Kidney Cancer Clinical Trial

Natural History and Biospecimen Acquisition for Children and Adults With Rare Solid Tumors

Summary

Background:

Approximately 150 cases of cancer per one million per year are considered rare cancers. While all tumors originate from genetic changes, a small percentage of these tumors are familial. Researchers want to study these changes in biological samples from people with rare tumors in order to learn more about how these tumors develop. The information obtained from this study may lead to improved screening, preventive guidelines, and treatments.

Objective:

To better understand rare cancers and hereditary cancer syndromes.

Eligibility:

People who have a rare tumor, a family history of a rare tumor, a hereditary cancer syndrome, or a mutation that leads to rare tumors.

Design:

Participants will be screened with questions about their medical history and/or that of their family members. They will give a saliva sample.

Participants who have a tumor will have their medical records and tests reviewed. They will answer questions about their wellbeing and needs. They may provide a tumor tissue sample.

Participants may also have:

Physical exam
Clinical photography
Blood, urine, saliva, and stool samples taken
Consultation with specialists
A scan that produces a picture of the body. Either one that uses a small amount of radiation, or one that uses a magnetic field.
Genetic testing/genetic counseling.

Participants will be contacted once a year. They will answer updated questions about their medical and family history.

Participants will be asked to contact the study team if there are changes in their tumors.

Participants may be invited to join focus groups for people with the same diagnosis of rare tumors.

Participants may be invited to participate in other NIH protocols.

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RARE TUMOR LIST:

Acinar cell carcinoma of the pancreas
Adamantinoma
Adenosqaumous carcinoma of the pancreas
Adrenocortical carcinoma
Alveolar soft part sarcoma
Anaplastic Thyroid Cancer
Angiosarcoma
Atypical Teratoid Rhabdoid Tumor/MRT
Carcinoid
Carcinoma of Unknown Primary
Chondrosarcoma
Chondromyxoid fibroma
Chordoma
Clear cell renal carcinoma
Clear Cell Sarcoma
Clear cell sarcoma of kidney
Conventional chordoma
Dedifferentiated chordoma
Desmoid
Desmoplastic small round cell tumor
Epithelioid hemangioendothelioma
Esthenioneuroblastoma
Ewing Sarcoma
Fibrolamellar carcinoma
Fusion negative rhabdomyosarcoma
Fusion positive renal cell carcinoma
Fusion positive rhabdomyosarcoma
Gastro-enteropancreatic neuroendocrine tumor
Hepatoblastoma
Hereditary Diffuse Gastric Cancer
Inflammatory myofibroblastic tumor
Kaposiform hemangioendothelioma
Malignant ectomesenchymal tumor
Malignant peripheral nerve sheath tumor
Malignant triton tumor
Medullary thyroid cancer
Mixed acinar adenocarcinoma
Mixed acinar neuroendocrine carcinoma
Myxoid Liposarcoma
Neuroblastoma
Neuroendocrine tumors
NUT midline carcinoma
Osteosarcoma
Pancreas ductal adenocarcinoma with squamous features
Pancreatic acinar cell carcinoma
Papillary renal cell carcinoma
Paraganglioma
Parosteal Osteosarcoma
Periosteal Osteosarcoma
Peripheral nerve sheath tumor
Peripheral primitive neuroectodermal tumor
Pheochromocytoma
Pituitary cancer
Poorly differentiated chordoma
Renal medullary carcinoma
Rhabdomyosarcoma
Round cell Liposarcoma
Schwannoma
Sclerosing Epithelioid Fibrosarcoma
SDH deficient GIST
SMARCB1 deficient tumors
SMARCA4 deficient tumors
Synovial sarcoma

Undifferentiated Sarcoma

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View Full Description

Full Description

Background:

Rare tumors are defined as fewer than 150 incident cases per one million per year. Consequently, only 11 tumor types are common in U.S. adults (prostate, breast, lung/bronchus, colon, uterus, bladder, melanoma, rectum, ovary, non-Hodgkin lymphoma, and kidney/renal pelvis neoplasms) and will not be studied in this trial. One-quarter of all adults with tumor have a rare tumor diagnosis.

All pediatric tumors meet this definition of rare affecting < 1% individuals younger than 20 years per year in the US.

Notably, there is a group of solid tumors that occur so infrequently in children and adults that little is known about the natural history of these tumors, their clinical behavior, molecular/genetic characteristics, optimal management, and drug response.

The NCI and the NIH Clinical Center infrastructure are uniquely suited to conduct studies of rare tumors. There is a precedent in the NCI when even non-interventional studies or initiatives were paradigm-changing. The NCI neurofibromatosis type 1 natural history study allowed the development of groundbreaking interventional trials in participants with plexiform neurofibromas. The Pediatric and Wild-Type Gastrointestinal Stromal Tumor (GIST) Clinic, which involves intramural and extramural experts, not only provided the background for discovery of the molecular features of a very rare disease such as succinate dehydrogenase deficient GIST, but also was able identify therapeutic strategies for this group of participants (for example, avoidance of unnecessarily aggressive surgery). Similarly, studies in adults at the CCR have tremendously advanced the understanding of rare solid tumors occurring primarily in adults such as thymoma, renal cell cancer, and endocrine tumors.

Systematic and longitudinal collection and annotation of clinical history, tissue samples, imaging studies, patient reported outcomes, and other pertinent information in participants with these rare tumors and return of results to participants will provide a service to the participants themselves and to the medical community, in line with the NIH mission of to seek fundamental knowledge about the nature and behavior of living systems and the application of that knowledge to enhance health, lengthen life, and reduce illness and disability .

Objective:

To comprehensively and longitudinally evaluate the natural history of participants with rare solid tumors or tumor predisposition syndromes, estimating and defining their clinical spectrum (e.g. disease course and survival).

Eligibility:

Participants with a diagnosis of a rare solid tumor (fewer than 15 cases in 100,000 people per year).

OR

Relatives of participants with diagnosis of rare solid tumors

OR

Carriers of germline genetic variants that predispose to rare solid tumor and their relatives.

Design:

This will be a long-term study to comprehensively study participants (and their relatives) with select rare tumors.

Initially participants will provide clinical information (medical history, family medical history, imaging studies and reports, surgical pathology reports, genetic test results, patient-reported outcomes) and biospecimens (archival pathology specimen and saliva) for review by and feedback from the study team.

If indicated, participants will be invited to the study site for additional evaluations and consultation, including clinical phenotyping, genotyping, imaging of tumor sites, and patient reported or other appropriate outcomes.

After evaluation, participants will be provided with recommendations about possible treatment options and might be enrolled into disease specific sub-protocols of this trial.

Since long-term follow-up of individuals with rare tumors, their family members at high risk for developing tumors, and carriers of germline genetic variants is a major feature of the study, we intend to maintain active contact with study subjects for as long as possible.

In addition to evaluating individual participants, this protocol will allow bringing groups of participants (approximately 10-20) with specific rare tumors for a rare tumor clinic on the same day to allow for development of a deeper understanding of rare tumors through the conduct of focus groups.

View Eligibility Criteria

Eligibility Criteria

INCLUSION CRITERIA:
Cohort 1: Participants with a diagnosis of a rare solid tumor (fewer than 15 cases in 100,000 people per year). There are no age restrictions beyond the neonatal period (4 weeks).

OR

-Cohort 2: Participants without a rare tumor who have a germline genetic variant that predisposes to a rare solid tumor

OR

-Cohort 3: Relatives of participants with diagnosis of rare solid tumors who do NOT have a known germline variant that predisposes to a rare solid tumor

OR

Cohort 4: Parent/guardian of child participating in a focus group if not already enrolled on the study.
Ability of subject or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.

EXCLUSION CRITERIA:

None

Study is for people with:

Kidney Cancer

Estimated Enrollment:

10000

Study ID:

NCT03739827

Recruitment Status:

Recruiting

Sponsor:

National Cancer Institute (NCI)

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There are 4 Locations for this study

See Locations Near You

Children's National Medical Center
Washington District of Columbia, 20010, United States More Info
AeRang Kim
Contact
301-451-7025
[email protected]
National Institutes of Health Clinical Center
Bethesda Maryland, 20892, United States More Info
For more information at the NIH Clinical Center contact National Cancer Institute Referral Office
Contact
888-624-1937
Oregon Health and Science University
Portland Oregon, 97239, United States More Info
Takumi Suzuki
Contact
503-494-3621
[email protected]
Texas Children's Hospital
Houston Texas, 77030, United States More Info
Gaylon Stevenson
Contact
(713) 798-495_
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Kidney Cancer

Estimated Enrollment:

10000

Study ID:

NCT03739827

Recruitment Status:

Recruiting

Sponsor:


National Cancer Institute (NCI)

How clear is this clinincal trial information?

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