O'Connor James P B, Jayson Gordon C, Jackson Alan, Ghiorghiu Dana, Carrington Bernadette M, Rose Chris J, Mills Samantha J, Swindell Ric, Roberts Caleb, Mitchell Claire L, Parker Geoffrey J M
Imaging Science and Biomedical Engineering, University of Manchester, Manchester, UK. james.o'
Clin Cancer Res. 2007 Oct 15;13(20):6130-5. doi: 10.1158/1078-0432.CCR-07-0331.
To define a simple radiologic biomarker of prognosis in patients with advanced epithelial ovarian carcinoma on first-line chemotherapy.
Twenty-seven patients receiving platinum-based chemotherapy with >2 cm residual disease [International Federation of Gynecology and Obstetrics (FIGO) stages IIIC or IV] after surgery were identified. The proportion of enhancing tumor tissue--the enhancing fraction--was calculated on pre-chemotherapy computed tomography scans at four Hounsfield unit (HU) thresholds and assessed for correlation with CA125 response, Response Evaluation Criteria in Solid Tumors (RECIST) radiologic response, and time to progression. Discriminative power was assessed by leave-one-out discriminant analysis.
Pre-chemotherapy residual tumor volume did not correlate with clinical outcome. Pre-chemotherapy enhancing fraction at all thresholds significantly correlated with CA125 response (P < 0.001, rho = 0.553 for 50 HU; P < 0.001, rho = 0.565 for 60 HU; P < 0.001, rho = 0.553 for 70 HU; P = 0.001, rho = 0.516 for 80 HU). Significant correlations were also shown for radiologic response at all thresholds. Enhancing fraction predicted CA125 response with 81.9% to 86.4% specificity and Response Evaluation Criteria in Solid Tumors response with 74.9% to 76.8% specificity at 95% sensitivity (dependent on threshold). Enhancing fraction correlated with time to progression at the 60 HU (P = 0.045, rho = 0.336) and 70 HU (P = 0.042; rho = 0.340) thresholds.
Pre-chemotherapy enhancing fraction is a simple quantitative radiologic measure. Further evaluation in larger trials is required to confirm the potential of enhancing fraction as a predictive factor, particularly for patients who may benefit from the addition of antiangiogenic therapy.
确定晚期上皮性卵巢癌患者一线化疗预后的一种简单的放射学生物标志物。
确定了27例术后接受铂类化疗且残留病灶>2 cm[国际妇产科联盟(FIGO)IIIC期或IV期]的患者。在四个亨氏单位(HU)阈值下,根据化疗前计算机断层扫描计算增强肿瘤组织的比例——增强分数,并评估其与CA125反应、实体瘤疗效评价标准(RECIST)放射学反应以及疾病进展时间的相关性。通过留一法判别分析评估判别能力。
化疗前残留肿瘤体积与临床结局无关。所有阈值下化疗前的增强分数均与CA125反应显著相关(50 HU时,P<0.001,rho=0.553;60 HU时,P<0.001,rho=0.565;70 HU时,P<0.001,rho=0.553;80 HU时,P=0.001,rho=0.516)。所有阈值下的放射学反应也显示出显著相关性。在95%的敏感度下(取决于阈值),增强分数预测CA125反应的特异性为81.9%至86.4%,预测实体瘤疗效评价标准反应的特异性为74.9%至76.8%。在60 HU(P=0.045,rho=0.336)和70 HU(P=0.042;rho=0.340)阈值下,增强分数与疾病进展时间相关。
化疗前增强分数是一种简单的定量放射学指标。需要在更大规模的试验中进一步评估,以确认增强分数作为预测因子的潜力,特别是对于可能从添加抗血管生成治疗中获益的患者。