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Fludarabine, Total-Body Irradiation, and Donor Stem Cell Transplant Followed By Cyclosporine and Mycophenolate Mofetil in Treating Patients With Chronic Myelogenous Leukemia

20 settembre 2010 aggiornato da: Fred Hutchinson Cancer Center

Fludarabine and Low-Dose TBI Dose Escalation to Determine the Optimal Regimen for Achieving High Rates Engraftment of Unrelated Donor Peripheral Blood Stem Cell in Patients With Chronic Myeloid Leukemia - A Multi-Center Trial

RATIONALE: Giving low doses of chemotherapy, such as fludarabine, and radiation therapy before a donor stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune system and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after transplant may stop this from happening.

PURPOSE: This phase I/II trial is studying the side effects and best dose of fludarabine, total-body irradiation, and donor stem cell transplant followed by cyclosporine and mycophenolate mofetil and to see how well they work in treating patients with chronic myelogenous leukemia.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

OBJECTIVES:

Primary

  • Determine whether increasing the intensity of a nonmyeloablative conditioning regimen comprising fludarabine and total body irradiation allows achievement of a donor T-cell chimerism level of > 40% on day 28 post-transplantation in 90% or more of patients with chronic myelogenous leukemia undergoing allogeneic peripheral blood stem cell transplantation and immunosuppression comprising cyclosporine and mycophenolate mofetil.
  • Determine the feasibility of reducing the day 84 graft rejection rate/graft failure to < 10% in patients treated with this regimen.
  • Determine the feasibility of maintaining the incidence of grade 4 acute graft-versus-host disease at < 10% in patients treated with this regimen.
  • Determine the feasibility of maintaining the day 200 nonrelapse mortality rate at < 15% in patients treated with this regimen.

Secondary

  • Determine the rate of complete cytogenetic remission in patients treated with this regimen.
  • Determine the probability of actuarial disease-free survival of patients treated with this regimen.
  • Determine the pharmacokinetics of mycophenolate mofetil and fludarabine in these patients.

OUTLINE: This is a multicenter, dose-escalation study of fludarabine and total-body irradiation (TBI).

  • Nonmyeloablative conditioning regimen: Patients receive fludarabine IV on days -4 to -2 OR days -6 to -2. Patients undergo TBI on day 0.
  • Allogeneic peripheral blood stem cell transplantation (PBSCT): After the completion of TBI, patients undergo allogeneic PBSCT on day 0.
  • Immunosuppression: Patients receive oral cyclosporine twice daily on days -3 to 100 followed by a taper to day 177 in the absence of graft-versus-host disease (GVHD). Beginning within 4-6 hours after the completion of PBSCT, patients receive oral mycophenolate mofetil 2-3 times daily on days 0-40 followed by a taper to day 96 in the absence of GVHD.

Cohorts of 5-25 patients receive cumulative doses of fludarabine and escalating doses of TBI until 2 of 5, 3 of 10-15, 4 of 20, or 5 of 25 patients experience a day 28 post-transplant T-cell chimerism level ≤ 40% and/or a day 84 post-transplant graft rejection rate of > 10%.

After completion of study transplantation, patients are followed 3 times weekly for 3 months, at 6, 12, and 18 months, annually for 5 years, and then periodically thereafter.

PROJECTED ACCRUAL: A total of 5-75 patients will be accrued for this study.

Tipo di studio

Interventistico

Iscrizione (Anticipato)

75

Fase

  • Fase 2
  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Washington
      • Seattle, Washington, Stati Uniti, 98108
        • Veterans Affairs Medical Center - Seattle
      • Seattle, Washington, Stati Uniti, 98109-1023
        • Seattle Cancer Care Alliance
      • Seattle, Washington, Stati Uniti, 98109-1024
        • Fred Hutchinson Cancer Research Center

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

DISEASE CHARACTERISTICS:

  • Diagnosis of chronic myelogenous leukemia (CML), meeting 1 of the following criteria:

    • First or second chronic phase

      • Philadelphia chromosome-positive (Ph+) disease by cytogenetics or fluorescent in situ hybridization (FISH)
    • First accelerated phase, meeting any of the following criteria:

      • More than 10% but < 30% myeloblasts and promyelocytes in bone marrow or peripheral blood
      • Any additional clonal cytogenetic abnormalities
      • Increasing splenomegally
      • Extramedullary tumor
      • WBC, platelet count, or hematocrit pertubations not controlled by therapy with hydroxyurea, interferon, or imatininb mesylate
      • Persistent unexplained fever or bone pain
  • Less than 5% blasts in marrow at time of transplant

    • No blast crisis
  • No other curative therapy exists
  • Received prior imatinib mesylate AND meets ≥ 1 of the following criteria:

    • Hematologic evidence of disease progression
    • Lack of complete hematologic response after 3 months of treatment with imatinib mesylate
    • Cytogenetic evidence of disease progression, defined as an increase in Ph+ cells or BCR/ABL-positive (BCR/ABL+) cells of > 25%
    • Lack of complete cytogenetic remission (no Ph+ cells by cytogenetic analysis or BCR/ABL+ cells by FISH) after 1 year of treatment with imatinib mesylate
    • At least 65% Ph+ cells by cytogenetic analysis or BCR/ABL+ cells by FISH after 6 months of treatment with imatinib mesylate
    • Less than 3-log reduction in BCR/ABL mRNA levels by quantitative polymerase chain reaction (Q-PCR) compared to a standard baseline level after 1 year of treatment with imatinib mesylate
    • Molecular evidence of disease progression, defined as > 1 log increase in BCR/ABL mRNA levels by Q-PCR, detected in 2 samples
    • Experienced adverse events with imatinib mesylate treatment that would preclude further administration of the drug
    • Patient refused further treatment with imatinib mesylate despite lack of disease progression
  • Refused conventional myeloablative allogeneic stem cell transplantation OR at high risk for regimen-related toxicity due to pre-existing medical conditions (for patients < 50 years of age)
  • Unrelated donor available

    • Matched at HLA-A, -B, -C, -DRB1, and -DQB1 by high-resolution typing

      • A single allele* disparity for HLA-A, -B, or -C allowed
    • Negative anti-donor cytotoxic crossmatch
    • Not a marrow donor NOTE: *Patient and donor pairs homozygous at a mismatched allele (e.g., the patient is A*0101 and the donor is A*0201) are considered a two-allele mismatch and are not allowed
  • No CNS involvement with disease that is refractory to intrathecal chemotherapy

PATIENT CHARACTERISTICS:

Age

  • Any age

Performance status

  • Karnofsky 70-100%
  • Lanksy 50-100% (for pediatric patients)

Life expectancy

  • Not specified

Hematopoietic

  • See Disease Characteristics

Hepatic

  • No fulminant liver failure
  • No cirrhosis of the liver with evidence of portal hypertension
  • No alcoholic hepatitis
  • No esophageal varices
  • No history of bleeding esophageal varices
  • No hepatic encephalopathy
  • No uncorrectable hepatic synthetic dysfunction evidenced by prolongation of PT
  • No ascites related to portal hypertension
  • No bacterial or fungal liver abscess
  • No biliary obstruction
  • No chronic viral hepatitis AND bilirubin > 3 mg/dL
  • No symptomatic biliary disease

Renal

  • Not specified

Cardiovascular

  • Ejection fraction ≥ 40%
  • No cardiac failure requiring therapy
  • No poorly controlled hypertension (i.e., blood pressure ≥ 150/90 mm Hg despite standard medication)

Pulmonary

  • DLCO ≥ 35% (corrected)
  • No requirement for supplementary continuous oxygen
  • Pulmonary nodules allowed at the discretion of the principal investigator

Immunologic

  • HIV negative
  • No uncontrolled systemic infection
  • No fungal infection with radiological progression after treatment with amphotericin B or active triazole for > 1 month

Other

  • Not pregnant or nursing
  • Fertile patients must use effective contraception during and for 12 months after completion of study treatment
  • No other active malignancy except nonmelanoma skin cancer
  • No prior localized malignancy at high risk (≥ 20%) of recurrence

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • See Disease Characteristics
  • See Chemotherapy

Chemotherapy

  • See Disease Characteristics
  • More than 3 weeks since prior cytotoxic chemotherapy

    • Imatinib mesylate and interferon are not considered cytotoxic chemotherapy

Endocrine therapy

  • Not specified

Radiotherapy

  • Not specified

Surgery

  • Not specified

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Increase number of patients with donor T-cell chimerism from > 40% to 90% on day 28 post-transplant
Reduce graft rejection rate to < 10% day 84 post-transplant
Maintain acute graft-vs-host disease (GVHD) incidence of 10%
Maintain nonrelapse mortality incidence of < 15% on day 200 post-transplant

Misure di risultato secondarie

Misura del risultato
Farmacocinetica
Rate of complete cytogenetic remission
Probability of actuarial disease-free survival

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Investigatori

  • Investigatore principale: Brenda Sandmaier, MD, Fred Hutchinson Cancer Center

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 aprile 2005

Completamento dello studio (Effettivo)

1 novembre 2007

Date di iscrizione allo studio

Primo inviato

12 luglio 2005

Primo inviato che soddisfa i criteri di controllo qualità

12 luglio 2005

Primo Inserito (Stima)

13 luglio 2005

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

21 settembre 2010

Ultimo aggiornamento inviato che soddisfa i criteri QC

20 settembre 2010

Ultimo verificato

1 settembre 2010

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .