Department of Radiation Oncology, UT MD Anderson Cancer Center, Houston, Texas.
Department of GI Medical Oncology, UT MD Anderson Cancer Center, Houston, Texas.
Cancer Med. 2018 Oct;7(10):4880-4892. doi: 10.1002/cam4.1734. Epub 2018 Aug 27.
To evaluate the effect of escalated dose radiation therapy (EDR, defined as doses >50.4 Gy in 28 fractions [59.5 Gy BED]) on overall survival (OS), freedom from local progression (FFLP), and freedom from distant progression (FFDP) of patients with unresectable extrahepatic cholangiocarcinoma (EHCC).
A consecutive cohort of 80 patients who underwent radiotherapy for unresectable EHCC from 2001 to 2015 was identified. Demographic, tumor, treatment, toxicity, and laboratory variables were collected. The maximal RT doses ranged from 30 to 75 Gy (median 50.4 Gy, at 1.8-4.5 Gy/fraction). Gross tumor volume (GTV) coverage by maximal dose in EDR group ranged from 38% to 100%. Kaplan-Meier method was used to estimate OS, FFLP, and FFDP. Univariate and multivariate Cox regression models were analyzed.
After radiotherapy, median OS, FFLP, and FFDP were 18.7, 22.6, and 24.3 months, respectively. There was no significant difference in OS or FFLP between patients who received EDR to portions of the GTV and patients who did not. On multivariate analysis, bigger GTV, age, and ECOG performance status were independently associated with shorter OS. Local progression on chemotherapy prior to RT was independently associated with shorter FFLP. High baseline neutrophil/lymphocyte ratio (>5.3) was independently associated with shorter FFDP. Toxicity grades were similar in EDR and lower doses except lymphopenia which was higher in EDR (P = 0.053).
EDR to selective portions of the GTV may not benefit patients with unresectable EHCC despite having acceptable toxicity. New methods to improve local control and survival for unresectable EHCC are needed.
评估递增剂量放疗(EDR,定义为 28 个分次中剂量>50.4Gy[59.5GyBED])对不可切除的肝外胆管癌(EHCC)患者的总生存(OS)、无局部进展(FFLP)和无远处进展(FFDP)的影响。
从 2001 年至 2015 年,确定了 80 例接受不可切除的 EHCC 放疗的连续队列患者。收集了人口统计学、肿瘤、治疗、毒性和实验室变量。最大 RT 剂量范围为 30-75Gy(中位数 50.4Gy,分次剂量为 1.8-4.5Gy)。在 EDR 组中,最大剂量的 GTV 覆盖率范围为 38%-100%。Kaplan-Meier 法用于估计 OS、FFLP 和 FFDP。采用单因素和多因素 Cox 回归模型进行分析。
放疗后,中位 OS、FFLP 和 FFDP 分别为 18.7、22.6 和 24.3 个月。接受 EDR 治疗的 GTV 部分和未接受 EDR 治疗的患者在 OS 或 FFLP 方面无显著差异。多因素分析显示,较大的 GTV、年龄和 ECOG 表现状态与较短的 OS 独立相关。在 RT 前化疗中出现局部进展与较短的 FFLP 独立相关。高基线中性粒细胞/淋巴细胞比值(>5.3)与较短的 FFDP 独立相关。EDR 和较低剂量的毒性分级相似,除 EDR 中更高的淋巴细胞减少症(P=0.053)外。
尽管毒性可接受,但对 GTV 的选择性部位进行 EDR 可能对不可切除的 EHCC 患者无益。需要新的方法来提高不可切除的 EHCC 的局部控制和生存率。