Klaeser Bernd, Nitzsche Egbert, Schuller Jan C, Köberle Dieter, Widmer Lucas, Balmer-Majno Sabine, Hany Thomas, Cescato-Wenger Corinne, Brauchli Peter, Zünd Michael, Pestalozzi Bernhard C, Caspar Clemens, Albrecht Susanne, von Moos Roger, Ruhstaller Thomas
Department of Nuclear Medicine, Inselspital Bern, Switzerland.
Onkologie. 2009 Dec;32(12):724-30. doi: 10.1159/000251842. Epub 2009 Nov 9.
Only responding patients benefit from preoperative therapy for locally advanced esophageal carcinoma. Early detection of non-responders may avoid futile treatment and delayed surgery.
In a multi-center phase ll trial, patients with resectable, locally advanced esophageal carcinoma were treated with 2 cycles of induction chemotherapy followed by chemoradiotherapy (CRT) and surgery. Positron emission tomography with 2[fluorine-18]fluoro-2-deoxy-d-glucose (FDG-PET) was performed at baseline and after induction chemotherapy. The metabolic response was correlated with tumor regression grade (TRG). A decrease in FDG tumor uptake of less than 40% was prospectively hypothesized as a predictor for histopathological non-response (TRG > 2) after CRT.
45 patients were included. The median decrease in FDG tumor uptake after chemotherapy correlated well with TRG after completion of CRT (p = 0.021). For an individual patient, less than 40% decrease in FDG tumor uptake after induction chemotherapy predicted histopathological non-response after completion of CRT, with a sensitivity of 68% and a specificity of 52% (positive predictive value 58%, negative predictive value 63%).
Metabolic response correlated with histopathology after preoperative therapy. However, FDG-PET did not predict non-response after induction chemotherapy with sufficient clinical accuracy to justify withdrawal of subsequent CRT and selection of patients to proceed directly to surgery.
只有有反应的患者才能从局部晚期食管癌的术前治疗中获益。早期发现无反应者可避免无效治疗和手术延迟。
在一项多中心II期试验中,可切除的局部晚期食管癌患者接受2个周期的诱导化疗,随后进行放化疗(CRT)和手术。在基线期和诱导化疗后进行2-[氟-18]氟-2-脱氧-D-葡萄糖正电子发射断层扫描(FDG-PET)。代谢反应与肿瘤退缩分级(TRG)相关。前瞻性假设FDG肿瘤摄取减少小于40%为CRT后组织病理学无反应(TRG>2)的预测指标。
纳入45例患者。化疗后FDG肿瘤摄取的中位减少与CRT完成后的TRG相关性良好(p = 0.021)。对于个体患者,诱导化疗后FDG肿瘤摄取减少小于40%可预测CRT完成后组织病理学无反应,敏感性为68%,特异性为52%(阳性预测值58%,阴性预测值63%)。
术前治疗后代谢反应与组织病理学相关。然而,FDG-PET在诱导化疗后预测无反应的临床准确性不足,无法证明取消后续CRT以及选择患者直接进行手术的合理性。