Carfilzomib in Treating Patients With Chronic Graft-Versus-Host Disease

Fred Hutchinson Cancer Center (FHCC)

Status and phase: Completed; Phase 2

Conditions: Chronic Graft Versus Host Disease

Treatments: Other: Laboratory Biomarker Analysis; Drug: Carfilzomib; Other: Quality-of-Life Assessment; Other: Questionnaire Administration

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT02491359

9228 (Other Identifier)

NCI-2015-00809 (Registry Identifier)

P30CA015704 (U.S. NIH Grant/Contract)

9228.00

Details and patient eligibility

About

This pilot phase II trial studies how well carfilzomib works in treating patients with chronic graft-versus-host disease. Chronic graft-versus-host disease is a complication of a donor bone marrow or blood cell transplant, usually occurring more than three months after transplant, in which donor cells damage the host tissue. Carfilzomib may be an effective treatment for chronic graft-versus-host disease.

Full description

PRIMARY OBJECTIVE:

I. Determine proportion of subjects with treatment failure by 6 months of carfilzomib therapy for chronic graft-versus-host disease (GVHD).

SECONDARY OBJECTIVES:

I. Determine 3 month overall (complete + partial), and complete response rate.

II. Determine 6 month overall (complete + partial), and complete response rate.

III. Report overall survival, non-relapse mortality, primary malignancy relapse, failure-free survival, treatment success, and discontinuation of immune suppression at 6 months and 1 year.

IV. Examine functional outcome (2-minute walk test) and patient-reported outcomes (Lee Chronic GVHD Symptom Scale, quality of life [Short Form Health Survey (SF)-36, Functional Assessment of Cancer Therapy Bone Marrow Transplant (FACT-BMT) Questionnaire], Human Activity Profile [HAP]) at study enrollment, 6 months, and 1 year.

V. Study biologic effects of proteasome inhibition.

OUTLINE:

Patients receive carfilzomib intravenously (IV) over approximately 30 minutes on days 1, 8, and 15. 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 3, 6, and 12 months.

Enrollment: 20 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of chronic GVHD according to National Institutes of Health (NIH) Consensus Criteria

  • May have either classic chronic GVHD or overlap subtype of chronic GVHD

• Failure of at least one prior line of systemic immune suppressive therapy for management of chronic GVHD

• Subject underwent transplantation at least 3 months prior to enrollment

• Anticipated life expectancy >= 6 months

• Alanine aminotransferase (ALT) =< 3.5 times the upper limit of normal, unless due to chronic GVHD

• Bilirubin =< 2 mg/dL, unless due to chronic GVHD

• Absolute neutrophil count (ANC) >= 1.0 × 10^9/L

• Hemoglobin >= 8 g/dL

• Platelet count >= 50 × 10^9/L

• Creatinine clearance (CrCl) >= 15 mL/minute, either measured or calculated

• Signed informed consent in accordance with federal, local, and institutional guidelines

• Females of childbearing potential (FCBP) must agree to a pregnancy test at study enrollment and to practice contraception during the study

• Male subjects must agree to practice contraception during the study

Exclusion criteria

• Evidence of recurrent or progressive underlying malignant disease

• Pregnant or lactating females

• Surgery within 21 days prior to enrollment

  • Does not include placement of venous access device, bone marrow biopsy, GVHD diagnostic biopsy, or other routine procedures in chronic GVHD or post-transplantation care

• Uncontrolled infection within 14 days prior to enrollment

  • Infection treated with appropriate antimicrobial therapy and without signs of progression/treatment failure does not constitute an exclusion criterion

• Documented human immunodeficiency virus (HIV) infection

• Active hepatitis B or C infection

• Documented unstable angina or myocardial infarction within 6 months prior to enrollment, New York Heart Association (NYHA) class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, sick sinus syndrome, or electrocardiographic evidence of acute ischemia or grade 3 conduction system abnormalities (unless subject has a pacemaker), left ventricular ejection fraction (LVEF) < 40%, history of torsade de pointe

• Uncontrolled hypertension or uncontrolled diabetes within 14 days prior to enrollment

  • Sustained systolic blood pressure > 160 or diastolic blood pressure > 100 despite medical therapy; sustained blood sugar > 300 despite medical therapy
  • Chronic hypertension or diabetes on appropriate medical therapy does not constitute an exclusion criterion

• Non-hematologic malignancy within the past 3 years with the exception of:

  • Adequately treated basal cell carcinoma, squamous cell skin cancer, or thyroid cancer
  • Carcinoma in situ of the cervix or breast
  • Prostate cancer of Gleason grade 6 or less with stable prostate-specific antigen levels
  • Cancer considered cured by surgical resection or unlikely to impact survival during the duration of the study

• Significant neuropathy per Common Terminology Criteria for Adverse Events (CTCAE) version (ver.) 4.03 or current version (grade 3 and above, or grade 2 with pain) within 14 days prior to enrollment

• History of allergy to Captisol (a cyclodextrin derivative used to solubilize carfilzomib)

• Contraindication to all available herpes simplex virus (HSV)/varicella prophylactic antiviral drugs

• Pleural effusions requiring thoracentesis, or ascites requiring paracentesis, within 14 days prior to enrollment

• Any other clinically significant medical or psychological disease or condition that, in the investigator's opinion, may interfere with protocol adherence or a subject's ability to give informed consent

• New systemic immune suppressive agent added for the treatment of chronic GVHD within 2 weeks prior to enrollment

• Treatment with a non-Food and Drug Administration (FDA) approved drug in the previous 4 weeks

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Treatment (carfilzomib)

Experimental group

Description:

Patients receive carfilzomib IV over approximately 30 minutes on days 1, 8, and 15. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Treatment:

Other: Quality-of-Life Assessment

Other: Laboratory Biomarker Analysis

Drug: Carfilzomib

Other: Questionnaire Administration