Annals of Oncology 15:504-510, 2004
© 2004 European Society for Medical Oncology
Original Paper |
Efficiency of in vivo purging with rituximab prior to autologous peripheral blood progenitor cell transplantation in B-cell non-Hodgkins lymphoma: a single institution study
Received 20 May 2003; revised 1 September 2003; accepted 7 November 2003;Background:
Rituximab induces clinical response in advanced B-cell lymphoma and is efficient in removing circulating B-cell from peripheral blood. We therefore postulated that rituximab might be a useful in vivo purging agent before high-dose therapy in this setting.
Patients and methods:
Fourteen patients with relapsed follicular, marginal zone and mantle cell lymphomas (11, two and one cases, respectively) and a PCR-detectable molecular marker were treated first with rituximab, then a mobilization chemotherapeutic regimen, followed by high-dose therapy with peripheral blood stem cell transplantation. PCR analyses were performed in peripheral blood before rituximab and during follow-up, and in harvest.
Results:
Harvests were free of PCR-detectable molecular marker in nine of the 11 studied cases (82%). After high-dose therapy, clinical complete remission was obtained in 13 (93%) patients and molecular remission in 11 (79%). With a median follow-up of 3 years, the 14 transplanted patients were alive, 11 of them remaining in clinical complete remission and eight in molecular remission at last follow-up.
Conclusion:
Rituximab treatment followed by high dose therapy appears to be effective in achieving complete clinical and molecular response. In vivo harvest purging is predictive of prolonged clinical and molecular remission.
1 CHU Henri Mondor, Service dHématologie Clinique; 2 CHU Henri Mondor, Laboratoire dImmunologie; 3 CHU Henri Mondor, Unité de Thérapie cellulaire EFS; 4 CHU Henri Mondor, Service de Radiothérapie; 5 CHU Henri Mondor, Service dAnatomo-pathologie, Créteil, France
Key words: B-NHL, high-dose therapy, PCR, purging, rituximab
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