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Spots Global Cancer Trial Database for Allogeneic Hematopoietic Stem Cell Transplantation After Reduced-intensity Conditioning for Relapsed Follicular Lymphoma

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Trial Identification

Brief Title: Allogeneic Hematopoietic Stem Cell Transplantation After Reduced-intensity Conditioning for Relapsed Follicular Lymphoma

Official Title: Safety and Efficacy of a Strategy of Allogeneic Hematopoietic Stem Cell Transplantation After Reduced-intensity Conditioning for Chemosensitive Relapsed Follicular Lymphoma

Study ID: NCT01208896

Study Description

Brief Summary: This trial will evaluate the efficacy and the safety of a strategy of allogeneic stem cell transplantation including Rituximab in the conditioning regimen for the treatment of relapsed follicular lymphoma. The rationale for using Rituximab relies on a better control of the disease and a better prophylaxis of the graft versus host disease.

Detailed Description: Follicular lymphomas are chemosensitive neoplasms characterized by a relentless succession of remissions and relapses when treated with conventional chemotherapy. The successive periods of remission are of shorter duration and patients invariably die of their disease. At first line, patients are treated with conventional chemotherapy. At first relapse, intensive chemotherapy with autologous stem cell transplantation (SCT) is often proposed. Allogeneic hematopoietic stem cell transplantation after reduced-intensity conditioning (RIC-allo) is an option for patients relapsing after autologous SCT, allowing long-term progression free survival of 50 to 60%. The toxic mortality related to severe acute graft versus host disease (GVHD) remains a critical issue. The goal of our study is to test in a multicentric approach a strategy of RIC-allo including rituximab in order to reduce the incidence of acute GVHD. Around half of patients with relapsed or refractory follicular lymphomas treated with allogeneic SCT achieve long-term progression free survival whatever the conditioning regimen. Because the median age of patients with follicular lymphoma is 55 years, a reduced intensity conditioning is the most appropriate option in this setting. The outcome of patients with a chemoresistant disease is usually poor because of a high toxic mortality. As a consequence, only patients with a chemosensitive disease will be included in this study. To further reduce the toxic mortality, it is critical to reduce the incidence of severe acute GVHD. A low incidence of acute GVHD could be obtained by the use of Rituximab before and after the transplantation as reported by the MD Anderson's experience in several hematological malignancies including follicular lymphoma. Their results are impressive in patients with follicular lymphoma with long-term survival of 85%. The favored hypothesis is a depletion of patient and donor B cells reducing the presentation of minor histocompatibility alloantigens. The benefit of Rituximab could also be explained by its anti-lymphoma effects that could compensate the putative reduction of a graft versus lymphoma effect due to a better control of GVHD. The primary objective is to estimate 2-year overall survival in this setting.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University Hospital Angers, Angers Cedex 01, Angers, France

Service Hématologie, Hôpital Minjoz, Besançon, , France

Service Hématologie, Hôpital Augustin Morvan, Brest, , France

University Hospital, Caen, Caen, , France

Service Hématologie et Thérapie cellulaire, Pavillon Villemin Pasteur, CHU Clermont-Ferrand, Clermont-Ferrand, , France

CHU Grenoble, Grenoble, , France

CHRU Lille, Lille, , France

CHU Limoges, Limoges, , France

Hôpital Edouard Herriot, Lyon, , France

Service Hématologie Oncologie, Hôpital Lapeyronie, CHU de Montpellier, Montpellier, , France

CHU Nancy, Nancy, , France

Service Hématologie Clinique, CHU -Hôtel Dieu, Nantes, , France

Service Hématologie Clinique, Hôpital Archet 1, Nice, , France

APHP Hôpital Necker-Enfants malades, Paris, , France

APHP Hôpital Saint Louis, Paris, , France

APHP Hôpital Pitié-Salpêtrière, Paris, , France

APHP Hôpital Henri-Mondor, Paris, , France

Service des maladies du sang - Hôpital Haut-Lévêque - avenue de magellan, Pessac, , France

CHU Poitiers - La Milétrie, Poitiers, , France

Service Hématologie Clinique, Hôpital Pontchaillou, Rennes, , France

Centre Henri Becquerel, Rouen, , France

Institut de Cancérologie de la Loire, Saint Etienne, , France

Département d'Hématologie et d'Oncologie, Hôpital CHRU de Hautepierre, Strasbourg, , France

Service Hématologie, Hôpital Purpan, Toulouse, , France

CHRU Tours, Tours, , France

Institut Gustave Roussy, Villejuif, , France

Contact Details

Name: Stéphane VIGOUROUX, MD

Affiliation: University Hospital, Bordeaux

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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