- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01014351
Study of Everolimus With Paclitaxel and Carboplatin in Patients With Metastatic Melanoma
10 febbraio 2014 aggiornato da: SCRI Development Innovations, LLC
A Phase II Study of Everolimus in Combination With Paclitaxel and Carboplatin in Patients With Metastatic Melanoma
Based on data demonstrating synergy between paclitaxel and mammalian target of rapamycin (mTOR) inhibition, the investigators propose that the addition of everolimus to paclitaxel with carboplatin should lead to improvements in efficacy as measured by progression-free survival and response rate.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Effettivo)
70
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
-
-
Florida
-
Fort Myers, Florida, Stati Uniti, 33901
- Florida Cancer Specialists
-
-
Georgia
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Gainesville, Georgia, Stati Uniti, 30501
- Northeast Georgia Medical Center
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Indiana
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Evansville, Indiana, Stati Uniti, 47630
- Oncology Hematology of SW Indiana
-
-
Louisiana
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Baton Rouge, Louisiana, Stati Uniti, 70809
- Hematology Oncology Clinic, LLP
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Maryland
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Bethesda, Maryland, Stati Uniti, 20817
- Center for Cancer and Blood Disorders
-
-
Michigan
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Grand Rapids, Michigan, Stati Uniti, 49503
- Grand Rapids Oncology Program
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-
Missouri
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Kansas City, Missouri, Stati Uniti, 64132
- Research Medical Center
-
-
Nebraska
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Omaha, Nebraska, Stati Uniti, 68114
- Nebraska Methodist Cancer Center
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-
Ohio
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Cincinnati, Ohio, Stati Uniti, 45242
- Oncology Hematology Care
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Tennessee
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Chattanooga, Tennessee, Stati Uniti, 37404
- Chattanooga Oncology Hematology Associates
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Nashville, Tennessee, Stati Uniti, 37023
- Tennessee Oncology, PLLC
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Virginia
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Newport News, Virginia, Stati Uniti, 23601
- Peninsula Cancer Institute
-
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
18 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Histologically confirmed metastatic melanoma.
- Stage III or IV disease that is not amenable to resection.
- Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. If the patient has had previous radiation to the target lesion(s), there must be evidence of progression since the radiation.
- ECOG Performance Status of 0 or 1.
- Life expectancy ≥12 weeks.
- No prior cytotoxic chemotherapy or targeted therapy. Immunotherapy is allowed (i.e., interleukin-2 or interferon).
Adequate hematological function:
- absolute neutrophil count (ANC) ≥1500/µL and
- platelets ≥100,000/µL and
- hemoglobin >9 g/dL
- Adequate renal function: serum creatinine ≤2.0 mg/dL or calculated (measured) GFR ≥50 mL/min.
Adequate hepatic function:
- serum bilirubin ≤1.5 x institutional upper limit of normal (ULN);
- aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × ULN, or ≤5 × ULN in patients with documented liver metastases.
- Normal PT, INR. Patients on coumadin anticoagulation are eligible if they are on a stable dose, with an INR in the therapeutic range.
- Fasting serum cholesterol ≤300 mg/dL OR ≤7.75 mmol/L AND fasting triglycerides ≤ 2.5 x ULN. NOTE: In case one or both of these thresholds are exceeded, the patient can be included after initiation of appropriate lipid lowering medication.
- Age ≥18 years.
- Ability to swallow whole pills.
- Patient must be accessible for treatment and follow-up.
- Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.
Exclusion Criteria:
- Previous treatment with an mTOR inhibitor (sirolimus, temsirolimus, everolimus), paclitaxel, or carboplatin.
- Treatment with any investigational agent ≤4 weeks of protocol treatment.
- Patients currently receiving anticancer therapies or who have received anticancer therapies ≤3 weeks of the start of the study drug (including radiation therapy, immunotherapy).
- Patients, who have had a major surgery or significant traumatic injury ≤4 weeks of start of study drug or patients who have not recovered from the side effects of any major surgery (defined as requiring general anesthesia).
- Patients receiving chronic, systemic treatment with corticosteroids (dose >10 mg daily of methylprednisolone or equivalent) or other immunosuppressive agents. Topical or inhaled steroids are allowed.
- Immunization with attenuated live vaccine ≤1 week of study or anytime during study treatment period.
- Patients with active brain metastases are ineligible. Patients with treated brain metastases are eligible if (1) radiation therapy was completed ≥4 weeks prior to study entry; (2) surgery was completed ≥4 weeks prior to study entry; (3) follow-up scan shows no disease progression; and (4) patient does not require steroids.
Any severe and/or uncontrolled medical conditions or other conditions that could affect participation in the study such as:
- severely impaired lung function defined as a DLCO ≤50% of the normal predicted value and/or O2 saturation ≤88% at rest on room air.
- symptomatic congestive heart failure of New York Heart Association Class III or IV.
- unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤6 months of start of study drug, serious uncontrolled cardiac arrhythmia or any other clinically significant disease.
- uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN.
- active (acute or chronic) uncontrolled severe infections.
- liver disease such as cirrhosis, chronic active hepatitis or chronic persistent hepatitis.
- Active, bleeding diathesis.
- Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of everolimus (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
- A known history of human immunodeficiency virus (HIV) seropositivity.
- Known hypersensitivity to everolimus or other rapamycins (sirolimus, temsirolimus) or to its excipients.
- Use of St. John's Wort is prohibited. Drugs or substances (e.g., grapefruits, star fruits, seville oranges, and their juices and products), known to be inhibitors or inducers of the isoenzyme CYP3A4 should be avoided. Co-administration with substrates, inducers, or inhibitors of P glycoprotein should also be avoided.
- Female patients who are pregnant or breastfeeding or adults of reproductive potential who are not using effective birth control methods. If barrier contraceptives are being used, these must be continued throughout the trial by both sexes. Hormonal contraceptives are not acceptable as a sole method of contraception. (Women of childbearing potential [WOCBP] must have a negative urine or serum pregnancy test within 7 days prior to administration of everolimus.) WOCBP should continue to use effective contraception for 8 weeks after ending everolimus treatment.
- Other malignancies within the past 3 years except for adequately treated carcinoma of the cervix or basal or squamous cell carcinomas of the skin.
- History of noncompliance to medical regimens. Patients unwilling to, or unable to, comply with the protocol.
- History of any other disease, physical examination finding, or clinical laboratory finding that gives reasonable suspicion of a disease or a condition that may render the patient at high risk for treatment complications using these agents.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Paclitaxel/Carboplatin/Everolimus
Systemic Therapy using everolimus, paclitaxel and carboplatin given during a 21-day treatment cycle
|
Paclitaxel, 175mg/m2 by IV infusion over 1-3 hours on day 1 of every 21 day cycle
Altri nomi:
Carboplatin, AUC 6 given by IV infusion over 20-30 minutes on day 1 of every 21 day cycle
Altri nomi:
Everolimus, 5 mg by mouth (PO) once a day, continuous dosing every 21-day cycle
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Progression-free Survival (PFS)
Lasso di tempo: 18 months
|
Progression-free survival (PFS) is defined as the time from randomization until objective tumor progression (PD) or death.
Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.
|
18 months
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Overall Survival (OS)
Lasso di tempo: 18 months
|
Overall survival (OS) is defined as the time from randomization until death from any cause.
|
18 months
|
|
Objective Response Rate (ORR)
Lasso di tempo: 18 months
|
Objective Response Rate (ORR) is defined as the Percentage of Patients Who Experience an Objective Benefit From Treatment.
Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI or CT: 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.
|
18 months
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
Investigatori
- Cattedra di studio: John D. Hainsworth, M.D., SCRI Development Innovations, LLC
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Collegamenti utili
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio
1 febbraio 2010
Completamento primario (Effettivo)
1 febbraio 2012
Completamento dello studio (Effettivo)
1 agosto 2013
Date di iscrizione allo studio
Primo inviato
16 novembre 2009
Primo inviato che soddisfa i criteri di controllo qualità
16 novembre 2009
Primo Inserito (Stima)
17 novembre 2009
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
26 marzo 2014
Ultimo aggiornamento inviato che soddisfa i criteri QC
10 febbraio 2014
Ultimo verificato
1 gennaio 2014
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Neoplasie per tipo istologico
- Neoplasie
- Tumori neuroectodermici
- Neoplasie, cellule germinali ed embrionali
- Neoplasie, tessuto nervoso
- Tumori neuroendocrini
- Nevi e melanomi
- Melanoma
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Agenti antineoplastici
- Agenti immunosoppressivi
- Fattori immunologici
- Modulatori della tubulina
- Agenti antimitotici
- Modulatori della mitosi
- Agenti antineoplastici, fitogenici
- Carboplatino
- Paclitaxel
- Everolimo
Altri numeri di identificazione dello studio
- SCRI MEL 19
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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