Oei Angèle L M, Sweep Fred C G J, Geurts-Moespot Anneke, van Tienoven Doorlène, Von Mensdorff-Pouilly Silvia, Thomas Chris M G, Massuger Leon F A G
Department of Obstetrics and Gynecology, Radboud University Nijmegen Medical Centre, the Netherlands.
Anticancer Res. 2008 Sep-Oct;28(5A):2721-5.
Human anti-mouse antibody (HAMA)-IgM and IgG in ovarian cancer patients treated with intraperitoneal (i.p.) 90Y-muHMFG1 as consolidating therapy were analyzed for a relationship with outcome of disease.
Serial serum samples from 208 ovarian cancer patients participating in a phase III trial of i.p. 90Y-muHMFG1 and 25 controls were analyzed for HAMA-IgM and HAMA-IgG. Results were correlated with time to, and location of, disease recurrence.
Patients receiving i.p. 90Y-muHMFG1 developed a rapid HAMA-IgM peak (week 4 to 8), followed by a HAMA-IgG peak 2-4 weeks later. HAMA levels in the control group remained unchanged. Early maximum HAMA-IgG peaks were associated with early relapse [hazard ratio (HR), 0.975; 95% confidence interval (CI) 0.956 to 0.995; p=0.012]. Patients with a HAMA-IgG maximum before or at 8 weeks were at significantly higher risk for disease recurrence (HR, 1.6; 95% CI 1.1 to 25;p=0.021) as compared to patients with a HAMA-IgG maximum after 8 weeks.
Besides time point of maximum HAMA-IgG, no evident relation could be found between HAMA-IgM or HAMA-IgG development and time to relapse or location of recurrence.
分析接受腹腔内(i.p.)注射90Y-muHMFG1巩固治疗的卵巢癌患者体内的人抗鼠抗体(HAMA)-IgM和IgG与疾病预后的关系。
对参与i.p. 90Y-muHMFG1 III期试验的208例卵巢癌患者及25例对照的系列血清样本进行HAMA-IgM和HAMA-IgG分析。结果与疾病复发时间及复发部位相关。
接受i.p. 90Y-muHMFG1治疗的患者出现快速的HAMA-IgM峰值(第4至8周),随后在2 - 4周后出现HAMA-IgG峰值。对照组的HAMA水平保持不变。早期最大HAMA-IgG峰值与早期复发相关[风险比(HR),0.975;95%置信区间(CI)0.956至0.995;p = 0.012]。与HAMA-IgG最大峰值出现在8周后相比,HAMA-IgG最大峰值出现在8周之前或8周时的患者疾病复发风险显著更高(HR,1.6;95% CI 1.1至2.5;p = 0.021)。
除了HAMA-IgG最大峰值的时间点外,未发现HAMA-IgM或HAMA-IgG的产生与复发时间或复发部位之间存在明显关系。