Department of Hematology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Department of Clinical Pharmaceutics, Faculty of Pharmaceutical Sciences, Doshisha Women's College of Liberal Arts, Kyotanabe City, Japan.
Clin Lymphoma Myeloma Leuk. 2020 Dec;20(12):813-819.e1. doi: 10.1016/j.clml.2020.07.005. Epub 2020 Jul 16.
The objective of the present retrospective study was to evaluate the effect of ponatinib administration as maintenance therapy on the outcomes after allogeneic hematopoietic stem cell transplantation in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.
We retrospectively analyzed the data from 34 consecutive patients treated at our institution from January 2008 to June 2019. We had administered post-transplant tyrosine kinase inhibitors preemptively before December 2017. Thereafter, we had initiated the prophylactic use of post-transplant ponatinib. The initial ponatinib dose was 15 mg/d. Ponatinib plasma trough levels were measured using the liquid chromatography-tandem mass spectrometry method 8 days after the first administration and subsequently.
Nine patients received ponatinib maintenance. The 2-year overall survival and leukemia-free survival in the ponatinib maintenance group tended to be better than that in the non-ponatinib group (100% vs. 70.5%, P = .10; and 100% vs. 50.8%, P = .02, respectively). In the first 7 of the 9 consecutive patients, the median plasma concentration after ponatinib administration (15 mg/d) was 15.6 ng/mL (range, 4.8-23.3 ng/mL). Although the treatment schedule for 1 patient was altered because of adverse effects (elevation of serum amylase and neutropenia), ponatinib administration was continued for all the patients, except for 1 patient with molecular relapse. One patient developed a transient elevation of serum lipase. No patient presented with any arterial occlusive events.
Our results have indicated that the strategy of ponatinib maintenance after allogeneic hematopoietic stem cell transplantation is safe, efficacious, and promising.
本回顾性研究的目的是评估 ponatinib 给药作为维持疗法对费城染色体阳性急性淋巴细胞白血病患者异基因造血干细胞移植后结局的影响。
我们回顾性分析了 2008 年 1 月至 2019 年 6 月在我院接受治疗的 34 例连续患者的数据。我们在 2017 年 12 月之前预先给予了移植后酪氨酸激酶抑制剂。此后,我们开始预防性使用移植后 ponatinib。初始 ponatinib 剂量为 15mg/d。在首次给药后第 8 天和随后使用液相色谱-串联质谱法测量 ponatinib 血浆谷浓度。
9 例患者接受 ponatinib 维持治疗。ponatinib 维持组的 2 年总生存率和无白血病生存率均倾向于优于非 ponatinib 组(100%比 70.5%,P=0.10;100%比 50.8%,P=0.02)。在连续 9 例患者中的前 7 例中,ponatinib 给药(15mg/d)后的中位血浆浓度为 15.6ng/mL(范围为 4.8-23.3ng/mL)。虽然 1 例患者因不良反应(血清淀粉酶升高和中性粒细胞减少)改变了治疗方案,但除 1 例分子复发患者外,所有患者均继续接受 ponatinib 治疗。1 例患者出现血清脂肪酶一过性升高。无患者发生任何动脉闭塞事件。
我们的结果表明,异基因造血干细胞移植后 ponatinib 维持治疗策略是安全、有效和有前景的。