About Chronic Graft-Versus-Host Disease


What is graft-versus-host disease?

Graft-versus-host disease (GVHD) is a serious complication that may affect people who have had a stem cell transplant using cells from a donor. This type of procedure is called an allogeneic (AL-oh-geh-NAY-ik) stem cell transplant. During an allogeneic stem cell transplant, a patient’s cells are replaced with donor cells. (Figure A)

GVHD occurs when donor cells (called the graft) attack the organs and tissues of the patient who received them (or the host). That’s why the condition is known as graft-versus-host disease. (Figure B)

Diagram to show how cGVHD occurs

There are two main types of GVHD—acute and chronic

Acute GVHD usually develops within the first 3 months after transplant. Symptoms are typically limited to the skin, liver, and gastrointestinal tract.

Many people who develop chronic GVHD have had acute GVHD in the past.

Chronic GVHD tends to develop more slowly than acute GVHD. In most cases, symptoms appear sometime in the first year after transplant. Chronic GVHD can also affect many more organs and tissues than acute GVHD, so it is important to keep watching for new signs and symptoms. (See below.)

Some of the effects of chronic GVHD include tissue thickening and scarring, known as fibrosis. These symptoms are similar to ones caused by certain autoimmune diseases. (Autoimmune diseases happen when the body’s immune system attacks healthy organs by mistake.) Other symptoms of chronic GVHD—such as dry eyes, muscle pain, and breathing trouble—are also common with other conditions.

How is chronic GVHD diagnosed?

Because chronic GVHD symptoms can be confused with other health conditions, your Healthcare Professional may do a thorough physical exam as well as various tests to diagnose it. This helps them make sure your symptoms are caused by chronic GVHD and not something else.


Signs and symptoms of chronic GVHD

Chronic GVHD can affect one or more of these areas of the body.

Circle icon of Roy

“Don’t put the symptoms off. Call your  oncologist, schedule an appointment, ask about  GVHD as early as possible.”

- Roy, a patient with cGVHD

 

Eyes

Dry eyes | Irritation that won’t go away | Blurred vision | Teary eyes

Lungs

Cough that doesn’t go away | Shortness of breath

Skin, Hair, and Nails

Skin texture changes (thickening) | Nail changes | Rash | Unusual hair loss or thinning | Itchy skin

Genitals

Irritation or dryness | Rash | Painful intercourse

Full body diagram

Mouth

Painless white lines on tongue or inner cheeks | Sores or irritation | Trouble opening your mouth | Sensitivity to spice | Dry mouth and lips

Nervous System

Weakness, tingling, numbness in legs or feet

Digestive System

Nausea or vomiting | Diarrhea | Belly pain or cramping | Liver symptoms, such as yellowing of the eyes or skin

Joints and Muscles

Arthritis-like symptoms (pain and stiffness) | Muscle aches or pain, cramps, or weakness

alt

Eyes

Dry eyes | Irritation that won’t go away | Blurred vision | Teary eyes

alt

Lungs

Cough that doesn’t go away | Shortness of breath

alt

Skin, Hair, and Nails

Skin texture changes (thickening) | Nail changes | Rash | Unusual hair loss or thinning | Itchy skin

alt

Genitals

Irritation or dryness | Rash | Painful intercourse

alt

Mouth

Painless white lines on tongue or inner cheeks | Sores or irritation | Trouble opening your mouth | Sensitivity to spice | Dry mouth and lips

alt

Nervous System

Weakness, tingling, numbness in legs or feet

alt

Digestive System

Nausea or vomiting | Diarrhea | Belly pain or cramping | Liver symptoms, such as yellowing of the eyes or skin

alt

Joints and Muscles

Arthritis-like symptoms (pain and stiffness) | Muscle aches or pain, cramps, or weakness

alt

Caregivers Play an Important Role

Caregivers can help monitor for any new or changing symptoms of GVHD—especially in areas like the back or the eyes, where patients may not notice their symptoms right away. These symptoms are important to talk about together and mention to your healthcare team since help may be available.

Family, friends, and other caregivers are essential for helping patients during transplant recovery and for supporting each other.

“Some days are better and some days are worse and it’s hard to know when to step into ‘situation-controlling mode’ and when to back off.”

-Kris, Roy's caregiver

Watch Roy's Story

Roy and Kris (Patient and caregiver)
Roy and Kris (Patient and caregiver)

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What is JAKAFI® or JAKAFI XR?

What is JAKAFI® or JAKAFI XR?

JAKAFI or JAKAFI XR (ruxolitinib) is a prescription medication used to treat adults with certain types of myelofibrosis (MF).
It is not known if JAKAFI or JAKAFI XR is safe or effective in children for treatment of myelofibrosis.

JAKAFI or JAKAFI XR is a prescription medication used to treat adults with polycythemia vera (PV) who have already taken a medicine called hydroxyurea and it did not work well enough or they could not tolerate it.
It is not known if JAKAFI or JAKAFI XR is safe or effective in children for treatment of polycythemia vera.

JAKAFI or JAKAFI XR is a prescription medication used to treat adults and children 12 years of age and older with acute graft-versus-host disease (GVHD) who have taken corticosteroids and they did not work well enough.

JAKAFI or JAKAFI XR is a prescription medication used to treat adults and children 12 years of age and older with chronic graft-versus-host disease (GVHD) who have taken one or two types of treatments and they did not work well enough.

Important Safety Information

JAKAFI or JAKAFI XR can cause serious side effects, including:

Low blood counts: JAKAFI or JAKAFI XR may cause low platelet, red blood cell, and white blood cell counts. If you develop bleeding, stop taking JAKAFI or JAKAFI XR and call your healthcare provider. Your healthcare provider will do a blood test to check your blood counts before you start and regularly during your treatment. Your healthcare provider may change your dose or stop your treatment based on the results of your blood tests.
Tell your healthcare provider right away if you develop or have worsening symptoms such as

  • unusual bleeding
  • bruising
  • tiredness
  • shortness of breath
  • a fever

Infection: You may be at risk for developing a serious infection during treatment with JAKAFI or JAKAFI XR. Tell your healthcare provider if you develop any of the following symptoms of infection:

  • chills
  • nausea
  • vomiting
  • aches
  • weakness
  • fever
  • painful skin rash or blisters

Worsening of symptoms after interrupting or stopping treatment. Signs and symptoms of myelofibrosis may worsen after you stop treatment.

Do not interrupt or stop treatment without talking to your healthcare provider. Tell your healthcare provider right away if you have any of the following after stopping treatment:

  • fever
  • trouble breathing
  • weakness
  • night sweats
  • feeling dizzy or lightheaded
  • pain in left upper stomach area or left shoulder

Cancer: Some people have had certain types of non-melanoma skin cancers during treatment with JAKAFI or JAKAFI XR. Your healthcare provider will regularly check your skin during your treatment. Tell your healthcare provider if you develop any new or changing skin lesions during treatment.

Increases in cholesterol: You may have changes in your blood cholesterol levels during treatment with JAKAFI or JAKAFI XR. Your healthcare provider will do blood tests to check your cholesterol levels about every 8 to 12 weeks after you start taking JAKAFI or JAKAFI XR and as needed.

Increased risk of major cardiovascular events such as heart attack, stroke or death in people who have cardiovascular risk factors and who are current or past smokers while using another JAK inhibitor to treat rheumatoid arthritis:

Get emergency help right away if you get any symptoms of a heart attack or stroke during treatment with JAKAFI or JAKAFI XR, including:

  • discomfort in the center of your chest that lasts for more than a few minutes or that goes away and comes back
  • severe tightness, pain, pressure, or heaviness in your chest, throat, neck, or jaw
  • pain or discomfort in your arms, back, neck, jaw, or stomach
  • shortness of breath with or without chest discomfort
  • breaking out in a cold sweat
  • nausea or vomiting
  • feeling lightheaded
  • weakness in one part or on one side of your body
  • slurred speech

Increased risk of blood clots: Blood clots in the veins of your legs (deep vein thrombosis, DVT) or lungs (pulmonary embolism, PE) have happened in people taking another JAK inhibitor for rheumatoid arthritis and may be life-threatening.

Tell your healthcare provider right away if you have any signs and symptoms of blood clots during treatment with JAKAFI or JAKAFI XR, including:

  • swelling, pain, or tenderness in one or both legs
  • sudden, unexplained chest or upper back pain
  • shortness of breath or difficulty breathing

Possible increased risk of new (secondary) cancers: People who take another JAK inhibitor for rheumatoid arthritis have an increased risk of new (secondary) cancers, including lymphoma and other cancers. People who smoke or who smoked in the past have an added risk of new cancers.

The most common side effects of JAKAFI or JAKAFI XR include:

  • for certain types of myelofibrosis (MF) – low platelet or red blood cell counts, bruising, dizziness, headache, and diarrhea
  • for certain types of polycythemia vera (PV) – low platelet or red blood cell counts, bruising, dizziness, headache, and diarrhea
  • for acute GVHD – low platelet counts, low red or white blood cell counts, infections, and swelling
  • for chronic GVHD – low red blood cell or platelet counts and infections, including viral infections

These are not all the possible side effects. Ask your pharmacist or healthcare provider for more information. Call your doctor for medical advice about side effects.

Before taking JAKAFI or JAKAFI XR, tell your healthcare provider about:

  • all the medications, vitamins, and herbal supplements you are taking
  • your medical conditions, including if you
    • have or had low white or red blood cell counts
    • have an infection
    • have or had tuberculosis (TB) or have been in close contact with someone who has TB
    • had shingles (herpes zoster)
    • have or had hepatitis B
    • have a high level of fat in your blood (high blood cholesterol or triglycerides)
    • have or have had a blood clot, heart attack, other heart problems, or stroke
    • are a current or past smoker
    • had cancer
    • have or had liver or kidney problems or are on dialysis. If you are on dialysis, JAKAFI or JAKAFI XR should be taken after your dialysis
    • have any other medical condition

Women should not take JAKAFI or JAKAFI XR while pregnant or planning to become pregnant. Do not breastfeed during treatment with JAKAFI or JAKAFI XR and for 2 weeks after the final dose.

How should I take JAKAFI or JAKAFI XR?

  • Take exactly as your healthcare provider tells you.
  • Do not change your dose or stop taking JAKAFI or JAKAFI XR without first talking to your healthcare provider. If you stop treatment, symptoms of your condition may return.
  • If you miss a dose, take your next dose at your regular time. Do NOT take 2 doses at the same time.
  • You may have regular blood tests during your treatment. Based on the results, your healthcare provider may change your dose or stop JAKAFI or JAKAFI XR.
  • IF YOU ARE PRESCRIBED JAKAFI:
    • Take JAKAFI 2 times a day with or without food.
    • JAKAFI may also be given through certain nasogastric tubes.
    • Tell your healthcare provider if you cannot take JAKAFI by mouth. Your healthcare provider will decide if you can take JAKAFI through a nasogastric tube. Ask your healthcare provider to give you specific instructions on how to properly take JAKAFI through a nasogastric tube.
  • IF YOU ARE PRESCRIBED JAKAFI XR:
    • Take JAKAFI XR 1 time a day with or without food.
    • Swallow JAKAFI XR whole. Do not split, crush, or chew.

Please see the Full Prescribing Information, including Patient Information, which includes a more complete discussion of the risks associated with JAKAFI or JAKAFI XR.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

You may also report side effects to Incyte Medical Information at 1-855-463-3463.