Nakao A, Takeda S, Shimoyama S, Kasuya H, Kimata H, Teshigahara O, Sawaki M, Kikumori T, Kodera Y, Nagasaka T, Goshima F, Nishiyama Y, Imai T
Department of Surgery II, Nagoya University, Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Curr Cancer Drug Targets. 2007 Mar;7(2):169-74. doi: 10.2174/156800907780058808.
We reviewed our clinical trial using mutant herpes simplex virus "HF10". We have evaluated the safety and effect of HF10 against recurrent breast cancer since 2003 and also applied HF10 to non-resectable pancreatic cancer since 2005. An oncolytic herpes simplex virus type 1, mutant HF10, has been isolated and evaluated for anti-tumor efficacy in syngeneic immunocompetent mouse models. From long time before clinical trial, we have found that the mutant virus can have remarkable potential to effectively treat cancer in experimental studies using animals, and that all of the surviving mice acquire resistance to rechallenge of the tumor cells. A number of studies have shown that HF10 is effective and safe for use in localized or peritoneally disseminated malignant tumors of non-neuronal origin in animals. Pilot studies using HF10 have been initiated in patients with metastatic breast cancer. For each patient, 0.5 ml HF10 diluents at various doses were injected into test nodule, and 0.5 ml sterile saline was injected into a second nodule. All patients were monitored for local and systemic adverse effects, and the nodules were excised 14 days after viral injection for histopathological studies. All patients tolerated the clinical trial well. While no adverse effects occurred, there was cancer cell death and 30-100% regression histopathologically in recurrent breast cancer. As mentioned above, intratumoral injection of mutant herpes simplex virus HF10 for recurrent metastatic breast cancer was safe and effective. Also a trial for non-resectable pancreatic cancer being carried out on the basis of the above result has proved to be innocuous and has been in progress to assess the clinical benefit and enhance the potentiality of HF10 against cancer.
我们回顾了使用突变型单纯疱疹病毒“HF10”的临床试验。自2003年以来,我们评估了HF10对复发性乳腺癌的安全性和疗效,并且自2005年起将HF10应用于不可切除的胰腺癌。一种溶瘤性1型单纯疱疹病毒,突变体HF10,已被分离出来,并在同基因免疫活性小鼠模型中评估其抗肿瘤疗效。在临床试验之前很长一段时间,我们发现在动物实验研究中,这种突变病毒具有有效治疗癌症的显著潜力,并且所有存活的小鼠都获得了对肿瘤细胞再次攻击的抗性。许多研究表明,HF10在动物体内用于治疗非神经源性的局部或腹膜播散性恶性肿瘤是安全有效的。已针对转移性乳腺癌患者开展了使用HF10的初步研究。对于每位患者,将不同剂量的0.5 ml HF10稀释液注射到测试结节中,并将0.5 ml无菌生理盐水注射到另一个结节中。对所有患者进行局部和全身不良反应监测,并在病毒注射14天后切除结节进行组织病理学研究。所有患者对临床试验耐受性良好。虽然未发生不良反应,但在复发性乳腺癌中出现了癌细胞死亡,并且组织病理学上有30% - 100%的消退。如上所述,瘤内注射突变型单纯疱疹病毒HF10治疗复发性转移性乳腺癌是安全有效的。此外,基于上述结果正在进行的不可切除胰腺癌试验已证明是无害的,并且正在进行以评估临床益处并增强HF10对抗癌症的潜力。