This can lead to a range of mild to severe symptoms, based on which organs are attacked.

A 2023 study of 3,542 people found that 40% experienced a GvHD diagnosis after transplant.

If GvHD symptoms develop, treatment can include steroidal and nonsteroidalimmune-suppressantsthat can temper and eventually control theautoimmune-like assault.

Graft-versus-host disease skin symptoms

lolostock / iStock / Getty Images

This article explains GvHD causes and symptoms of the condition.

It discusses who may be more at risk of GvHD and how the condition is treated and prevented.

Acute vs.

Rash on the palms is a common early symptom of GvHD in transplant recipients

It can sometimes manifest with features of acute and chronic GvHD, referred to as “overlap syndrome.”

With chronic GvHD, the affected organ systems tend to be more diverse.

The symptoms of acute and chronic GvHD can range from mild to severe.

A doctor with a tablet and a senior woman

If no matches are available, unrelated donors are used on the basis ofHLA blood test results.

But even with a genetic match, the risk of GvHD remains high.

The rate is even higher when an unrelated HLA-matched donor is involved.

Doctor running CT scan from control room

Beyond HLA typing, there are other factors that can increase the risk of acute or chronic GvHD.

How Is GVHD Diagnosed?

It may seem reasonable todiagnose GvHDbased on symptoms alone in an allogeneic transplant recipient.

Black healthcare worker looking pensive

In such cases, symptoms alone are enough to render a diagnosis.

The NIH defines diagnostic symptoms as defining features that do not require any form of confirmatory testing.

Chronic GvHD

The grading system of chronic GvHD is slightly different.

Woman cancer patient talking to her doctor

To this end, healthcare providers will explore other explanations for the symptoms to ensure the correct diagnosis.

There are several types used in the treatment of GvHD.

Corticosteroids

Corticosteroid drugs(a.k.a.

steroids) are the cornerstone of treatment for both acute and chronic GvHD.

Mild cutaneous GvHD may only require atopical steroidto control skin symptoms.

Severe symptoms in people with GvHD are typically treated with intravenous corticosteroids likeprednisoneand methylprednisone.

Some people may require no further treatment.

These include:

Even if symptoms aren’t entirely resolved, there are some benefits to having mild GvHD.

What Is the Survival Rate for GvHD?

A number of factors affect graft-versus-host disease outcomes and life expectancy.

Of those who do respond to corticosteroid therapy, anywhere from 20% to 25% will relapse.

Skin Care

Regular moisturizing is key to improving the tightness and dryness of the skin.

Use anemollient-rich moisturizerwithout perfumes or fragrance, applied immediately after showering and throughout the day as needed.

Diet

GvHD occurring in the gastrointestinal tract can cause significant diarrhea and weight loss.

Sex

GvHD can sometimes affect the genitals and libido of both women and men.

Testosterone replacement therapycan often help improve libido in men.

Other stress management techniques include meditation, progressive muscle relaxation (PMR), and guided imagery.

Symptoms typically begin in the skin but spread across the body and into other organs.

GvHD is a serious and often fatal development.

Treatment is possible, however, and GvHD symptoms can be effectively controlled medications.

While some people require lifelong treatment, a great many don’t.

Diagnosis and Staging Working Group report.Biol Blood Marrow Transplant.2015;21(3):389-401.e1.

doi:10.1016/j.bbmt.2014.12.001

Lee SJ.Classification systems for chronic graft-versus-host disease.Blood.

2017;129(1):30-7. doi:10.1182/blood-2016-07-686642

Wolfe D, Lawitschka A.Chapter 44: Chronic graft-versus-host disease.

In: The EBMT Handbook: Hematopoietic Stem Cell Transplantation and Cellular Therapies [Internet].

American Cancer Society.Stem cell or bone marrow transplant side effects.

2020 Jul;34(7):1898-1906. doi: 10.1038/s41375-020-0726-z.

2019 Jan;54(1):68-75. doi:10.1038/s41409-018-0221-6

Cancer Research UK.Treatment for chronic GvHD.

2016;51(6):833-40. doi:10.1038/bmt.2015.342