Department of Hepatobiliary Surgery and Liver Transplantation, Vanderbilt University, Nashville, TN 37232, USA.
Hum Gene Ther. 2010 Sep;21(9):1119-28. doi: 10.1089/hum.2010.020.
This multicenter phase I/II study evaluated the safety, pharmacokinetics, and antitumor effects of repeated doses of NV1020, a genetically engineered oncolytic herpes simplex virus, in patients with advanced metastatic colorectal cancer (mCRC). Patients with liver-dominant mCRC received four fixed NV1020 doses via weekly hepatic artery infusion, followed by two or more cycles of conventional chemotherapy. Phase I included cohorts receiving 3 × 10(6), 1 × 10(7), 3 × 10(7), and 1 × 10(8) plaque-forming units (PFU)/dose to determine the optimal biological dose (OBD) for phase II. Blind independent computed tomography scan review was based on RECIST (response evaluation criteria in solid tumors) to assess hepatic tumor response. Phase I and II enrolled 13 and 19 patients, respectively. Patients experienced transient mild-moderate febrile reactions after each NV1020 infusion. Grade 3/4 virus-related toxicity was limited to transient lymphopenia in two patients. NV1020 shedding was not detected. Simultaneous cytokine and grade 1 coagulation perturbations were dose-limiting at 1 × 10(8) PFU/dose, considered the OBD. All 22 OBD patients had previously received 5-fluorouracil; most had received oxaliplatin or irinotecan (50% had both), many with at least one targeted agent. After NV1020 administration, 50% showed stable disease. The best overall tumor control rate after chemotherapy was 68% (1 partial response, 14 stable disease); this did not correlate with baseline variables or chemotherapy. Median time to progression was 6.4 months (95% confidence interval: 2, 8.9); median overall survival was 11.8 months (95% confidence interval: 8.3, 20.7). One-year survival was 47.2%. We conclude that NV1020 stabilizes liver metastases with minimal toxicity in mCRC. It may resensitize metastases to salvage chemotherapy and extend overall survival. A randomized phase II/III trial now appears justified.
这项多中心的 I/II 期研究评估了 NV1020(一种基因工程的溶瘤单纯疱疹病毒)在晚期转移性结直肠癌(mCRC)患者中的安全性、药代动力学和抗肿瘤作用。肝脏为主的 mCRC 患者接受每周一次的肝动脉内输注 4 个固定剂量的 NV1020,然后进行两个或更多周期的常规化疗。I 期包括接受 3×10(6)、1×10(7)、3×10(7)和 1×10(8)噬菌斑形成单位(PFU)/剂量的队列,以确定 II 期的最佳生物学剂量(OBD)。盲法独立计算机断层扫描(CT)评估基于 RECIST(实体瘤反应评价标准)来评估肝肿瘤反应。I 期和 II 期分别纳入了 13 名和 19 名患者。患者在每次 NV1020 输注后出现短暂的轻度至中度发热反应。两名患者出现了 3/4 级与病毒相关的毒性,仅限于短暂的淋巴细胞减少。未检测到 NV1020 脱落。同时发生的细胞因子和 1 级凝血紊乱是剂量限制在 1×10(8)PFU/剂量,被认为是 OBD。所有 22 名接受 OBD 治疗的患者均接受过氟尿嘧啶治疗;大多数患者接受过奥沙利铂或伊立替康治疗(50%的患者同时接受了这两种药物治疗),许多患者还至少接受了一种靶向药物治疗。接受 NV1020 治疗后,50%的患者病情稳定。化疗后最佳的总体肿瘤控制率为 68%(1 例部分缓解,14 例病情稳定);这与基线变量或化疗无关。中位无进展生存期为 6.4 个月(95%置信区间:2,8.9);中位总生存期为 11.8 个月(95%置信区间:8.3,20.7)。一年生存率为 47.2%。我们得出结论,NV1020 在 mCRC 中稳定肝脏转移灶,毒性最小。它可能使转移灶对挽救化疗重新敏感,并延长总生存期。目前看来,进行一项随机的 II/III 期试验是合理的。