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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01195714
Other study ID # LNH09-7B
Secondary ID
Status Completed
Phase Phase 2
First received September 3, 2010
Last updated March 6, 2018
Start date May 2010
Est. completion date April 2014

Study information

Verified date March 2018
Source The Lymphoma Academic Research Organisation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a multicentric, phase II, open-label, non-randomized trial evaluating the efficacy of O-miniCHOP in patients aged over 80 years with non previously treated CD20+ diffuse large B-cell lymphoma (age-adjusted IPI=0 to3), stage I, II, III or IV with a performance status ECOG from 0 to 4.

The anticipated study dates (start / end) are: 2010 - 2013. The study will evaluate a cohort of 120 patients (approximately 95 in France, 15 in Belgium, 5 in Switzerland and 5 in Portugal).

Patients will be recruited over 30 months and followed at least one year after the last patient has been included.

The duration of the treatment period is approximately 20 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender All
Age group 81 Years and older
Eligibility Inclusion Criteria:

Patient with histologically proven CD20+ diffuse large B-cell lymphoma (DLBCL) (WHO classification 2008) including clinical subtypes (primitive mediastinal, intravascular, etc.) May also be included : de Novo Transformed DLBCL from low grade lymphoma (Follicular, other...) and DLBCL associated with some small cell infiltration in bone marrow

- Or CD20+ B-cell lymphoma, with intermediate features between DLBCL and Burkitt or with intermediate features between DLBCL and classical Hodgkin lymphoma

- Or CD20+ Follicular lymphoma grade 3B

- Or CD20+ Aggressive B-cell lymphoma unclassifiable Aged over 80 years. Ann Arbor stage I, II, III or IV. All aaIPI Patient non previously treated. All ECOG performance status With a minimum life expectancy of 3 months. Negative HIV, HBV and HCV serologies test < 4 weeks (except after vaccination). Patient able to give his consent and having previously signed a written informed consent.

Patient affiliated to social security system, if applicable

Exclusion Criteria:

Any other histological type of lymphoma, Burkitt included. Any history of treated or non-treated small-B cell lymphoma. Central nervous system or meningeal involvement by lymphoma. Contra-indication to any drug contained in the chemotherapy regimens. Any serious active disease (according to the investigator's decision). Poor renal function (creatinin level>150µmol/l), poor hepatic function (total bilirubin level>30mmol/l, transaminases>2.5 maximum normal level) unless these abnormalities are related to the lymphoma.

Poor bone marrow reserve as defined by neutrophils <1.5 G/l or platelets <100 G/l, unless related to bone marrow infiltration.

Any history of cancer during the last 5 years with the exception of non-melanoma skin tumors or stage 0 (in situ) cervical carcinoma. Patients previously diagnosed with prostate cancer are eligible if (1) their disease was T1-T2a, N0, M0, with a Gleason score <7, and a prostate specific antigen (PSA) <10 ng/mL prior to initial therapy, (2) they had definitive curative therapy (ie, prostatectomy or radiotherapy) >2 years before Day 1 of Cycle 1, and (3) at a minimum 2 years following therapy they had no clinical evidence of prostate cancer, and their PSA was undetectable if they underwent prostatectomy or <1 ng/mL if they did not undergo prostatectomy.

Treatment with any investigational drug within 30 days before planned first cycle of chemotherapy and during the study.

Prior treatment with anti-CD20 monoclonal antibody or alemtuzumab within 3 months prior to start of therapy Adult patient under tutelage.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ofatumumab
solution for perfusion, 1000mg per cycle, 1 cycle every 3 weeks, total 6 cycles

Locations

Country Name City State
Belgium Zna Stuivenberg Antwerpen
Belgium RHMS Baudour
Belgium Az Sint Jan Av Bruges
Belgium Chu de Liege Bruxelles
Belgium Institut Jules Bordet Bruxelles
Belgium Ucl de Louvain St Luc Bruxelles
Belgium Universite Libre de Bruxelles - Hopital Erasme Bruxelles
Belgium Grand Hopital de Charleroi Charleroi
Belgium Universitair Ziekenhuis Gent Gent
Belgium Clinique Notre Dame de Grace Gosselies
Belgium Hopital Jolimont Haine Saint Paul
Belgium Ch Hutois Huy
Belgium Az Groeninge - Campus Maria'S Voorzienigheid Kortrijk
Belgium Chu Tivoli La Louvière
Belgium Chr de La Citadelle Liège
Belgium Clinique Saint Pierre Ottignies
Belgium Universite Catholique de Louvain Mont Godinne Yvoir
France Ch Du Pays D'Aix Aix En Provence
France Ch Antibes Antibes
France Ch Henri Duffaut Avignon
France Hopital de Bayonne Bayonne
France Hopital Avicenne Bobigny
France Polyclinique Bordeaux Nord Aquitaine Bordeaux
France Ch Du Dr Duchenne Boulogne sur Mer
France Ch de Bour En Bresse Bourg en Bresse
France Chu de Brive Brive la Gaillarde
France Centre Henri Baclesse Caen
France Chu Cote de Nacre Caen
France Ch de Cannes Cannes
France Hopital de Chalon Chalon sur Saone
France Ch Chambery Chambery
France Ch de Chartres - Hopital Louis Pasteur Chartres
France Hopital Antoine Beclere Clamart
France Hopital D'Instruction Des Armees Percy Clamart
France Hopital Pasteur Colmar
France Ch Compiege Compiegne
France Ch Sud Francilien Corbeil-Essonnes
France Hopital Henri Mondor Creteil
France Chu Le Bocage Dijon
France Ch de Dunkerque Dunkerque
France Ch Dunkerque Dunkerque
France Ch Frejus St Raphael Frejus
France CH GERET Gueret
France Hopital Saint Louis La Rochelle
France Hopital Andre Mignot Le Chesnay
France Hopital Bicetre Le Kremlin-Bicêtre
France Ch de Meulan Les Mureaux
France Chu Claude Hurriez Lille
France Hopital St Vincent de Paul Lille
France Chu Dupuytren Limoges
France Centre Leon Berard Lyon
France Hopital Des Chanaux Macon
France Chu Hopital Nord Marseille
France Institut Paoli Calmette Marseille
France Chu de Meaux Meaux
France Chu Marc Jacquet Melun
France Hopital Bon Secours Metz
France Crlc Val D'Aurelle - Paul Lamarque Montpellier
France Centre Azureen de Cancerologie Mougins
France Hopital Americain de Paris Neuilly sur Seine
France Centre Antoine Lacassagne Nice
France Hopital de La Pitie Salpetriere Paris
France Hopital Necker Paris
France Hopital St Antoine Paris
France Hopital St Louis Paris
France Hotel Dieu Paris
France Institut Curie Paris
France Ch Marechal Joffre Perpignan
France Chu Lyon Sud Pierre Bénite
France Chu de Poitiers - Hopital de Miletrie Poitiers
France Ch Rene Dubos Pontoise
France Ch Annecy Pringy
France Chu Robert Debre Reims
France Ch de Roubaix - Hopital Victor Provo Roubaix
France Centre Henri Becquerel Rouen
France Clinique Mathilde Rouen
France Centre Rene Hugenin Saint Cloud
France Ch de Saint Germain Saint Germain en Laye
France Hopital Font Pre Toulon
France Chu de Toulouse Toulouse
France Ch de Troyes Troyes
France Hopital de Valence Valence
France Chu Brabois Vandoeuvre Les Nancy
France Institut Gustave Roussy Villejuif

Sponsors (1)

Lead Sponsor Collaborator
The Lymphoma Academic Research Organisation

Countries where clinical trial is conducted

Belgium,  France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Survival 2 years