Tobias Joseph, Abou Azar Sara, Gujarathi Rushabh, Nordgren Rachel, Vaghaiwalla Tanaz, Millis J Michael, Feinberg Nicholas, Liao Chih-Yi, Keutgen Xavier M
Division of General Surgery and Surgical Oncology, Department of Surgery, University of Chicago, Chicago, IL.
Division of General Surgery and Surgical Oncology, Department of Surgery, University of Chicago, Chicago, IL.
Surgery. 2025 Jan;177:108834. doi: 10.1016/j.surg.2024.06.065. Epub 2024 Oct 11.
With the advent of peptide receptor radionuclide therapy, the timing and sequence of surgery in the treatment of metastatic gastroenteropancreatic neuroendocrine tumors merits further study. We hypothesized that surgery before peptide receptor radionuclide therapy might enhance its effectiveness in patients with metastatic gastroenteropancreatic neuroendocrine tumors.
Eighty-nine patients with metastatic well-differentiated gastroenteropancreatic neuroendocrine tumors treated with Lutetium-dotatate peptide receptor radionuclide therapy between 2018 and 2023 were included. Fifty-six patients underwent surgery (primary tumor resection and/or liver debulking) before peptide receptor radionuclide therapy and 33 patients did not. Primary outcome was progression-free survival according to Response Evaluation Criteria in Solid Tumors. Pretreatment dotatate positron emission tomography/computed tomography was used to calculate tumor volumes.
The surgery and no-surgery groups were well-matched. Median progression-free survival after peptide receptor radionuclide therapy was 15.6 months (interquartile range, 9.1-22.7 months) in the no-surgery group compared with 26.1 months (interquartile range, 12.7-38.1 months) in the surgery group (P = .04). On subgroup analysis, median progression-free survival was 18.1 months (interquartile range, 11.9-38.4 months) in patients who underwent primary tumor resection only compared with 26.2 months (interquartile range, 14.0-38.1 months) in patients who underwent liver debulking (P = .04). Tumor volume was lowest in patients who underwent liver debulking (median 146.07 mL) compared with no surgery (median 626.42 mL) (P = .001). On univariable analysis, a tumor volume <138.8 mL was associated with longer progression-free survival (hazard ratio, 2.03; 95% confidence interval, 0.95-4.34, P = .05), with a median progression-free survival of 38.1 months (interquartile range, 16.9-41.3 months) compared with 17.8 months (interquartile range, 10.8-28.7 months).
Surgery may enhance the effectiveness of Lutetium-dotatate in the treatment of metastatic well-differentiated gastroenteropancreatic neuroendocrine tumors. This positive effect may be the result of a lower tumor volume in patients after surgery. Our findings fortify the concept of using surgical debulking to improve systemic therapies such as peptide receptor radionuclide therapy.
随着肽受体放射性核素治疗的出现,转移性胃肠胰神经内分泌肿瘤治疗中手术的时机和顺序值得进一步研究。我们假设在肽受体放射性核素治疗前进行手术可能会提高其对转移性胃肠胰神经内分泌肿瘤患者的疗效。
纳入2018年至2023年间接受镥[177Lu]奥曲肽肽受体放射性核素治疗的89例转移性高分化胃肠胰神经内分泌肿瘤患者。56例患者在肽受体放射性核素治疗前接受了手术(原发肿瘤切除和/或肝脏减瘤),33例患者未接受手术。主要结局是根据实体瘤疗效评价标准得出的无进展生存期。治疗前奥曲肽正电子发射断层扫描/计算机断层扫描用于计算肿瘤体积。
手术组和非手术组匹配良好。肽受体放射性核素治疗后,非手术组的中位无进展生存期为15.6个月(四分位间距,9.1 - 22.7个月),而手术组为26.1个月(四分位间距,12.7 - 38.1个月)(P = 0.04)。亚组分析显示,仅接受原发肿瘤切除的患者中位无进展生存期为18.1个月(四分位间距,11.9 - 38.4个月),而接受肝脏减瘤的患者为26.2个月(四分位间距,14.0 - 38.1个月)(P = 0.04)。接受肝脏减瘤的患者肿瘤体积最小(中位值146.07 mL),与未手术患者(中位值626.42 mL)相比(P = 0.001)。单因素分析显示,肿瘤体积<138.8 mL与更长的无进展生存期相关(风险比,2.03;95%置信区间,0.95 - 4.34,P = 0.05),中位无进展生存期为38.1个月(四分位间距,16.9 - 41.3个月),而肿瘤体积≥138.8 mL的患者为17.8个月(四分位间距,10.8 - 28.7个月)。
手术可能会提高镥[177Lu]奥曲肽对转移性高分化胃肠胰神经内分泌肿瘤的治疗效果。这种积极作用可能是手术患者肿瘤体积较小的结果。我们的研究结果强化了通过手术减瘤来改善肽受体放射性核素治疗等全身治疗的概念。