Li Xingxin, Shi Jun, Wang Min, Nie Neng, Shao Yingqi, Ge Meili, Huang Jinbo, Huang Zhendong, Zhang Jing, Zheng Yizhou
Severe Aplastic Anemia Studying Program, State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, PR China.
Acta Haematol. 2015;134(3):138-45. doi: 10.1159/000370097. Epub 2015 Apr 24.
Clinical and experimental evidence suggests an immune-mediated pathophysiology in subjects with lower-risk myelodysplastic syndromes (MDS) in whom immunosuppressive therapy may be effective. The novel immunosuppressive strategy of cyclosporine A (CsA) alternately combined with levamisole (LMS; CsA + LMS regimen) can dramatically improve the response rate and survival in aplastic anemia from those of our previous study. Herein, we retrospectively analyzed the data of 89 lower-risk MDS patients who received the CsA + LMS regimen. A total of 63 patients (70.8%) achieved either complete remission or hematological improvement at 4 months. Overall, 51, 41 and 19 patients had erythroid, platelet and neutrophil responses, respectively. Following the CsA + LMS regimen, 6 patients progressed to more advanced MDS at a median interval of 5 months (range, 3-42 months). The estimated 24-month progression-free survival was 82.2% (95% CI, 72.84-91.56) for all patients. Within the median follow-up of 18.5 months (range, 7.0-61.0), 6 patients died. In conclusion, the CsA + LMS regimen alleviated cytopenias and improved survival and freedom from evolution, suggesting that it could be reserved as an alternative choice for lower-risk MDS.
临床和实验证据表明,免疫介导的病理生理学在低危骨髓增生异常综合征(MDS)患者中存在,免疫抑制治疗对这类患者可能有效。环孢素A(CsA)与左旋咪唑交替联合使用的新型免疫抑制策略(CsA + LMS方案)可显著提高再生障碍性贫血的缓解率和生存率,优于我们之前研究中的方案。在此,我们回顾性分析了89例接受CsA + LMS方案治疗的低危MDS患者的数据。共有63例患者(70.8%)在4个月时达到完全缓解或血液学改善。总体而言,分别有51例、41例和19例患者出现红系、血小板和中性粒细胞反应。接受CsA + LMS方案治疗后,6例患者进展为更晚期的MDS,中位间隔时间为5个月(范围3 - 42个月)。所有患者的估计24个月无进展生存率为82.2%(95%CI,72.84 - 91.56)。在中位随访18.5个月(范围7.0 - 61.0)内,6例患者死亡。总之,CsA + LMS方案减轻了血细胞减少,提高了生存率并延缓了病情进展,表明它可作为低危MDS的一种替代选择。