医学
粘膜炎
全身照射
梅尔法兰
中性粒细胞减少症
多发性骨髓瘤
恶心
自体干细胞移植
移植
造血干细胞移植
外科
毒性
临床研究阶段
内科学
耐受性
胃肠病学
不利影响
化疗
环磷酰胺
作者
Axel Cailleteau,Philippe Maingon,Sylvain Choquet,Rémi Bourdais,Delphine Antoni,Bruno Lioure,Cyrille Hulin,Stéphanie Batard,Camille Llagostera,Valentine Guimas,Cyrille Touzeau,Philippe Moreau,Marc-André Mahé,Stéphane Supiot
标识
DOI:10.1016/j.ijrobp.2022.09.069
摘要
A second intensification is an option at first relapse in multiple myeloma (MM) after more than 36 months of initial remission. Many conditioning regimens have been tested, with or without total body irradiation (TBI). Recently, it was found that TBI could be replaced by total marrow irradiation (TMI) using helical tomotherapy, with promising results.This study was a prospective multicenter phase 1 trial that aimed to determine the maximum tolerated dose (MTD) of TMI administered in association with melphalan 140 mg/m², followed by autologous stem cell transplantation as consolidation at first relapse in MM. Four dose levels were explored: 8 Gy, 10 Gy, 12 Gy, and 14 Gy. The dose-limiting toxicity (DLT) was defined as grade 4 neutropenia >15 days, grade 4 thrombopenia >28 days, and all other grade 4 nonhematologic toxic effects except nausea, vomiting, alopecia, mucositis, and reaction to autologous stem cell infusion.Thirteen patients were included; only 1 DLT at the third escalated dose level (12 Gy) was observed, whereas 1 patient was treated at 14 Gy with no adverse events. The MTD was not reached. The rate of acute toxicity was low: 38% of grade 3-4 diarrhea, mucositis, or unexplained fever. Regarding the lungs, the mean dose administered was systematically less than 8 Gy. After a median follow-up of 55 months, 70% of participants were alive. Of these 13 patients, 38.5% were in very good partial response and 30.8% were in complete response. Three of them were progression-free. Six patients were long survivors, still alive after 55 months of follow-up.Total marrow irradiation provides good results with a good tolerance profile at first relapse in MM and makes it possible to increase the dose delivered to the planning target volume while sparing organs at risk. This technique could be discussed for all regimens before auto- or allo-stem cell rescue when TBI is required.
科研通智能强力驱动
Strongly Powered by AbleSci AI