Effect of combined adoptive immunotherapy and radiotherapy on tumor growth

✍ Scribed by R. Sumareva; G. Ukrainsky; L. Kiremidjian-Schumacher; M. Roy; H.I. Wishe; A.D. Steinfeld; J.S. Cooper

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 352 KB
• Volume: 7
• Category: Article
• ISSN: 1065-7541
• DOI: 10.1002/(sici)1520-6823(1999)7:1<22::aid-roi3>3.0.co;2-6

✦ Synopsis

Advanced squamous cell carcinomas of the head and neck are difficult to control despite optimal surgery, radiotherapy and/or chemotherapy, and the tumors are usually not immunogenic. Because of the anatomic accessibility of the tumors, local adoptive immunotherapy of these tumors is feasable and may interact with radiotherapy to retard tumor growth. It is hypothesized that antigens released from tumor cells injured by radiation may stimulate, in the presence of interleukin-2, an enhanced immunocytodestruction of live tumor cells by adoptively transferred lymphokine activated killer cells and recruited tumor cytotoxic cells. DBA/2 mice were injected subcutaneously with 5 × 10 5 syngeneic squamous cell carcinoma cells in the thigh and the resulting tumors were treated for two weeks with daily peritumoral injections of interleukin-2 (1,000 International Units) or saline, four radiation treatments of 625 cGy each, and four peritumoral injections of 10 7 lymphokine activated killer cells. The results suggested that radiotherapy combined with peritumoral injection of lymphokine activated killer cells and interleukin-2 resulted in a significant reduction (P < 0.01) of tumor size whereas radiation alone, at the same dose, failed to produce a significant effect. Such results may have direct clinical application in enhancing the response of tumors to radiotherapy and in reducing the incidence of tumor recurrence.