Department of Endoscopy, Nagoya University Hospital, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan.
Cancer Immune Therapy Research Center, Nagoya University Graduate School of Medicine, Nagoya, Japan.
BMC Cancer. 2018 May 25;18(1):596. doi: 10.1186/s12885-018-4453-z.
Prognosis of pancreatic cancer is poor with a 5-year survival rate of only 7%. Although several new chemotherapy treatments have shown promising results, all patients will eventually progress, and we need to develop newer chemotherapy treatments to improve response rates and overall survival (OS). HF10 is a spontaneously mutated oncolytic virus derived from a herpes simplex virus-1, and it has potential to show strong antitumor effect against malignancies without damaging normal tissue. We aimed to evaluate the safety and anti-tumor effectiveness in phase I dose-escalation trial of direct injection of HF10 into unresectable locally advanced pancreatic cancer under endoscopic ultrasound (EUS)-guidance in combination with erlotinib and gemcitabine administration. The mid-term results have been previously reported and here we report the final results of our study.
This was a single arm, open-label Phase I trial. HF10 was injected once every 2 weeks and continued up to four times in total unless dose-limiting toxicity (DLT) appears. A total of nine subjects in three Cohorts with dose-escalation were planned to be enrolled in this trial. The primary endpoint was the safety assessment and the secondary endpoint was the efficacy assessment.
Twelve patients enrolled in this clinical trial, and ten subjects received this therapy. Five patients showed Grade III myelosuppression and two patients developed serious adverse events (AEs) (perforation of duodenum, hepatic dysfunction). However, all of these events were judged as AEs unrelated to HF10. Tumor responses were three partial responses (PR), four stable diseases (SD), and two progressive diseases (PD) out of nine subjects who completed the treatment. Target lesion responses were three PRs and six SDs. The median progression free survival (PFS) was 6.3 months, whereas the median OS was 15.5 months. Two subjects from Cohort 1 and 2 showed downstaging and finally achieved surgical complete response (CR).
HF10 direct injection under EUS-guidance in combination with erlotinib and gemcitabine was a safe treatment for locally advanced pancreatic cancer. Combination therapy of HF10 and chemotherapy should be explored further in large prospective studies.
This study was prospectively registered in UMIN-CTR (UMIN000010150) on March 4th, 2013.
胰腺癌的预后很差,5 年生存率仅为 7%。尽管几种新的化疗治疗方法显示出了有希望的结果,但所有患者最终都会进展,我们需要开发新的化疗方法来提高反应率和总生存率(OS)。HF10 是一种源自单纯疱疹病毒-1 的自发突变溶瘤病毒,它有可能对恶性肿瘤产生强烈的抗肿瘤作用,而不会损伤正常组织。我们旨在评估在超声内镜(EUS)引导下直接注射 HF10 联合厄洛替尼和吉西他滨治疗不可切除的局部晚期胰腺癌的安全性和抗肿瘤效果。中期结果已在前一份报告中报道,在此我们报告本研究的最终结果。
这是一项单臂、开放标签的 I 期试验。HF10 每 2 周注射一次,最多共注射四次,除非出现剂量限制毒性(DLT)。该试验计划招募三个剂量递增队列共 9 名受试者。主要终点是安全性评估,次要终点是疗效评估。
本临床试验共纳入 12 例患者,10 例患者接受了该治疗。5 例患者出现 III 级骨髓抑制,2 例患者发生严重不良事件(AE)(十二指肠穿孔,肝功能障碍)。然而,所有这些事件均被判定为与 HF10 无关的 AE。9 名完成治疗的受试者中,肿瘤反应为 3 例部分缓解(PR)、4 例稳定疾病(SD)和 2 例进展疾病(PD)。靶病灶反应为 3 例 PR 和 6 例 SD。中位无进展生存期(PFS)为 6.3 个月,中位总生存期(OS)为 15.5 个月。2 例来自队列 1 和 2 的患者降期,最终达到手术完全缓解(CR)。
EUS 引导下 HF10 直接注射联合厄洛替尼和吉西他滨治疗局部晚期胰腺癌是一种安全的治疗方法。HF10 与化疗的联合治疗应在大型前瞻性研究中进一步探索。
本研究于 2013 年 3 月 4 日在 UMIN-CTR(UMIN000010150)前瞻性注册。