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| ID | Type | Description | Link |
|---|---|---|---|
| U01CA233056 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
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The primary aim of this study is to collect and store data, tissue, and personal and family histories from patients being screened for colorectal cancer and/or endometrial cancer at NYPH and WCM for routine clinical care and to make these available for future use for molecular and mechanistic studies.
Colorectal cancer (CRC) and endometrial cancer (EC) have a highly heritable component. Approximately 25% of CRC or EC patients have another first or second degree relative who are also affected by CRC or EC, and there are at least 32 known high penetrance CRC/EC germline predisposition genes. The overarching goal of this protocol is to (a) facilitate the discoveries of novel mechanisms in intestinal carcinogenesis and genes inducing genetic predisposition, (b) to help identify new genes and proteins that are amenable to targeted therapy and precision prevention drug intervention and biomarker development in Hereditary Cancer Syndromes, (c) to facilitate understanding and learning about ways of how the immune system can be used to recognize and kill tumor cells that carry mutations. To accomplish these goals, we plan to pursue the following aims:
To accomplish these goals, we will obtain normal mucosa, polyp tissue and carcinoma (tumor tissue) arising in the upper gastrointestinal tract (mainly the duodenum, but also other potential locations such as the esophagus, GE junction, stomach, and small bowel), lower gastrointestinal tract (mainly the colorectum), paired normal mucosa samples, endometrial tissue, and blood and as a source of genomic DNA, RNA, and protein.
The biospecimen samples will be collected in the context of standard of care (SOC) endoscopic procedure(s) and/or from pathologic specimens obtained during gastrointestinal (GI) endoscopy procedures and surgery performed at Weill Cornell or New York Presbyterian Hospital, including diagnostic testing, clinic and/or treatment visit and/or from residual blood. These tissue samples and blood samples were collected in the context of routine care and procedures performed at Weill-Cornell and NYPH. Biospecimen samples will also be collected in the context of SOC transvaginal ultrasound, hysteroscopy and endometrium biopsy performed at Weill Cornell or New York Presbyterian Hospital, including diagnostic testing, clinic and/or treatment visit.
Blood samples will be collected at the time blood is taken for clinical care. We will register, collect, process and store frozen blood, frozen normal and diseased tissue and FFPE (formalin fixed paraffin embedded) specimens.
This will be an invaluable annotated hereditary CRC/EC registry and tissue repository that will be available to the Weill Cornell Community upon appropriate approval. Subjects that provide informed consent will agree to collection and storage of clinical data. For the purposes of this project, clinical data includes all data collected for standard clinical purposes (e.g., demographics, medical issues, prognostic data, treatment data, outcomes).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| FAP without treatment with NSAIDs | Patients with the Hereditary Cancer Syndrome known as Familial Adenomatous Polyposis (FAP) undergoing upper or lower endoscopy/surgery without treatment with NSAIDs | ||
| FAP on treatment with NSAIDs | Patients with the Hereditary Cancer Syndrome known as Familial Adenomatous Polyposis (FAP) undergoing upper or lower endoscopy/surgery on treatment with NSAIDs | ||
| HNPCC without treatment with NSAIDs | Patients with the Hereditary Cancer Syndrome known as Hereditary Non-Polyposis Colorectal Cancer (HNPCC) undergoing lower endoscopy/surgery without treatment with NSAIDs | ||
| HNPCC on treatment with NSAIDs | Patients with the Hereditary Cancer Syndrome known as Hereditary Non-Polyposis Colorectal Cancer (HNPCC) undergoing lower endoscopy/surgery on treatment with NSAIDs | ||
| Other Hereditary Colorectal Cancer Syndromes | Other Hereditary Colorectal Cancer Syndromes undergoing lower endoscopy/surgery | ||
| Average-risk population | Average-risk population undergoing lower endoscopy/surgery in the lower gastrointestinal tract. |
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| Measure | Description | Time Frame |
|---|---|---|
| Novel mechanisms and genes inducing genetic predisposition to Hereditary Cancer Syndromes | Discover novel mechanisms in intestinal carcinogenesis and genes inducing genetic predisposition to Hereditary Cancer Syndromes. | 7 years |
| New genes and proteins for targeted therapy in Hereditary Cancer Syndromes | Identify new genes and proteins that are amenable to targeted therapy and precision prevention drug intervention and biomarker development in Hereditary Cancer Syndromes. | 7 years |
| Understanding and learning about the immune system's ability to recognize and kill tumor cells | To facilitate understanding and learning about ways of how the immune system can be used to recognize and kill tumor cells that carry mutations. | 7 years |
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The following eligibility criteria must be met as follows:
Age ≥ 18 years old.
One of the following must be met:
Willingness and ability to sign informed consent.
Ability to read/understand English, Spanish, and/or simplified Chinese.
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New York Presbyterian Hospital (NYPH) and Weill Cornell Medicine (WCM) Gastroenterology and Gynecologic Oncology Patients
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Steven M Lipkin, MD, PhD | Contact | 212-746-4014 | stl2012@med.cornell.edu | |
| Melissa K Frey, MD, MS | Contact | 646-697-6621 | mkf2002@med.cornell.edu |
| Name | Affiliation | Role |
|---|---|---|
| Steven M Lipkin, MD | Weill Medical College of Cornell University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| NYP/Weill Cornell Medicine | Recruiting | New York | New York | 10065 | United States |
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| D016889 | Endometrial Neoplasms |
| D009386 | Neoplastic Syndromes, Hereditary |
| D011127 | Polyps |
| D002277 | Carcinoma |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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BLOOD COLLECTION. Collection of 3-5 tubes of up to 10 ml each will be performed during standard of care blood draws.
POLYP/TUMOR COLLECTION DURING PROCEDURE. Removal of polyps and/or tumor tissue will be performed according to standard clinical practices during standard clinical care procedures.
NORMAL MUCOSA/TISSUE COLLECTION DURING PROCEDURE. Removal of normal mucosa will be performed according to standard clinical practices.
INCOMPLETELY REMOVED POLYP/TUMOR SAMPLES. Lesions that are not or cannot be completely removed will undergo standard biopsy prior to the acquisition of research biopsies.
RETROSPECTIVELY COLLECTED SAMPLES. The research team member will coordinate with the pathology team or research laboratory personnel to obtain the tissue and/or samples.
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |
| D014594 | Uterine Neoplasms |
| D005833 | Genital Neoplasms, Female |
| D014565 | Urogenital Neoplasms |
| D014591 | Uterine Diseases |
| D005831 | Genital Diseases, Female |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D000091662 | Genital Diseases |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |