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Chronic Myeloproliferative DisordersPhase 2/3NCT00003816

Combination Chemotherapy and Donor Stem Cell Transplant in Treating Patients With Aplastic Anemia or Hematologic Cancer

A Phase 2/3 study testing anti-thymocyte globulin, busulfan and carboplatin in people with Chronic Myeloproliferative Disorders and Leukemia, run by Roswell Park Cancer Institute at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

RATIONALE: Giving chemotherapy drugs and total-body irradiation before a donor stem cell helps stop the growth of cancer or abnormal cells. It may also stop the patient's immune system from rejecting the donor's stem cells. Read more about this study

Who is it for?
Ages 4 to 70 years
What is being tested?
anti-thymocyte globulin, busulfan and carboplatin
Could I receive a placebo?
No, everyone receives an active treatment
How many people
361 participants
Where
1 siteUnited States
Study dates
19 Oct 1998to 12 Jul 2019
Phase
Phase 2/3

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 4 to 70 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

DISEASE CHARACTERISTICS:

  • Diagnosis of one of the following:
  • Severe aplastic anemia as defined by either of the following:
  • Marrow cellularity (< 25% [or 25-50% cellularity with < 30% of remaining cells hematopoietic in origin])
  • At least 2 of the following abnormal peripheral blood counts:
  • Reticulocyte count < 1% (corrected for hematocrit)
  • Platelet count < 20,000/mm^3
  • Neutrophil count < 500/mm^3
  • Histologically confirmed hematologic malignancy, including any of the following:
  • Acute leukemia
  • Resistant or recurrent disease after combination chemotherapy with at least one standard regimen OR in first remission and at high risk of relapse
  • Acute myeloid leukemia (AML) (antecedent myelodysplastic syndromes [MDS], secondary AML, or high-risk cytogenetic abnormalities)
  • Acute lymphoblastic leukemia (ALL) (high-risk cytogenetic abnormalities)
  • Chronic myeloid leukemia (CML)
  • Chronic phase, accelerated phase, or blast phase
  • Myeloproliferative disorders or MDS, including any of the following:
  • Myelofibrosis
  • Polycythemia vera*
  • Essential thrombocythemia*
  • Refractory anemia
  • Refractory anemia with excess blasts
  • Refractory anemia with excess blasts in transformation
  • Chronic myelomonocytic leukemia NOTE: * Only if transformed to AML or MDS
  • Lymphoproliferative disease
  • Recurrent or persistent, symptomatic disease after first-line chemotherapy, including any of the following:
  • Chronic lymphocytic leukemia (CLL) (≥ 20% marrow involvement)
  • Waldenstrom macroglobulinemia
  • Low-grade non-Hodgkin lymphoma
  • Intermediate or high-grade non-Hodgkin lymphoma, meeting 1 of the following criteria:
  • Resistant or recurrent disease after combination chemotherapy with one standard regimen
  • Lymphoblastic lymphoma or small noncleaved cell lymphoma in first remission and at high risk of relapse
  • CNS disease
  • Bone marrow disease and LDH greater than 300
  • Solid tumor that would otherwise be treated on RPCI-DS-9115 (or equivalent autologous stem transplant protocol) AND has a syngeneic donor
  • Autologous bone marrow transplant not possible (or desirable) due to 1 of the following:
  • History of marrow tumor
  • Inadequate marrow dose
  • Abnormal marrow histology or function prior to storage
  • Thrombocytopenia or leukopenia
  • Marrow cellularity < 20%
  • Histocompatible donor identified
  • Well-matched donor, as defined by 1 of the following:
  • Family member matched for 5 or 6 HLA specificities (A, B, DR)*
  • Unrelated donor meeting compatibility criteria of the National Marrow Donor Program (matched for HLA A, B, and DRB1 antigens)*
  • Identical twin sibling
  • If a compatible cord blood donor is identified and there is no suitable unrelated donor available, patient may receive cord blood transplant NOTE: *Patients ≤ 25 years of age may be singly mismatched at the A or B loci

NOTE: A new classification scheme for adult non-Hodgkin's lymphoma has been adopted by PDQ. The terminology of "indolent" or "aggressive" lymphoma will replace the former terminology of "low", "intermediate", or "high" grade lymphoma. However, this protocol uses the former terminology.

PATIENT CHARACTERISTICS:

Age:

  • 4 to 70

Performance status:

  • Zubrod 0-2 OR
  • Karnofsky 70-100%

Life expectancy:

  • Not specified

Hematopoietic:

  • See Disease Characteristics

Hepatic:

  • Bilirubin < 3 times normal (unless due to disease)
  • Alkaline phosphatase < 3 times normal (unless due to disease)
  • SGOT < 3 times normal (unless due to disease)
  • Hepatitis B surface antigen negative
  • No severe hepatic disease that would preclude study participation

Renal:

  • Creatinine normal
  • Creatinine clearance ≥ 50 mL/min
  • No severe renal disease that would preclude study participation

Cardiovascular:

  • Cardiac ventricular ejection fraction ≥ 50% by MUGA or echocardiogram
  • No uncontrolled or severe cardiovascular disease (e.g., myocardial infarction, congestive heart failure, symptomatic angina, life threatening arrhythmia, or hypertension within the past 6 months)

Pulmonary:

  • DLCO or DLVA ≥ 50% predicted (corrected for hemoglobin or alveolar ventilation)

Other:

  • No serious concurrent medical or psychiatric illness
  • No other serious organ dysfunction (unless due to underlying disease), including the following:
  • Uncontrolled bacterial, viral, or fungal infection
  • Uncontrolled peptic ulcer disease
  • Uncontrolled diabetes mellitus
  • HIV negative
  • Cytomegalovirus status known
  • Not pregnant

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • See Disease Characteristics
  • Pretransplant cytoreductive chemotherapy allowed for patients with relapsed or refractory disease

Endocrine therapy:

  • Not specified

Radiotherapy:

  • Not eligible for total-body irradiation if prior radiotherapy exceeded the following limits:
  • Mediastinum: 3,600 cGy
  • Heart: 3,600 cGy
  • Whole lungs: 1,200 cGy
  • Small bowel: 3,600 cGy
  • Kidneys: 1,200 cGy
  • Whole liver: 1,600 cGy
  • Cranial spinal: 3,600 cGy
  • Brain: 4,000 cGy
  • Retina: 4,000 cGy

Surgery:

  • Not specified

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Roswell Park Cancer Institute

    Buffalo, New York, 14263-0001

Other trials in United States

About this study

Official title: Allogeneic Blood or Marrow Transplantation for Hematologic Malignancy and Aplastic Anemia

RATIONALE: Giving chemotherapy drugs and total-body irradiation before a donor stem cell helps stop the growth of cancer or abnormal cells. It may also stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. It is not yet known which combination chemotherapy regimen is most effective when given before a donor stem cell transplant in treating aplastic anemia or hematologic cancer.

PURPOSE: This phase II/III trial is studying different combination chemotherapy regimens to compare how well they work when given before donor stem cell transplant in treating patients with aplastic anemia or hematologic cancer.

Read the detailed description

OBJECTIVES:

  • Compare the morbidity, mortality, and overall outcome of patients with severe aplastic anemia or hematologic malignancy treated with standard vs novel conditioning regimens followed by allogeneic stem cell transplantation.
  • Examine the influence of donor histocompatibility on outcome by comparing matched/related, mismatched/related (with or without T-cell depletion), and matched/unrelated transplants with stratification for type of preparative regimen.
  • Ensure that patients with uncommon diagnoses will be treated in a uniform fashion with the best therapy available.

OUTLINE: Patients are stratified according to risk of relapse (standard-risk: acute leukemia in first complete remission, chronic myelogenous leukemia in first chronic phase, lymphoma in sensitive first relapse or second remission, primary or untreated myelodysplastic syndromes, or untreated severe aplastic anemia vs high-risk: all others).

Patients are assigned to one of the following conditioning regimens based on diagnosis, risk of relapse, and donor relatedness:

  • Regimen 1: Patients receive busulfan IV over 2 hours every 6 hours on days -7 to -4 and cyclophosphamide IV over 2 hours on days -3 and -2.
  • Regimen 2: Patients receive cyclophosphamide IV over 2 hours on days -5 to -2 and anti-thymocyte globulin IV over 4-8 hours on days -5 to -3.
  • Regimen 3: Patients receive cyclophosphamide IV over 2 hours on days -5 and -4 and total-body irradiation (TBI) twice daily on days -3 to -1.
  • Regimen 4: Patients receive fludarabine IV over 30 minutes on days -6 to -2 and melphalan IV over 1 hour on days -3 and -2.
  • Regimen 5: Patients receive etoposide IV over 26 hours beginning on day -5, cyclophosphamide IV over 2 hours on day -4, and TBI twice daily on days -3 to -1.
  • Regimen 6: Patients receive cyclophosphamide IV over 24 hours, carboplatin IV over 24 hours, and thiotepa IV over 24 hours on days -7 to -4.
  • Regimen 7: Patients receive fludarabine IV over 30 minutes on days -5 to -1 and anti-thymocyte globulin IV over 4-8 hours on days -5 to -2.
  • Regimen 8: Patients receive cyclophosphamide IV over 2 hours on days -5 and -4, TBI twice daily on days -3 to -1, and anti-thymocyte globulin IV over 4-8 hours on days -3 to -1.
  • Regimen 9: Patients receive busulfan IV over 2 hours every 6 hours and anti-thymocyte globulin IV over 4-8 hours on days -7 to -4 and cyclophosphamide IV over 2 hours on days -3 and -2.

All patients then receive donor stem cell infusions on day 0. Some patients may undergo involved-field radiotherapy 4-8 weeks after transplant.

Patients will be taken off study after a minimum of 4 years of follow up.

PROJECTED ACCRUAL: At least 405 patients will be accrued for this study within 5 years.

Being tested
anti-thymocyte globulin, busulfan, carboplatin, cyclophosphamide, etoposide
Keywords
recurrent childhood acute lymphoblastic leukemia, recurrent cutaneous T-cell non-Hodgkin lymphoma, Burkitt lymphoma, Waldenstrom macroglobulinemia, recurrent childhood lymphoblastic lymphoma, recurrent childhood acute myeloid leukemia, recurrent adult acute myeloid leukemia, recurrent adult acute lymphoblastic leukemia, relapsing chronic myelogenous leukemia, refractory chronic lymphocytic leukemia, chronic phase chronic myelogenous leukemia, accelerated phase chronic myelogenous leukemia, blastic phase chronic myelogenous leukemia, adult acute myeloid leukemia in remission, adult acute lymphoblastic leukemia in remission, childhood acute myeloid leukemia in remission, childhood acute lymphoblastic leukemia in remission, polycythemia vera, essential thrombocythemia, refractory anemia
Medical subject headings
Myeloproliferative Disorders, Leukemia, Lymphoma, Myelodysplastic Syndromes, Myelodysplastic-Myeloproliferative Diseases, Neoplasms, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Lymphoma, T-Cell, Cutaneous

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00003816
Study groupRoleWhat they receive
Regimen 1ExperimentalPatients receive busulfan IV over 2 hours every 6 hours on days -7 to -4 and cyclophosphamide IV over 2 hours on days -3 and -2.
Receives: Drug: busulfan; Drug: cyclophosphamide
Regimen 2ExperimentalPatients receive cyclophosphamide IV over 2 hours on days -5 to -2 and anti-thymocyte globulin IV over 4-8 hours on days -5 to -3.
Receives: Biological: anti-thymocyte globulin; Drug: cyclophosphamide
Regimen 3ExperimentalPatients receive cyclophosphamide IV over 2 hours on days -5 and -4 and total-body irradiation (TBI) twice daily on days -3 to -1.
Receives: Drug: cyclophosphamide; Radiation: total-body irradiation
Regimen 4ExperimentalPatients receive fludarabine IV over 30 minutes on days -6 to -2 and melphalan IV over 1 hour on days -3 and -2.
Receives: Drug: fludarabine phosphate; Drug: melphalan
Regimen 5ExperimentalPatients receive etoposide IV over 26 hours beginning on day -5, cyclophosphamide IV over 2 hours on day -4, and TBI twice daily on days -3 to -1.
Receives: Drug: cyclophosphamide; Drug: etoposide; Radiation: total-body irradiation
Regimen 6ExperimentalPatients receive cyclophosphamide IV over 24 hours, carboplatin IV over 24 hours, and thiotepa IV over 24 hours on days -7 to -4.
Receives: Drug: carboplatin; Drug: cyclophosphamide; Drug: thiotepa
Regimen 7ExperimentalPatients receive fludarabine IV over 30 minutes on days -5 to -1 and anti-thymocyte globulin IV over 4-8 hours on days -5 to -2.
Receives: Biological: anti-thymocyte globulin; Drug: fludarabine phosphate
Regimen 8ExperimentalPatients receive cyclophosphamide IV over 2 hours on days -5 and -4, TBI twice daily on days -3 to -1, and anti-thymocyte globulin IV over 4-8 hours on days -3 to -1.
Receives: Biological: anti-thymocyte globulin; Drug: cyclophosphamide; Radiation: total-body irradiation
Regimen 9ExperimentalPatients receive busulfan IV over 2 hours every 6 hours and anti-thymocyte globulin IV over 4-8 hours on days -7 to -4 and cyclophosphamide IV over 2 hours on days -3 and -2.
Receives: Biological: anti-thymocyte globulin; Drug: busulfan; Drug: cyclophosphamide

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. CR Rate

    Rate of Complete Remission by Day +100

    Measured: day 100

Secondary outcomes (3)
  1. Toxicity/TRM at Day 100

    Death due to treatment related causes before day +100 after BMT

    Measured: Day +100

  2. 4 Year PFS

    progression free survival estimate at 4 years post BMT (events are disease progression/relapse and death due to any cause)

    Measured: 4 years

  3. 4 yr OS

    Overall survival estimate at 4 years post BMT

    Measured: 4-year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2003 (estimated)
  2. Study start19 Oct 1998
  3. Primary completion12 Jul 2019
  4. Study completion12 Jul 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
361 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00003816
Sponsor's protocol ID
RP 98-15
Other IDs
RP 98-15
Status last verified
Jul 2021
First submitted
1 Nov 1999
Last updated
13 Aug 2021
Data monitoring committee
Yes

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