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DOI 10.1200/jco.2003.10.005

Медицинская библиотека · Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2003

Clinical and immunologic results of a randomized phase II trial of vaccination using four melanoma peptides either administered in granulocyte-macrophage colony-stimulating factor in adjuvant or pulsed on dendritic cells.

Slingluff Craig L, Petroni Gina R, Yamshchikov Galina V, Barnd Donna L, Eastham Shannon, Galavotti Holly, Patterson James W, Deacon Donna H, Hibbitts Sarah, Teates David, Neese Patrice Y, Grosh William W, Chianese-Bullock Kimberly A, Woodson Elizabeth M H, Wiernasz Catherine J, Merrill Priscilla, Gibson Jennifer, Ross Maureen, Engelhard Victor H

Клиническое исследованиеСтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПоддержка службы здравоохранения СШАПеревод пока не подготовлен

Аннотация

PURPOSE: To determine clinical and immunologic responses to a multipeptide melanoma vaccine regimen, a randomized phase II trial was performed.

PATIENTS AND

METHODS

Twenty-six patients with advanced melanoma were randomly assigned to vaccination with a mixture of four gp100 and tyrosinase peptides restricted by HLA-A1, HLA-A2, and HLA-A3, plus a tetanus helper peptide, either in an emulsion with granulocyte-macrophage colony-stimulating factor (GM-CSF) and Montanide ISA-51 adjuvant (Seppic Inc, Fairfield, NJ), or pulsed on monocyte-derived dendritic cells (DCs). Systemic low-dose interleukin-2 (Chiron, Emeryville, CA) was given to both groups. T-lymphocyte responses were assessed, by interferon gamma ELIspot assay (Chiron, Emeryville, CA), in peripheral-blood lymphocytes (PBLs) and in a lymph node draining a vaccine site (sentinel immunized node [SIN]).

RESULTS

In patients vaccinated with GM-CSF in adjuvant, T-cell responses to melanoma peptides were observed in 42% of PBLs and 80% of SINs, but in patients vaccinated with DCs, they were observed in only 11% and 13%, respectively. The overall immune response was greater in the GM-CSF arm (P <.02). Vitiligo developed in two of 13 patients in the GM-CSF arm but in no patients in the DC arm. Helper T-cell responses to the tetanus peptide were detected in PBLs after vaccination and correlated with T-cell reactivity to the melanoma peptides. Objective clinical responses were observed in two patients in the GM-CSF arm and one patient in the DC arm. Stable disease was observed in two patients in the GM-CSF arm and one patient in the DC arm.

CONCLUSION

The high frequency of cytotoxic T-lymphocyte responses and the occurrence of clinical tumor regressions support continued investigation of multipeptide vaccines administered with GM-CSF in adjuvant.

Для цитирования: Slingluff Craig L, Petroni Gina R, Yamshchikov Galina V, Barnd Donna L, Eastham Shannon, Galavotti Holly, Patterson James W, Deacon Donna H, Hibbitts Sarah, Teates David, Neese Patrice Y, Grosh William W, Chianese-Bullock Kimberly A, Woodson Elizabeth M H, Wiernasz Catherine J, Merrill Priscilla, Gibson Jennifer, Ross Maureen, Engelhard Victor H. Clinical and immunologic results of a randomized phase II trial of vaccination using four melanoma peptides either administered in granulocyte-macrophage colony-stimulating factor in adjuvant or pulsed on dendritic cells.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2003. DOI: 10.1200/jco.2003.10.005.

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