Etude : IFM2017_03 /



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Acronyme
Nom
Traitement
Type d'étude
MÀJ
Présentation de l'étude
Acronyme : IFM2017_03

Nom :

Traitement :

Type d'étude : Hors ciblage moléculaire

Dernière MÀJ : 17/10/2019
Titre
Spécialité(s)
CIM10 - Localisation(s)
Informations principales
Titre : A Phase III Study Comparing Lenalidomide and Subcutaneous Daratumumab (R-Dara SC) vs Lenalidomide and Dexamethasone (Rd) in Frail Subjects With Previously Untreated Multiple Myeloma Who Are Ineligible for High Dose Therapy

Spécialité : Tissus lymphoïde, hématopoïétique et apparentés
Localisation : C90 - Myélome multiple et tumeurs malignes à plasmocytes
Schéma
Phase
Stade
Ligne(s)
Informations complémentaires
Schéma : This is a Phase 3, randomized (study drug assigned by chance), open-label (participants and researchers are aware about the treatment, participants are receiving), active-controlled (study in which the experimental treatment or procedure is compared to a standard treatment or procedure), parallel-group (each group of participants will be treated at the same time), and multicenter (when more than one hospital team work on a medical research study) study in participants with newly diagnosed multiple myeloma (a blood cancer of plasma cells) and who are not candidates for high dose chemotherapy (treatment of disease, usually cancer, by chemical agents) and autologous stem cell transplant (ASCT). The primary hypothesis of this study is that subcutaneous Daratumumab in combination with Lenalidomide will prolong progression-free survival and likely induce less toxicity as compared with Lenalidomide and dexamethasone, in elderly frail subjects with newly diagnosed Multiple myeloma who are ineligible for high dose chemotherapy and ASCT


Study arms:
- Experimental: Arm 1: Experimental group
Daratumumab SC 1800 mg
* once every week for 8 weeks
* then once every other week for 16 weeks
* thereafter once every 4 weeks, until progression Lenalidomide PO (25mg): days 1 through 21 of each 28-day cycle, until progression Dexamethasone PO (20mg): days 1, 8, 15, 22 of a 28-day cycle, for the first 2 cycles, then discontinued
Interventions:
Drug: Daratumumab SC in combination with Lenalidomide
Drug: Lenalidomide PO (25mg)
Drug: Dexamethasone PO (20mg): days 1, 8, 15, 22 of each 28-day cycle, until progression

- Sham Comparator: Arm 2: Control group
Lenalidomide PO (25mg): days 1 through 21 of each 28-day cycle, until progression Dexamethasone PO (20mg): days 1, 8, 15, 22 of each 28-day cycle, until progression
Interventions:
Drug: Lenalidomide PO (25mg)
Drug: Dexamethasone PO (20mg): days 1, 8, 15, 22 of each 28-day cycle, until progression


Current primary outcome:
Comparison of the efficacy of Daratumumab SC injection when combined with Lenalidomide (R-Dara SC) vs Lenalidomide and Dexamethasone (Rd): PFS [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]

Current secondary outcomes:
- Time-to-treatment failure [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Time-to-next treatment [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- PFS2 time [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Overall survival (OS) time [ Time Frame: From date of randomization until the date of death from any cause, whichever came first, assessed up to 84months ]
- Overall survival (OS) time,
- Complete remission (CR) [ Time Frame: From date of randomization until the date of first documented progression whichever came first, assessed up to 84months ]
- Percentage of participants with CR, as defined by the IMWG criteria, will be reported.
- Very good partial response (VGPR) or better. [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- VGPR or better, defined as VGPR or CR according to the IMWG criteria during or after the study treatment at the time of data cutoff.
- Overall response (CR + VGPR + partial response [PR]). [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Overall response, defined as CR or VGPR or PR, according to the IMWG criteria
- Occurrence of grade 3 or more side effects. [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Collecting all AE (grade 3 or more)
- Safety and tolerability of Daratumumab SC when administered in combination with Revlimid: NCI-CTCAE V5.0. [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Evaluation of safety data by type, frequency, severity, relation to study drug, according to NCI-CTCAE V5.0.
- Evaluation of quality of life based on MY20 questionnaires [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Treatment effects on patient reported outcomes and heath economic/resource utilization.
- Evaluation of quality of life based on EORTC C30 questionnaires [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Treatment effects on patient reported outcomes and heath economic/resource utilization.
- Evaluation of quality of life based on EQ-5D questionnaires [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months ]
- Treatment effects on patient reported outcomes and heath economic/resource utilization.
- Minimal residual disease (MRD) negative rate at 12 months. [ Time Frame: after 12 months of treatment ]
- Proportion of participants assessed as MRD negative
- Event Free Survival [ Time Frame: From date of randomization until the date of first documented progression or date of toxicity or date of death from any cause, whichever came first, assessed up to 84months

Phase : III

Stade : NA

1
Informations libres de droit
Critères d'inclusion
Critères de non-inclusion
Informations libres de droit
Critères d'inclusion et de non-inclusion
Critères d'inclusion : - Subject must be at least 65 years of age.
- Subject must have documented multiple myeloma satisfying the CRAB criteria and measurable disease.
- Newly diagnosed and not considered candidate for high-dose chemotherapy with SCT.
- Subject must have a Frailty Score ≥ 2
- Subject must have within 5 days prior to first drug intake (C1D1) pretreatment clinical laboratory values meeting the following criteria during the Screening Phase:
* hemoglobin ≥7.5 g/dL
* absolute neutrophil count ≥1.0 x 109/L
* platelet count ≥70 x 109/L
* aspartate aminotransferase (AST) ≤2.5 x upper limit of normal (ULN)
* alanine aminotransferase (ALT) ≤2.5 x ULN
* total bilirubin ≤2.0 x ULN
* creatinine clearance≥30mL/min
- Measurable ISS with β2-microglobulin and albumin values for randomization
- A man who is sexually active with a woman of childbearing potential must agree to use a latex or synthetic condom, even if they had a successful vasectomy. All men must also not donate sperm during the study, for 4 weeks after the last dose of lenalidomide, and for 4 months after the last dose of daratumumab. Women participating in this study must be postmenopausal.
- Each subject must sign an informed consent form (ICF) indicating that he or she understands the purpose of and procedures required for the study and are willing to participate in the study. Subject must be willing and able to adhere to the prohibitions and restrictions specified in this protocol, as referenced in the ICF.
- Subjects affiliated with an appropriate social security system.

Critères de non-inclusion : - Subject has a diagnosis of primary amyloidosis, monoclonal gammopathy of undetermined significance, or smoldering multiple myeloma.
- Subject has a diagnosis of Waldenström's disease, or other conditions in which IgM M-protein is present in the absence of a clonal plasma cell infiltration with lytic bone lesions.
- Subject has prior or current systemic therapy or SCT for multiple myeloma
- Subject has a history of malignancy (other than multiple myeloma) within 5 years before the date of randomization
- Subject has had radiation therapy within 14 days of randomization.
- Subject has had plasmapheresis within 28 days of randomization.
- Subject is exhibiting clinical signs of meningeal involvement of multiple myeloma.
- Subject has known chronic obstructive pulmonary disease (COPD) (defined as a forced expiratory volume [FEV] in 1 second <60% of predicted normal), persistent asthma, or a history of asthma within the last 2 years (intermittent asthma is allowed).
- Subject is known to be seropositive for history of human immunodeficiency virus (HIV)
- Seropositive for hepatitis B.
- (Known to be) seropositive for hepatitis C
- Subject has any concurrent medical or psychiatric condition or disease that is likely to interfere with the study procedures or results, or that in the opinion of the investigator, would constitute a hazard for participating in this study.
- Subject has clinically significant cardiac disease, including:
* myocardial infarction within 1 year before randomization, or an unstable or uncontrolled disease/condition related to or affecting cardiac function
* uncontrolled cardiac arrhythmia or clinically significant ECG abnormalities
* screening 12-lead ECG showing a baseline QT interval as corrected by Fridericia's formula (QTcF) >470 msec
- Subject has known allergies, hypersensitivity, or intolerance to corticosteroids, monoclonal antibodies or human proteins, or their excipients
- Subject has plasma cell leukemia or POEMS syndrome
- Subject is known or suspected of not being able to comply with the study protocol. Subject has any condition for which, in the opinion of the investigator, participation would not be in the best interest of the subject or that could prevent, limit, or confound the protocol-specified assessments.
- Subject has had major surgery within 2 weeks before randomization or has not fully recovered from surgery, or has surgery planned during the time the subject is expected to participate in the study.
- Subject has received an investigational drug (including investigational vaccines) or used an invasive investigational medical device within 4 weeks before randomization or is currently enrolled in an interventional investigational study.
- Refusal to consent or protected by legal regime ( guardianship, trusteeship)
- Subject has contraindications to required prophylaxis for deep vein thrombosis and pulmonary embolism
- Incidence of gastrointestinal disease that may significantly alter the absorption f oral drugs.
NCT
Promoteur
Coordonnateur
Informations relatives au promoteur
NCT :
NCT03993912
Promoteur :
CHU de Lille
Type de sponsor : Institutionnel
CHU de Lille
59000 LILLE

Coordonnateur :
professeur Thierry FACON
Centre investigateur
Investigateur
TEC / ARC / IDE
État
MÀJ
Informations relatives aux investigateurs
Centre investigateur :
Centre Hospitalier Universitaire de Lille - 2 Avenue Oscar Lambret - 59000 LILLE

Investigateur :
Professeur Thierry FACON

TEC / ARC / IDE :
Secrétariat de recherche
fanny.miquel@
chru-lille.fr
03.20.44.57.13

Ouverture de l'essai : OUVERT

MAJ : 10/10/2019

Centre investigateur :
Centre hospitalier de Dunkerque - 130, avenue Louis Herbeaux - CS 76367 - 59140 DUNKERQUE

Investigateur :
Docteur Hélène DEMARQUETTE

TEC / ARC / IDE :
Viginie EL AZOUZI - PAQUEZ
Virginie.Paquez@
ch-dunkerque.fr
03 28 28 59 00 poste 6485

Ouverture de l'essai : OUVERT

MAJ : 17/10/2019