Li Yan, Liu Kai-Qi, Gong Ben-Fa, Wang Ying, Wei Hui, Lin Dong, Liu Bing-Cheng, Zhou Chun-Lin, Wei Shu-Ning, Zhang Guang-Ji, Liu Yun-Tao, Gong Xiao-Yuan, Wang Jian-Xiang, Mi Ying-Chang
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College,State Key Laboratory of Experimental Hematology, Tianjin 300020, China,National Clinical Research Center for Blood Diseases, Tianjin 300020, China.
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College,State Key Laboratory of Experimental Hematology, Tianjin 300020, China,National Clinical Research Center for Blood Diseases, Tianjin 300020, China,Tianjin Clinical Research Center for Blood Diseases, Tianjin 300020, China,E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Feb;28(1):1-6. doi: 10.19746/j.cnki.issn.1009-2137.2020.01.001.
To investigate the efficacy and safety of arsenic trioxide combined with ATRA and chemo- therapy for treatment of relapsed acute promyelocytic leukemia (APL) patients.
The clinic data of 25 patients with relapse APL treated in our hospital from 1996 to 2013 were collected and analyzed. Among the 25 patients, 15 patients suffered first-time hematological relapse (HR), and the other 10 patients showed first-time molecular relapse (MR). The patients with first-time replase were treated with ATO+ATRA+Anthracycline re-induction chemotherapy. The clinical features, complete remission (CR) rate, overall survival (OS), disease-free survival (DFS) and adverse events after re-induction therapy were analyzed.
Fourteen of 15 hematological relapsed patients achieved the second-time hematological complete remission (CR2) after re-induction therapy except one patient died of bleeding complication during the re-induction. 8 of 14 patient showed molecular complete remission (CRm) after two cycles of therapy with this regimen. Totally, eleven out of the 14 HR patients were alive without disease till the last follow-up, and 3 of the 14 HR patients died because of bleeding complications. All of the 10 molecular relapsed patients received the second CRm after treated by the regimen. Among these 10 patients, 6 patients suffered only once relapse and continued with the molecular CR2 status, and for the other 4 patients with more than two-relapses, only 1 survived untill 89.3 months after achieved second-time CRm, and other 3 patients died because of bleeding complications.
For relapsed APL patients, the treatment with ATO+ATRA+chemotherapy regimen after relapse still shows encouraging efficacy, no matter whether or not the application of ATO in the previous regimens. In addition, patients with more than two molecular relapses show a poor prognosis.
探讨三氧化二砷联合全反式维甲酸(ATRA)及化疗治疗复发急性早幼粒细胞白血病(APL)患者的疗效及安全性。
收集并分析我院1996年至2013年收治的25例复发APL患者的临床资料。25例患者中,15例为首次血液学复发(HR),另外10例为首次分子学复发(MR)。首次复发患者采用三氧化二砷(ATO)+ATRA+蒽环类药物再诱导化疗。分析再诱导治疗后的临床特征、完全缓解(CR)率、总生存期(OS)、无病生存期(DFS)及不良事件。
15例血液学复发患者中,除1例在再诱导治疗期间死于出血并发症外,其余14例在再诱导治疗后达到第二次血液学完全缓解(CR2)。14例患者中有8例在该方案治疗两个周期后达到分子学完全缓解(CRm)。14例HR患者中,共有11例在最后一次随访时无病存活,14例HR患者中有3例因出血并发症死亡。所有10例分子学复发患者经该方案治疗后均获得第二次CRm。在这10例患者中,6例仅复发一次并持续处于分子学CR2状态,另外4例复发两次以上的患者中,只有1例在达到第二次CRm后存活至89.3个月,其他3例患者因出血并发症死亡。
对于复发APL患者,复发后采用ATO+ATRA+化疗方案治疗仍显示出令人鼓舞的疗效,无论既往方案中是否应用ATO。此外,分子学复发两次以上的患者预后较差。