Ott Katja, Fink Ulrich, Becker Karen, Stahl Alexander, Dittler Hans-Joachim, Busch Raymonde, Stein Hubert, Lordick Florian, Link Thomas, Schwaiger Markus, Siewert Jörg-Rüdiger, Weber Wolfgang A
Department of Surgery, Technische Universitä München, Munich, Germany.
J Clin Oncol. 2003 Dec 15;21(24):4604-10. doi: 10.1200/JCO.2003.06.574.
We prospectively evaluated the predictive value of therapy-induced reduction of tumor glucose use for subsequent response and patient survival in patients with gastric cancer treated by preoperative chemotherapy.
Forty-four consecutive patients with locally advanced gastric carcinomas were studied by positron emission tomography with the glucose analog fluorine-18 fluorodeoxyglucose (FDG-PET) at baseline and 14 days after initiation of cisplatin-based polychemotherapy. On the basis of a previous study, a reduction of tumor FDG uptake by more than 35% was used as a criterion for a metabolic response. The metabolic response in FDG-PET was correlated with histopathologic response after completion of therapy (< 10% viable tumor cells in the resected specimen) and patient survival.
Thirty-five (80%) of the 44 tumors were visualized with sufficient contrast for quantitative analysis (two of 19 intestinal and seven of 25 nonintestinal tumors showed only low FDG uptake). In the 35 assessable patients, PET imaging after 14 days of therapy correctly predicted histopathologic response after 3 months of therapy in 10 (77%) of 13 responders and 19 (86%) of 22 nonresponders. Median overall survival for patients with a metabolic response has not been reached (2-year survival rate, 90%); for patients without a metabolic response, median survival was only 18.9 months (2-year survival rate, 25%; P =.002)
This study prospectively demonstrates that in patients with gastric cancer, response to preoperative chemotherapy can be predicted by FDG-PET early during the course of therapy. By avoiding the morbidity and costs of ineffective therapy, FDG-PET imaging may markedly facilitate the use of preoperative chemotherapy.
我们前瞻性评估了术前化疗的胃癌患者中,治疗引起的肿瘤葡萄糖利用减少对后续反应和患者生存的预测价值。
连续44例局部晚期胃癌患者在基线时以及基于顺铂的多药化疗开始14天后,通过正电子发射断层扫描及葡萄糖类似物氟-18氟脱氧葡萄糖(FDG-PET)进行研究。根据先前的一项研究,将肿瘤FDG摄取减少超过35%作为代谢反应的标准。FDG-PET中的代谢反应与治疗完成后的组织病理学反应(切除标本中存活肿瘤细胞<10%)及患者生存相关。
44个肿瘤中的35个(80%)显影对比度充足,可进行定量分析(19个肠型肿瘤中的2个以及25个非肠型肿瘤中的7个仅显示低FDG摄取)。在35例可评估患者中,治疗14天后的PET成像正确预测了3个月治疗后的组织病理学反应,13例反应者中有10例(77%),22例无反应者中有19例(86%)。有代谢反应患者的中位总生存期尚未达到(2年生存率90%);无代谢反应患者的中位生存期仅为18.9个月(2年生存率25%;P = 0.002)
本研究前瞻性表明,在胃癌患者中,治疗过程早期通过FDG-PET可预测术前化疗反应。通过避免无效治疗的发病率和成本,FDG-PET成像可能显著促进术前化疗的应用。