- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01490866
A Trial of Single Agent Axitinib as Maintenance Therapy for Patients With First Line Metastatic Colorectal Cancer (mCRC)
A Phase II Trial of Single Agent Axitinib as Maintenance Therapy for Patients With First Line Metastatic Colorectal Cancer (mCRC)
Aperçu de l'étude
Statut
Les conditions
Description détaillée
Type d'étude
Inscription (Réel)
Phase
- Phase 2
Contacts et emplacements
Lieux d'étude
-
-
Arkansas
-
Jonesboro, Arkansas, États-Unis, 72401
- NEA Baptist Clinic
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-
Florida
-
Fort Myers, Florida, États-Unis, 33916
- Florida Cancer Specialists-South
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Pensacola, Florida, États-Unis, 32503
- Woodlands Medical Specialists
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Saint Petersburg, Florida, États-Unis, 33705
- Florida Cancer Specialists-North
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-
Georgia
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Gainesville, Georgia, États-Unis, 30501
- Northeast Georgia Medical Center
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-
Indiana
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Newburgh, Indiana, États-Unis, 47630
- Oncology Hematology of SW Indiana
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Terre Haute, Indiana, États-Unis, 47802
- Hope Cancer Center
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-
Michigan
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Grand Rapids, Michigan, États-Unis, 49503
- Grand Rapids Oncology Program
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-
Nebraska
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Omaha, Nebraska, États-Unis, 68114
- Nebraska Methodist Hospital
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New Jersey
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Summit, New Jersey, États-Unis, 07901
- Atlantic Health System
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Tennessee
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Nashville, Tennessee, États-Unis, 37203
- Tennessee Oncology
-
-
Texas
-
Dallas, Texas, États-Unis, 75243
- Texas Health Physician Group
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Histologically or cytologically confirmed metastatic adenocarcinoma of the colon or rectum.
- Patients must have measurable disease per RECIST Version 1.1.
- No previous systemic therapy for metastatic colorectal cancer. Previous radiosensitizing chemotherapy is allowed, if completed at least 4 weeks prior to Cycle 1 Day 1 of study treatment, and previous neoadjuvant and/or adjuvant chemotherapy is allowed, if completed at least 6 months prior to diagnosis of metastatic disease.
- Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 to 1.
- Life expectancy >=12 weeks.
- Adequate hematologic, renal and hepatic function
- Patients who are on coumadin should have an INR value within the therapeutic range (i.e., 2 to 3 x ULN). Patients who are on stable, chronic doses of coumadin are eligible.
- Male patients willing to use adequate contraceptive measures. Female patients who are not of child-bearing potential, and female patients of child-bearing potential who agree to use adequate contraceptive measures, who are not breastfeeding, and who have a negative serum or urine pregnancy test performed within 72 hours prior to start of treatment.
- Willingness and ability to comply with the trial and follow-up procedures.
- Ability to understand the investigative nature of this trial and give written informed consent.
Exclusion Criteria:
- History or known presence of central nervous system (CNS) metastases.
- Patients who have had a major surgical procedure (not including mediastinoscopy), or significant traumatic injury <=4 weeks prior to beginning treatment.
- Women who are pregnant or lactating. All females of child-bearing potential must have negative serum or urine pregnancy tests within 72 hours prior to study treatment (see Appendix D)
- History of hypersensitivity to active or inactive excipients of any component of treatment (5 fluorouracil, bevacizumab, oxaliplatin, or axitinib), or known dipyrimidine dehydrogenase deficiency.
Patients with proteinuria at screening as demonstrated by:
- Urine dipstick for proteinuria >=2+ (patients discovered to have >=2+ proteinuria on dipstick urinalysis at baseline should undergo a 24-hour urine collection, and must demonstrate <=1 g of protein/24 hours to be eligible)
- Patients with a serious non healing wound, active ulcer, or untreated bone fracture.
- Patients with evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation).
- Patients with history of hematemesis or hemoptysis (defined as having bright red blood of ½ teaspoon or more per episode) <=1 month prior to study enrollment.
- Patients requiring concomitant treatment with potent CYP3A4 or CYP1A2 inducers and CYP3A4 inhibitors.
- History of myocardial infarction or unstable angina <=6 months prior to beginning treatment.
- Inadequately controlled hypertension (defined as systolic blood pressure >150 mmHg and/or diastolic blood pressure >100 mmHg while on antihypertensive medications). Initiation of antihypertensive agents is permitted provided adequate control is documented at least 1 week prior to Day 1 of study treatment.
- New York Heart Association Grade II or greater congestive heart failure.
- Serious cardiac arrhythmia requiring medication. Patients with chronic, rate-controlled atrial fibrillation are eligible.
- Significant vascular disease (e.g., aortic aneurysm requiring surgical repair, or recent peripheral arterial thrombosis) <=6 months prior to Day 1 of treatment.
- History of stroke or transient ischemic attack <=6 months prior to beginning treatment.
- Any prior history of hypertensive crisis or hypertensive encephalopathy.
- History of abdominal fistula or gastrointestinal perforation <=6 months prior to Day 1 of beginning treatment.
- Concurrent severe, intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.
- Any known positive test for human immunodeficiency virus, hepatitis C virus or acute or chronic hepatitis B infection.
- Mental condition that would prevent patient comprehension of the nature of, and risk associated with, the study.
- Use of any non-approved or investigational agent <=28 days prior to administration of the first dose of study drug. Patients may not receive any other investigational or anti-cancer treatments while participating in this study.
- Past or current history of neoplasm other than the entry diagnosis with the exception of treated non-melanoma skin cancer or carcinoma in situ of the cervix, or other cancers cured by local therapy alone and a disease free survival >=5 years.
- Infection requiring IV antibiotics.
- Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter drug absorption (e.g. active inflammatory bowel disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or significant small bowel resection).
- Inability to swallow whole tablets.
- Patients with > Grade 2 peripheral neuropathy.
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: FOLFOX/bevacizumab and Axitinib
Phase II trial investigating axitinib as a single-agent maintenance therapy following standard first-line FOLFOX/bevacizumab therapy for patients with mCRC. (FOLFOX is a combination of 5-Fluorouracil, Leucovorin and Oxaliplatin.) All patients will receive FOLFOX/bevacizumab for four 28-day cycles (a total of 16 weeks). After 4 cycles, maintenance axitinib will be started. |
5-mg tablets PO BID
Autres noms:
5 mg/kg Days 1 and 15; IV
Autres noms:
400 mg/m2 Days 1 and 15; IV
Autres noms:
2400 mg/m2 over 46-48 hours Days 1 and 15; Continuous Intravenous
Autres noms:
400 mg/m2 Days 1 and 15; IV
Autres noms:
85 mg/m2 Days 1 and 15; IV
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Progression-free Survival
Délai: 24 months
|
Defined as the time from first treatment until objective tumor progression or death from any cause, assessed according to Response Evaluation Criteria for Solid Tumors (RECIST) v1.1.
|
24 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Objective Response Rate
Délai: every 8 weeks, assessed up to approximately 24 months
|
Defined as the percentage of evaluable patients showing a complete or partial response (CR or PR) per RECIST v1.1 criteria.
CR = disappearance of all lesions.
PR = at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD.
Stable disease (SD) = neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest (nadir) sum LD since start of treatment.
|
every 8 weeks, assessed up to approximately 24 months
|
|
Time To Progression (TTP)
Délai: every 8 weeks, assessed approximately up to 24 months
|
Defined as the time after a disease is diagnosed (or treated) until worsening of the disease.
|
every 8 weeks, assessed approximately up to 24 months
|
|
Overall Survival (OS)
Délai: every 8 weeks until progression then every 3 months for up to 5 years.
|
Defined as the time from first treatment until death from any cause.
|
every 8 weeks until progression then every 3 months for up to 5 years.
|
|
Frequency of Adverse Events as a Measure of Safety
Délai: Every 4 weeks plus 30 days during treatment and up to 5 years thereafter.
|
The frequency of adverse events (AEs) was analyzed in 2 groups of patients, those receiving FOLFOX/bevacizumab (N=70), and patients who received axitinib maintenance (N = 48).
AEs were assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.0.
|
Every 4 weeks plus 30 days during treatment and up to 5 years thereafter.
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chaise d'étude: Johanna Bendell, M.D., SCRI Development Innovations, LLC
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
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
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies du système digestif
- Tumeurs
- Tumeurs par site
- Tumeurs gastro-intestinales
- Tumeurs du système digestif
- Maladies gastro-intestinales
- Maladies du côlon
- Maladies intestinales
- Tumeurs intestinales
- Maladies rectales
- Tumeurs colorectales
- Effets physiologiques des médicaments
- Mécanismes moléculaires de l'action pharmacologique
- Inhibiteurs d'enzymes
- Antimétabolites, Antinéoplasique
- Antimétabolites
- Agents antinéoplasiques
- Agents immunosuppresseurs
- Facteurs immunologiques
- Agents protecteurs
- Agents antinéoplasiques immunologiques
- Inhibiteurs de l'angiogenèse
- Agents modulateurs de l'angiogenèse
- Substances de croissance
- Inhibiteurs de croissance
- Micronutriments
- Inhibiteurs de protéine kinase
- Vitamines
- Antidotes
- Complexe de vitamine B
- Fluorouracile
- Oxaliplatine
- Bévacizumab
- Leucovorine
- Axitinib
Autres numéros d'identification d'étude
- SCRI GI 154
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