Tumor-directed immunotherapy: combined radiotherapy and oncothermia
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1 Tumor-directed immunotherapy: combined radiotherapy and oncothermia Kwan-Hwa Chi Professor, National Yang-Ming Medical University Chairman, Department of Radiation Therapy& Oncology, Shin-Kong Memorial Hospital, Taipei Presented at 36 th ICHS, Budapest, 2018 Cite this article as: Chi KH. (2018): Tumor-directed immunotherapy: combined radiotherapy and oncothermia; Oncothermia Journal 24: Oncothermia Journal, Volume 24, October
2 Tumor-directed immunotherapy: combined radiotherapy and oncothermia Kwan-Hwa Chi Chairman, Department of Radiation Therapy & Oncology, Shin Kong Wu Ho- Su Memorial Hospital Professor, National Yang-Ming University Objective Radiotherapy is an important part of cancer treatment. Hyperthermia has long been regarded as one of the best radiosensitization method. Oncothermia is a new kind of hyperthermia machine emphasizing energy absorbed on tumor cell membrane instead of nonspecific temperature rising around the treatment region. We proposed that oncothermia may have immune potentiation effect besides its radio(chemo)-sensitization effect Methods We aimed to examine, how real the abscopal events and what is the therapeutic effect of combined oncothermia and RT. Patients treated with combined RT and oncothermia since January 2017 till December 2017 at Shin-Kong Hospital, Taipei were retrospectively reviewed. We analyzed those who have measurable disease, performance status 2, a minimal RT dose of 30Gy and at least 4 times of oncothermia treatments. The primary prostate cancers were excluded. Results There were 60 patients evaluable, 27 patients with localized disease, in whom RT were the main treatment. Among them the CR rate was 22.2%, PR rate was 55.5%, SD with 14.8%. Two patients (one phylloid tumor of breast and one pancreatic cancer) were progressive disease after treatment. Most patients had acceptable local control for a median follow-up time of 9 months. Thirty-three patients with metastatic disease received palliative RT for a total of 38 sites, with a median dose of 44Gy/22fx to major disease sites. Patients with CR/PR has much longer survival than those not (SD+PD) (P<0.001). Shallower tumor (<5cm below skin) seemed to have batter effect than deeper tumor, but not significant (P>0.1). The objective response (CR+PR) in treated area is 60.7%. Most strikingly, there were obvious abscopal response in 3 patients. All of them had autoimmune reaction from treatment. One patient had autoimmune hepatitis the other one had dermatitis hapefiforms, and one patient had severe myasthenia gravis. They all had long duration of response without systemic treatment. Conclusion We reported that the combination of RT and oncothermia is effective and well tolerated. Oncothermia seems to have efficient radiosensitization effect in combined with RT or CCRT. Only randomized trial can answer the real clinical benefit of combined RT+HT on advanced cancer. However, a connection of autoimmune response is an evidence of immune boosting from oncothermia. Oncothermia activates lymphocyte in situ and provoked abscopal effect with RT. How oncothermia treatment provokes autoimmune reaction can pave the way antitumor immunity is underway Oncothermia Journal, Volume 24, October
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