Department of Surgical Oncology, Peter MacCallum Cancer Centre, St. Andrew's Place, East Melbourne, Victoria, Australia.
Dis Colon Rectum. 2011 May;54(5):518-25. doi: 10.1007/DCR.0b013e31820b36f0.
Complete pathological response has proven prognostic benefits in patients with locally advanced rectal cancer treated with neoadjuvant chemoradiotherapy. Sequential 18-FDG PET may be an early surrogate for pathological response to chemoradiotherapy.
The aim of this study was to identify whether metabolic response measured by FDG PET following chemoradiotherapy is prognostic for tumor recurrence and survival following neoadjuvant therapy and surgical treatment for primary rectal cancer.
Patients with primary rectal cancer treated by long-course neoadjuvant chemoradiotherapy followed by surgery had FDG PET performed before and 4 weeks after treatment, before surgical resection was performed. Retrospective chart review was undertaken for patient demographics, tumor staging, recurrence rates, and survival.
: Between 2000 and 2007, 78 patients were identified (53 male, 25 female; median age, 64 y). After chemoradiotherapy, 37 patients (47%) had a complete metabolic response, 26 (33%) had a partial metabolic response, and 14 (18%) had no metabolic response as assessed by FDG PET (1 patient had missing data). However, only 4 patients (5%) had a complete pathological response. The median postoperative follow-up period was 3.1 years during which 14 patients (19%) had a recurrence: 2 local, 9 distant, and 3 with both local and distant. The estimated percentage without recurrence was 77% at 5 years (95% CI 66%-89%). There was an inverse relationship between FDG PET metabolic response and the incidence of recurrence within 3 years (P = .04). Kaplan-Meier analysis of FDG PET metabolic response and overall survival demonstrated a significant difference in survival among patients in the 3 arms: complete, partial, and no metabolic response (P = .04); the patients with complete metabolic response had the best prognosis.
Complete or partial metabolic response on PET following neoadjuvant chemoradiotherapy and surgery predicts a lower local recurrence rate and improved survival compared with patients with no metabolic response. Metabolic response may be used to stratify prognosis in patients with rectal cancer.
新辅助放化疗治疗局部晚期直肠癌患者完全病理缓解已被证明具有预后益处。连续 18-FDG PET 可能是放化疗后病理反应的早期替代指标。
本研究旨在确定新辅助治疗和直肠癌手术治疗后,放化疗后 FDG PET 测量的代谢反应是否与肿瘤复发和生存有关。
对接受长程新辅助放化疗后手术的原发性直肠癌患者进行 FDG PET 检查,分别在治疗前和治疗后 4 周进行,然后进行手术切除。回顾性图表审查了患者的人口统计学、肿瘤分期、复发率和生存率。
2000 年至 2007 年间,共确定了 78 例患者(53 例男性,25 例女性;中位年龄 64 岁)。放化疗后,37 例(47%)患者完全代谢缓解,26 例(33%)患者部分代谢缓解,14 例(18%)患者 FDG PET 无代谢反应(1 例患者数据缺失)。然而,只有 4 例(5%)患者完全病理缓解。术后中位随访时间为 3.1 年,14 例患者(19%)出现复发:2 例局部复发,9 例远处转移,3 例局部和远处均有转移。5 年无复发率估计为 77%(95%CI 66%-89%)。FDG PET 代谢反应与 3 年内复发率呈负相关(P =.04)。FDG PET 代谢反应和总生存率的 Kaplan-Meier 分析显示,在完全、部分和无代谢反应的患者之间生存存在显著差异(P =.04);完全代谢反应的患者预后最好。
新辅助放化疗和手术后 PET 上的完全或部分代谢反应与无代谢反应的患者相比,局部复发率较低,生存预后较好。代谢反应可用于分层直肠癌患者的预后。