Association of Velcade to R-CHOP in the Treatment of B Cell Lymphoma

B Cell Lymphoma Clinical Trial

Official title:

Phase II Study of the Association of Velcade to R-CHOP in the Treatment of B Cell Lymphoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00169468
• Other study ID #: R-CHOP VELCADE
• Status: Completed
• Phase: Phase 2
• Start date: January 2005
• Est. completion date: January 2006

Study information

• Verified date: August 2018
• Source: Lymphoma Study Association
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to evaluate the response rate and toxicity of the association R-CHOP with two schedules of administration of Velcade, in B-cell CD 20 + lymphoma patients, aged from 18 to 80 years

The goal is to get a response rate at least at what observed with R-CHOP alone and will be evaluates with a sequential test.

The other objective is to evaluate the toxicity

Description:

The association of the monoclonal antibody Rituximab to chemotherapy regimen of B-cell lymphoma is associated with an increase response rate and event free survival when compared to chemotherapy alone (Coiffier et al NEJM 2002). It has been observed in almost all histological type of B-cell lymphomas. No significant increase of toxicity was observed especially in the most used regimen CHOP and the association R-CHOP is a standard for most B-cell malignancies CD20 positive.

However, in patients with diffuse large cell lymphoma progress should be made as the complete response rate is below 75% in most situation and in low grade lymphoma, although patients respond well to chemotherapy complete remission rate averaged generally 50% (Marcus et al 2003), Czuczman et al 1999) .

There is a need to improve this association with new innovative agent. Before running randomized study it is important to evaluate the like hood of getting improvement by phase 2 study testing tolerance and efficacy on a well established regimen.

Bortezomib (Velcade formerly PS 341) is a proteasome inhibitor which has shown promising activity in the treatment of refractory myeloma. As single agent in indolent lymphomas, administered twice per weeks for 2 weeks followed by one week rest period it has already showed activity in phase 2 study. It is well tolerated and main toxicity was neuropathy and thrombocytopenia.

Proteasome inhibitors can act through multiple mechanisms to arrest tumor growth, tumor spread, and angiogenesis. In vitro studies have shown a synergistic effect of the association of Velcade and doxorubicin on myeloma cell lines resistant to chemotherapy.

Association of Velcade to standard chemotherapy regimen is under study with the aim of improving on the results.

Association of Velcade to one of the most efficient treatment of B-cell lymphoma, R-CHOP, might increase the response rate.

However, different schedules should be explored in order to better appreciate efficacy and toxicity.

This randomized phase 2 study is designed to evaluate the response rate and the toxicity of two schedules of administration of Velcade in association with R-CHOP. The aim of the study is to establish a well tolerated regimen giving a response rate in the limit upper/lower of what is observed with conventional R-CHOP used in all the different histological subtypes of B cell lymphomas patients requiring treatment.

The heterogeneity of the population will preclude any meaningful subgroup analysis.

It is important to evaluate tolerability before exploring the efficacy of this new regimen in large randomized studies or in specific phases II study which will need 50 patients for each subgroup of patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: January 2006
• Est. primary completion date: January 2006
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Patients with one of the following B-cell Lymphoma CD 20 positive : Mantle cell, Marginal zone, lymphocytic, follicular requiring treatment, Histological transformation from low grade to high grade, diffuse large cell without adverse prognostic factors defined by the international prognostic index (IPI)

• Aged from 18 to 80 years

• Untreated with chemotherapy except with Chlorambucil or Cyclophosphamide per os alone less than 6 months

• Previous radiotherapy except if localized

• Performance status < 3

• Signed inform consent

Exclusion Criteria:

• Other type of lymphomas: Burkitt, T cell, CD 20 negative

• Central nervous system or meningeal involvement

• Contraindication to any drug contained in the chemotherapy regimen

• HIV disease, active hepatitis B or C

• Treatment with polychemotherapy before except with Chlorambucil or Cyclophosphamide per os less than 6 months

• Prior extended radiotherapy

• Any serious active disease or co-morbid medical condition (according to investigator's decision )

• Renal deficiency (clearance < 30 ml/mn), liver deficiency (bilirubin > 30 mmol/l) unless related to lymphoma

• Neuropathy> grade 2 within 14 days before enrollment

• Platelets < 30.109/l within 14 days before enrollment

• Neutrophils < 1.0 109/l within 14 days before enrollment

• Women with pregnancy or without adequate method of contraception

• Any history of active cancer during the last two years

Related Conditions & MeSH terms

• B Cell Lymphoma
• Lymphoma
• Lymphoma, B-Cell

Intervention

Drug:
• Rituximab -CHOP plus Velcade

Locations

Country	Name	City	State
France	Hôpital Henri Mondor	Créteil
France	Hôpital Saint-Louis	Paris	Paris 10
France	Hôpital Lyon Sud	Pierre Bénite
France	Institut Gustave Roussy	Villejuif	Villejuif Cedex

Sponsors (2)

Lead Sponsor	Collaborator
Lymphoma Study Association	Association pour le Développement de la Recherche Clinique et Informatique en Onco-Hématologie

Country where clinical trial is conducted

France, 

References & Publications (4)

44. Marcus R, et al. (2003). An International Multi-Centre, Randomized, Open-Label, Phase III Trial Comparing Rituximab Added to CVP Chemotherapy to CVP Chemotherapy Alone in Untreated Stage III/IV Follicular Non-Hodgkins Lymphoma. Blood, 102, issue 11, (abstract 87).

Coiffier B, Lepage E, Briere J, Herbrecht R, Tilly H, Bouabdallah R, Morel P, Van Den Neste E, Salles G, Gaulard P, Reyes F, Lederlin P, Gisselbrecht C. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. N Engl J Med. 2002 Jan 24;346(4):235-42. — View Citation

Czuczman MS, Grillo-López AJ, White CA, Saleh M, Gordon L, LoBuglio AF, Jonas C, Klippenstein D, Dallaire B, Varns C. Treatment of patients with low-grade B-cell lymphoma with the combination of chimeric anti-CD20 monoclonal antibody and CHOP chemotherapy. J Clin Oncol. 1999 Jan;17(1):268-76. — View Citation

O'Connor O, Wright J, Moskowitz CH et al. Promising Activity of the Proteasome Inhibitor Bortezomib (Velcade) in the Treatment of Indolent Non-Hodgkin's Lymphoma and Mantle Cell Lymphoma. Session Type: Poster Session 517-II. Blood, Volume 102, issue 11, November 16, 2003 (abstract 2346)

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of complete remission		1 year
Primary	Number of SAE		1 year
Secondary	Duration of response		1 year
Secondary	Progression free survival		1 year
Secondary	Overall survival		1 year