Houard Clémence, Pinaquy Jean-Baptiste, Mesguich Charles, Henriques de Figueiredo Bénédicte, Cazeau Anne-Laure, Allard Jean-Baptiste, Laharie Hortense, Bordenave Laurence, Fernandez Philippe, Vendrely Véronique
Nuclear Medicine Department, CHU de Bordeaux, F-33000 Bordeaux, France.
Nuclear Medicine Department, CHU de Bordeaux, F-33000 Bordeaux, France
J Nucl Med. 2017 Sep;58(9):1414-1420. doi: 10.2967/jnumed.116.185280. Epub 2017 Mar 9.
The aim of this study was to evaluate the relevance of PET/CT and F-FDG as a strategy for response evaluation after chemoradiotherapy for anal cancer. For this, the performance of posttreatment F-FDG PET/CT, the impact on patient care, and the predictive value of metabolic response were assessed. This was a retrospective and multicenter analysis of 87 patients treated by chemoradiotherapy for anal squamous cell carcinoma between October 2007 and October 2013. All patients underwent systematic posttreatment F-FDG PET/CT and were followed with at least a clinical examination every 4 mo for 2 y and every 6 mo thereafter. Disease progression was confirmed by biopsy for all patients in the case of local recurrence before surgery. Kaplan-Meier and Cox regression models were used to test for associations between metabolic or clinical endpoints and progression-free survival (PFS) or cause-specific survival (CSS). The median follow-up was 25 mo. F-FDG PET/CT was performed 1-8 mo (median, 4 mo) after completion of chemoradiotherapy. Overall, 25 patients relapsed and 13 died. The posttherapy F-FDG PET/CT did not show any abnormal F-FDG uptake (complete metabolic response [CMR]) in 55 patients whereas 32 displayed incomplete response (non-CMR): 15 patients with partial response and 17 with disease progression. The sensitivity of F-FDG PET/CT to detect residual tumor tissue was 92% (95% confidence interval [CI], 75%-97%), specificity was 85% (95% CI, 75%-92%), positive predictive value was 72% (95% CI, 61%-90%), and negative predictive value was 96.4% (95% CI, 90%-98.7%). The 2-y PFS was 96% (95% CI, 90-100) for patients with CMR and 28% (95% CI, 14-47) for non-CMR patients ( < 0.0001). The 2-y CSS was 100% for patients with CMR and 59% (95% CI, 42-84) for those without CMR ( < 0.0001). F-FDG PET/CT changed patient management in 14 cases (16%), with relevant modifications in 12 (14%). A Cox proportional hazards model of survival outcome indicated that a CMR was the only significant predictor of PFS and CSS ( < 0.0001). F-FDG PET/CT shows good accuracy in posttreatment evaluation of anal cancer and has a relevant impact on patient management. Moreover, CMR is associated with good survival outcome. Thus, F-FDG PET/CT may play a significant role during posttreatment follow-up of anal cancer.
本研究的目的是评估正电子发射断层显像/计算机断层扫描(PET/CT)及氟代脱氧葡萄糖(F-FDG)作为肛管癌放化疗后疗效评估策略的相关性。为此,评估了治疗后F-FDG PET/CT的性能、对患者治疗的影响以及代谢反应的预测价值。这是一项对2007年10月至2013年10月期间接受肛管鳞状细胞癌放化疗的87例患者进行的回顾性多中心分析。所有患者均接受了系统性治疗后F-FDG PET/CT检查,并在2年内每4个月至少进行一次临床检查,此后每6个月进行一次。对于所有术前局部复发的患者,均通过活检确认疾病进展。采用Kaplan-Meier法和Cox回归模型检验代谢或临床终点与无进展生存期(PFS)或特定病因生存期(CSS)之间的关联。中位随访时间为25个月。F-FDG PET/CT在放化疗结束后1 - 8个月(中位时间为4个月)进行。总体而言,25例患者复发,13例死亡。治疗后F-FDG PET/CT显示55例患者没有任何异常F-FDG摄取(完全代谢缓解[CMR]),而32例显示不完全缓解(非CMR):15例部分缓解患者和17例疾病进展患者。F-FDG PET/CT检测残留肿瘤组织的敏感性为92%(95%置信区间[CI],75% - 97%),特异性为85%(95% CI,75% - 92%),阳性预测值为72%(95% CI,61% - 90%),阴性预测值为96.4%(95% CI,90% - 98.7%)。CMR患者的2年PFS为96%(95% CI,90 - 100),非CMR患者为28%(95% CI,14 - 47)(P < 0.0001)。CMR患者的2年CSS为100%,非CMR患者为59%(95% CI,42 - 84)(P < 0.0001)。F-FDG PET/CT改变了14例(16%)患者的治疗管理,其中12例(14%)有相关调整。生存结局的Cox比例风险模型表明,CMR是PFS和CSS的唯一显著预测因素(P < 0.0001)。F-FDG PET/CT在肛管癌治疗后评估中显示出良好的准确性,并且对患者治疗管理有相关影响。此外,CMR与良好的生存结局相关。因此,F-FDG PET/CT可能在肛管癌治疗后随访中发挥重要作用。