Shaikh Mohammad Usman, Ali Natasha, Karim Farheen, Raheem Ahmed, Sarwar Shahzad
Department of Pathology and Laboratory Medicine/Oncology, Aga Khan University Karachi, Pakistan.
New Cross Hospital, Royal Wolverhampton NHS Trust UK.
Am J Blood Res. 2020 Aug 25;10(4):82-89. eCollection 2020.
Acute promyelocytic leukemia (APL) is a unique subtype of acute myeloid leukemia with characteristic morphology and clinical features. Early mortality rate of 30% has been reported in developed countries despite prompt initiation of treatment. We have previously reported an early induction mortality of approximately 62% in our cohort. Based on this mortality rate, we made changes in our treatment protocol. The objective of this follow-up study was to report the early induction mortality and overall survival of patients with APL after incorporating changes in chemotherapy and supportive care regimen.
This was a prospective descriptive study conducted at Aga Khan University Karachi, Pakistan from October 2012 till October 2019. Data of patients included clinical features, morphological findings, cytogenetic and PCR studies, cytotoxic protocols, overall outcome and causes of early induction mortality. The changes in treatment protocol included prophylactic infusion of fresh frozen plasma, dexamethasone therapy and other changes in supportive care regimen. Results were recorded as frequencies and percentages. Statistical Package for the Social Sciences version 19.0 (SPSS Inc., Chicago, IL, USA) was used to analyze patient's data. Survival curves were calculated using the Kaplan-Meier method.
During the study period, total of 447 patients presented with acute myeloid leukemia at our institution out of which 40 patients were diagnosed with acute promyelocytic leukemia (9%). Out of these 40 patients 24 were males and 16 were females. The median age was 37 years. Twenty-five patients were in low risk group whereas 15 were high-risk. Differentiation syndrome was seen in 14 patients. As a part of induction chemotherapy, 13 patients received only ATRA because they were not eligible for chemotherapy and 17 patients received a combination of ATRA and anthracycline. Among the remaining patients, four received ATRA, arsenic and anthracycline while two received ATRA and arsenic only. Four patients did not receive any treatment because of rapid deterioration of clinical condition and death. The overall survival was 65% and early induction mortality was 30%.
The early induction mortality decreased to 30% from 62% in this study and the overall survival was 65%. With the introduction of prophylactic infusion of fresh frozen plasma, dexamethasone and appropriate supportive treatment during the induction chemotherapy, we were able to improve the induction mortality and overall survival of patients.
急性早幼粒细胞白血病(APL)是急性髓系白血病的一种独特亚型,具有特征性的形态学和临床特征。尽管发达国家在治疗开始后立即进行了治疗,但早期死亡率仍报告为30%。我们之前报告过我们队列中的早期诱导死亡率约为62%。基于这一死亡率,我们对治疗方案进行了调整。这项随访研究的目的是报告在化疗和支持治疗方案发生变化后,APL患者的早期诱导死亡率和总生存率。
这是一项前瞻性描述性研究,于2012年10月至2019年10月在巴基斯坦卡拉奇的阿迦汗大学进行。患者数据包括临床特征、形态学检查结果、细胞遗传学和聚合酶链反应研究、细胞毒性方案、总体结局以及早期诱导死亡原因。治疗方案的变化包括预防性输注新鲜冰冻血浆、地塞米松治疗以及支持治疗方案的其他变化。结果以频率和百分比记录。使用社会科学统计软件包第19.0版(SPSS公司,美国伊利诺伊州芝加哥)分析患者数据。采用Kaplan-Meier方法计算生存曲线。
在研究期间,我们机构共有447例急性髓系白血病患者就诊,其中40例被诊断为急性早幼粒细胞白血病(9%)。在这40例患者中,24例为男性,16例为女性。中位年龄为37岁。25例患者为低风险组,15例为高风险组。14例患者出现分化综合征。作为诱导化疗的一部分,13例患者仅接受全反式维甲酸(ATRA)治疗,因为他们不符合化疗条件,17例患者接受了ATRA和蒽环类药物联合治疗。在其余患者中,4例接受了ATRA、砷剂和蒽环类药物治疗,2例仅接受了ATRA和砷剂治疗。4例患者因临床状况迅速恶化和死亡未接受任何治疗。总生存率为65%,早期诱导死亡率为30%。
本研究中早期诱导死亡率从62%降至30%,总生存率为65%。通过在诱导化疗期间引入预防性输注新鲜冰冻血浆、地塞米松和适当的支持治疗,我们能够提高患者的诱导死亡率和总生存率。