Acute myeloid leukemia with t(9;11)(p22;q23)

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Overview

Acute myeloid leukemia with t(9;11)(p22;q23), also known as AML with KMT2A-MLLT3 rearrangement, is a specific type of blood cancer. In this disease, the bone marrow (the spongy tissue inside your bones that makes blood cells) starts producing too many immature white blood cells called myeloid blasts. These abnormal cells crowd out healthy blood cells, leading to problems like infections, anemia, and bleeding. The name refers to a specific genetic change where pieces of chromosomes 9 and 11 swap places (called a translocation), creating an abnormal fusion gene that drives the cancer. This subtype is recognized by the World Health Organization as a distinct form of AML because it behaves differently from other types. Symptoms often come on quickly and can include fatigue, frequent infections, easy bruising or bleeding, fevers, and bone pain. Some patients may notice swollen gums or skin changes. This subtype is more common in children than adults and is generally considered to have an intermediate prognosis compared to other AML subtypes. Treatment typically involves intensive chemotherapy given in phases: induction therapy to achieve remission, followed by consolidation therapy to prevent relapse. In some cases, a bone marrow (stem cell) transplant may be recommended, especially if the leukemia comes back or is considered higher risk. Newer targeted therapies and clinical trials are also being explored. With modern treatment, many patients—especially children—can achieve long-term remission, though the journey is often challenging and requires close medical follow-up.

Also known as:

Key symptoms:

Extreme tiredness and fatigueFrequent or severe infectionsEasy bruisingUnusual or prolonged bleedingUnexplained feversBone or joint painPale skinShortness of breathSwollen gumsLoss of appetite and weight lossSmall red or purple spots on the skin (petechiae)Swollen lymph nodesFeeling of fullness or discomfort in the abdomen due to enlarged spleen or liverNight sweats

Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Variable

Can begin at different ages, from infancy through adulthood

Orphanet ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Acute myeloid leukemia with t(9;11)(p22;q23).

View clinical trials →

No actively recruiting trials found for Acute myeloid leukemia with t(9;11)(p22;q23) at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Acute myeloid leukemia with t(9;11)(p22;q23) community →

Specialists

7 foundView all specialists →
JL
Jeffrey Lancet
TAMPA, FL
Specialist
PI on 2 active trials

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Acute myeloid leukemia with t(9;11)(p22;q23).

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Community

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Latest news about Acute myeloid leukemia with t(9;11)(p22;q23)

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

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Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.What is the exact genetic profile of my leukemia, and how does the t(9;11) translocation affect my treatment plan?,What are the chances of achieving remission with the recommended chemotherapy, and what happens if the first treatment doesn't work?,Will I need a bone marrow transplant, and if so, when should we start looking for a donor?,Are there any clinical trials available for KMT2A-rearranged AML, such as menin inhibitor trials?,What are the short-term and long-term side effects of the proposed treatment?,How will treatment affect my fertility, and are there options to preserve fertility before starting?,What support services are available to help with the emotional, financial, and practical challenges of treatment?

Common questions about Acute myeloid leukemia with t(9;11)(p22;q23)

What is Acute myeloid leukemia with t(9;11)(p22;q23)?

Acute myeloid leukemia with t(9;11)(p22;q23), also known as AML with KMT2A-MLLT3 rearrangement, is a specific type of blood cancer. In this disease, the bone marrow (the spongy tissue inside your bones that makes blood cells) starts producing too many immature white blood cells called myeloid blasts. These abnormal cells crowd out healthy blood cells, leading to problems like infections, anemia, and bleeding. The name refers to a specific genetic change where pieces of chromosomes 9 and 11 swap places (called a translocation), creating an abnormal fusion gene that drives the cancer. This subty

How is Acute myeloid leukemia with t(9;11)(p22;q23) inherited?

Acute myeloid leukemia with t(9;11)(p22;q23) follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

Which specialists treat Acute myeloid leukemia with t(9;11)(p22;q23)?

7 specialists and care centers treating Acute myeloid leukemia with t(9;11)(p22;q23) are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.