Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
Division of Radiation Oncology, Department of Radiology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
J Radiat Res. 2020 Nov 16;61(6):969-976. doi: 10.1093/jrr/rraa078.
Total body irradiation using intensity-modulated radiation therapy total body irradiation (IMRT-TBI) by helical tomotherapy in allogeneic hematopoietic stem cell transplantation (allo-HSCT) allows for precise evaluation and adjustment of radiation dosage. We conducted a single-center pilot study to evaluate the safety of IMRT-TBI for allo-HSCT recipients. Patients with hematological malignancies in remission who were scheduled for allo-HSCT with TBI-based myeloablative conditioning were eligible. The primary endpoint was the incidence of adverse events (AEs). Secondary endpoints were engraftment rate, overall survival, relapse rate, non-relapse mortality, and the incidence of acute and chronic graft-versus-host disease (aGVHD and cGVHD, respectively). Between July 2018 and November 2018, ten patients were recruited with a median observation duration of 571 days after allo-HSCT (range, 496-614). D80% for planning target volume (PTV) in all patients was 12.01 Gy. Average D80% values for lungs, kidneys and lenses (right/left) were 7.50, 9.03 and 4.41/4.03 Gy, respectively. Any early AEs (within 100 days of allo-HSCT) were reported in all patients. Eight patients experienced oral mucositis and gastrointestinal symptoms. One patient experienced Bearman criteria grade 3 regimen-related toxicity (kidney and liver). All cases achieved neutrophil engraftment. There was no grade III-IV aGVHD or late AE. One patient died of sinusoidal obstruction syndrome 67 days after allo-HSCT. The remaining nine patients were alive and disease-free at final follow-up. Thus, IMRT-TBI was well tolerated in terms of early AEs in adult patients who underwent allo-HSCT; this warrants further study with longer observation times to monitor late AEs and efficacy.
采用螺旋断层放疗全身调强放疗(IMRT-TBI)进行异基因造血干细胞移植(allo-HSCT)中的全身照射可精确评估和调整辐射剂量。我们进行了一项单中心的试点研究,以评估 IMRT-TBI 用于 allo-HSCT 受者的安全性。符合条件的患者为处于缓解期的血液系统恶性肿瘤患者,计划接受基于全身照射的 TBI 清髓性预处理 allo-HSCT。主要终点是不良事件(AE)的发生率。次要终点是植入率、总生存率、复发率、非复发死亡率以及急性和慢性移植物抗宿主病(aGVHD 和 cGVHD)的发生率。2018 年 7 月至 2018 年 11 月期间,共纳入 10 例患者,allo-HSCT 后中位观察时间为 571 天(范围 496-614 天)。所有患者的计划靶区(PTV)D80%为 12.01Gy。肺、肾脏和晶状体(右/左)的平均 D80%值分别为 7.50、9.03 和 4.41/4.03Gy。所有患者均报告了任何早期 AE(allo-HSCT 后 100 天内)。8 例患者发生口腔黏膜炎和胃肠道症状。1 例患者发生 Bearman 标准 3 级与治疗相关的毒性(肾和肝)。所有病例均实现中性粒细胞植入。无 3-4 级 aGVHD 或晚期 AE。1 例患者在 allo-HSCT 后 67 天死于窦阻塞综合征。其余 9 例患者在最终随访时存活且无疾病。因此,在接受 allo-HSCT 的成年患者中,IMRT-TBI 在早期 AE 方面具有良好的耐受性;这需要进一步研究更长的观察时间来监测晚期 AE 和疗效。