news banner
 

pediatric views

other publications

news room

giving

 
 

Program spotlight: Pediatric Cancer Risk Program

The Pediatric Cancer Risk Program (PCRP) at Dana-Farber/Children's Hospital Cancer Center provides multidisciplinary consultative care to patients and their families whose condition or family history suggests an increased risk of cancer. The program offers patients access to expert pediatric geneticists, genetic counselors and other specialists at Children's, as well as world-renowned pediatric oncologists from Dana-Farber/Children's Hospital Cancer Center.

Program basics
The first of its kind in New England, our program accepts referrals, second opinions and consultations for evaluation of children who have cancers with known hereditary links, genetic defects associated with cancer development, or children with family histories that place them at a higher risk for cancer development.

An integrated approach
Our integrated approach to care offers a comprehensive evaluation and follow-up for children at risk. Cases are reviewed in a multidisciplinary clinic conference; if needed, we recommend referrals to additional specialists. Adult family members of at-risk children may be referred to Dana-Farber Cancer Institute's Cancer Genetics and Prevention Program.

A cancer risk assessment can provide you and your patient with more information about cancer risk and appropriate screening. A certified genetic counselor assesses each case according to individual needs, coordinates all patient visits and determines if the patient should be seen by an oncologist at Dana-Farber Cancer Institute and/or a geneticist at Children's Hospital Boston.

When to refer
Referral to the PCRP is recommended for children with a history of cancers with known hereditary links or for children with the following genetic syndromes or history:

  • ataxia telangiectasia
  • Beckwith-Wiedemann syndrome
  • children whose parents have known cancer predisposition syndromes
  • Cowden syndrome
  • familial adenomatous polyposis
  • Li-Fraumeni syndrome
  • multiple endocrine neoplasia
  • multiple family members with colon cancer
  • pheochromocytoma
  • retinoblastoma
  • strong family history of cancer
  • Von Hippel-Lindau syndrome
  • X-linked lymphoproliferative syndrome

Materials may be sent to:
Pediatric Cancer Risk Program,
Fax: 617-730-0466 Children's Hospital Boston,
Hunnewell 5 300 Longwood Avenue,
Boston, MA 02115

More information: childrenshospital.org/cancer, childrenshospital.org/genetics

Make a referral: 617-355-4388

 


Meet the team

Our team includes members from the Dana-Farber/Children's Hospital Cancer Center, Division of Genetics at Children's Hospital Boston and the Cancer Risk and Prevention Program at Dana-Farber Cancer Institute.


diller

Lisa R. Diller, MD
Chief Medical Director
Dana-Farber/Children's Hospital Cancer Center




diller

Mira B. Irons, MD
Associate Chief, Division of Genetics,
Children's Hospital Boston




diller

Stephen Huang, MD
Director, Thyroid Program,
Children's Hospital Boston




diller

Victor L. Fox, MD
Director, Center for Pediatric Polyposis,
Children's Hospital Boston




diller

Jill Brace O'Neill, MS, RN-CS, PN
Pediatric Nurse Practitioner
Dana-Farber/Children's Hospital Cancer Center




diller

Wen-Hann Tan, BMBS
Geneticist
Children's Hospital Boston




diller

Katherine Schneider
Genetic Counselor
Dana-Farber Cancer Institute




diller

Carly Grant
Genetic Counselor
Dana-Farber Cancer Institute




diller

Sharyn Lincoln, MS
Genetic Counselor
Children's Hospital Boston




 
 
 

Dana-Farber/Children's Hospital Cancer Center

Division of Genetics

 
  mouse  

Subscribe to our monthly
e-newsletter, eDose

   

Subscribe to our RSS feed

 

  Contact Us
 

Share

 

Share