University of Texas, M.D. Anderson Cancer Center, Houston, TX, USA.
SWOG Statistical Center, Seattle, WA, USA.
Eur J Cancer. 2014 Jun;50(9):1638-48. doi: 10.1016/j.ejca.2014.03.005. Epub 2014 Apr 4.
Vandetanib is an oral tyrosine kinase inhibitor of VEGFR-2/3, EGFR and RET, which has demonstrated clinical activity as a single agent and in combination with taxanes. We explored the efficacy, safety and toxicity of docetaxel and vandetanib in women with recurrent ovarian cancer (OC).
Women with refractory or progressive OC were randomised 1:1 to docetaxel (75 mg/m(2), IV)+vandetanib (100mg daily, PO, D+V) or docetaxel (75 mg/m(2), D). Up to three additional cytotoxic regimens for recurrence and prior anti-angiogenic agents (as primary therapy) were allowed. The primary end-point was progression free survival (PFS). The study had 84% power to detect a PFS hazard ratio of 0.65, using a one-sided P of 0.1. This corresponds to an increase in median PFS from 3.6 months to 5.6 months. Patients progressing on D were allowed to receive single agent vandetanib (D → V).
131 Patients were enrolled; two were excluded. 16% had received prior anti-angiogenic therapy. The median PFS estimates were 3.0 mos (D+V) versus 3.5 (D); HR: 0.99 (80% CI: 0.79-1.26). 61 Patients on D+V were assessable for toxicity; 20(33%) had treatment-related Grade (G) 4 events, primarily haematologic. Similarly, 17 (27%) of 64 patients receiving D had G4 events, primarily haematologic. 27 Evaluable patients crossed-over to V. 1/27(4%) experienced a G4 event. G3 diarrhoea was observed in 4% D → V patients. Median OS was 14 mos (D+V) versus 18 mos (D → V); HR(OS): 1.25 (80% CI: 0.93-1.68). Crossover vandetanib response was 4% (1/27 evaluable patients). High plasma IL-8 levels were associated with response to D+V.
Combination docetaxel+vandetanib did not prolong PFS relative to docetaxel alone in OC patients. No unexpected safety issues were identified.
凡德他尼是一种口服的血管内皮生长因子受体-2/3(VEGFR-2/3)、表皮生长因子受体(EGFR)和转染期间重排(RET)酪氨酸激酶抑制剂,作为单一药物以及与紫杉烷类联合应用均显示出临床疗效。我们探索了多西他赛联合凡德他尼治疗复发性卵巢癌(OC)患者的疗效、安全性和毒性。
难治性或进展性 OC 患者按 1:1 随机分为多西他赛(75mg/m2,IV)+凡德他尼(100mg 每日,PO,D+V)或多西他赛(75mg/m2,D)组。允许患者在复发时接受最多三种额外的细胞毒性治疗方案和先前的抗血管生成药物(作为一线治疗)。主要终点是无进展生存期(PFS)。该研究有 84%的效能检测单侧 P 值为 0.1 时 PFS 风险比为 0.65,这对应于中位 PFS 从 3.6 个月增加到 5.6 个月。接受 D 治疗后进展的患者可接受单药凡德他尼(D→V)治疗。
共纳入 131 例患者,其中 2 例被排除。16%的患者接受过抗血管生成治疗。D+V 组和 D 组的中位 PFS 估计值分别为 3.0 个月和 3.5 个月;HR:0.99(80%CI:0.79-1.26)。61 例接受 D+V 治疗的患者可评估毒性;20 例(33%)患者出现治疗相关的 4 级事件,主要是血液学毒性。同样,64 例接受 D 治疗的患者中有 17 例(27%)发生 4 级事件,主要是血液学毒性。27 例可评估患者交叉至 V 组。1/27(4%)例患者发生 4 级事件。D→V 组有 4%的患者发生 3 级腹泻。D+V 组的中位 OS 为 14 个月,D→V 组为 18 个月;(OS)HR:1.25(80%CI:0.93-1.68)。交叉至凡德他尼治疗的患者中有 1 例(27 例可评估患者的 4%)出现 4 级事件。高血浆白细胞介素-8(IL-8)水平与 D+V 反应相关。
与单独使用多西他赛相比,多西他赛联合凡德他尼并未延长 OC 患者的 PFS。未发现新的安全性问题。