Abstract | BACKGROUND: METHODS: Autologous DCs were generated from monocytes, loaded with ATCs, and delivered intranodally. Delayed-type hypersensitivity (DTH) and immunological endpoints were measured prevaccination and postvaccination. Clinical follow-up was required. RESULTS:
Tumors obtained from 30 patients yielded 2 × 10(6) to 2 × 10(8) tumor cells. Only 19 of 30 (63%) were sterile. Ten of 30 patients (33%) had ≥1 × 10(7) sterile tumor cells required for vaccine production. Eight of 10 patients had positive recall DTH. Five of 10 patients were leukapheresed to generate DCs. Four of 5 patients were vaccinated. ATC-reactive T cells were detected in 3 of 4 patients. All 4 patients survived >5 years. The trial failed to enroll the projected 12 patients and was terminated. CONCLUSION: This vaccine was safe and immunogenic but feasible only in patients with HNSCC with positive prevaccine DTH and ≥1 × 10(7) sterile tumor cells. All vaccinated patients were long-term disease-free survivors. © 2015 Wiley Periodicals, Inc. Head Neck 38: E494-E501, 2016.
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Authors | Theresa L Whiteside, Robert L Ferris, Miroslaw Szczepanski, Mitchell Tublin, Joseph Kiss, Rita Johnson, Jonas T Johnson |
Journal | Head & neck
(Head Neck)
Vol. 38 Suppl 1
Pg. E494-501
(04 2016)
ISSN: 1097-0347 [Electronic] United States |
PMID | 25735641
(Publication Type: Journal Article)
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Copyright | © 2015 Wiley Periodicals, Inc. |
Chemical References |
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Topics |
- Apoptosis
- Cancer Vaccines
(therapeutic use)
- Carcinoma, Squamous Cell
(prevention & control)
- Dendritic Cells
- Disease-Free Survival
- Feasibility Studies
- Head and Neck Neoplasms
(prevention & control)
- Humans
- Hypersensitivity, Delayed
- Pilot Projects
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