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Researchers describe new condition involving numerous GI polyps in cancer survivors

February 12, 2020

BOSTON - In a paper published online today, Dana-Farber Cancer Institute researchers provide new details about a recently discovered condition in which childhood cancer survivors develop numerous colorectal growths called polyps despite not having a hereditary susceptibility to the condition.

The condition, known as therapy-associated polyposis, or TAP, was first described by Dana-Farber scientists in 2014 based on a group of five patients. The new study presents a deeper look at the condition, based on data from 34 patients at eight cancer centers around the US.

The development of colorectal polyps - abnormal bump-like growths of tissue - in any individual is a risk factor for colorectal cancer. Polyposis, a condition in which many polyps grow in the intestinal tract, often signals a predisposition to colorectal cancer and other malignancies. People diagnosed with polyposis, as well as their relatives, are typically advised to undergo increased screening and other invasive procedures to detect the abnormal growths at the earliest stage possible. By knowing the specific signs of TAP - and knowing that it isn't part of a familial syndrome - physicians can spare family members unnecessary screenings and ensure patients receive proper treatment.

"Survivors of cancer in childhood or young adulthood have an increased risk for a variety of cancers and noncancerous conditions, including colorectal cancers and polyps, in the years after treatment," says Leah Biller, MD, physician-researcher at Dana-Farber Cancer Institute and Brigham and Women's Hospital (BWH), first author of the study, published online today by the journal Cancer Prevention Research. "When they develop polyposis, we often are concerned about a hereditary cause and recommend testing to see if they have an inherited link to the condition. TAP patients, however, develop polyposis without a known hereditary susceptibility. This suggested that while their condition mimicked the symptoms of hereditary polyposis syndromes, it was a separate phenomenon."

To pin down the characteristics of TAP - and potentially distinguish it from hereditary polyposis - researchers needed data from numerous patients with the condition. Aided by colleagues at Dana-Farber, Brigham and Women's and seven other treatment centers across the U.S., they gathered data from 34 patients with TAP who didn't have a hereditary or known genetic link to the condition but had been treated with chemotherapy and/or radiation therapy for childhood cancers.

The patients with TAP developed polyposis a median of 27 years after their cancer treatment. Investigators also found that 35% of the patients had more than 50 colorectal polyps, and 94% had multiple types of polyps, including adenomas, serrated polyps, hyperplastic polyps, and hamartomas. This contrasts with other hereditary polyposis syndromes in which all the polyps are generally of the same type.

Investigators also found that 74% of the patients had experienced other complications associated with cancer treatment: 50% had been diagnosed with cancerous conditions outside the colon; and 47% had been diagnosed with non-cancerous conditions indicative of prior cancer treatment. These findings suggest that people who develop TAP may be especially susceptible to treatment-related conditions in general, the study authors say.

"TAP appears to be an acquired condition that imitates various familial colorectal cancer syndromes but is biologically distinct from them," says Matthew Yurgelun, MD, an oncologist at Dana-Farber specializing in gastrointestinal cancer and Director of the Lynch Syndrome Center at Dana-Farber. "The fact that it takes different forms and involves different types of polyps suggests that there may be multiple biological pathways involved in its development. We're working to better understand these pathways in order to improve treatment of it and other treatment-related conditions."
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Co-authors of the study are Chinedu Ukaegbu, MBBS, MPH, Tara G. Dhingra, and Anuradha Chittenden, MS, of Dana-Farber; Ramona M. Lim, MD, and Sapna Syngal, MD, of Dana-Farber and BWH; Carol A. Burke, MD, Brandie H. Leach, MS, James M. Church, MD, and Matthew F. Kalady, MD, of the Cleveland Clinic; Yana Chertock, MA, and Michael J. Hall, MD, MS, of Fox Chase Cancer Center; Erika S. Koeppe, MS, and Elena Stoffel, MD, of the University of Michigan; Elana Levinson, MS, MPH, and Fay Kastrinos, MD, of New York Presbyterian Hospital; Megan Lutz, MD, and Jennifer M. Weiss, MD, of the University of Wisconsin School of Medicine; Erin Salo-Mullen, MS, Rania Sheikh, MS, and Zsofia K. Stadler, MD, of Memorial Sloan Kettering Cancer Center; and Gregory Idos, MD, of the University of Southern California.

The study was upported by the National Institutes of Health (grants K24CA113433, R01CA132829, and K07CA151769); The Pussycat Foundation Helen Gurley Brown Presidential Initiative; and an American Cancer Society Mentored Research Scholar Grant (MRSG-13-144-01-CPHPS).

About Dana-Farber Cancer Institute

Dana-Farber Cancer Institute is one of the world's leading centers of cancer research and treatment. It is one of the only hospitals ranked in the top five by U.S. News and World Report in both adult and pediatric cancer care. Dana-Farber's mission is to reduce the burden of cancer through scientific inquiry, clinical care, education, community engagement, and advocacy. We provide the latest in cancer for adults through Dana-Farber/Brigham and Women's Cancer Care and for children through Dana-Farber/Boston Children's Cancer and Blood Disorders Center. Dana-Farber is dedicated to a unique and equal balance between cancer research and care, translating the results of discovery into new treatments for patients locally and around the world.

Dana-Farber Cancer Institute

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