CC-4047 in Treating Patients With Myelofibrosis

Chronic Myeloproliferative Disorders Clinical Trial

Official title:

A Phase I/II, Prospective, Open-Label Study to Determine the Safety and Efficacy of CC-4047 in Patients With Primary, Post Polycythemia Vera, or Post Essential Thrombocythemia Myelofibrosis®

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00669578
• Other study ID #: MC078B
• Secondary ID: P30CA015083MC078
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: May 2008
• Est. completion date: December 12, 2019

Study information

• Verified date: December 2019
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Biological therapies, such as CC-4047, may stimulate the immune system in different ways and stop cancer cells from growing. CC-4047 may also stop the growth of cancer cells by blocking blood flow to the cancer.

PURPOSE: This trial is studying the side effects and best dose of CC-4047 and to see how well it works in treating patients with myelofibrosis.

Description:

OBJECTIVES:

Phase I:

Primary

• To determine the Maximum Tolerated Dose of CC-4047 in the treatment of Primary, Post Polycythemia Vera, or Post Essential Thrombocythemia Myelofibrosis (PMF, post-PV MF, or post-ET MF).

Phase II:

Primary

• Best overall response as determined by International Working Group Criteria over the first 6 cycles (168 days) of study treatment.

Secondary

• Safety (type, frequency, severity [National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0] of adverse events (AEs), and relationship of AEs to CC-4047.

• Duration of response.

• Time to response.

• Best overall response as determined by International Working Group Criteria over the first 12 cycles (336 days) of study treatment.

OUTLINE: Patients receive oral CC-4047. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed at 28 days and then every 6 months for up to 3 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 77
• Est. completion date: December 12, 2019
• Est. primary completion date: July 7, 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 120 Years

Eligibility

DISEASE CHARACTERISTICS:

• Diagnosis of primary and post essential thrombocythemia (ET) or post polycythemia vera (PV) myelofibrosis requiring therapy

• De novo presentation (i.e., agnogenic myeloid metaplasia AND post ET or post PV myelofibrosis)

• Developed after an antecedent history of PV (i.e., post polycythemic myeloid metaplasia) or essential polycythemia (i.e., post thrombocythemic myeloid metaplasia)

• Total hemoglobin < 10 g/dL OR transfusion dependent anemia (defined by a history of = 2 units of red blood cell (RBC) transfusions within the past 28 days for hemoglobin < 8.5 g/dL that was not associated with overt bleeding) OR marked splenomegaly (e.g., = 10 cm below costal margin)

PATIENT CHARACTERISTICS:

• Eastern Cooperative Oncology Group (ECOG) performance status 0-2

• Absolute neutrophil count (ANC) = 500/µL

• Platelet count = 20,000/µL

• Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) = 3 times upper limit of normal (ULN) (= 5 times ULN if attributed to hepatic extramedullary hematopoiesis)

• Total bilirubin = 3 times ULN OR direct bilirubin = 2 times ULN

• Serum creatinine = 2.0 mg/dL

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective double-method contraception for = 28 days before, during, and for = 28 days after completion of study treatment

• Agrees to abstain from donating blood, semen, or sperm during and for = 28 days after completion of study treatment

• Willing to undergo transfusion of blood products (if applicable)

• Able to complete questionnaire(s) alone or with assistance

• No known HIV positivity, hepatitis B carrier, or active hepatitis C infection

• No serious medical condition, psychiatric illness, or any other condition, including the presence of laboratory abnormalities, that (as judged by the treating physician) would preclude giving informed consent or participating in the study or confound the ability to interpret data from the study

• No other active malignancies, except basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast

• No active deep vein thrombosis or pulmonary embolism that has not been therapeutically anticoagulated

PRIOR CONCURRENT THERAPY:

• Recovered from all prior therapy

• No prior CC-4047

• More than 28 days since prior growth factors, cytotoxic chemotherapeutic agents (e.g., hydroxyurea or anagrelide), corticosteroids, or experimental drugs or therapies

• No other concurrent experimental drugs or therapies or cytotoxic chemotherapeutic agents (e.g., hydroxyurea or anagrelide) for myelofibrosis

• No concurrent growth factors (including erythropoietin) for myelofibrosis, except G-CSF or pegfilgrastim

• No concurrent chronic use (i.e., > 2 weeks) of more than physiologic doses of corticosteroids (dose equivalent to > 10 mg/day of prednisone)

Related Conditions & MeSH terms

• Chronic Myeloproliferative Disorders
• Myeloproliferative Disorders
• Polycythemia Vera
• Primary Myelofibrosis
• Secondary Myelofibrosis

Intervention

Drug:
• CC-4047
CC-4047: taken orally each day in a 28 day cycle.

Locations

Country	Name	City	State
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (2)

Lead Sponsor	Collaborator
Mayo Clinic	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determine the Maximum Tolerated Dose of CC-4047	Starting at a dose level of 2.5 mg/d on days 1-21 in every 28 day cycle, participants were accrued in cohorts of three to assess dose limiting toxicities (DLT) and determine the maximum tolerated dose (MTD). Dose escalation at increments of 0.5 mg/d was done if no subject had a DLT (a grade 4 or higher hematologic toxicity or a grade 3 or higher febrile neutropenia or a grade 3 or higher non-hematologic toxicity) in cycle 1. Subsequent cohorts were treated until the maximum tolerated dose (MTD) was reached (dose level before that which results in a DLT in >1 of 6 subjects). Subsequent participants were treated at the MTD, those without response at the MTD after 3 cycles were lowered to the minimal efficacious dose (MED) of 0.5 mg daily. Here, we are reporting the percentage of participants in Phase I with a DLT at each dose level.	The first 28-day cycle of treatment.
Primary	Best Overall Response Over the First 6 Cycles of Treatment	Response evaluation: Complete Remission (CR): Neutrophil count between 1 to 10 x 10^9/L without peripheral blasts in blood or bone marrow.; Partial Hematologic Response/Partial Remission (PR): Increase in neutrophil by 50% + above 10^9/L for neutropenia); Clinical Improvement (CI): Increase in Neutrophil count, hemoglobin, platelet count or reduction in blood/marrow blasts.	Every cycle of treatment for 6 cycles. Each cycle is 28 days.
Secondary	Number of Participants With Treatment Related Adverse Events.	Adverse events (AE) that are classified as either possibly, probably, or definitely related to study treatment according to the National Cancer Institute Common Toxicity Criteria for Adverse Events (NCI CTCAE version 3.0). The maximum grade for each type of AE will be recorded for each patient. The number of participants with grade 3 or higher adverse events at least possibly related to study treatment are reported here.	During treatment and every 6 months until 3 years from registration or progression.
Secondary	Duration of Response Time	Duration of response is defined as the date at which the patient's objective status is first noted to be a CR, PR or CI to the date progression is documented (if one has occurred) or to the date of last follow-up(for those patients who have not progressed).	Time from response to disease progression, intolerance of study drug, or death.
Secondary	Time to Response	The time to response is defined as the time from study registration to the first date at which the patient's objective status was classified as a response (CR, PR or CI). In patients who do not achieve a response, time to response will be censored at the patient's last evaluation date. The distribution for each of these event-time variables (duration of response and time to response) will be estimated by Kaplan-Meier curves.	Time from registration to the first date of response within twelve 28-day cycles of treatment.