Splenic irradiation prior to allogeneic transplant conditioning in myelofibrosis: A pilot experience

IF 3.2 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Current Research in Translational Medicine Pub Date : 2023-07-01 DOI:10.1016/j.retram.2023.103400
Edoardo Campodonico , Elisabetta Xue , Simona Piemontese , Anna Chiara , Alessandro Bruno , Gianluca Scorpio , Rosamaria Nitti , Daniele Sannipoli , Giorgio Orofino , Paolo Fiore , Maria Chiara Quattrocchi , Elisa Diral , Daniela Clerici , Francesca Farina , Consuelo Corti , Francesca Lunghi , Maria Teresa Lupo-Stanghellini , Nadia Di Muzio , Fabio Ciceri , Raffaella Greco , Jacopo Peccatori
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Abstract

Introduction

In the era of JAK inhibitors, allogeneic stem cell transplantation (HSCT) remains the only curative treatment for patients with Myelofibrosis (MF). Splenic irradiation (SI) may be used to reduce spleen size and related symptoms.

Methods

We conducted a retrospective analysis on 14 patients with MF who underwent HSCT with SI from any donor source at our center between June 2016 and March 2021. All patients received a conditioning backbone based on treosulfan and fludarabine, with post-transplant cyclophosphamide (PTCy) and sirolimus as graft-versus-host disease (GvHD) prophylaxis. Patients received SI with 10 Gy involved-field radiotherapy in five 2-Gy fractions over the course of a week prior to the beginning of conditioning.

Results

At transplant all patients were transfusion-dependent and had splenomegaly (median bipolar diameter by ultrasound: 20.75 cm). Overall, 12 patients had received ruxolitinib prior to transplant. Re-evaluation of spleen dimensions was available for 13 patients: median splenic bipolar diameter after at least 3 months from transplant decreased by a median of 25%. With a median post-transplant follow-up of 25 months, 6 patients remain in CR with full-donor chimerism, 3 patients died due to NRM. Overall, 4 patients relapsed. At last follow-up, nine patients are currently alive and achieved transfusion-independence.

Conclusions

In a small cohort of mostly ruxolitinib pre-treated patients, SI and treosulfan-based conditioning appeared a safe and effective tool to reduce spleen dimensions and ameliorate symptoms. Future prospective studies with adequate sample size are warranted to further investigate the usefulness and safety of this approach in MF.

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骨髓纤维化异基因移植前脾照射:一项试点经验。
引言:在JAK抑制剂时代,异基因干细胞移植(HSCT)仍然是骨髓纤维化(MF)患者的唯一治疗方法。脾脏照射(SI)可用于减少脾脏大小和相关症状。方法:我们对2016年6月至2021年3月期间在我们中心接受任何供体来源的SI HSCT的14名MF患者进行了回顾性分析。所有患者均接受了以曲磺芬和氟达拉滨为基础的调节骨干,移植后环磷酰胺(PTCy)和西罗莫司作为移植物抗宿主病(GvHD)的预防药物。在开始调理前的一周内,患者接受了10 Gy的SI,包括五次2 Gy的现场放射治疗。结果:在移植时,所有患者都是输血依赖性的,并有脾肿大(超声显示双极直径中位数:20.75cm)。总的来说,12名患者在移植前接受了鲁索利替尼治疗。对13名患者的脾脏尺寸进行了重新评估:移植后至少3个月,脾脏双极直径中位数下降了25%。中位移植后随访25个月,6名患者仍处于完全供体嵌合状态,3名患者死于NRM。总的来说,4名患者复发。在最后的随访中,有9名患者目前还活着,并实现了输血独立性。结论:在一小群主要是鲁索利替尼预治疗的患者中,基于SI和treosulfan的调理似乎是一种安全有效的工具,可以缩小脾脏尺寸并改善症状。未来有足够样本量的前瞻性研究有必要进一步研究这种方法在MF中的有用性和安全性。
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来源期刊
Current Research in Translational Medicine
Current Research in Translational Medicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
7.00
自引率
4.90%
发文量
51
审稿时长
45 days
期刊介绍: Current Research in Translational Medicine is a peer-reviewed journal, publishing worldwide clinical and basic research in the field of hematology, immunology, infectiology, hematopoietic cell transplantation, and cellular and gene therapy. The journal considers for publication English-language editorials, original articles, reviews, and short reports including case-reports. Contributions are intended to draw attention to experimental medicine and translational research. Current Research in Translational Medicine periodically publishes thematic issues and is indexed in all major international databases (2017 Impact Factor is 1.9). Core areas covered in Current Research in Translational Medicine are: Hematology, Immunology, Infectiology, Hematopoietic, Cell Transplantation, Cellular and Gene Therapy.
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