Sakura Kazuma, Kuroyama Muneyoshi, Shintani Yasushi, Funaki Soichiro, Atagi Shinji, Kadota Yoshihisa, Kuribayashi Kozo, Kijima Takashi, Nakano Takashi, Nakajima Toshihiro, Sasai Masao, Okumura Meinoshin, Kaneda Yasufumi
Respiratory Center, Osaka University Hospital, Suita, 5650871, Japan.
Department of Surgery, Osaka University Graduate School of Medicine, Suita, 5650871, Japan.
Cancer Immunol Immunother. 2024 Oct 3;73(12):243. doi: 10.1007/s00262-024-03815-1.
The hemagglutinating virus of Japan envelope (HVJ-E) is an inactivated Sendai virus particle with antitumor effect and inducing antitumor immunity. However, its dosage and efficacy have not been verified. We conducted a phase I clinical study on chemotherapy-resistant malignant pleural mesothelioma (MPM) aiming to determine the recommended dosage for a phase II study through dose-limiting toxicity and evaluate HVJ-E's preliminary efficacy. HVJ-E was administered intratumorally and subcutaneously to the patients with chemotherapy-resistant MPM. While no serious adverse events occurred, known adverse events of HVJ-E were observed. In the preliminary antitumor efficacy using modified response evaluation criteria in solid tumors (RECIST) criteria, three low-dose patients exhibited progressive disease, while all high-dose patients achieved stable disease, yielding disease control rates (DCRs) of 0% and 100%, respectively. Furthermore, the dose-dependent effect of HVJ-E revealed on DCR modified by RECIST and the baseline changes in target lesion size (by CT and SUL-peak; p < 0.05). Comparing targeted lesions receiving intratumoral HVJ-E with non-injected ones, while no clear difference existed at the end of the study, follow-up cases suggested stronger antitumor effects with intratumoral administration. Our findings suggest that HVJ-E could be safely administered to patients with chemotherapy-resistant MPM at both study doses. HVJ-E exhibited some antitumor activity against chemotherapy-resistant MPM, and higher doses tended to have stronger antitumor effects than lower doses. Consequently, a phase II clinical trial with higher HVJ-E doses has been conducted for MPM treatment. Trial registration number: UMIN Clinical Trials Registry (#UMIN000019345).
日本血凝病毒包膜(HVJ-E)是一种具有抗肿瘤作用并能诱导抗肿瘤免疫的灭活仙台病毒颗粒。然而,其剂量和疗效尚未得到验证。我们针对化疗耐药的恶性胸膜间皮瘤(MPM)进行了一项I期临床研究,旨在通过剂量限制性毒性确定II期研究的推荐剂量,并评估HVJ-E的初步疗效。将HVJ-E瘤内注射和皮下注射给化疗耐药的MPM患者。虽然未发生严重不良事件,但观察到了HVJ-E已知的不良事件。在使用实体瘤改良反应评估标准(RECIST)标准的初步抗肿瘤疗效中,三名低剂量患者出现疾病进展,而所有高剂量患者病情稳定,疾病控制率(DCR)分别为0%和100%。此外,HVJ-E对经RECIST修改的DCR的剂量依赖性效应以及靶病变大小的基线变化(通过CT和SUL-峰值;p<0.05)得以显现。将接受瘤内HVJ-E注射的靶病变与未注射的靶病变进行比较,虽然在研究结束时没有明显差异,但随访病例表明瘤内给药具有更强的抗肿瘤作用。我们的研究结果表明,在两个研究剂量下,HVJ-E均可安全地用于化疗耐药的MPM患者。HVJ-E对化疗耐药的MPM表现出一定的抗肿瘤活性,且高剂量往往比低剂量具有更强的抗肿瘤作用。因此,已针对MPM治疗开展了更高剂量HVJ-E的II期临床试验。试验注册号:UMIN临床试验注册库(#UMIN000019345)。