Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00504491

R-CHOP and Alemtuzumab in Patients With Chronic Lymphocytic Leukemia

Rescue Treatment With Rituximab-CHOP Therapy and Alemtuzumab (R-CHOP-A) in Refractory or Recidivant Patients With Chronic Lymphocytic Leukemia After Purine-analogous Treatment

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
CABYC · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Since there is no standard rescue therapy for refractory CLL or relapsed to the purine analogous, our target is to carry out a rescue therapy combining several chemotherapy agents (CHOP) adding the synergistic effect of Rituximab in order to act against tumour-like CLL forms, with assessable size lymph nodes. Afterwards, based in other studies, we shall study the role of Alemtuzumab as drug for consolidation or improvement of responses obtained with the initial therapy (CHOP-R), acting by "cleaning" from peripheral blood and bone marrow the CLL lymphocytes that may have had remain as residual after chemotherapy induction therapy. More precisely, the addition of Alemtuzumab as maintenance treatment would increase the complete responses with negative residual disease number and may prolong the duration of the response. For this, it is necessary to have not only an adequate and rigorous clinical follow-up but also biological, i.e. being able to analyze minimal residual disease by molecular biology techniques. This is the reason of writing this phase II clinical trial protocol.

Detailed description

OBJECTIVES The objectives of this clinical trial are the following: * Main objective of the study: Overall response rate obtained after R-CHOP regime followed by Alemtuzumab consolidation as second line therapy * Secondary objectives * Determine the molecular complete response rate after R-CHOP regimen * Determine the efficacy of Alemtuzumab in response improvement after R-CHOP regimen: conversion of PR to CR and of MRD+ to MRD-. * Applicability (toxicity profile) of Alemtuzumab consolidation therapy. * As additional objectives will be considered: 1. Prognostic value of several biological variables (ZAP-70 and cytogenetics) having influence on the response 2. Response duration 3. Progression free survival 4. Overall survival

Conditions

Interventions

TypeNameDescription
DRUGRituximab-CHOP-AlemtuzumabFour Rituximab - CHOP courses will be given The courses will be given every 21 days

Timeline

Start date
2007-07-01
Primary completion
2012-01-01
Completion
2012-06-01
First posted
2007-07-20
Last updated
2011-12-30

Locations

32 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT00504491. Inclusion in this directory is not an endorsement.