Department of Surgery, IRCCS - Ospedale Sacro Cuore Don Calabria, Via Don A. Sempreboni 5, 37024, Negrar, Verona, Italy.
Department of Advanced Radiation Oncology, IRCCS - Ospedale Sacro Cuore Don Calabria, Via Don A. Sempreboni 5, 37024, Negrar, Verona, Italy.
Radiol Med. 2020 Oct;125(10):990-998. doi: 10.1007/s11547-020-01189-9. Epub 2020 Apr 10.
The potential role of neoadjuvant radiation dose intensification in locally advanced rectal cancer (LARC) is still largely debated. In the present study, a comparative analysis between radiation dose intensification and conventional fractionation was performed.
In the current prospective observational study (protocol ID RT-03/2011), 56 patients diagnosed with LARC were enrolled between January 2013 and December 2016. More specifically, 25 patients underwent preoperative conventional radiation dose [i.e., 50.4 Gy in 28 fractions here defined as standard dose radiotherapy (SDR)-group 1], whereas 31 patients were candidate for radiation dose intensification (RDI) (i.e., 60 Gy in 30 fractions-group 2). The primary endpoint was the complete pathological response (pCR) rate. Secondary endpoints were postoperative complications and ChT-RT-related toxicity.
No statistical significance was observed in pCR rate (20.8% and 22.6% in SDR and RDI group, respectively, p = 0.342). Of contrast, the RDI group showed a significantly higher primary tumor downstaging in case of T3 tumor compared to SDR group (p = 0.049). Sphincter-preserving surgery was 84% and 93.5% in SDR and RDI groups, respectively (p = 0.25). All patients had R0 margins. No surgical-related death was recorded. No statistically significant difference was observed regarding surgical complications and incomplete mesorectal excision. Acute genitourinary toxicity was significantly higher in RDI group (p = 0.015).
The intensification of the neoadjuvant radiotherapy for LARC seems to produce a major pathological response in T3 tumors. The radiation dose intensification appears probably associated with a higher rate of genitourinary toxicity.
新辅助放疗剂量强化在局部进展期直肠癌(LARC)中的作用仍存在较大争议。本研究对放疗剂量强化与常规分割进行了比较分析。
本前瞻性观察性研究(方案 ID RT-03/2011)纳入了 2013 年 1 月至 2016 年 12 月期间诊断为 LARC 的 56 例患者。具体而言,25 例患者接受术前常规放疗剂量(即定义为标准剂量放疗(SDR)的 50.4Gy/28 次),而 31 例患者适合放疗剂量强化(即 60Gy/30 次-组 2)。主要终点是完全病理缓解(pCR)率。次要终点是术后并发症和化疗联合放疗相关毒性。
pCR 率在 SDR 组和 RDI 组分别为 20.8%和 22.6%,差异无统计学意义(p=0.342)。相比之下,RDI 组 T3 肿瘤的原发肿瘤降期明显高于 SDR 组(p=0.049)。保肛手术在 SDR 组和 RDI 组分别为 84%和 93.5%(p=0.25)。所有患者均达到了 R0 切缘。无手术相关死亡病例。手术并发症和不完全直肠系膜切除方面无统计学差异。RDI 组急性泌尿生殖毒性明显更高(p=0.015)。
LARC 的新辅助放疗强化似乎能使 T3 肿瘤产生更大的病理反应。放疗剂量强化可能与更高的泌尿生殖毒性发生率相关。