Clinical Trials /

Inotuzumab Ozogamicin and Chemotherapy in Treating Patients With Leukemia or Lymphoma Undergoing Stem Cell Transplant

NCT03856216

Description:

This phase II trial studies the side effects of inotuzumab ozogamicin with chemotherapy in treating patients with leukemia or lymphoma undergoing stem cell transplant. Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a chemotherapy drug called ozogamicin. Inotuzumab attaches to CD22-positive cancer cells in a targeted way and delivers ozogamicin to kill them. Giving chemotherapy before a bone marrow or peripheral blood stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. Sometimes the transplanted cells from a donor attack the body's normal cells (called graft-versus-host disease). Giving tacrolimus and filgrastim before or after the transplant may stop this from happening. Giving inotuzumab ozogamicin with chemotherapy may work better in treating patients with leukemia or lymphoma undergoing stem cell transplant.

Related Conditions:
  • Acute Lymphoblastic Leukemia
  • Leukemia
  • Lymphoma
Recruiting Status:

Not yet recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: Inotuzumab Ozogamicin and Chemotherapy in Treating Patients With Leukemia or Lymphoma Undergoing Stem Cell Transplant
  • Official Title: Addition of Inotuzumab Ozogamicin Pre- and Post-Allogeneic Transplantation

Clinical Trial IDs

  • ORG STUDY ID: 2018-0860
  • SECONDARY ID: NCI-2019-00531
  • SECONDARY ID: 2018-0860
  • SECONDARY ID: P30CA016672
  • NCT ID: NCT03856216

Conditions

  • Acute Lymphoblastic Leukemia
  • Allogeneic Hematopoietic Stem Cell Transplantation Recipient
  • B Acute Lymphoblastic Leukemia
  • CD22 Positive
  • Lymphocytic Neoplasm
  • Lymphoma

Interventions

DrugSynonymsArms
Anti-Thymocyte GlobulinAntithymocyte Globulin, Antithymocyte Serum, ATG, ATGAM, ATS, ThymoglobulinGroup I (inotuzumab ozogamicin, chemotherapy, transplant)
BendamustineSDX-105Group II (inotuzumab ozogamicin, chemotherapy, transplant)
Filgrastim-sndzFilgrastim Biosimilar Filgrastim-sndz, ZarxioGroup I (inotuzumab ozogamicin, chemotherapy, transplant)
FludarabineFluradosaGroup I (inotuzumab ozogamicin, chemotherapy, transplant)
Inotuzumab OzogamicinBesponsa, CMC-544, Way 207294, WAY-207294Group I (inotuzumab ozogamicin, chemotherapy, transplant)
MelphalanAlanine Nitrogen Mustard, CB-3025, L-PAM, L-Phenylalanine Mustard, L-sarcolysin, L-Sarcolysin Phenylalanine mustard, L-Sarcolysine, Melphalanum, Phenylalanine Mustard, Phenylalanine nitrogen mustard, Sarcoclorin, Sarkolysin, WR-19813Group I (inotuzumab ozogamicin, chemotherapy, transplant)
MethotrexateAbitrexate, Alpha-Methopterin, Amethopterin, Brimexate, CL 14377, CL-14377, Emtexate, Emthexat, Emthexate, Farmitrexat, Fauldexato, Folex, Folex PFS, Lantarel, Ledertrexate, Lumexon, Maxtrex, Medsatrexate, Metex, Methoblastin, Methotrexate LPF, Methotrexate Methylaminopterin, Methotrexatum, Metotrexato, Metrotex, Mexate, Mexate-AQ, MTX, Novatrex, Rheumatrex, Texate, Tremetex, Trexeron, Trixilem, WR-19039Group I (inotuzumab ozogamicin, chemotherapy, transplant)
RituximabABP 798, BI 695500, C2B8 Monoclonal Antibody, Chimeric Anti-CD20 Antibody, CT-P10, IDEC-102, IDEC-C2B8, IDEC-C2B8 Monoclonal Antibody, MabThera, Monoclonal Antibody IDEC-C2B8, PF-05280586, Rituxan, Rituximab Biosimilar ABP 798, Rituximab Biosimilar BI 695500, Rituximab Biosimilar CT-P10, Rituximab Biosimilar GB241, Rituximab Biosimilar IBI301, Rituximab Biosimilar PF-05280586, Rituximab Biosimilar RTXM83, Rituximab Biosimilar SAIT101, RTXM83Group I (inotuzumab ozogamicin, chemotherapy, transplant)
TacrolimusFK 506, Fujimycin, Hecoria, Prograf, ProtopicGroup I (inotuzumab ozogamicin, chemotherapy, transplant)

Purpose

This phase II trial studies the side effects of inotuzumab ozogamicin with chemotherapy in treating patients with leukemia or lymphoma undergoing stem cell transplant. Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a chemotherapy drug called ozogamicin. Inotuzumab attaches to CD22-positive cancer cells in a targeted way and delivers ozogamicin to kill them. Giving chemotherapy before a bone marrow or peripheral blood stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. Sometimes the transplanted cells from a donor attack the body's normal cells (called graft-versus-host disease). Giving tacrolimus and filgrastim before or after the transplant may stop this from happening. Giving inotuzumab ozogamicin with chemotherapy may work better in treating patients with leukemia or lymphoma undergoing stem cell transplant.

Detailed Description

      PRIMARY OBJECTIVES:

      I. To assess the safety of the addition of inotuzumab ozogamicin (IO) pre- and
      post-allogeneic transplantation in patients with CD22-positive hematological malignancies.

      SECONDARY OBJECTIVES:

      I. Overall survival, progression-free survival and relapse rates. II. Treatment-related
      mortality. III. Cumulative incidence of acute and chronic graft-versus-host disease (GVHD).

      PRIMARY OBJECTIVES:

      I. To assess the safety of the addition of inotuzumab ozogamicin (IO) pre- and
      post-allogeneic transplantation in patients with CD22-positive hematological malignancies.

      SECONDARY OBJECTIVES:

      I. Overall survival, progression-free survival and relapse rates. II. Treatment-related
      mortality. III. Cumulative incidence of acute and chronic graft-versus-host disease (GVHD).

      OUTLINE: Patients are assigned to 1 of 2 groups.

      GROUP I: Patients with acute lymphoblastic leukemia (ALL) receive inotuzumab ozogamicin
      intravenously (IV) over 1 hour on day -13, fludarabine IV over 1 hour on days -5 to -2,
      melphalan IV over 30 minutes on day -2, and tacrolimus IV continuously beginning on day -2
      then orally (PO) once daily (QD) or twice daily (BID) for about 6 months. Patients receiving
      stem cells from a matched unrelated donor (MUD), receive anti-thymocyte globulin IV over 3-4
      hours on days -2 to -1 and not receive chemotherapy drugs. Patients also receive bone marrow
      or peripheral blood progenitor cells IV on day 0. Patients then receive methotrexate IV over
      30 minutes on days 1, 3, 6, and 11 and filgrastim-sndz subcutaneously (SC) QD beginning 1
      week after the transplant until blood cell levels return to normal. Patients with
      CD22-positive cancer, receive rituximab IV over 4-6 hours on days 1 and 8.

      GROUP II: Patients with lymphoma receive inotuzumab ozogamicin IV over 1 hour on day -13,
      fludarabine IV over 1 hour and bendamustine IV over 30 minutes to 1 hour on days -5 to -3,
      and tacrolimus IV continuously beginning on day -2 then PO QD or BID for about 6 months.
      Patients receiving stem cells from a MUD, receive anti-thymocyte globulin IV over 3-4 hours
      on days -2 to -1 and not receive chemotherapy drugs. Patients also receive bone marrow or
      peripheral blood progenitor cells IV on day 0. Patients then receive rituximab IV over 4-6
      hours on days 1 and 8, methotrexate IV over 30 minutes on days 1, 3, and 6, and
      filgrastim-sndz SC once a day beginning 1 week after the transplant. Patients who received a
      stem cell transplant from a MUD also receive methotrexate IV over 30 minutes on day 11.

      MAINTENANCE: Between 45 and 100 days after stem cell transplant, all patients receive
      inotuzumab ozogamicin IV over 1 hour on days 1 and 2. Beginning 28 to 100 days after start of
      first cycle, patients receive inotuzumab ozogamicin IV over 1 hour on days 1 and 2 in the
      absence of disease progression or unacceptable toxicity.

      After completion of study treatment, patients are followed up periodically.
    

Trial Arms

NameTypeDescriptionInterventions
Group I (inotuzumab ozogamicin, chemotherapy, transplant)ExperimentalSee Detailed Description.
  • Anti-Thymocyte Globulin
  • Filgrastim-sndz
  • Fludarabine
  • Inotuzumab Ozogamicin
  • Melphalan
  • Methotrexate
  • Rituximab
  • Tacrolimus
Group II (inotuzumab ozogamicin, chemotherapy, transplant)ExperimentalSee Detailed Description.
  • Anti-Thymocyte Globulin
  • Bendamustine
  • Filgrastim-sndz
  • Fludarabine
  • Inotuzumab Ozogamicin
  • Methotrexate
  • Rituximab
  • Tacrolimus

Eligibility Criteria

        Inclusion Criteria:

          -  Patient age 18 to 70; young adults (age 18-35) with ALL will be included only if they
             are not eligible for myeloablative transplants.

          -  CD22+ lymphoid malignancies including B acute lymphoblastic leukemia (B-ALL).

          -  Eligible to receive a reduced-intensity allogeneic hematopoietic stem cell
             transplantation (alloSCT).

          -  Donor: HLA compatible related or matched unrelated donor (HLA-A, B, C, DRB1).

          -  Performance status of 0 to 2.

          -  Creatinine less than or equal to 1.6 mg/dL (at time of study entry).

          -  Bilirubin less than 1.6 mg/dL (at time of study entry).

          -  Serum glutamate pyruvate transaminase (SGPT) < 2 x upper limit of normal (ULN) (at
             time of study entry).

          -  Ejection fraction >= 40% (at time of study entry).

          -  Forced expiratory volume in one second (FEV1), forced vital capacity (FVC) and
             diffusion capacity of the lung for carbon monoxide (DLCO) >= 40% (at time of study
             entry).

          -  Negative beta human chorionic gonadotropin (HCG) test in a woman with child bearing
             potential defined as not post-menopausal for 12 months or no previous surgical
             sterilization) or currently breast-feeding. Pregnancy testing is not required for post
             menopausal or surgically sterilized women.

        Exclusion Criteria:

          -  Philadelphia chromosome (Ph)-positive ALL.

          -  Active and uncontrolled disease/infection.

          -  Unable or unwilling to sign consent.

          -  Current active hepatic or biliary disease (with exception of Gilbert's syndrome).

          -  Active hepatitis B or C.

          -  Recent chemotherapy or radiation within 3 weeks of study entry. Exception: ibrutinib
             and venetoclax are allowed to within 3 days.

          -  Prior inotuzumab ozogamicin within 3 weeks of study entry.
      
Maximum Eligible Age:70 Years
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Incidence of grade 3 or higher renal, hepatic, cardiac, pulmonary, or neurologic toxicity
Time Frame:At the end of Cycle 1 (each cycle is 28 days)
Safety Issue:
Description:Will be assessed using the Bayesian method of Thall, Simon, and Estey. At the end of the trial, the rates of severe toxicity will be summarized, and analyses will be performed to assess the relationship between each toxicity endpoint and covariates of interest using logistic regression.

Secondary Outcome Measures

Measure:Treatment-related mortality (TRM)
Time Frame:Up to 2 years
Safety Issue:
Description:The cumulative incidence of TRM will be assessed in a competing risks framework with the competing risk of disease relapse. Regression models will be fit to assess the relationship between each and covariates of interest using the method of Fine and Gray.
Measure:Relapse Rates
Time Frame:Up to 2 years
Safety Issue:
Description:The cumulative incidence of TRM will be assessed in a competing risks framework with the competing risk of disease relapse. Regression models will be fit to assess the relationship between each and covariates of interest using the method of Fine and Gray.
Measure:Overall survival (OS)
Time Frame:Up to 2 years
Safety Issue:
Description:The distribution of OS will be assessed using the Kaplan-Meier method, and distributions will be compared using the log-rank test. Cox proportional hazards regression models will be fit to assess the relationship between OS and covariates of interest.
Measure:Progression-free survival (PFS)
Time Frame:Up to 2 years
Safety Issue:
Description:The distribution of PFS will be assessed using the Kaplan-Meier method, and distributions will be compared using the log-rank test. Cox proportional hazards regression models will be fit to assess the relationship between PFS and covariates of interest.
Measure:Acute graft versus host disease (GVHD)
Time Frame:Up to 2 years
Safety Issue:
Description:The cumulative incidence of acute GvHD will be assessed in a competing risks framework with competing risks of death without relapse and disease relapse. The method of Fine and Gray will be used to assess the association between GvHD and covariates of interest.
Measure:Chronic GVHD
Time Frame:Up to 2 years
Safety Issue:
Description:The cumulative incidence of chronic GvHD will be assessed in a competing risks framework with competing risks of death without relapse and disease relapse. The method of Fine and Gray will be used to assess the association between GvHD and covariates of interest.

Details

Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Not yet recruiting
Lead Sponsor:M.D. Anderson Cancer Center

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