Gastric Ca Registry IDs Those With CDH1 Mutation

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Oncology NEWS InternationalOncology NEWS International Vol 16 No 6
Volume 16
Issue 6

A registry for patients with gastric cancer who have early-onset or familial disease and their relatives may eventually lead to strategies for early detection and prevention of this cancer

LAS VEGAS—A registry for patients with gastric cancer who have early-onset or familial disease and their relatives may eventually lead to strategies for early detection and prevention of this cancer, according to one institution's experience. Gastric cancer disproportionately affects poor and minority populations, and this pattern cannot be fully explained by environmental factors, Jennifer Randazzo, RN, BSN, reported at the 2007 Annual Congress of the Oncology Nursing Society (abstract 2170). Moreover, 30% of families with hereditary diffuse gastric cancer have a mutation in the CDH1 gene that downregulates expression of e-cadherin, reducing cell-cell adhesion and thereby promoting invasion.

To better study the genetic contributors to gastric cancer, Ms. Randazzo and her colleagues at Memorial Sloan-Kettering Cancer Center established the "Early-Onset and Familial Gastric Cancer Registry," Ms. Randazzo told ONI in an interview.

Patients with gastric cancer are eligible if they have early-onset disease (onset before age 50 years), a family history of the disease (at least one affected first-degree relative or two affected second-degree relatives), or a known CDH1 mutation in their family. Relatives without gastric cancer are eligible if they have at least one first-degree relative with early-onset disease, at least two relatives with gastric cancer (one of whom must be a first-degree relative), or at least three second-degree relatives with gastric cancer.

Questionnaires

Participants complete family history and gastric cancer risk factor questionnaires, and are invited to contribute samples for a blood and tissue repository, Ms. Randazzo said. They are then offered genetic counseling to discuss the risks, benefits, and limitations of genetic testing; relatives are also offered an evaluation for the need for a screening upper endoscopy exam.

Since January 2006, the registry has enrolled 118 participants: 47 are patients with early-onset gastric cancer, 26 are patients with familial gastric cancer, 30 are relatives, and 15 are individuals at low risk included as a control group. "So far, 70 patients or families worldwide have indeed had the CDH1 mutation. Prophylactic gastrectomies have shown that they do also have cancer in situ," Ms. Randazzo said. "So it looks like we are headed in the right direction."

Although the registry is currently open only at Memorial Sloan-Kettering Cancer Center, individuals from across the United States can nonetheless participate, she said.

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