Thalidomide in Treating Patients With Myelofibrosis

Primary Myelofibrosis Clinical Trial

Official title:

A Pilot Study of Thalidomide as an Inhibitor of Angiogenesis in the Treatment of Myelofibrosis With Myeloid Metaplasia (MMM)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00015821
• Other study ID #: NCI-2012-01853
• Secondary ID: NCI-2012-01853CD
• Status: Completed
• Phase: Phase 2
• First received: May 6, 2001
• Last updated: October 7, 2013
• Start date: May 2000

Study information

• Verified date: October 2013
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Phase II trial to study the effectiveness of thalidomide in treating patients who have myelofibrosis. Thalidomide may stop the growth of myelofibrosis by stopping blood flow to the cancer cells.

Description:

PRIMARY OBJECTIVES:

I. To investigate whether thalidomide, a potent inhibitor of angiogenic and fibrogenic growth factors, is an effective therapeutic agent in patients with MMM. Specifically, to assess whether thalidomide improves anemia and/or organomegaly in patients with MMM.

II. To assess the effects of thalidomide on the myelofibrotic stroma with respect to microvascular architecture and angiogenesis, collagen and reticulin deposition, and the expression of the mediating growth factors bFGF, TGF-b, and PDGF, and their respective receptors.

OUTLINE: This is a multicenter study.

Patients receive oral thalidomide once daily for 1 year in the absence of disease progression or unacceptable toxicity. Patients with stable or responding disease may receive 1 additional year of therapy.

Patients are followed every 6 months until 5 years from study entry.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 43
• Est. primary completion date: December 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed myelofibrosis with myeloid metaplasia

• Agnogenic myeloid metaplasia

• Post-polycythemic myeloid metaplasia

• Post-thrombocythemic myeloid metaplasia

• No metastatic carcinoma, lymphoma, myelodysplasia, hairy cell leukemia, mast cell disease, acute leukemia (including M7), or acute myelofibrosis

• No chromosomal translocation t(9;22) or bcr/abl gene rearrangement

• Presence of reticulin fibrosis in bone marrow and leukoerythroblastosis and dacrocytosis in peripheral blood

• Presence of anemia (hemoglobin less than 10 g/dL), palpable splenomegaly, or hepatomegaly

• Performance status - ECOG 0-2

• Absolute neutrophil count greater than 750/mm^3

• Platelet count less than 400,000/mm^3

• WBC less than 50,000/mm^3

• Bilirubin no greater than 2 mg/dL (if total bilirubin elevated, direct bilirubin must be normal)

• AST no greater than 3 times upper limit of normal (ULN)

• Alkaline phosphatase no greater than 3 times ULN

• Creatinine no greater than 1.5 mg/dL

• Creatinine clearance at least 60 mL/min

• Not pregnant or nursing

• Negative pregnancy test

• Fertile women must use at least 1 highly active method AND 1 additional effective method of contraception for at least 4 weeks before study, during study, and for at least 4 weeks after study

• Fertile men must use effective contraception during study and for at least 4 weeks after study

• No uncontrolled infection

• No concurrent condition that would preclude study

• No peripheral neuropathy

• At least 1 month since prior interferon, pirfenidone, anagrelide, or epoetin alfa

• At least 1 month since prior hydroxyurea or other chemotherapy

• At least 1 month since prior corticosteroids or androgen derivatives

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Primary Myelofibrosis

Intervention

Drug:
• thalidomide
Given PO

Other:
• laboratory biomarker analysis
Correlative studies

Locations

Country	Name	City	State
United States	North Central Cancer Treatment Group	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Confirmed Response, i.e., an objective status of complete or partial response, recorded on 2 consecutive evaluations at least 4 weeks apart.	The proportion of successes will be estimated using the Binomial point estimator (number of successes divided by the total number of evaluable patients) and 95% confidence intervals calculated using the Duffy-Santner algorithm for multi-stage designs.	Up to 5 years	No
Secondary	Survival	Kaplan-Meier survival curves will be generated to estimate survival.	Number of days from registration date to the date of death or last follow-up, assessed up to 5 years	No
Secondary	Time to progression	Kaplan-Meier survival curves will be generated to estimate time to progression.	Number of days from registration date to the date of disease progression or last follow-up, assessed up to 5 years	No
Secondary	Response duration	Kaplan-Meier survival curves will be generated to estimate response duration.	Number of days from the first date that objective status = complete or partial response was recorded to the date of disease progression or date of death, whichever comes first, assessed up to 5 years	No