Ogawa Yasuhiro, Kubota Kei, Ue Hironobu, Kataoka Yuko, Tadokoro Michiko, Miyatake Kana, Tsuzuki Kazuhiro, Yamanishi Tomoaki, Itoh Satoshi, Hitomi Jiro, Hamada Norihiko, Kariya Shinji, Fukumoto Mitsutaka, Nishioka Akihito, Inomata Taisuke
Department of Diagnostic Radiology and Radiation Oncology, Medical School, Kochi University, Oko-cho, Nankoku-shi, Kochi 783-8505, Japan.
Int J Oncol. 2009 Mar;34(3):609-18. doi: 10.3892/ijo_00000186.
Using a currently employed linear accelerator, our intent was to inactivate peroxidase/catalase in tumor tissue by the application of hydrogen peroxide, which is degraded to produce oxygen, thus re-oxygenizing the tumor tissue. In this way, we can convert radioresistant tumors into radiosensitive ones. On the basis of this strategy, we previously developed a new enzyme-targeting radiosensitization treatment named KORTUC I, which remarkably enhances the radiotherapeutic effect on various types of superficially exposed and locally advanced malignant neoplasms. Based on our clinical experience using KORTUC I, we also developed a new radiosensitizer containing hydrogen peroxide and sodium hyaluronate for injection into various types of tumors that are not superficially exposed (KORTUC II; described herein). KORTUC II was approved by our local ethics committee for advanced skin cancer, including malignant melanoma, bone/soft tissue malignant neoplasms, breast cancer, and metastatic lymph nodes. A maximum of 6 ml of the agent was injected into tumor tissue one to two times per week under ultrasonographic guidance, just prior to each administration of radiation therapy. Eleven patients, including seven with breast cancer, were enrolled in the KORTUC II trial upon fully informed consent. KORTUC II was well tolerated, with a minimum of adverse effects. Nine of the 11 patients showed a complete response (CR), and no severe complications occurred in any of the 11 patients. This new enzyme-targeting radiosensitization treatment may be indicated for various types of locally advanced neoplasms, including soft tissue neoplasms and breast cancers.
我们的目的是使用目前使用的直线加速器,通过应用过氧化氢来灭活肿瘤组织中的过氧化物酶/过氧化氢酶,过氧化氢降解后会产生氧气,从而使肿瘤组织重新充氧。通过这种方式,我们可以将抗辐射肿瘤转化为对辐射敏感的肿瘤。基于这一策略,我们之前开发了一种名为KORTUC I的新型酶靶向放射增敏治疗方法,该方法能显著增强对各种类型的浅表暴露和局部晚期恶性肿瘤的放射治疗效果。基于我们使用KORTUC I的临床经验,我们还开发了一种新的放射增敏剂,其含有过氧化氢和透明质酸钠,用于注射到各种非浅表暴露的肿瘤中(KORTUC II;本文所述)。KORTUC II已获得我们当地伦理委员会的批准,可用于治疗晚期皮肤癌,包括恶性黑色素瘤、骨/软组织恶性肿瘤、乳腺癌和转移性淋巴结。在每次放疗前,在超声引导下每周向肿瘤组织注射最多6毫升该药物,注射一至两次。11名患者,包括7名乳腺癌患者,在充分知情同意后参加了KORTUC II试验。KORTUC II耐受性良好,不良反应最少。11名患者中有9名出现完全缓解(CR),11名患者中均未发生严重并发症。这种新型酶靶向放射增敏治疗可能适用于各种类型的局部晚期肿瘤,包括软组织肿瘤和乳腺癌。