Efficacy and Safety of Pegylated Interferon Alfa in Polycythemia Vera
Primary Purpose
Polycythemia Vera
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
pegylated interferon-alfa 2a
Sponsored by
About this trial
This is an interventional treatment trial for Polycythemia Vera focused on measuring myeloproliferative disorder, polycythemia vera, interferon
Eligibility Criteria
Inclusion Criteria: polycythemia vera diagnosed according to PVSG criteria, modified by Pearson Previously untreated patients or patients treated by phlebotomy only or HU or pipobroman for less than 2 years Age 18 to 65 years Signed informed consent Exclusion Criteria: Contra indication for interferon Severe renal or liver disease ECOG performance status > 2 Pregnancy Uncontrolled endocrine disorders except well regulated hyperthyroidism and diabetes Severe concomitant heart failure or psychiatric disorder Patients receiving an other investigational treatment
Sites / Locations
- Hopital Avicenne
- Hopital Huriez
- Hopital Dupuytren
- Hopital Lariboisiere
- Hopital Saint-Louis
Outcomes
Primary Outcome Measures
response rate after one year of treatment
Secondary Outcome Measures
safety
molecular response
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00241241
Brief Title
Efficacy and Safety of Pegylated Interferon Alfa in Polycythemia Vera
Official Title
Multicenter Phase 2 Study of Efficacy and Safety of Pegylated Interferon-alfa 2a in Polycythemia Vera Patients
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
September 2004 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
January 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
PV-Nord
4. Oversight
5. Study Description
Brief Summary
Interferon alfa is an effective treatment of polycythemia vera (PV), but about 20% of patients discontinue their treatment because of side effects and treatment schedule (three times per week administration). The pegylated form of interferon alfa-2a has shown a better tolerance in hepatitis patients and is administered only once a week. The purpose of this study is to determine efficacy and safety of pegylated interferon alfa-2a in the treatment of PV patients.
Detailed Description
The aim of PV treatment is to reduce the risk of vascular thrombosis without enhancing the long-term risk of evolution toward myelofibrosis or MDS/AL. Although currently controversial, phlebotomies have been shown in the old PVSG01 study to increase the risk of both thrombosis and myelofibrosis. On the other hand, currently available cytoreductive treatments have been shown to efficiently reduce the thrombotic risk, but were demonstrated (32P, busulfan, chlorambucil) or suspected (pipobroman, hydroxyurea) to enhance the risk of evolution to MDS/AL. In fact, the main widely used cytoreductive treatment, when indicated, is hydroxyurea (HU). This drug is very efficient to control myeloproliferation with a response rate of 80 to 90%. It is generally well tolerated, even if long term toxicity leads to treatment change in 10% of cases. Although no prospective study has yet clearly demonstrated its leukemogenic potential in PV, a non-leukemogenic alternative treatment is highly warranted, especially for younger patient.
Interferon (IFN) alpha is a promising agent in PV both because of good efficacy and absence of leukemogenic risk. Expanded experience with IFN-alpha was recently reported, showing a control of erythrocytosis in approximately 75% of patients. A similar percentage of patients also have resolution of disease-related symptoms, in particular a reduction in spleen size and relief from intractable pruritus. In some cases, long-term persisting remissions after treatment discontinuation have been observed as well as demonstration of eradication of the myeloproliferative clone. However, 20% of patients may not tolerate the treatment because of side effects. Furthermore, the treatment schedule (three times per week administration) may be a factor reducing long-term compliance to this drug.
In this regard, pegylated-IFN could be a major drug in PV. The weekly administration and better tolerance by comparison to IFN reported in hepatitis patients could allow to obtain results similar to chemotherapy in terms of compliance to treatment and efficacy, with a major advantage, its lack of mutagenicity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycythemia Vera
Keywords
myeloproliferative disorder, polycythemia vera, interferon
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
pegylated interferon-alfa 2a
Primary Outcome Measure Information:
Title
response rate after one year of treatment
Secondary Outcome Measure Information:
Title
safety
Title
molecular response
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
polycythemia vera diagnosed according to PVSG criteria, modified by Pearson
Previously untreated patients or patients treated by phlebotomy only or HU or pipobroman for less than 2 years
Age 18 to 65 years
Signed informed consent
Exclusion Criteria:
Contra indication for interferon
Severe renal or liver disease
ECOG performance status > 2
Pregnancy
Uncontrolled endocrine disorders except well regulated hyperthyroidism and diabetes
Severe concomitant heart failure or psychiatric disorder
Patients receiving an other investigational treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Jacques Kiladjian, MD
Organizational Affiliation
PV-Nord
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pierre Fenaux, MD, PhD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Christine Chomienne, MD, PhD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Sylvia Bellucci, MD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Bruno Cassinat, MD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Marie-Jose Grange, MD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nathalie Cambier, MD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jean-Francois Bernard, MD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Philippe Rousselot, MD
Organizational Affiliation
PV-Nord
Official's Role
Study Chair
Facility Information:
Facility Name
Hopital Avicenne
City
Bobigny
Country
France
Facility Name
Hopital Huriez
City
Lille
Country
France
Facility Name
Hopital Dupuytren
City
Limoges
Country
France
Facility Name
Hopital Lariboisiere
City
Paris
Country
France
Facility Name
Hopital Saint-Louis
City
Paris
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
3704665
Citation
Berk PD, Goldberg JD, Donovan PB, Fruchtman SM, Berlin NI, Wasserman LR. Therapeutic recommendations in polycythemia vera based on Polycythemia Vera Study Group protocols. Semin Hematol. 1986 Apr;23(2):132-43.
Results Reference
background
PubMed Identifier
9025158
Citation
Fruchtman SM, Mack K, Kaplan ME, Peterson P, Berk PD, Wasserman LR. From efficacy to safety: a Polycythemia Vera Study group report on hydroxyurea in patients with polycythemia vera. Semin Hematol. 1997 Jan;34(1):17-23. No abstract available.
Results Reference
background
PubMed Identifier
15866263
Citation
Kiladjian JJ, Bernard JF, Fenaux P. Is life expectancy of polycythemia vera patients clearly different from that of the general population? Am J Med. 2005 May;118(5):565; author reply 565-6. doi: 10.1016/j.amjmed.2004.12.026. No abstract available.
Results Reference
background
PubMed Identifier
10803930
Citation
Lengfelder E, Berger U, Hehlmann R. Interferon alpha in the treatment of polycythemia vera. Ann Hematol. 2000 Mar;79(3):103-9. doi: 10.1007/s002770050563.
Results Reference
background
PubMed Identifier
11830459
Citation
Streiff MB, Smith B, Spivak JL. The diagnosis and management of polycythemia vera in the era since the Polycythemia Vera Study Group: a survey of American Society of Hematology members' practice patterns. Blood. 2002 Feb 15;99(4):1144-9. doi: 10.1182/blood.v99.4.1144.
Results Reference
background
PubMed Identifier
18650451
Citation
Kiladjian JJ, Cassinat B, Chevret S, Turlure P, Cambier N, Roussel M, Bellucci S, Grandchamp B, Chomienne C, Fenaux P. Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera. Blood. 2008 Oct 15;112(8):3065-72. doi: 10.1182/blood-2008-03-143537. Epub 2008 Jul 23.
Results Reference
derived
PubMed Identifier
16709929
Citation
Kiladjian JJ, Cassinat B, Turlure P, Cambier N, Roussel M, Bellucci S, Menot ML, Massonnet G, Dutel JL, Ghomari K, Rousselot P, Grange MJ, Chait Y, Vainchenker W, Parquet N, Abdelkader-Aljassem L, Bernard JF, Rain JD, Chevret S, Chomienne C, Fenaux P. High molecular response rate of polycythemia vera patients treated with pegylated interferon alpha-2a. Blood. 2006 Sep 15;108(6):2037-40. doi: 10.1182/blood-2006-03-009860. Epub 2006 May 18.
Results Reference
derived
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Efficacy and Safety of Pegylated Interferon Alfa in Polycythemia Vera
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