Outcomes and patterns of relapse with ponatinib-based therapy in patients with chronic myeloid leukemia in myeloid blast phase.

IF 2.2 4区 医学 Q3 HEMATOLOGY
Omer Karrar, Hagop Kantarjian, Fadi G Haddad, Roberta S Azevedo, Ghayas Issa, Farhad Ravandi, Koji Sasaki, Jayastu Senapati, Hussein Abbas, Sara Dellasala, Elias Jabbour, Nicholas J Short
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引用次数: 0

Abstract

We analyzed 76 patients who received a ponatinib-based regimen, either as monotherapy or in combination with chemotherapy, for chronic myeloid leukemia in myeloid blast phase (CML-MBP). The rate of morphological remission with or without count recovery (i.e. overall response rate [ORR]) was 49%. Patients who received a ponatinib-based regimen as their first therapy for CML-MBP had better ORR than those received ponatinib as salvage (60% versus 27%, respectively; p = 0.006). ORR was also higher with ponatinib combination therapy than monotherapy (54% versus 29%, respectively; p = 0.06). For the entire cohort, the median RFS and OS were 11.9 and 8.5 months, respectively. Responding patients who underwent allogeneic HSCT had superior outcomes to those who did not (2-year OS 79% versus 38%, respectively; p = 0.05). After ponatinib failure, outcomes were dismal (median OS: 3.9 months). Ponatinib-based regimens are effective in CML-MBP, especially when used as first therapy and in combination with chemotherapy, followed by HSCT.

以波纳替尼为基础的治疗在髓细胞期慢性髓性白血病患者的复发的结果和模式。
我们分析了76例接受以波纳替尼为基础的方案的患者,无论是作为单一治疗还是联合化疗,治疗髓细胞期慢性髓性白血病(CML-MBP)。无论有无计数恢复,形态学缓解率(即总有效率[ORR])为49%。接受以波纳替尼为基础的方案作为CML-MBP首次治疗的患者的ORR优于接受波纳替尼作为挽救性治疗的患者(分别为60%对27%;p = 0.006)。波纳替尼联合治疗的ORR也高于单药治疗(分别为54%对29%;p = 0.06)。对于整个队列,中位RFS和OS分别为11.9个月和8.5个月。接受同种异体造血干细胞移植的患者预后优于未接受移植的患者(2年生存率分别为79%和38%;p = 0.05)。波纳替尼失败后,结果令人沮丧(中位OS: 3.9个月)。以ponatinib为基础的方案对CML-MBP有效,特别是当作为第一次治疗和与化疗联合使用时,随后进行HSCT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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