Benz Matthias R, Armstrong Wesley R, Ceci Francesco, Polverari Giulia, Donahue Timothy R, Wainberg Zev A, Quon Andrew, Auerbach Martin, Girgis Mark D, Herrmann Ken, Czernin Johannes, Calais Jeremie
Ahmanson Translational Theranostics Division, Department of Molecular and Medical Pharmacology, UCLA, Los Angeles, California;
Clinic of Radiology and Nuclear Medicine, University Hospital of Basel, Basel, Switzerland.
J Nucl Med. 2022 Feb;63(2):199-204. doi: 10.2967/jnumed.121.261952. Epub 2021 Jul 16.
The purpose of this study was to evaluate F-FDG PET/CT as an early and late interim imaging biomarker in patients with pancreatic ductal adenocarcinoma who undergo first-line systemic therapy. This was a prospective, single-center, single-arm, open-label study (IRB12-000770). Patient receiving first-line chemotherapy were planned to undergo baseline F-FDG PET/CT, early interim F-FDG PET/CT, and late interim F-FDG PET/CT. Cutoffs for metabolic and radiographic tumor response assessment as selected and established by receiver-operating-characteristic analysis were applied (modified PERCIST/RECIST1.1). Patients were followed to collect data on further treatments and overall survival. The study population consisted of 28 patients who underwent baseline F-FDG PET/CT. Twenty-three of these (82%) underwent early interim F-FDG PET/CT, and 21 (75%) underwent late interim F-FDG PET/CT. Twenty-three deaths occurred during a median follow-up period of 14 mo (maximum follow-up, 58.3 mo). The median overall survival was 36.2 mo (95% CI, 28 mo to not yet reached [NYR]) in early metabolic responders (6/23 [26%], = 0.016) and 25.4 mo (95% CI, 19.6 mo-NYR) in early radiographic responders (7/23 [30%], = 0.16). The median overall survival was 27.4 mo (95% CI, 21.4 mo-NYR) in late metabolic responders (10/21 [48%], = 0.058) and 58.2 mo (95% CI, 21.4 mo-NYR) in late radiographic responders (7/21 [33%], = 0.008). F-FDG PET may serve as an early interim imaging biomarker (at ∼4 wk) for evaluation of response to first-line chemotherapy in patients with pancreatic ductal adenocarcinoma. Radiographic changes might be sufficient for response evaluation after the completion of first-line chemotherapy.
本研究的目的是评估F-FDG PET/CT作为接受一线全身治疗的胰腺导管腺癌患者的早期和晚期中期成像生物标志物。这是一项前瞻性、单中心、单臂、开放标签研究(IRB12-000770)。计划接受一线化疗的患者要进行基线F-FDG PET/CT、早期中期F-FDG PET/CT和晚期中期F-FDG PET/CT检查。应用通过受试者操作特征分析选择和确定的代谢和影像学肿瘤反应评估临界值(改良的PERCIST/RECIST1.1)。对患者进行随访,以收集关于进一步治疗和总生存期的数据。研究人群包括28例接受基线F-FDG PET/CT检查的患者。其中23例(82%)接受了早期中期F-FDG PET/CT检查,21例(75%)接受了晚期中期F-FDG PET/CT检查。在中位随访期14个月(最长随访期58.3个月)内发生了23例死亡。早期代谢反应者(6/23 [26%],P = 0.016)的中位总生存期为36.2个月(95% CI,28个月至尚未达到[NYR]),早期影像学反应者(7/23 [30%],P = 0.16)的中位总生存期为25.4个月(95% CI,19.6个月至NYR)。晚期代谢反应者(10/21 [48%],P = 0.058)的中位总生存期为27.4个月(95% CI,21.4个月至NYR),晚期影像学反应者(7/21 [33%],P = 0.008)的中位总生存期为58.2个月(95% CI,21.4个月至NYR)。F-FDG PET可作为一种早期中期成像生物标志物(约4周时),用于评估胰腺导管腺癌患者对一线化疗的反应。影像学变化可能足以在一线化疗完成后进行反应评估。