IMRT-TMI With Fludarabine as Myeloablative Conditioning for Allogeneic HSCT

A Dose Escalation Study of Intensity Modulated Total Marrow Irradiation (IMRT-TMI) With Fludarabine as a Myeloablative Conditioning Regimen for Allogeneic Hematopoietic Stem Cell Transplantation for Patients With Relapsed and Refractory Hematologic Malignancies

This is a phase I/II clinical trial on the use of total marrow irradiation (TMI) given concurrently with fludarabine, a chemotherapy drug commonly used to treat leukemia, as a myeloablative therapy for patients undergoing Allo-HSCT. TMI is a targeted technique to deliver radiation to the bone marrow while minimizing dose to other normal organs in the body. In phase I of the clinical study, the dose of radiation to the bone marrow will be incrementally increased to determine the highest tolerated TMI dose. In phase II, the effectiveness of the TMI-fludarabine conditioning regimen utilizing that dose of radiation will be studied. Acute and long-term toxicity data as well as quality of life data will also be studied.

*Stopping criteria was met during the first dose level cohort in Phase l. The trial will not continue into Phase II as originally planned.

Study Overview

• Status: Terminated
• Conditions: Acute Myeloid Leukemia; Myelodysplastic Syndromes; Chronic Myeloid Leukemia; Acute Lymphocytic Leukemia
• Intervention / Treatment: Drug: Fludarabine; Radiation: Total Marrow Irradiation (TMI)

Detailed Description

This is a phase I/II clinical trial to determine the maximum tolerated dose (MTD) of intensity modulated radiation therapy based total marrow irradiation (TMI) concurrent with fludarabine as a myeloablative conditioning regimen for allogeneic hematopoietic stem cell transplantation (Allo-HSCT), as well as to determine the efficacy of the regimen in patients with high-risk and relapsed or refractory leukemia and myelodysplasia. TMI, which allows for conformal dosing of target bone marrow tissue while giving lower doses to organs at risk, is considered by many to be a superior alternative to conventional total body irradiation (TBI)

Primary Objectives:

Phase I:

Determine the MTD of TMI given concurrently with fludarabine (fixed at 150 mg/m2) as a conditioning regimen for Allo-HSCT for patients with high risk (relapsed/refractory) acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and chronic myelogenous leukemia (CML).

Phase II:

Single-arm exploratory study to expand the cohort at the MTD level to estimate 1- year overall survival (OS), with the objective of increasing the OS from the historical rate of 30% (null hypothesis ) to 50% (alternate hypothesis) with 80% power and a one-sided type I error of 0.05.

Secondary Objectives

1. Describe the extramedullary toxicity and the incidence of complications, including mucositis, acute and chronic graft versus host disease (GvHD), sinusoidal obstruction syndrome (SOS), and pneumonitis.
2. Describe the time to engraftment of neutrophils and platelets
3. Describe the disease response rate at day 30 after transplantation
4. Describe the overall survival and disease-free survival
5. Describe the cumulative incidence of relapse and non-relapse mortality
6. Determine the correlation between plasma/serum markers and radiation induced acute and long term toxicities.

7. Describe the quality of life metrics of participating subjects

   • Stopping criteria was met during the first dose level cohort in Phase l. The trial will not continue into Phase II as originally planned.

• Study Type: Interventional
• Enrollment (Actual): 6
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Indiana
    • Indianapolis, Indiana, United States, 46202
      • Indiana University Melvin & Bren Simon Cancer Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Patients must be diagnosed with one of the following conditions:

   Acute Myeloid Leukemia (AML) who are not in complete remission, and who have either primary refractory or relapsed disease, and who do not have more than one of the following adverse factors:

   1. Duration of first CR < 6 months (if previously in CR)
   2. Poor risk karyotype including any of the following: complex karyotype with ≥3 clonal abnormalities, 5q-/-5, 7q-/-7, 11q23 abnormalities, inv(3q), 20q or 21q abnormalities, t(6;9), t(9;22), 17p abnormalities [or TP53 mutations] or monosomal karyotype. Molecular typing (except for TP53 mutation) will not be used for eligibility criteria determination.
   3. Circulating peripheral blood blasts at time of enrollment
   4. Karnofsky performance status <90%

   Acute Lymphocytic Leukemia (ALL) who are not in complete remission, and who have either primary refractory or relapsed disease, and who do not have more than one of the following adverse factors:

   1. First refractory relapse. Patients in second or subsequent relapse are excluded.
   2. Donor is CMV seropositive
   3. Bone marrow blasts >25% (within 30 days of admission)
   4. Age >40 years

   Myelodysplasia with a Revised International Prognostic Score (IPSS-R) of greater than 4.5 (i.e., high- or very-high risk).

   Chronic Myelogenous Leukemia (CML) in either

   1. Accelerated phase, defined by any of the following:

      • 10-19% blasts in peripheral blood white cells or bone marrow
      • Peripheral blood basophils at least 20%
      • Persistent thrombocytopenia (<100 x 109/l) unrelated to therapy, or persistent thrombocytosis (>1000 x 109/l) unresponsive to therapy
      • Increasing spleen size and increasing white blood cell (WBC) count unresponsive to therapy
      • Cytogenetic evidence of clonal evolution (i.e., the appearance of an additional genetic abnormality that was not present in the initial specimen at the time of diagnosis of chronic phase)
   2. Chronic phase provided a complete hematologic remission was not achieved by 3 months or a complete cytogenetic remission by 18 months and the patient had received at least 2 tyrosine kinase inhibitors.
2. Patient age 18-65 years old at time of consent
3. Availability of a consenting human leukocyte antigens(HLA) -matched donor
4. Karnofsky Performance Status 70% or higher

5. Required baseline laboratory values:

   1. Estimated creatinine clearance ≥ 60 ml/min
   2. Aspartate aminotransferase and alanine aminotransferease ≤ 2.5 x upper limit of normal value
   3. Bilirubin ≤ 1.5 x upper limit of normal value

6. Required baseline cardiac function of left ventricular ejection fraction (LVEF) > 45

   • corrected
7. Required baseline pulmonary function of lung diffusing capacity (DLCO) > 45 % predicted (corrected for hemoglobin)
8. Patient must be capable of understanding the investigational nature of this study, potential risks and benefits of the study, and be able to provide a valid informed consent.

Exclusion Criteria:

1. Patients with ALL who are in second or subsequent relapse
2. HIV seropositive patients.
3. Pregnant or nursing females are excluded from this study.
4. Prior radiation therapy
5. Patients who have had a prior autologous or allogeneic bone marrow or stem cell transplantation

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Sequential Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Fludarabine + Total Marrow Irradiation	Drug: Fludarabine; Fludarabine 30 mg/m2/day IV (total 5 doses) administered days -7 through -3 of conditioning regimen; Radiation: Total Marrow Irradiation (TMI); TMI will be delivered twice a day, at least 6 hours apart, on days -7 through -3 (total of 10 fractions) of conditioning regimen

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Overall survival (OS) rate 1 year post transplant-Phase II only	1 year
Dose limiting toxicity (DLT) of Total Marrow Irradiation (TMI) in combination with 150 mg/m2 fludarabine- Phase I only	Day -7 of conditioning regimen through 30 days post transplant (37 days)
Maximum-tolerated dose (MTD) of Total Marrow Irradiation (TMI) in combination with 150 mg/m2 fludarabine-Phase I only	Day -7 of conditioning regimen through 30 days post transplant (37 days)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Disease-Free Survival		2 years
Incidence of mucositis		100 days
Incidence of pneumonitis		100 days
Incidence of non-relapse mortality		30 days
Incidence of non-relapse mortality		100 days
Incidence of non-relapse mortality		1 year
Incidence of relapse mortality		1 year
Incidence of relapse mortality		30 days
Incidence of relapse mortality		100 days
Frequency of non hematologic toxicities		100 days
Incidence of infection		100 days
Type of infections		100 days
Incidence of graft versus host disease (GvHD)		100 days
Incidence of chronic graft versus host disease (GvHD)		2 years
Incidence of sinusoidal obstruction syndrome (SOS)		100 days
Time to engraftment of neutrophils		from date of transplant to the first of three consecutive days after transplantation during which the absolute neutrophil count (ANC) is greater than or equal to 0.5 x 10^9/liter
Time to engraftment of platelets		from date of transplant until he first of seven consecutive days after transplantation during which the platelet count is greater than or equal to 20 x10^9/liters without transfusion.
Disease response rate		Day 30 after transplant (30 days)
Mean Quality of Life (QOL) as measured by Functional Assessment of Cancer Therapy-Bone Marrow Transplant (FACT-BMT) version 4	50 item likert type scale with responses measuring from 0-4 (where 0 = not at all; 1 = a little bit; 2 = somewhat, 3 = quite; and 4 = very much) with higher scores correlating to higher QOL	Screening (at simulation), day +180, day +365, + 2 years from transplant (approximately 2 years)

Collaborators and Investigators

• Sponsor: Naoyuki G. Saito, M.D., Ph.D.
• Collaborators: Indiana University
• Investigators: Principal Investigator: Naoyuki G Saito, MD PhD, Indiana University

Study record dates

Study Major Dates

• Study Start (Actual): August 29, 2018
• Primary Completion (Actual): July 8, 2020
• Study Completion (Actual): April 13, 2021

Study Registration Dates

• First Submitted: October 2, 2018
• First Submitted That Met QC Criteria: October 3, 2018
• First Posted (Actual): October 4, 2018

Study Record Updates

• Last Update Posted (Actual): March 9, 2022
• Last Update Submitted That Met QC Criteria: February 22, 2022
• Last Verified: February 1, 2022

More Information

Terms related to this study

• Keywords: Bone Marrow Transplantation; Fludarabine; Radiation; Total Marrow Irradiation
• Additional Relevant MeSH Terms: Immune System Diseases; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Bone Marrow Diseases; Hematologic Diseases; Myeloproliferative Disorders; Leukemia, Lymphoid; Myelodysplastic Syndromes; Leukemia; Leukemia, Myeloid; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Antineoplastic Agents; Fludarabine
• Other Study ID Numbers: IUSCC-0652

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No