Department of Radiation Oncology, College of Medicine, University of Florida, Jacksonville, Florida.
Department of Radiation Oncology, College of Medicine, University of Florida, Jacksonville, Florida.
Int J Radiat Oncol Biol Phys. 2020 Apr 1;106(5):968-976. doi: 10.1016/j.ijrobp.2019.12.036. Epub 2020 Jan 25.
This study aimed to report on the institutional outcomes after proton therapy for pelvic rhabdomyosarcoma (RMS).
Thirty-one children (≤21 years old) with group III pelvic RMS were enrolled on a prospective outcome study and treated between 2007 and 2018. Patients with vaginal/cervical RMS were excluded. The median age was 2.6 years. Twenty-four patients had embryonal RMS. At diagnosis, the median tumor volume was 185 cm and the median maximum diameter was 9.4 cm. Seven patients had N1 disease. Nineteen and 12 patients received European Pediatric Soft Tissue Sarcoma Study Group- and Children's Oncology Group-based chemotherapy, respectively. Fourteen patients underwent resection of the primary tumor after induction chemotherapy, including 6 patients who had a total cystectomy. The median radiation dose was 50.4 Gy relative biological effectiveness.
With a median follow-up of 4.2 years, the 5-year local control, progression-free survival, and overall survival rates were 83%, 80%, and 84%, respectively. Patients <3 years old had better local control (100% vs 68%; P = .02), and patients with embryonal histology had better survival (96% vs 54%; P = .02). No other factors were significantly associated with disease control or survival. Specifically, no statistically significant difference was observed in local control, progression-free survival, or overall survival when comparing patients who underwent biopsy versus gross total resection (75% vs 93%, 68% vs 93%, 75% vs 93%, respectively). Excluding patients who underwent cystectomy, urinary toxicity was limited to 2 patients with nocturnal enuresis. Exploratory surgery to address a persistent mass or thickened bladder wall after radiation was the most common source of serious toxicity.
This cohort of young children with large pelvic tumors treated with proton therapy demonstrates similar local control with less toxicity than historic reports. Functional bladder preservation is possible in most patients. Exploratory biopsy in the 18 months after radiation should be approached with caution.
本研究旨在报告质子治疗盆腔横纹肌肉瘤(RMS)的机构治疗结果。
31 名(≤21 岁)患有 III 期盆腔 RMS 的儿童参与了一项前瞻性结局研究,并于 2007 年至 2018 年接受治疗。排除阴道/宫颈 RMS 患者。中位年龄为 2.6 岁。24 例患者患有胚胎性 RMS。诊断时,肿瘤体积中位数为 185cm³,最大直径中位数为 9.4cm。7 例患者患有 N1 疾病。19 名和 12 名患者分别接受了欧洲儿科软组织肉瘤研究组和儿童肿瘤组为基础的化疗。14 名患者在诱导化疗后行原发性肿瘤切除术,其中 6 名患者行全膀胱切除术。中位放疗剂量为 50.4Gy 相对生物效应。
中位随访时间为 4.2 年,5 年局部控制率、无进展生存率和总生存率分别为 83%、80%和 84%。<3 岁的患者局部控制更好(100%比 68%;P=0.02),胚胎组织学患者的生存率更高(96%比 54%;P=0.02)。其他因素与疾病控制或生存均无显著相关性。具体而言,在比较活检与大体全切除的患者时,在局部控制、无进展生存率或总生存率方面未观察到统计学显著差异(75%比 93%、68%比 93%、75%比 93%)。不包括行膀胱切除术的患者,尿液毒性仅限于 2 例夜间遗尿。放疗后持续肿块或膀胱壁增厚的探索性手术是最常见的严重毒性来源。
本队列中接受质子治疗的年轻、骨盆大肿瘤患儿的局部控制效果与历史报告相似,但毒性更小。大多数患者的膀胱功能可保留。在放疗后 18 个月内进行探索性活检时应谨慎。