Experimental Clinical Abdominal Oncology, IRCCS Istituto Nazionale Tumori "Fondazione Giovanni Pascale," Naples, Italy
Nuclear Medicine, IRCCS Istituto Nazionale Tumori "Fondazione Giovanni Pascale," Naples, Italy.
J Nucl Med. 2019 Nov;60(11):1560-1568. doi: 10.2967/jnumed.118.222604. Epub 2019 Mar 15.
There is an unmet need for predictive biomarkers of the clinical benefit of antiangiogenic drugs. The aim of the present study was to prospectively evaluate the value of F-FDG PET/CT performed during and after preoperative chemoradiotherapy with bevacizumab for the prediction of complete pathologic tumor regression and survival in patients with MRI-defined high-risk locally advanced rectal cancer. Sixty-one patients treated in a nonrandomized phase II study (BRANCH) with concomitant or sequential (4 d before chemoradiotherapy) administration of bevacizumab with preoperative chemoradiotherapy were included. F-FDG PET/CT was performed at baseline, 11 d after the beginning of chemoradiotherapy (early), and before surgery (late). Metabolic changes were compared with pathologic complete tumor regression (TRG1) versus incomplete tumor regression (TRG2-TRG5), progression-free survival, cancer-specific survival, and overall survival. Receiver-operating-characteristic curves were calculated for those F-FDG PET/CT parameters that significantly correlated with TRG1. Early total-lesion glycolysis and its percentage change compared with baseline (ΔTLG-early) could discriminate TRG1 from TRG2-TRG5. Only receiver-operating-characteristic analysis of ΔTLG-early showed an area under the curve greater than 0.7 (0.76), with an optimal cutoff at 59.5% (80% sensitivity, 71.4% specificity), for identifying TRG1. Late metabolic assessment could not discriminate between the 2 groups. After a median follow-up of 98 mo (range, 77-132 mo), metabolic responders (ΔTLG-early ≥ 59.5%) demonstrated a significantly higher 10-y progression-free survival (89.3% vs. 63.6%, = 0.02) and cancer-specific survival (92.9% vs. 72.6%, = 0.04) than incomplete metabolic responders. Our results suggest that early metabolic response can act as a surrogate marker of the benefit of antiangiogenic therapy. The findings provide further support for the use of early F-FDG PET/CT evaluation to predict pathologic response and survival in the preoperative treatment of patients with locally advanced rectal cancer. ΔTLG-early showed the best accuracy in predicting tumor regression and may be particularly useful in guiding treatment-modifying decisions during preoperative chemoradiotherapy based on expected response.
目前,临床上对抗血管生成药物疗效的预测性生物标志物仍有需求。本研究旨在前瞻性评估在接受贝伐单抗联合术前放化疗的 MRI 定义的局部晚期直肠癌患者中,在放化疗期间和之后进行 F-FDG PET/CT 检查对完全病理肿瘤消退和生存的预测价值。本研究共纳入 61 例在非随机 II 期 BRANCH 研究中接受治疗的患者,这些患者接受了贝伐单抗的同期或序贯(放化疗前 4 天)治疗。F-FDG PET/CT 分别在基线、放化疗开始后 11 天(早)和手术前(晚)进行。代谢变化与病理完全肿瘤消退(TRG1)与不完全肿瘤消退(TRG2-TRG5)、无进展生存期、癌症特异性生存期和总生存期进行比较。对与 TRG1 显著相关的 F-FDG PET/CT 参数进行受试者工作特征曲线分析。早期全病灶糖酵解及其与基线相比的百分比变化(ΔTLG-early)可区分 TRG1 与 TRG2-TRG5。只有 ΔTLG-early 的受试者工作特征曲线分析显示曲线下面积大于 0.7(0.76),最佳截断值为 59.5%(80%敏感性,71.4%特异性),可用于识别 TRG1。晚期代谢评估不能区分这两组。中位随访 98 个月(范围 77-132 个月)后,代谢反应者(ΔTLG-early≥59.5%)的 10 年无进展生存率(89.3%比 63.6%,P=0.02)和癌症特异性生存率(92.9%比 72.6%,P=0.04)显著更高。我们的结果表明,早期代谢反应可以作为抗血管生成治疗获益的替代标志物。这些发现为术前治疗局部晚期直肠癌患者时使用早期 F-FDG PET/CT 评估预测病理反应和生存提供了进一步支持。ΔTLG-early 在预测肿瘤消退方面具有最佳准确性,并且可能特别有助于指导术前放化疗期间基于预期反应的治疗调整决策。