- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01743859
Azacitidine and Lenalidomide for Relapsed and Refractory Patients With Acute Myeloid Leukemia
Sequential Treatment With Azacitidine and Lenalidomide for Relapsed and Refractory Patients With Acute Myeloid Leukemia
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Réel)
Phase
- Phase 2
Contacts et emplacements
Lieux d'étude
-
-
Colorado
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Aurora, Colorado, États-Unis, 80045
- University of Colorado Cancer Center
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
• World Health Organization (WHO)-confirmed AML, other than Acute Promyelocytic Leukemia (APL)
- Age >18 years
White blood cell count (WBC) at initiation of treatment ≤ 10,000/L
o If WBC is > 10,000/L patients may be started on an appropriate dose of hydroxyurea (to be determined by the investigators), until WBC < 10,000/L, at which time the hydroxyurea will be discontinued for 12 hours prior to enrollment
Relapsed or refractory (resistant) disease, as defined by standard criteria21:
- Relapsed: Bone marrow blasts ≥5%; reappearance of blasts in the blood; development of extramedullary disease
- Refractory (resistant): Failure to achieve Complete Remission (CR) or complete remission with incomplete recovery of blood counts (CRi) in patients who survive ≥7 days following completion of initial treatment, with evidence of persistent leukemia by blood and/or bone marrow examination
- Failure of at least one prior therapy
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (See Appendix D: ECOG Performance Status Scale)
- Life expectancy > 2 months
- All study participants must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist® (RevAssist is a restricted distribution program for receiving lenalidomide)
- Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 million International Units per milliliter (mIU/mL) 10 - 14 days prior to study enrollment and again within 24 hours of prescribing lenalidomide (prescriptions must be filled within 7 days) and must either commit to continued abstinence from heterosexual intercourse or begin two acceptable methods of birth control, one highly effective method and one additional effective method at the same time, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. See Appendix F: Risks of Fetal Exposure, Pregnancy Testing Guidelines and Acceptable Birth Control Methods
- Willing and able to understand and voluntarily sign a written informed consent
- Able to adhere to the study visit schedule and other protocol requirements
Exclusion Criteria:
• Known or suspected hypersensitivity to azacitidine or mannitol
- Patients with advanced malignant hepatic tumors.
- Treatment less than four weeks prior to enrollment with other experimental therapies or antineoplastic agents, with the exception of hydroxyurea
- Inability to swallow or absorb drug
- Prior treatment with lenalidomide for AML
- Active opportunistic infection or treatment for opportunistic infection within four weeks of first day of study drug dosing
- New York Heart Association Class III or IV heart failure
- Unstable angina pectoris
- Significant uncontrolled cardiac arrhythmias
- Uncontrolled psychiatric illness that would limit compliance with requirements
- Known Human immunodeficiency virus (HIV) infection
- Graft vs. host disease ≥ grade 2
- Relapse after allogeneic stem cell transplantation prior to post-transplant day 30
- Pregnant or breast feeding females; lactating females must agree not to breast feed while taking lenalidomide
- Other medical or psychiatric illness or organ dysfunction or laboratory abnormality which in the opinion of the investigator would compromise the patient's safety or interfere with data interpretation
Laboratory abnormalities:
- Either creatinine >2.0 mg/dL or creatinine clearance <30 mL/min
- Total bilirubin > 2 x institutional upper limit of normal (ULN) (unless documented Gilbert's syndrome)
- Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) > 3 x institutional ULN
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Azacitidine + Lenalidomide + Off Therapy
Patients will receive 7 days of azacitidine followed by 3 weeks of lenalidomide.
They will then have 2 weeks off therapy, for a maximum of 12 cycles.
|
Enrolled patients will receive 75 mg/m2 of azacitidine subcutaneously (SC) or intravenously (IV) on days 1-7 alone.
Autres noms:
Beginning on day 8, patients will receive 50 mg of lenalidomide PO, and will take this daily from day 8 through 28.
Autres noms:
2 weeks off therapy, then begin sequence again for 12 weeks.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Percentage of Participants With Complete Remission or Complete Remission With Incomplete Recovery Blood Counts
Délai: Interim assessment after 18 patients (estimated 2 years) and full assessment after 37 patients (estimated 3-4 years)
|
Change in baseline to end of study.
To be assessed by standard criteria based on bone marrow examination.
Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR
|
Interim assessment after 18 patients (estimated 2 years) and full assessment after 37 patients (estimated 3-4 years)
|
|
Overall Response Rate
Délai: Planned assessment after enrollment of all 37 patients (estimated 3-4 years)
|
Change in baseline to end of study.
To be assessed by standard criteria based on bone marrow examination
|
Planned assessment after enrollment of all 37 patients (estimated 3-4 years)
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Response or Remission Duration
Délai: Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
|
Change in baseline to end of study.
To be assessed by standard criteria based on bone marrow examination
|
Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
|
|
Toxicity and SAEs Related to Treatment
Délai: Will begin assessment with first patient and will continue until completion of study, estimated to be 4 years
|
Change in baseline to end of study.
To be measured based on Common Terminology Criteria for Adverse Events (CTCAE) criteria
|
Will begin assessment with first patient and will continue until completion of study, estimated to be 4 years
|
|
Overall Survival
Délai: Depending on outcomes, will begin assessment at 2 years and will continue until completion of study, estimated to be at four years
|
Change in baseline to end of study
|
Depending on outcomes, will begin assessment at 2 years and will continue until completion of study, estimated to be at four years
|
|
Progression-free Survival
Délai: Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
|
Change in baseline to end of study.
To be assessed by standard criteria based on bone marrow examination
|
Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
|
|
Determine Biomarkers That Predict Response/Toxicity
Délai: Three years after initiating study
|
Change in baseline to end of study.
Planned assessments of methylation changes and other biomarkers.
Computational biology modeling used to identify biomarkers and predict response.
|
Three years after initiating study
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs par type histologique
- Tumeurs
- Leucémie
- Leucémie myéloïde
- Leucémie, myéloïde, aiguë
- Effets physiologiques des médicaments
- Mécanismes moléculaires de l'action pharmacologique
- Inhibiteurs d'enzymes
- Antimétabolites, Antinéoplasique
- Antimétabolites
- Agents antinéoplasiques
- Facteurs immunologiques
- Inhibiteurs de l'angiogenèse
- Agents modulateurs de l'angiogenèse
- Substances de croissance
- Inhibiteurs de croissance
- Lénalidomide
- Azacitidine
Autres numéros d'identification d'étude
- 12-1283.cc
- NCI-2012-03191 (Autre identifiant: National Cancer Institute)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
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