Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, USA. Electronic address: https://twitter.com/DianaLinMed.
Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: https://twitter.com/EricLehrer.
Radiother Oncol. 2019 Jun;135:147-152. doi: 10.1016/j.radonc.2019.03.006. Epub 2019 Mar 27.
To investigate the incidence of radiotherapy-related acute and late toxicities among patients with pro-inflammatory comorbidities.
PICOS/PRISMA/MOOSE methods were used to identify studies on PubMed and MEDLINE, 1970-2018. The following were extracted: location, cancer, sample size, age, follow-up duration, medical contraindication, treatment, and toxicity. A weighted random effects model with the DerSimonian and Laird method was used in the meta-analysis. The primary endpoint was the grade ≥ 3 acute toxicity, and the secondary endpoint was late toxicity.
There were 1137 articles screened and 18 included, assessing 621 patients. Among the 18 articles, 10 had collagen vascular disease (n = 417) and 8 had inflammatory bowel disease (n = 204). Median follow-up was 52.8 months. 457 patients received radiotherapy alone, and 153 received concurrent chemo-radiotherapy. The random effects estimate for incidence of grade ≥ 3 toxicity in collagen vascular disease patients (95% confidence interval) was 11.7% (5.4-19.6%) and 6.1% (1.4-12.6%) for acute and late toxicities, respectively. Incidence of grade ≥ 3 toxicity in inflammatory bowel disease patients was 14.0% (7.1-22.4%) and 10.2% (3.2-19.7%) for acute and late toxicities, respectively. Average grade 4 toxicity across both diseases was 1.5% and 4.5% for acute and late toxicities, respectively. Average grade 5 toxicity across both diseases was negligible (<1%).
Patients with historically accepted contraindications to radiation therapy have a 10-15% risk of any grade ≥ 3 toxicity, <5% risk of grade 4 toxicity, and <1% risk for grade 5 toxicity, suggesting that collagen vascular disease and inflammatory bowel disease are not absolute contraindications to radiotherapy.
本研究旨在调查伴有炎症性合并症的患者接受放疗后发生急性和晚期毒性的情况。
本研究通过 PICOS/PRISMA/MOOSE 方法检索 1970 年至 2018 年在 PubMed 和 MEDLINE 发表的研究。提取的内容包括:研究地点、癌症类型、样本量、年龄、随访时间、医学禁忌证、治疗方法和毒性反应。采用随机效应模型进行荟萃分析,并采用 DerSimonian 和 Laird 法进行加权处理。主要终点为≥3 级急性毒性,次要终点为晚期毒性。
共筛选出 1137 篇文章,最终纳入 18 项研究,共纳入 621 例患者。其中 10 项研究为胶原血管疾病(n=417),8 项研究为炎症性肠病(n=204)。中位随访时间为 52.8 个月。457 例患者接受单纯放疗,153 例患者接受同步放化疗。胶原血管疾病患者≥3 级毒性发生率的随机效应估计值(95%置信区间)分别为急性毒性 11.7%(5.4-19.6%)和晚期毒性 6.1%(1.4-12.6%)。炎症性肠病患者≥3 级毒性发生率分别为急性毒性 14.0%(7.1-22.4%)和晚期毒性 10.2%(3.2-19.7%)。两种疾病的平均 4 级毒性发生率分别为急性毒性 1.5%和晚期毒性 4.5%。两种疾病的平均 5 级毒性发生率可忽略不计(<1%)。
既往被认为对放疗有禁忌证的患者,发生任何级别≥3 级毒性的风险为 10%-15%,发生 4 级毒性的风险<5%,发生 5 级毒性的风险<1%,提示胶原血管疾病和炎症性肠病并不是放疗的绝对禁忌证。