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What My Sister's Keeper Can Teach Us About Leukemia
In My Sister's Keeper, Kate lives with acute promyelocytic leukemia, a type of acute myeloid leukemia. Here's what leukemia really is.
A plain-language summary based on public reporting and trusted sources, linked below.

Please note: this page is educational only — it is not medical advice, and it does not speculate about anyone’s health beyond reliable public reporting. For questions about your own health, talk with your healthcare team.
A diagnosis chosen for a reason
Jodi Picoult's novel gives Kate Fitzgerald a specific illness. Kirkus Reviews, summarizing the book, says Kate was diagnosed at age 2 with acute promyelocytic leukemia. Her younger sister Anna was conceived to be a genetic match. Anna gives platelets, bone marrow, and cord blood stem cells over the years, then sues to stop.
The legal fight is the story. The blood disease behind it is real, well understood, and worth knowing about on its own.
What the words actually mean
Leukemia is cancer of the blood-forming tissue, mostly the bone marrow. Acute means it moves fast. Myeloid points to the family of blood cells it starts in.
Acute promyelocytic leukemia, or APL, is a subtype of acute myeloid leukemia. NCI explains it clearly. Genes on chromosome 15 swap places with genes on chromosome 17. That swap builds an abnormal gene called PML-RARA. The faulty gene stops promyelocytes, a young type of white blood cell, from growing up.
Those stalled cells pile up in the marrow and blood. They crowd out healthy white cells, red cells, and platelets. NCI notes that severe bleeding and blood clots can both happen in APL, and calls it a serious problem that needs treatment as soon as possible. That bleeding risk is the reason APL is an emergency the day it is suspected.
How it is found
The first clue is often a routine blood count that comes back wrong. Too few red cells, too few platelets, or a strange white cell count sends the sample onward.
Confirming it takes a look at the marrow itself. A doctor draws a small sample from the hip bone with a needle. Lab tests then hunt for the specific gene change. In APL that means testing for PML-RARA. Finding it does two things at once. It names the disease, and it points to the treatment. Our overview of leukemia walks through the wider family of blood cancers.
Why APL is treated its own way
Most acute leukemias start with intensive chemotherapy. APL does not have to.
NCI lists tretinoin, also called all-trans retinoic acid or ATRA, and arsenic trioxide as the drugs used in APL. They are not standard chemotherapy. They push the stalled promyelocytes to finish maturing, or they kill them directly. For newly diagnosed childhood APL, NCI lists tretinoin with arsenic trioxide, or tretinoin plus chemotherapy with or without arsenic trioxide.
NCI's health-professional summary adds that APL has a specific sensitivity to ATRA, and that high remission rates and long disease-free survival can follow either ATRA with chemotherapy or an arsenic-based regimen without chemotherapy. This is the part of the story medicine got right in the decades since the novel was written.
Where a sibling donor really fits
The book turns on Anna being a match. That idea is grounded in something real.
An allogeneic stem cell transplant uses blood-forming stem cells from another person. NCI explains that donors are matched on HLAs, which are protein markers found on most cells in the body. The more HLA markers two people share, the better the odds the body accepts the graft. A brother or sister is often the closest match. The cells can come from the bloodstream, the bone marrow, or blood collected from an umbilical cord at birth.
A transplant is not a simple gift. NCI describes months of treatment, long stays at a specialized center, and a risk of graft-versus-host disease, in which donor immune cells attack the recipient's skin, liver, gut, or other organs. Our page on stem cell transplant covers what the weeks around day zero involve.
Worth saying plainly: most people with APL today are treated with drugs, not transplants.
Signs worth an appointment
NCI lists these signs of childhood acute myeloid leukemia and related conditions:
- fever, with or without an infection
- drenching night sweats
- shortness of breath
- weakness, tiredness, or looking pale
- easy bruising or bleeding
- petechiae, which are flat pinpoint spots under the skin caused by bleeding
- bone or joint pain
- pain or fullness below the ribs
- painless lumps in the neck, underarm, stomach, or groin
Any one of these has ordinary causes far more often than cancer. The combination that should move fast is bruising or bleeding that makes no sense together with tiredness and fever. A blood count is a cheap, fast test, and it is the right first step.
What this story cannot tell you
- The novel is fiction. Kate's course was written for a plot, not drawn from a case.
- Treatment for APL changed a great deal after the book appeared in 2004. Today's approach leans on tretinoin and arsenic trioxide.
- SEER records five-year relative survival for acute myeloid leukemia as a whole at 33.4 percent for people diagnosed from 2016 to 2022. APL sits inside that figure and behaves differently, so the number does not describe APL, and it describes no individual at all.
- Being a tissue match does not decide anything by itself. Donation is a choice, and living donors in the United States give consent for each procedure.
Sources
- Kirkus Reviews: My Sister's Keeper
- NCI: Childhood Acute Myeloid Leukemia Treatment (PDQ) — Patient Version
- NCI: Adult Acute Myeloid Leukemia Treatment (PDQ) — Health Professional Version
- NCI: Stem Cell Transplant
- SEER Cancer Stat Facts: Acute Myeloid Leukemia
How this page was made
An AI-assisted editorial system helped prepare this page. This article has not been reviewed by a healthcare professional unless a named reviewer is specifically shown. Cancer Explained is published by the National Cancer Information Foundation as a nonprofit-oriented public-interest education project. It is not a diagnostic service, does not recommend treatments, and is not for emergencies.
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Put the story in context
Prevention, possible warning signs, screening, and diagnosis
This story relates to Leukemia. The information below is general: it does not reveal anything else about a public person’s health, and not every point applies to every cancer. Personal advice depends on age, symptoms, family history, exposures, and medical history.
Prevention and risk reduction
Not every cancer can be prevented. Avoiding tobacco, protecting skin from ultraviolet radiation, limiting alcohol, staying active, and receiving recommended HPV or hepatitis B vaccination can lower the risk of certain cancers. A risk factor is not a prediction or a cause in one individual.
Symptoms and possible early signs
Possible signs vary and are often caused by conditions other than cancer. Changes worth discussing include a new lump, unexplained bleeding or weight loss, a persistent cough, lasting bowel or bladder changes, a changing skin spot, or symptoms that persist or worsen. Some early cancers cause no symptoms.
Screening and early detection
Screening looks for certain cancers before symptoms begin. Recommended tests exist only for some cancers and depend on age and risk. Screening can have benefits and harms; it is not the same as evaluating a new symptom, and there is no single routine scan or blood test that reliably screens for every cancer.
How cancer is diagnosed
Diagnosis may involve a history and exam, imaging, laboratory tests, and often a biopsy. Pathology can identify the cancer type and may test biomarkers that guide treatment. Symptoms, screening results, tumor markers, or online stories alone cannot confirm cancer.
Learn about this story’s cancer topic
A public story may encourage questions, but it should not be used to estimate your risk or choose testing. Contact a healthcare professional about a persistent or concerning change. Seek urgent care for severe or rapidly worsening symptoms.