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同种异体造血干细胞移植中螺旋断层调强放疗全身照射的安全性:一项前瞻性的初步研究。

Safety of total body irradiation using intensity-modulated radiation therapy by helical tomotherapy in allogeneic hematopoietic stem cell transplantation: a prospective pilot study.

机构信息

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.

出版信息

J Radiat Res. 2020 Nov 16;61(6):969-976. doi: 10.1093/jrr/rraa078.

DOI:10.1093/jrr/rraa078
PMID:32888029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7674702/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd89/7674702/ed567ccc2fe2/rraa078f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd89/7674702/ed567ccc2fe2/rraa078f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd89/7674702/ed567ccc2fe2/rraa078f1.jpg

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