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Master Screening and Reassessment Protocol (MSRP) for the NCI MyeloMATCH Clinical Trials
Cancer Categories
Hematologic (Blood Cancers)
Karmanos Trial ID
MYELOMATCH
NCT ID
NCT05564390
Age Group
Adult
Scope
National
Phase
Questions, please contact us
N/A
Principal Investigator
Vijendra
Singh, M.D.
Oncology - Medical
View Profile
Objective:
Primary Objectives:
Screening and Reassessment (MSRP): To evaluate the feasibility of MATCHBox receiving and organizing all data needed for assignment to a myeloMATCH clinica >trial or Tier Advancement Pathway (TAP) within 72 hours of MDNet receipt of al >required specimens for initial therapy and within 10 days for subsequent therapy.
Tier Advancement Pathway (TAP): To enable participants who are not matched to an investigational myeloMATCH treatment substudy to receive standard of care (SOC) while remaining on the MSRP to maintain access to later tiers of treatment substudies.
Secondary Objectives:
Screening and Reassessment (MSRP)
To describe the time to generation of all data required for treatment substudy (or TAP) assignment, time to treatment substudy (or TAP) assignment, percent assigned to a myeloMATCH treatment substudy, and the percent of screened participants who register to a myeloMATCH investigational treatment substudy or are assigned to TAP:
Separately within each tier of myeloMATCH treatment substudy and analogous TAP assignment (see Section 2.1 for tier definitions)
Separately within each clinical basket of myeloMATCH treatment substudies (see Section 2.2 for clinical basket definitions).
Over time, across and within the categories above.
Tier Advancement Pathway (TAP)
To evaluate participants for assignment to higher tier treatment substudies within myeloMATCH.
To describe, within tier- and basket- levels of TAP, measurable residual disease (MRD) rates and clonal evolution.
To describe, within tier- and basket- levels of TAP, remission status and overall survival of participants who receive standard of care therapy.
To obtain MDNet specimens for translational medicine and biobanking.
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Eligibility
Locations
Applicable Disease Site
Therapies | Drugs | Devices
Eligibility
Eligibility
Inclusion Criteria:
Participants must be suspected to have previously untreated acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Participants with AML cannot have a history of previously treated myeloproliferative neoplasms (MPN) or MDS.
Participants must be >= 18 years of age.
Participants must not have received prior anti-cancer therapy for AML or MDS.
Note: Hydroxyurea to control the white blood cell count (WBC) is allowed.
Note: Prior erythroid stimulating agent (ESA) is not considered prior therapy for the purposes of eligibility. Participants must not be currently receiving any cytarabine-containing therapy other than up to 1 g/m^2 of cytarabine, which is allowed for urgent cytoreduction.
Participants are allowed prior use of hydroxyurea, all-trans retinoic acid (ATRA), BCR-ABL directed tyrosine kinase inhibitor, erythropoiesis-stimulating agent, thrombopoietin receptor agonist and lenalidomide, with a maximum limit of 1 month of exposure.
Note: Participants receiving hydroxyurea prior to treatment substudy or TAP assignment must agree to discontinue hydroxyurea within 24 hours before beginning substudy or TAP treatment.
Participants must not have a prior or concurrent malignancy that requires concurrent anti-cancer therapy
Note: active hormonal therapy is allowed
Participants must have a Zubrod Performance Status evaluation within 28 days prior to registration.
Participants must agree to have translational medicine specimens submitted.
Participants must be offered the opportunity to participate in specimen banking.
Note: Specimens must be collected and submitted following the initial paper-based process and subsequently via the Precision Medicine Specimen Tracking Forms in Medidata Rave instance for the MyeloMATCH MSRP.
Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines.
Note: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system.
Locations
Locations
Karmanos Cancer Institute - Detroit Headquarters
4100 John R
Detroit, MI 48201
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Phone:
1-800-527-6266
Karmanos Cancer Institute at Weisberg Cancer Center - Farmington Hills
31995 Northwestern Hwy
Farmington Hills, MI 48334
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Phone:
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Applicable Disease Site
Applicable Disease Site
Myeloid and Monocytic Leukemia
Therapies, Drugs, Devices
Therapies | Drugs | Devices
Therapies
Chemotherapy
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