MYELOMATCH: A Screening Study to Assign People With Myeloid Cancer to a Treatment Study or Standard of Care Treatment Within myeloMATCH (MyeloMATCH Screening Trial)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Cancer Institute (NCI)

About this trial

This MyeloMATCH Master Screening and Reassessment Protocol (MSRP) evaluates the use of a screening tool and specific laboratory tests to help improve participants' ability to register to clinical trials throughout the course of their myeloid cancer (acute myeloid leukemia or myelodysplastic syndrome) treatment. This study involves testing patients' bone marrow and blood for certain biomarkers. A biomarker (sometimes called a marker) is any molecule in the body that can be measured. Doctors look at markers to learn what is happening in the body. Knowing about certain markers can give doctors more information about what is driving the cancer and how to treat it. Testing patients' bone marrow and blood will show doctors if patients have markers that specific drugs can target. The marker testing in this study will let doctors know if they can match patients with a treatment study (myeloMATCH clinical trial) that tests treatment for the type of cancer they have or continue standard of care treatment with their doctor on the Tier Advancement Pathway (TAP).

Eligibility criteria

Qualifiers

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.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Allogeneic Hematopoietic Stem Cell Transplantation
  • Azacitidine
  • Best Practice
  • Biopsy Procedure
  • Biospecimen Collection
  • Bone Marrow Aspiration
  • Bone Marrow Biopsy
  • Busulfan
  • Chest Radiography
  • Computed Tomography
  • Cytarabine
  • Daunorubicin Hydrochloride
  • Decitabine and Cedazuridine
  • Echocardiography Test
  • Emavusertib
  • Enasidenib
  • Epoetin Alfa
  • Fludarabine
  • Gemtuzumab Ozogamicin
  • Gilteritinib
  • Liposome-encapsulated Daunorubicin-Cytarabine
  • Luspatercept
  • Melphalan
  • Multigated Acquisition Scan
  • Mutation Carrier Screening
  • Olutasidenib
  • Placebo Administration
  • Positron Emission Tomography
  • Total-Body Irradiation
  • Venetoclax

Treatment groups

2,000 Participants
are divided into 39 treatment groups

39

Treatment groups

See each treatment group below.