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

NCT ID: NCT05201183

Last Updated: 2023-12-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

PHASE1/PHASE2

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-31

Study Completion Date

2029-04-30

Brief Summary

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This is a phase I/II clinical trial to determine the maximum tolerated dose (MTD) of total marrow irradiation (TMI) followed by fludarabine in the context of 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 leukemia and myelodysplasia.

Detailed Description

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This is a phase I/II clinical trial to determine the maximum tolerated dose (MTD) of total marrow irradiation (TMI) followed by fludarabine in the context of 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 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). Through the use of TMI, it is possible to escalate the dose of radiation to the bone marrow while keeping the dose to normal organs at acceptable levels, effectively widening the therapeutic window of this modality. This conditioning regimen will be tried in patients with relapsed or refractory hematologic malignancies.

Primary Objectives:

Phase I: Determine the MTD of TMI (delivered twice a day for 5 days) followed by fludarabine (fixed at 150 mg/m2 given over 5 days) 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
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

Conditions

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Acute Myeloid Leukemia Chronic Myeloid Leukemia Acute Lymphocytic Leukemia Myelodysplastic Syndromes

Keywords

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Radiation Total Marrow Irradiation Fludarabine Bone Marrow Transplant

Study Design

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Allocation Method

NA

Intervention Model

SEQUENTIAL

A standard "3+3" phase I design of dose escalation using 3 patients per dose level cohort with an expansion to 6 patients at the MTD will be used in Phase I. We will treat 3 patients at the initial dose level of TMI. If no dose-limiting toxicity (DLT) is observed, the next cohort of three patients is treated at the next higher dose level. If 1 of the 3 patients demonstrates DLT, an additional 3 patients are treated at that dose level. If only 1 of the 6 shows DLT, the next cohort of three patients is entered at the next dose level. If 2 or more of the 6 demonstrate DLT, the MTD is defined as the previous dose level. If no DLT is observed in the final dose level, the number of patients treated will be expanded to 6. In phase II, we will enroll additional patients at the defined MTD level.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Fludarabine + Total Marrow Irradiation

Fludarabine will be administered sequentially after the administration of TMI. TMI will be delivered on Days -11, -10, -9, -8, and -7 (1.4-2.2 gray (GY)/fraction, twice a day) followed by fludarabine on Days -6, -5, -4, -3, and -2 (150 mg/m2, 30 mg/m2/day)

Group Type EXPERIMENTAL

Fludarabine + Total Marrow Irradiation

Intervention Type COMBINATION_PRODUCT

Patients will receive total marrow irradiation TMI on Day -11 to Day -7 in two fractions per day. The TMI dose will be escalated in successive cohorts compromised of 3-6 patients as follows:

Cohort 1 1.4 (Gy/fraction) Cohort 2: 1.6 (Gy/fraction) Cohort 3 1.8 (Gy/fraction) Cohort 4 2.0 (Gy/fraction) Cohort 5 2.2 (Gy/fraction)

Patients will receive Fludarabine (30 mg/m2/day) on Day -6 to Day -2 followed by allo-HSCT on Day 0.

Interventions

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Fludarabine + Total Marrow Irradiation

Patients will receive total marrow irradiation TMI on Day -11 to Day -7 in two fractions per day. The TMI dose will be escalated in successive cohorts compromised of 3-6 patients as follows:

Cohort 1 1.4 (Gy/fraction) Cohort 2: 1.6 (Gy/fraction) Cohort 3 1.8 (Gy/fraction) Cohort 4 2.0 (Gy/fraction) Cohort 5 2.2 (Gy/fraction)

Patients will receive Fludarabine (30 mg/m2/day) on Day -6 to Day -2 followed by allo-HSCT on Day 0.

Intervention Type COMBINATION_PRODUCT

Eligibility Criteria

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Inclusion Criteria

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

1. Acute Myeloid Leukemia (AML), with no history of extramedullary disease, who are not in complete remission, who have either primary refractory or relapsed disease, and who do not have more than one of the following adverse factors:

* Duration of first CR \< 6 months (if previously in CR), based on the best overall clinical assessment of the disease course, not solely based on blood test or bone marrow biopsy results
* 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.
* Circulating peripheral blood blasts at time of enrollment
* Karnofsky performance status \<90%
2. Acute Lymphocytic Leukemia (ALL) who are not in complete remission, who have either primary refractory or relapsed disease, and who do not have more than one of the following adverse factors:

* Primary refractory or first relapse. Patients in second or subsequent relapse are excluded.
* Bone marrow blasts \>25% within 30 days before the start of the conditioning regimen
* Age \>40 years
3. Myelodysplasia with a Revised International Prognostic Score (IPSS-R) of greater than 4.5 (i.e., high- or very-high risk).
4. Chronic Myelogenous Leukemia (CML) in 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. The patient must be 18-65 years old at time of consent
3. Signed written informed consent: 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.
4. Availability of a consenting human leukocyte antigens (HLA)-matched donor
5. Karnofsky Performance Status 70% or higher
6. Required baseline laboratory values:

* Estimated creatinine clearance ≥ 60 ml/min
* Aspartate aminotransferase and alanine aminotransferase ≤ 2.5 x upper limit of normal value
* Bilirubin ≤ 1.5 x upper limit of normal value (unless determined to be related to Gilbert's disease)
7. Required baseline cardiac function values:

* Required baseline cardiac function of left ventricular ejection fraction (LVEF) \> 45 % corrected
8. Required baseline pulmonary function values:

* Required baseline pulmonary function of lung diffusing capacity (DLCO) \> 45 % predicted (corrected for hemoglobin))

Exclusion Criteria

1. HIV seropositive patients
2. Pregnant or nursing females.
3. Prior radiation therapy
4. Patients who have had a prior autologous or allogeneic bone marrow or stem cell transplantation
5. Gemtuzumab ozogamicin (trade name: Mylotarg) and/or inotuzumab ozogamicin (trade name: Besponsa) use within 60 days before start of the conditioning regimen
6. Though this is NOT an exclusion criterion, we strongly recommend discontinuation of any steroidal oral contraceptives at least 7 days before start of the conditioning regimen. Use of therapeutic alternatives, including leuprolide should be considered to reduce the risk of SOS/VOD. Of note, for patients already on steroidal oral contraceptives for excessive menorrhagia, the switch to leuprolide should occur at least 2 weeks before the start of the conditioning regimen
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Naoyuki G. Saito, M.D., Ph.D.

OTHER

Sponsor Role lead

Responsible Party

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Naoyuki G. Saito, M.D., Ph.D.

Assistant Professor of Radiation Oncology

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Naoyuki Saito, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Indiana University

Locations

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Indiana University Melvin and Bren Simon Comprehensive Cancer Center

Indianapolis, Indiana, United States

Site Status

Countries

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United States

Other Identifiers

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CTO-IUSCCC-0747

Identifier Type: -

Identifier Source: org_study_id