We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Large Scale Program Launched to Scan Tumors for Mutations and Establish Genomic Database

By LabMedica International staff writers
Posted on 07 Nov 2011
Focused on speeding the development of cancer treatments that target the genetic flaws in each patient’s tumor, two internationally known medical institutions based in Boston, MA, USA, have launched Profile, a major research effort to scan tumor tissue from adult cancer patients for hundreds of gene mutations linked to cancer.

The program, undertaken by investigators from Dana-Farber Cancer Institute and Brigham and Women’s Hospital, almost two years in development, is one of the most extensive research projects in cancer genomics yet undertaken nationally. More...
Open to every adult cancer patient seen in the Brigham and Women’s and Dana-Farber Longwood Medical Area clinics, the program aims to build a comprehensive database for research into the genetic composition of different cancer types, and ultimately, into treatments that are most effective against individual tumors. (The program will be extended to pediatric cancer patients at Dana-Farber and Children’s Hospital Boston in 2012.)

Clinicians at Dana-Farber/Brigham and Women’s Cancer Center currently use targeted therapies that pinpoint genetic mutations in a select number of cancers, including colon, lung, breast, and some leukemias and sarcomas. The new research program is focused on identifying a far greater number of mutations for a wider array of cancers, ultimately enabling clinicians to treat more cancers with targeted therapies in the future.

“Profile will put us firmly on the path to realizing the promise of personalized medicine. By ‘genotyping’ each tumor--identifying the set of mutations that drive it--we’ll be able to design therapies geared specifically to those mutations, depriving the tumor of the ability to sustain itself while producing a minimum of side effects,” says Dana-Farber’s Chief Scientific Officer Barrett Rollins, MD, PhD, one of the architects of the program. “We’re laying the foundation for the development, testing, and implementation of such therapies, and we expect the project to grow as we discover new cancer-related gene mutations and with the development of new technologies.”

Tissue testing for the program will be performed with OncoMap, a system custom designed for genomic research in cancer by investigators at Dana-Farber, the Broad Institute of the Massachusetts Institute of Technology (MIT) and Harvard University (Boston, MA, USA; Cambridge, MA, USA). Using high-speed, high-capacity robotic machinery to prepare, sort, and scan tumor tissue, the system makes it possible to process rapidly large numbers of tumor tissue samples with a high degree of accuracy.

“We’ve learned a great deal about the role of specific mutated genes in cancer, and we now have technology for testing large numbers of tumor samples for those mutations,” said Janina Longtine, MD, director of molecular diagnostics at Brigham and Women’s Hospital and a senior leader of the research program. “For the first time, we have the opportunity to build a critical mass of genomic data that can be used to bring better treatments to patients.”

Studies have shown that tumors that look and act alike can carry different sets of mutations, which influence how cancers grow, metastasize, and respond to treatment. Only by gathering data on a mass scale can researchers expect to capture the huge diversity of cancer at the genetic level, according to the program leaders. By identifying a tumor’s molecular characteristics, clinicians will be able to select the appropriate treatment for the each patient. A patient whose tumor carries a specific mutation would receive a drug known to be effective against that mutation in specific types of tissue. Although this currently occurs in a minority of cancer cases, the aim of the Dana-Farber/Brigham and Women’s project is to find ways to apply this to many more patients.

In contrast to programs that scan specific types of tumors for a small number of gene mutations, Profile tests tumor samples for nearly 500 cancer mutations in 41 genes. Program researchers anticipate that well over 10,000 people will participate in the program during the first year and every year thereafter.

Study participants will have their tumor tissue scanned and data from their medical record--on the course of their disease, its response to treatment, relapse, and side effects--will be placed in a second, separate database. By connecting data from these two sources, researchers will be able to study which therapies are most effective against particular tumor types.

The study participants also can have the results of their OncoMap testing sent to their Dana-Farber or Brigham physician. The tumor-testing program was developed mainly for research purposes, but leaders expect that some participants may immediately benefit by learning of their eligibility for current clinical trials.

Drs. Longtine and Rollins anticipate that Profile will expand with the discovery of additional cancer-related mutations and the development of more sophisticated screening technologies.

Related Links:
Dana-Farber Cancer Institute
Brigham and Women’s Hospital
Broad Institute



Platinum Member
Xylazine Immunoassay Test
Xylazine ELISA
Verification Panels for Assay Development & QC
Seroconversion Panels
Anti-Cyclic Citrullinated Peptide Test
GPP-100 Anti-CCP Kit
Gold Member
Blood Glucose Reference Analyzer
Nova Primary
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image: QIP-MS could predict and detect myeloma relapse earlier compared to currently used techniques (Photo courtesy of Adobe Stock)

Mass Spectrometry-Based Monitoring Technique to Predict and Identify Early Myeloma Relapse

Myeloma, a type of cancer that affects the bone marrow, is currently incurable, though many patients can live for over 10 years after diagnosis. However, around 1 in 5 individuals with myeloma have a high-risk... Read more

Immunology

view channel
Image: The cancer stem cell test can accurately choose more effective treatments (Photo courtesy of University of Cincinnati)

Stem Cell Test Predicts Treatment Outcome for Patients with Platinum-Resistant Ovarian Cancer

Epithelial ovarian cancer frequently responds to chemotherapy initially, but eventually, the tumor develops resistance to the therapy, leading to regrowth. This resistance is partially due to the activation... Read more

Technology

view channel
Image: Ziyang Wang and Shengxi Huang have developed a tool that enables precise insights into viral proteins and brain disease markers (Photo courtesy of Jeff Fitlow/Rice University)

Light Signature Algorithm to Enable Faster and More Precise Medical Diagnoses

Every material or molecule interacts with light in a unique way, creating a distinct pattern, much like a fingerprint. Optical spectroscopy, which involves shining a laser on a material and observing how... Read more

Industry

view channel
Image: The collaboration aims to leverage Oxford Nanopore\'s sequencing platform and Cepheid\'s GeneXpert system to advance the field of sequencing for infectious diseases (Photo courtesy of Cepheid)

Cepheid and Oxford Nanopore Technologies Partner on Advancing Automated Sequencing-Based Solutions

Cepheid (Sunnyvale, CA, USA), a leading molecular diagnostics company, and Oxford Nanopore Technologies (Oxford, UK), the company behind a new generation of sequencing-based molecular analysis technologies,... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.