Kapoor Jyotsna, Mirgh Sumeet Prakash, Agrawal Narendra, Khushoo Vishvdeep, Tejwani Narender, Singh Reema, Mehta Pallavi, Bhurani Dinesh, Ahmed Rayaz
Department of Hematology and BMT Unit, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, Delhi 110085 India.
Present Address: Adult Hematolymphoid and BMT unit, Department of Medical Oncology, Tata Memorial Hospital ACTREC, Navi Mumbai, India.
Indian J Hematol Blood Transfus. 2022 Apr;38(2):394-402. doi: 10.1007/s12288-021-01478-x. Epub 2021 Sep 3.
Management of Acute Promyelocytic Leukemia (APML) has improved drastically after the introduction of ATRA (-trans-retinoic acid) and Arsenic trioxide (ATO). The use of APML-4 protocol has shown its effectiveness in Australian population. We know that high-risk APML represents a subset with poor outcomes. There is scarcity of literature reporting outcomes of high-risk APML from India. We present a 5-year retrospective analysis of the safety and efficacy of APML-4 protocol in our 28 high-risk patients. Of 28 patients, there were 8(28.5%) early deaths; all 20 patients (100%) who were alive achieved hematologic complete remission post-induction and molecular complete remission post-consolidation. The 5-year disease free survival, failure free survival (FFS) and overall survival were 100%, 69% and 69% respectively. Factors affecting FFS were age > 45 years ( = 0.008), baseline ECOG-PS > 1 ( < 0.0001), and grade 3-4 differentiation syndrome ( = 0.008). APML-4 protocol in high-risk patients is capable of achieving excellent disease control with less toxicities. While early induction deaths in high-risk APML still remain an issue, protocol modifications (for steroid and anthracyclines) are important considering high frequency of infections at baseline and during induction therapy in our population.
在引入全反式维甲酸(ATRA)和三氧化二砷(ATO)后,急性早幼粒细胞白血病(APML)的治疗有了显著改善。APML-4方案在澳大利亚人群中已显示出其有效性。我们知道,高危APML是一个预后较差的亚组。目前缺乏来自印度的关于高危APML预后的文献报道。我们对28例高危患者采用APML-4方案的安全性和有效性进行了为期5年的回顾性分析。28例患者中,有8例(28.5%)早期死亡;所有20例存活患者(100%)诱导后均达到血液学完全缓解,巩固后达到分子学完全缓解。5年无病生存率、无失败生存率(FFS)和总生存率分别为100%、69%和69%。影响FFS的因素包括年龄>45岁(P = 0.008)、基线ECOG-PS>1(P<0.0001)和3-4级分化综合征(P = 0.008)。APML-4方案在高危患者中能够实现良好的疾病控制且毒性较小。虽然高危APML的早期诱导死亡仍然是一个问题,但考虑到我们人群中基线和诱导治疗期间感染的高发生率,对方案进行修改(针对类固醇和蒽环类药物)很重要。