Publicações científicas

Clinical benefit associated with idiotypic vaccination in patients with follicular lymphoma

Inogés S [ES]., Rodríguez-Calvillo M., Zabalegui N., López-Díaz de Cerio A., Villanueva H., Soria E., Suárez L., Rodríguez-Caballero A., Pastor F., García-Muñóz R., Panizo C., Pérez-Calvo J., Melero I [ES]., Rocha E., Orfao A., Bendandi M.
Grupo Español de Linfomas/Trasplante Autologo de Medula Oseo study group, Programa para el Estudio y Tratamiento de Hemopatias Malignas study group.
Lab of Immunotherapy, Oncology Division, Center for Applied Medical Research (CIMA), Avda. Pío XII, 55, 31008 Pamplona (Navarra), Spain.

Revisão:Journal of the National Cancer Institute

Data: 1/Set/2006

Imunologia e Imunoterapia [ES] Área de Terapia Celular [ES]

BACKGROUND
Follicular lymphoma is considered incurable, although cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy can induce sequential remissions. A patient's second complete response is typically shorter than that patient's first complete response. Idiotype vaccines can elicit specific immune responses and molecular remissions in patients with follicular lymphoma. However, a clinical benefit has never been formally proven.

METHODS
Thirty-three consecutive follicular lymphoma patients in first relapse received six monthly cycles of CHOP-like chemotherapy. Patients who achieved a second complete response were vaccinated periodically for more than 2 years with autologous lymphoma-derived idiotype protein vaccine. Specific humoral and cellular responses were assessed, and patients were followed for disease recurrence. Statistical tests were two-sided.

RESULTS
Idiotype vaccine could be produced for 25 patients who had a second complete response. In 20 patients (80%), a humoral (13/20) and/or a cellular (18/20) idiotype-specific response was detected. The median duration of the second complete response has not been reached, but it exceeds 33 months (range = 20+ to 51+ months).

None of the 20 responders relapsed while undergoing active vaccination. All responders with enough follow-up for the comparison to be made experienced a second complete response that was statistically significantly (P<.0001) longer than both their first complete response (18 of 18 patients) and than the median duration of a CHOP-induced second complete response, i.e., 13 months (20 of 20 patients). The five nonresponders all had a second complete response that was shorter (median = 10 months; range = 8-13 months) than their first complete response (median = 17 months; range = 10-39 months).

CONCLUSIONS
Idiotypic vaccination induced a specific immune response in the majority of patients with follicular lymphoma. Specific immune response was associated with a dramatic and highly statistically significant increase in disease-free survival. This is the first formal demonstration of clinical benefit associated with the use of a human cancer vaccine.

CITAÇÃO DO ARTIGO J Natl Cancer Inst. 2006 Sep 20;98(18):1292-301

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