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对骨髓移植后复发的日本慢性粒细胞白血病患者进行有效且安全的干扰素治疗。名古屋血液与骨髓移植小组。

Effective and safe interferon treatment for Japanese patients with chronic myelogenous leukemia relapse after bone marrow transplantation. The Nagoya Blood and Marrow Transplantation Group.

作者信息

Sao H, Kato C, Kitaori K, Adachi T, Yano K, Kobayashi M, Kojima H, Tanimoto M, Hirabayashi N, Minami S, Yamada H, Morishita G Y, Morishima Y, Kodera Y

机构信息

Department of Hematology, Meitetsu Hospital, Nagoya, Japan.

出版信息

Int J Hematol. 2000 Aug;72(2):237-42.

Abstract

The purpose of this study was to assess the efficacy and safety of interferon (IFN) treatment in patients with a relapse of chronic myelogenous leukemia (CML) after bone marrow transplantation in Japan. Accordingly, we retrospectively analyzed the results obtained from 8 patients treated with IFN by the Nagoya Blood and Marrow Transplantation Group. One of 3 patients with hematologic relapse and all 5 patients with cytogenetic relapse achieved complete cytogenetic response (CCR). The median time to achieve CCR was 8 months (range, 3-16 months). One patient relapsed 9 months after starting IFN and died of blast crisis. CCR was maintained for a median duration of 47 months (range, 9-79 months) in the remaining 5 patients. The median duration of survival of these 5 patients after starting IFN was 58 months (range, 12-89 months). At the time of this report, 2 patients who did not attain CCR have survived for 81 months and 142 months after starting IFN, respectively. During IFN treatment, 1 patient showed a transient deterioration of chronic graft-versus-host disease, and no treatment-related deaths were observed. These results suggest that treatment with IFN for CML patients who relapse after bone marrow transplantation is effective and safe. A prospective study to compare IFN with donor lymphocyte infusion is necessary to establish the optimal strategy for the treatment of CML patients who relapse after bone marrow transplantation.

摘要

本研究的目的是评估在日本接受骨髓移植后慢性粒细胞白血病(CML)复发患者中干扰素(IFN)治疗的疗效和安全性。因此,我们回顾性分析了名古屋血液和骨髓移植组对8例接受IFN治疗患者的结果。3例血液学复发患者中的1例以及所有5例细胞遗传学复发患者均获得了完全细胞遗传学缓解(CCR)。达到CCR的中位时间为8个月(范围3 - 16个月)。1例患者在开始IFN治疗9个月后复发,并死于原始细胞危象。其余5例患者的CCR维持中位持续时间为47个月(范围9 - 79个月)。这5例患者开始IFN治疗后的中位生存时间为58个月(范围12 - 89个月)。在本报告时,2例未达到CCR的患者在开始IFN治疗后分别存活了81个月和142个月。在IFN治疗期间,1例患者慢性移植物抗宿主病出现短暂恶化,未观察到与治疗相关的死亡。这些结果表明,对于骨髓移植后复发的CML患者,IFN治疗是有效且安全的。有必要进行一项前瞻性研究,比较IFN与供体淋巴细胞输注,以确立骨髓移植后复发的CML患者的最佳治疗策略。

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