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
{"title":"Splenic irradiation prior to allogeneic transplant conditioning in myelofibrosis: A pilot experience","authors":"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","doi":"10.1016/j.retram.2023.103400","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>In the era of JAK inhibitors<span><span><span><span>, allogeneic stem cell transplantation (HSCT) remains the only curative </span>treatment for patients with </span>Myelofibrosis (MF). Splenic irradiation (SI) may be used to reduce </span>spleen size and related symptoms.</span></p></div><div><h3>Methods</h3><p><span><span><span><span>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 </span>backbone based on </span>treosulfan and </span>fludarabine<span>, with post-transplant cyclophosphamide (PTCy) and </span></span>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.</p></div><div><h3>Results</h3><p><span>At transplant all patients were transfusion-dependent and had splenomegaly (median bipolar diameter by ultrasound: 20.75 cm). Overall, 12 patients had received </span>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.</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":54260,"journal":{"name":"Current Research in Translational Medicine","volume":"71 3","pages":"Article 103400"},"PeriodicalIF":3.2000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Translational Medicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452318623000247","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
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.
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.