- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02020941
Carfilzomib in Treating Patients With Multiple Myeloma in First Relapse or Refractory to First-Line Therapy
A Phase 2 Study of Carfilzomib and Bone Metabolism in Patients With Multiple Myeloma in First Relapse or Refractory to First Line Therapy
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
PRIMARY OBJECTIVES:
I. To assess the overall response rate of carfilzomib after 8 cycles of treatment in patients with first-relapsed myeloma.
SECONDARY OBJECTIVES:
I. To assess the overall response rate to single agent carfilzomib after 4 cycles of treatment.
II. To assess progression-free survival (PFS). III. To assess time to progression (TTP). IV. To assess duration of response (DOR). V. To assess toxicities.
TERTIARY OBJECTIVES:
I. To examine the effect of carfilzomib alone or in combination with dexamethasone on the following biologic end points and their correlation with response: measurements of bone remodeling (sodium fluoride F 18 positron emission tomography [PET], serum markers of bone remodeling and the bone marrow osteoblastic and osteoclastic differentiation and function) with the measurement of disease response and proteasome activity in the bone marrow microenvironment.
II. To describe recapture of response after progression in the maintenance phase.
OUTLINE:
TREATMENT PHASE (COURSES 1-8): Patients receive carfilzomib intravenously (IV) over 30 minutes on days 1, 2, 8, 9, 15, and 16. Treatment repeats every 28 days for 8 courses in the absence of disease progression or unacceptable toxicity. Patients achieving less than partial response (PR) also receive dexamethasone orally (PO) or IV weekly in courses 4-8.
MAINTENANCE PHASE (COURSES 9-14): Patients receive carfilzomib IV over 30 minutes on days 1, 2, 15, and 16. Patients who received dexamethasone in the Treatment Phase continue to receive dexamethasone PO or IV weekly. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at 30 days and then every 3 months.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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Indiana
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Indianapolis, Indiana, Stati Uniti, 46202
- Indiana University Cancer Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
Multiple myeloma (MM) in first relapse or refractory to first line therapy; the previous line of therapy should include either an immunomodulatory agent or a proteasome inhibitor
- Refractory disease is defined as =< 25% response or progression during therapy or within 60 days after completion
The number of prior lines of anti-myeloma therapy will be determined as follows:
- Induction chemotherapy for peripheral-blood stem cell harvest followed by planned mobilization and subsequent high-dose chemotherapy with autologous stem cell transplant (ASCT) is considered one therapy regardless of the induction regimen
- Planned maintenance therapy after stem cell transplantation or other induction therapy is not considered a separate line of therapy, as long as there is no evidence of progression in the time between the induction or transplantation and the initiation of maintenance therapy
- Two ASCTs within 6 months of each other is considered as one line unless different agents were used in the high-dose therapy-conditioning regimens
- If the same regimen is repeated after a 6-month interval, they are considered to be two separate therapeutic lines
- If cyclophosphamide is used for reasons other than planned stem cell mobilization, its use is considered to be a separate line of therapy
- Dose modification of steroid and altering choices of steroid (i.e. from dexamethasone to prednisone) due to side effects, is not considered a line of therapy, as long as there is no evidence of progression
- If a regimen was stopped for more than 2 months, its re-initiation is counted as another line of therapy
- Presence of existing lytic bone lesions either by skeletal X-ray, computed tomography (CT) scan or magnetic resonance imaging (MRI) scan
Measurable MM disease, defined as one of the following:
- A monoclonal immunoglobulin (Ig) concentration on serum electrophoresis of >= 0.5 g/dL for an IgG myeloma, >= 0.1 g/dL for an IgD myeloma or >= 0.5 g/dL for an IgA myeloma
- Measurable urinary light chain secretion by quantitative analysis of >= 200 mg/24 hours
- Involved serum free light chain (FLC) level >= 10 mg/dL, provided the serum FLC ratio is abnormal
- Patients with oligo- or non-secretory disease must have bone marrow involvement with at least 30% plasmacytosis on aspiration
- Life expectancy >= 3 months as determined by the treating physician
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1 or 2
- Absolute neutrophil count (ANC) >= 1.0 × 10^9/L (without transfusion support and without hematological growth factor support within 2 weeks of cycle 1 day 1)
- Platelets >= 50 × 10^9/L; if the bone marrow contains >= 50% plasma cells, a platelet count of >= 30 × 10^9/L is allowed (without transfusion support and without hematological growth factor support within 2 weeks of cycle 1 day 1)
- Aspartate aminotransferase (AST)/serum glutamic oxaloacetic transaminase (SGOT) and/or alanine aminotransferase (ALT)/serum glutamic pyruvic transaminase (SGPT) =< 2.5 × the upper limit of normal (ULN)
- Bilirubin < 2.0 mg/dL
- Serum creatinine =< 3.0 mg/dL or a calculated creatinine clearance of at least 15 mL/min (using the Cockcroft and Gault method)
Adequate cardiac function defined as left ventricular ejection fraction (LVEF) >= 40%
- NOTE: 2-dimensional (2-D) transthoracic echocardiogram (ECHO) is the preferred method of evaluation
- Multigated acquisition scan (MUGA) is acceptable if ECHO is not available
- Written informed consent in accordance with federal, local, and institutional guidelines
- Females of childbearing potential (FCBP) must agree to ongoing pregnancy testing and to practice contraception; females are considered of childbearing potential unless they are surgically sterile (they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are naturally postmenopausal for at least 12 consecutive months
- Male subjects must agree to practice contraception
Exclusion Criteria:
- No primary amyloidosis
- No plasma cell leukemia (> 2.0 × 10^9/L circulating plasma cells by standard differential)
- No treatment with an investigational product or device within 21 days of cycle 1 day 1
- No history of allergic reaction/hypersensitivity to any of the study medications, their analogues or excipients in the various formulations
- No treatment with cytotoxic therapy or monoclonal antibodies within 21 days prior to cycle 1 day 1
- No treatment with a steroid intended to treat myeloma within 14 days prior to cycle 1 day 1
- No autologous or allogeneic stem cell transplant within 3 months prior to cycle 1 day 1
- No radiotherapy within 21 days prior to cycle 1 day 1; however, if the radiation portal covered =< 5% of the bone marrow reserve, the patient may be enrolled irrespective of the end date of radiotherapy
- No major surgery within 14 days and minor surgery within 7 days prior to cycle 1 day 1
- No pregnant or lactating females
- No acute active infection requiring treatment (systemic antibiotics, antivirals, or antifungals) within 14 days prior to cycle 1 day 1
- No known human immunodeficiency virus (HIV) infection
- No active hepatitis B or C infection
- No unstable angina or myocardial infarction within 4 months prior to cycle 1 day 1, New York Heart Association (NYHA) class III or IV heart failure, uncontrolled angina, history of severe coronary artery disease, severe uncontrolled ventricular arrhythmias, sick sinus syndrome, or electrocardiographic evidence of acute ischemia or grade 3 conduction system abnormalities unless subject has a pacemaker
- No uncontrolled hypertension or uncontrolled diabetes (as determined by the treating physician) within 14 days prior to cycle 1 day 1
- No nonhematologic malignancy within the past 3 years with the exception of a) adequately treated basal cell carcinoma, squamous cell skin cancer, or thyroid cancer; b) carcinoma in situ of the cervix or breast; c) prostate cancer of Gleason grade 6 or less with stable prostate-specific antigen levels; or d) cancer considered cured by surgical resection or unlikely to impact survival during the duration of the study, such as localized transitional cell carcinoma of the bladder or benign tumors of the adrenal or pancreas
- No significant neuropathy (grades 3-4, or grade 2 with pain) within 14 days prior to cycle 1 day 1
- No known history of allergy to Captisol (a cyclodextrin derivative used to solubilize carfilzomib)
- No contraindication to any of the required concomitant drugs or supportive treatments, including hypersensitivity to all anticoagulation and antiplatelet options, antiviral drugs, or intolerance to hydration due to preexisting pulmonary or cardiac impairment
- No subjects with pleural effusions requiring thoracentesis or ascites requiring paracentesis within 14 days prior to cycle 1 day 1
- Any other clinically significant medical disease or condition that, in the Investigator's opinion, may interfere with protocol adherence or a subject's ability to give informed consent
Piano di studio
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 |
|---|---|
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Sperimentale: Treatment (carfilzomib, dexamethasone)
TREATMENT PHASE (COURSES 1-8): Patients receive carfilzomib IV over 30 minutes on days 1, 2, 8, 9, 15, and 16. Treatment repeats every 28 days for 8 courses in the absence of disease progression or unacceptable toxicity. Patients achieving less than PR also receive dexamethasone PO or IV weekly in courses 4-8. MAINTENANCE PHASE (COURSES 9-14): Patients receive carfilzomib IV over 30 minutes on days 1, 2, 15, and 16. Patients who received dexamethasone in the Treatment Phase continue to receive dexamethasone PO or IV weekly. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity. |
Dato IV o PO
Altri nomi:
Dato IV
Altri nomi:
Studi correlati
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Overall Response Rate (ORR) After 8 Courses of Treatment
Lasso di tempo: At 32 weeks
|
: Evaluate the overall response rate of patients receiving therapy.
Patients are considered as having a response if their overall response is Partial Response or better.
The percentage of patients achieving this and the exact 95% confidence interval will be calculated.
Responses will be defined using the International Myeloma Working Group-Uniform Response Criteria (IMWG-URC).
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At 32 weeks
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Overall Response Rate (ORR) After 4 Courses of Treatment
Lasso di tempo: At 16 weeks
|
Evaluate the overall response rate of patients receiving therapy.
Patients are considered as having a response if their overall response is Partial Response or better.
The percentage of patients achieving this and the exact 95% confidence interval will be calculated.
Responses will be defined using the International Myeloma Working Group-Uniform Response Criteria (IMWG-URC).
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At 16 weeks
|
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Progression-free Survival (PFS)
Lasso di tempo: Time from first dose to first observed disease progression or death, assessed up to 2 years
|
Analysis will be performed using Kaplan-Meier estimates.
Time from date on treatment to date of progression for patients who progressed or date of death for patients who died without progressing.
The observations of patients remaining alive and progression free were censored at date of last disease evaluation.
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Time from first dose to first observed disease progression or death, assessed up to 2 years
|
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Time to Progression (TTP)
Lasso di tempo: Time from first dose to disease progression, assessed up to 2 years
|
Analysis will be performed using Kaplan-Meier estimates.
Time from date on treatment to date of progression.
The observations of patients who died or remained alive and progression free were censored at date of death or last disease evaluation, respectively.
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Time from first dose to disease progression, assessed up to 2 years
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Duration of Response (DOR)
Lasso di tempo: Time from first evidence of PR or better to disease progression or death, assessed up to 2 years
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Analysis will be performed using Kaplan-Meier estimates.
Time from date of first confirmed response of partial response or better to date of progression or death.
Only patients who had a response of partial response or better will be included in this analysis.
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Time from first evidence of PR or better to disease progression or death, assessed up to 2 years
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Treatment Related Adverse Events Grade 3 or Higher
Lasso di tempo: Up to 30 days after completion of study treatment, up to 2 years
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Number of unique patients who had a treatment related (possible, probable or definite) adverse events that were graded 3 or greater.
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Up to 30 days after completion of study treatment, up to 2 years
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Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Attaya Suvannasankha, Indiana University School of Medicine
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattia cardiovascolare
- Malattie vascolari
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Neoplasie
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Malattie ematologiche
- Disturbi emorragici
- Disturbi emostatici
- Paraproteinemie
- Disturbi delle proteine del sangue
- Mieloma multiplo
- Neoplasie, plasmacellule
- Effetti fisiologici delle droghe
- Agenti autonomi
- Agenti del sistema nervoso periferico
- Agenti antinfiammatori
- Agenti antineoplastici
- Antiemetici
- Agenti gastrointestinali
- Glucocorticoidi
- Ormoni
- Ormoni, sostituti ormonali e antagonisti ormonali
- Agenti antineoplastici, ormonali
- Desametasone
Altri numeri di identificazione dello studio
- IUCRO-0414 (Altro identificatore: Indiana University Cancer Center)
- P30CA082709 (Sovvenzione/contratto NIH degli Stati Uniti)
- NCI-2013-01771 (Identificatore di registro: CTRP (Clinical Trial Reporting Program))
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 .
Prove cliniche su desametasone
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