Schneider Ralf A, Schultze Jürgen, Jensen Johannes M, Hebbinghaus Dieter, Galalae Razvan, Kimmig Bernhard N
Department of Radiotherapy (Radiation Oncology), University Hospital of Schleswig-Holstein, Campus Kiel (UHK), Kiel, Germany.
Strahlenther Onkol. 2007 Oct;183(10):545-51. doi: 10.1007/s00066-007-1656-7.
To analyze lung complications after allogeneic or autologous transplantation following total-body irradiation (TBI) with compensators, so-called sIMRT (static intensity-modulated radiotherapy).
Between 1983 and 1998, 257 patients with different hematologic malignancies underwent TBI in six fractions to a total dose of 12 Gy within 3 consecutive days (212 with 11 Gy lung dose) prior to allogeneic (n=174) or autologous (n=83) transplantation. 40 patients were <16 years of age. Minimum follow-up time was 5 years. Median follow-up period was 110 months (13-231 months).
5-year survival rate was 47.9%, 5-year tumor-related mortality 23%, 5-year treatment-related mortality 29.2% (12 Gy lung dose: 53.3%+/-14.6%, 11 Gy: 24.1%+/-5.7%). Interstitial pneumonitis (IP) developed in 28 of 257 patients (10.9% +/- 3.8%). IP incidences in the allogeneic and autologous groups were 14.4% (+/-5.6%) and 3.6% (0-7.6%), respectively. IP incidences with 12/11 Gy lung dose were 22% (+/-12%)/8.5% (+/-3.7%). IP mortality was 9.3% (+/-3.6%). 13 of 28 patients with IP had a cytomegalovirus infection, five an acute graft-versus-host disease grade IV of the lungs. IP incidences with 12/11 Gy lung dose were 25% (9-50%)/4.2% (0.2-19.1%) in patients <16 years, and 20.7% (9.4-37.4%) and 13.3% (+/-6.5%) in older patients after allogeneic transplantation.
Compensator-generated static intensity-modulated TBI with a total dose of 12 Gy and a lung dose of 11 Gy is a modern and comfortable treatment with moderate lung toxicity, small dose inhomogeneities and little setup failure before transplantation. Especially patients <16 years of age benefit from lung dose reduction.
分析使用补偿器进行全身照射(TBI)(即所谓的静态调强放疗,sIMRT)后同种异体或自体移植后的肺部并发症。
1983年至1998年间,257例不同血液系统恶性肿瘤患者在同种异体移植(n = 174)或自体移植(n = 83)前,连续3天内分6次接受TBI,总剂量为12 Gy(212例肺部剂量为11 Gy)。40例患者年龄小于16岁。最短随访时间为5年。中位随访期为110个月(13 - 231个月)。
5年生存率为47.9%,5年肿瘤相关死亡率为23%,5年治疗相关死亡率为29.2%(肺部剂量12 Gy:53.3%±14.6%,11 Gy:24.1%±5.7%)。257例患者中有28例发生间质性肺炎(IP)(10.9%±3.8%)。同种异体组和自体组的IP发生率分别为14.4%(±5.6%)和3.6%(0 - 7.6%)。肺部剂量为12/11 Gy时的IP发生率分别为22%(±12%)/8.5%(±3.7%)。IP死亡率为9.3%(±3.6%)。28例IP患者中有13例发生巨细胞病毒感染,5例发生肺部急性移植物抗宿主病IV级。年龄小于16岁患者肺部剂量为12/11 Gy时的IP发生率分别为25%(9 - 50%)/4.2%(0.2 - 19.1%),同种异体移植后老年患者的发生率分别为20.7%(9.4 - 37.4%)和13.3%(±6.5%)。
总剂量为12 Gy、肺部剂量为11 Gy的补偿器产生的静态调强TBI是一种现代且舒适的治疗方法,肺部毒性适中,剂量不均匀性小,移植前设置失败率低。尤其是年龄小于16岁的患者受益于肺部剂量的降低。