21.2%)和18.2%(95%CI,6.6%至29.8%)。在4例可评估的骨髓瘤患者中有2例以及5例可评估的骨髓增生异常综合征患者中有2例也观察到完全缓解。DLI的并发症包括急性移植物抗宿主病(GVHD)(60%;95%CI,51.4%至68.6%)、慢性GVHD(60.7%;95%CI,50.3%至71.1%)和全血细胞减少(18.6%;95%CI,12.2%至25.0%)。CML患者中预测完全缓解的DLI前特征为BMT后慢性GVHD、DLI前慢性期疾病状态以及BMT至DLI的时间间隔小于2年。DLI后的急性和慢性GVHD与疾病反应高度相关(P <.00001)。

结论

DLI可使高比例复发的慢性期CML患者实现完全缓解。晚期CML和急性白血病患者中完全缓解较少见。GVHD和全血细胞减少常见;GVHD与反应高度相关。

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