Combination Chemotherapy With or Without Thalidomide in Treating Patients With Multiple Myeloma

Last updated: September 16, 2013
Sponsor: Commissie Voor Klinisch Toegepast Onderzoek
Overall Status: Trial Status Unknown

Phase

3

Condition

Multiple Myeloma

Lymphoproliferative Disorders

Leukemia

Treatment

N/A

Clinical Study ID

NCT00028886
CDR0000069144
HOVON-CKVO-2001-02
EU-20133
HOVON-50MM
CKTO-2001-02
  • Ages 18-65
  • All Genders

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Thalidomide may stop the growth of cancer cells by stopping blood flow to the cancer. Peripheral blood stem cell transplant using stem cells from the patient or a donor may be able to replace immune cells that were destroyed by chemotherapy used to kill cancer cells. The donated stem cells may also help destroy any remaining cancer cells (graft-versus-tumor effect). It is not yet known whether chemotherapy followed by peripheral blood stem cell transplant is more effective with or without thalidomide in treating multiple myeloma.

PURPOSE: This randomized phase III trial is studying giving combination chemotherapy with thalidomide to see how well it works compared with giving combination chemotherapy without thalidomide in treating patients with multiple myeloma.

Eligibility Criteria

Inclusion

DISEASE CHARACTERISTICS:

  • Histologically confirmed multiple myeloma

  • Stage II or III

  • No systemic amyloid light-chain amyloidosis

PATIENT CHARACTERISTICS:

Age:

  • 18 to 65

Performance status:

  • WHO 0-3

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • No significant hepatic dysfunction*

  • Bilirubin less than 1.75 mg/dL*

  • AST/ALT less than 2.5 times normal* NOTE: *Unless related to myeloma

Renal:

  • Not specified

Cardiovascular:

  • No severe cardiac dysfunction

  • No New York Heart Association class II, III, or IV heart disease

Other:

  • HIV negative

  • No active uncontrolled infection

  • No other malignancy within the past 5 years except basal cell skin cancer or carcinoma in situ of the cervix

  • No known intolerance to thalidomide

  • Not pregnant

  • Negative pregnancy test

  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Patients 18 to 55 years of age must not have been allocated before study randomization to allogeneic stem cell transplantation with an HLA-identical sibling donor

Chemotherapy:

  • No more than 2 prior courses of melphalan and prednisone therapy for local myeloma progression

  • No other prior chemotherapy

Endocrine therapy:

  • Not specified

Radiotherapy:

  • Prior local radiotherapy for local myeloma progression allowed

  • No other prior radiotherapy

Surgery:

  • Not specified

Study Design

Total Participants: 450
Study Start date:
March 01, 2001
Estimated Completion Date:

Study Description

OBJECTIVES:

  • Compare the efficacy of doxorubicin, dexamethasone, and high-dose melphalan with versus without thalidomide, in terms of event-free survival, of patients with multiple myeloma.

  • Determine the response rate, complete response rate, overall survival, and progression-free survival of patients treated with these regimens.

  • Determine the safety and toxicity of thalidomide in combination with intensive chemotherapy in these patients.

  • Assess the value of prognostic factors at diagnosis in individual patients treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center and treatment policy (1 course vs 2 courses of high-dose melphalan). Patients are randomized to 1 of 2 treatment arms.

Arm I:

  • Patients receive induction chemotherapy (AD) comprising doxorubicin IV on days 1-4 and oral dexamethasone on days 1-4, 9-12, and 17-20. Patients receive oral thalidomide daily beginning on day 1 and continuing until 2 weeks before start of stem cell mobilization. Treatment repeats every 28 days for 3 courses in the absence of disease progression or unacceptable toxicity.

  • Patients receive stem cell mobilization with chemotherapy comprising cyclophosphamide IV on day 1 and doxorubicin IV and oral dexamethasone on days 1-4 (CAD). Patients also receive filgrastim (G-CSF) subcutaneously (SC) beginning on day 5 and continuing until last apheresis.

  • Beginning 8-10 weeks after stem cell collection, patients receive low-dose oral thalidomide daily and high-dose melphalan IV on days -3 and -2 as intensification. Patients undergo stem cell infusion on day 0. Patients may receive a second course of high-dose melphalan 2-3 months after the first course, in which case, stem cell infusion follows the second course of melphalan.

  • Patients receive maintenance therapy with oral thalidomide daily until disease progression or after 3 months if no response.

  • Beginning 2 months after the last course, patients with an HLA-identical sibling donor undergo nonmyeloablative stem cell transplantation after radiotherapy.

Arm II:

  • Patients receive induction chemotherapy (VAD) comprising vincristine IV and doxorubicin IV on days 1-4 and dexamethasone on days 1-4, 9-12, and 17-20. Treatment repeats every 28 days for 3 courses in the absence of disease progression or unacceptable toxicity.

  • Patients receive stem cell mobilization with CAD chemotherapy as in arm I. G-CSF is given as in arm I.

  • Patients receive high-dose melphalan and undergo stem cell infusion as in arm I.

  • Patients receive maintenance therapy with interferon alfa SC 3 times weekly until progression or after 3 months if no partial response.

  • Beginning 2 months after the last course, patients with an HLA-identical sibling donor undergo nonmyeloablative stem cell transplantation after radiotherapy.

All patients are followed every 6 months for 3 years and then annually thereafter.

PROJECTED ACCRUAL: A total of 450 patients (225 per treatment arm) will be accrued for this study within 4 years.

Connect with a study center

  • U.Z. Gasthuisberg

    Leuven, B-3000
    Belgium

    Site Not Available

  • HagaZiekenhuis - Locatie Leyenburg

    's-Gravenhage, 2545 CH
    Netherlands

    Site Not Available

  • Jeroen Bosch Ziekenhuis

    's-Hertogenbosch, 5211 NL
    Netherlands

    Site Not Available

  • Meander Medisch Centrum

    Amersfoort, 3816 CP
    Netherlands

    Site Not Available

  • Academisch Medisch Centrum at University of Amsterdam

    Amsterdam, 1105 AZ
    Netherlands

    Site Not Available

  • Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital

    Amsterdam, 1066 CX
    Netherlands

    Site Not Available

  • Vrije Universiteit Medisch Centrum

    Amsterdam, 1081HV
    Netherlands

    Site Not Available

  • Medisch Spectrum Twente

    Enschede, 7500 KA
    Netherlands

    Site Not Available

  • University Medical Center Groningen

    Groningen, 9713 EZ
    Netherlands

    Site Not Available

  • Medisch Centrum Leeuwarden - Zuid

    Leeuwarden, 8934 AD
    Netherlands

    Site Not Available

  • Leiden University Medical Center

    Leiden, 2300 RC
    Netherlands

    Site Not Available

  • Academisch Ziekenhuis Maastricht

    Maastricht, 6202 AZ
    Netherlands

    Site Not Available

  • Sint Antonius Ziekenhuis

    Nieuwegein, 3435 CM
    Netherlands

    Site Not Available

  • Universitair Medisch Centrum St. Radboud - Nijmegen

    Nijmegen, NL-6500 HB
    Netherlands

    Site Not Available

  • Daniel Den Hoed Cancer Center at Erasmus Medical Center

    Rotterdam, 3008 AE
    Netherlands

    Site Not Available

  • University Medical Center Utrecht

    Utrecht, 3584 CX
    Netherlands

    Site Not Available

  • Isala Klinieken - locatie Sophia

    Zwolle, 8000 GK
    Netherlands

    Site Not Available

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