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NCT02896582CompletedPhase 2

Efficacy of Upfront and Maintenance Obinutuzumab in Mantle Cell Lymphoma Treated by DHAP and MRD Driven Maintenance

Phase II Study to Evaluate the Efficacy of Upfront Obinutuzumab in Mantle Cell Lymphoma Patients Treated by DHAP Followed by Autologous Transplantation Plus Obinutuzumab Maintenance Then MRD Driven Maintenance

Source: ClinicalTrials.gov · Last updated 14 Jan 2026

Brief summary (registry, in English)

This study is a multicentric, single arm phase II trial to evaluate the efficacy of upfront obinutuzumab in mantle cell lymphoma patients treated by Cisplatinum-Cytarabine-Dexamethasone (DHAP) followed by autologous transplantation plus obinutuzumab maintenance then Molecular Residual Disease (MRD) driven maintenance

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
86 (actual)
First submitted
6 Sept 2016
Start date
29 Nov 2016
Primary completion date
Mar 2019
Lead sponsor
The Lymphoma Academic Research Organisation
NCT number
NCT02896582

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 86
  • From 29 Nov 2016 to the primary completion date, Mar 2019
  • 30 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with a malignancy that has been treated but not with curative intent, unless the malignancy has been in remission without treatment for ≥ 5 years prior to enrollment. Patients with a history of curatively treated basal or squamous cell carcinoma or melanoma of the skin or in situ carcinoma of the cervix are eligible.
  • Prior history of Progressive Multifocal Leukoencephalopathy (PML)
  • Vaccination with a live vaccine a minimum of 28 days prior to inclusion (Prolonged B cell depletion)

Other illness

  • Severe cardiac disease: York Heart Association (NYHA) grade 3-4
  • History of chronic liver disease
  • Hepatic veno-occlusive disease or sinusoidal obstruction syndrome
  • Known seropositivity for Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV) or other active infection uncontrolled by treatment.
  • Viral infection with hepatitis B virus (HBV) defined as hepatitis B surface antigen (HBsAg) positive and/or Hepatitis B core antibody (anti-HBc) positive Note: Patients who are immune due to hepatitis B vaccination or natural infection (HBs Ag and anti-HBc negative, anti-HBs positive) are eligible. But the patients who are immune due to hepatitis B natural infection should consult liver disease experts before start of treatment and should be monitored and managed following local medical standards to prevent hepatitis reactivation
  • History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies. Known sensitivity or allergy to murine products
  • Psychiatric illness or condition which could interfere with their ability to understand the requirements of the study.

Lab values

  • Impaired liver (ALanine Amino Transferase (ALAT)/ASparagin Amino Transferase (ASAT) ≥ 2.5 Upper Limit of Normal (ULN), bilirubin ≥ 1.5 ULN), renal (calculated creatinine clearance \< 50 ml/min) or other organ function which will interfere with the treatment, if not related to lymphoma.
  • Any of the following laboratory abnormalities, if not result of a BM infiltration:
  • Absolute Neutrophils Count (ANC) \<1,500 /mm3 (1.5 x 109/L)
  • Platelet counts \< 75,000/mm3 (75 x 109/L)

Age

  • surgically sterile or ≥ 2 years after the onset of menopause

Other

  • Pregnancy/Nursing mothers
  • Fertile men or women of childbearing potential unless:
  • willing to use a highly effective contraceptive method
  • Person deprived of his/her liberty by a judicial or administrative decision
  • Person hospitalized without consent
  • Adult person under legal protection

Who the study is looking for

  • Age ≥ 18 and age ≤ 65
  • Histologically confirmed (according to the World Health Organization (WHO) classification) mantle cell lymphoma. The diagnosis has to be confirmed by phenotypic expression of CD5, CD20 and cyclin D1 or the t(11;14) translocation.
  • Bone marrow aspiration performed at inclusion for MRD analyses
  • Eligible for autologous stem cell transplant
  • Previously untreated MCL
  • Stage Ann Arbor II-IV in need of treatment
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2
  • Life expectancy of more than 3 months
  • Written informed consent
  • Patient affiliated by any social security system

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (30)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CHU D'amiens
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AmiensFranceUnknown status
CHU d Angers
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AngersFranceUnknown status
CH d'Avignon
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AvignonFranceUnknown status
CHU de CAEN
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CaenFranceUnknown status
CHU de Clermont-Ferrand
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Clermont-FerrandFranceUnknown status
Hopital Henri Mondor
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CréteilFranceUnknown status
CHU de Dijon - Hôpital le Bocage
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DijonFranceUnknown status
CHU de Grenoble
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GrenobleFranceUnknown status
CHD Vendée
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La Roche-sur-YonFranceUnknown status
Clinique Victor Hugo
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Le MansFranceUnknown status
Chru Lille - Hopital Claude Huriez
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LilleFranceUnknown status
CHU Limoges
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LimogesFranceUnknown status
CHU Montpellier
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MontpellierFranceUnknown status
CHU Nantes
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NantesFranceUnknown status
APHP - Hôpital Necker
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ParisFranceUnknown status
Hopital Saint Louis
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ParisFranceUnknown status
Ch Perpignan
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PerpignanFranceUnknown status
CHU de Haut Leveque
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PessacFranceUnknown status
CHU Lyon Sud
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Pierre-BéniteFranceUnknown status
CHU de Poitiers
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PoitiersFranceUnknown status
Centre Hospitalier Annecy Genevois
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PringyFranceUnknown status
CHU Robert Debré
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ReimsFranceUnknown status
CHU Pontchaillou
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RennesFranceUnknown status
Centre Henri Becquerel
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RouenFranceUnknown status
Institut de Cancérologie de Loire
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Saint-Priest-en-JarezFranceUnknown status
CHU de Strasbourg
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StrasbourgFranceUnknown status
I.U.C.T Oncopole
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ToulouseFranceUnknown status
CHRU Bretonneau
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ToursFranceUnknown status
CHU de Brabois
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Vandœuvre-lès-NancyFranceUnknown status
Gustave Roussy Cancer Campus
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VillejuifFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.