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Follows people with KSHV-associated Castleman disease over time to learn its course

Studies how Castleman disease linked to KSHV virus develops in adults over time.

Plain-language title generated from the registry record
Registry title: Natural History of KSHV-Associated Multicentric Castleman s Disease

Key facts

Where
Bethesda, United StatesSee the site

Where in United States

  • National Institutes of Health Clinical CenterBethesda, United StatesTaking people

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  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
National Cancer Institute (NCI)
Trial code
NCT04968288
Record updated
16 October 2026
Original description
Background:Read full original descriptionShow less

Natural History Study of KSHV-Associated Multicentric Castleman's Disease

Background:

Kaposi s sarcoma herpes virus (KSHV) causes several kinds of cancer, Kaposi sarcoma (KS), a form of Multicentric Castleman s Disease (MCD) and a type of lymphoma known as Primary Effusion Lymphoma (PEL). These cancers can occur alone or at the same time in the same patient. MCD can cause a lot of symptoms and problems with various organs in the body, making patients feel quite unwell. If unrecognized, the disease can be fatal. Medications such as rituximab alone or in combination with chemotherapy may help treat MCD but there is little known about the long term effects and the natural course of MCD.

Objective:

To better understand the biology of KSHV-MCD to help identify how this disease causes illness and how cancer treatments known to be effective in MCD may help patients with this condition. This study also aims to help identify ways to treat the disease by providing other standard cancer treatments that would be useful to use to treat MCD based on what we know about this condition.

Eligibility:

People 18 years of age and older with KSHV-MCD.

Design:

Participants will be screened with:

Medical history

Physical exam

CT scan

Blood and heart tests

Participants will have an initial evaluation. This will include:

Review of participants symptoms and ability to perform their normal activities

Blood and urine tests

Imaging studies such as CT and PET scans. Participants may have a contrast agent injected into their arm.

Photographs to document skin lesions

Optional skin biopsy. For this, a small piece of the skin will be removed.

Optional lymph node needle biopsy

Optional samples of the fluid in the space around the lungs, intestines, or heart

Optional sample of the liquid that surrounds the brain and spinal cord

Saliva samples

DEXA scan to examine the bones

Questionnaires

Optional limb measurements or cognitive tests

Physicians will give participants recommendations about treatment.

After their initial evaluation and any treatment, participants will have additional visits. These will occur every 3 months for the first year, then every 6 months for the second year, and then once a year for up to 1 year.

Exclusion: Any condition or set of circumstances that in the opinion of the investigators would make participation in this study unsafe or otherwise inappropriate for a given individual; Pregnancy.

INCLUSION CRITERIA:; Biopsy proven KSHV-associated MCD, confirmed in the Laboratory of Pathology (LP), CCR; Age >=18 years; ECOG performance status <=4 (Karnofsky >=20%); Ability of subject to understand and the willingness to sign a written informed consent document; Participants may be co-enrolled in other protocols, including investigational studies to treat KSHV-associated malignancies.

ClinicalTrials.gov NCT04968288