New lab test could identify imatinib resistance

Results are published in Clinical Cancer Research, a journal of the American Association for Cancer Research.

Imatinib, currently sold as Gleevec by Novartis, revolutionized the treatment of leukemia when it was approved in 2001. Yet imatinib comes with its own set of problems, chiefly resistance. Although resistance is relatively rare, occurring among 2 percent and 10 percent depending on the definition, it can cause unwanted problems both biologically and psychologically.

New drugs under development for the treatment of CML often tout their ability to overcome imatinib resistance, but determining who will develop resistance remains a challenge.

At the Hokkaido University Graduate School of Medicine, Yusuke Ohba, M.D., Ph.D., an associate professor, and colleagues tested the feasibility of a fluorescence resonance energy transfer biosensor in measuring the activity of leukemia cells.

“Using this test, we are now able to identify and predict the most suitable treatment option for individual chronic myeloid leukemia patients,” said Ohba. “This technique is both sensitive and practical to use; it is especially useful for patients who are in relapse, a case in which the clinician's important decision regarding the next step in treatment must be made quickly and accurately.”

Working with laboratory cells, the researchers developed a series of assays that measured protein levels and known activity markers within CML lines. Using these measurements, they were able to identify not only the drug-resistant cells within the cultures, but also accurately determine the next therapeutic option, including dose escalation, combination therapy or second generation inhibitors.

“The most critical issue in dealing with imatinib resistance is what to switch over to,” said Ohba. “If the patient is switched to another drug to which they are also resistant, then the treatment will just be a waste of time and detrimental to the patient's condition.”

In an accompanying editorial also published in Clinical Cancer Research, Yingxiao Wang, Ph.D., an assistant professor in the bioengineering department at the University of Illinois Urbana-Champaign, said this study is a “pioneer work.”

“The entire cancer community is talking about personalized medicine, and key to that is knowing when an individual person will have a unique response,” said Wang. “This project is an important step forward.”

The trial was funded by the Japanese government, and none of the authors had a conflict of interest. The test is not available clinically in the United States.

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The mission of the American Association for Cancer Research is to prevent and cure cancer. Founded in 1907, the AACR is the world's oldest and largest professional organization dedicated to advancing cancer research. The membership includes 31,000 basic, translational and clinical researchers; health care professionals; and cancer survivors and advocates in the United States and more than 90 other countries. The AACR marshals the full spectrum of expertise from the cancer community to accelerate progress in the prevention, diagnosis and treatment of cancer through high-quality scientific and educational programs. It funds innovative, meritorious research grants, research fellowship and career development awards. The AACR Annual Meeting attracts more than 17,000 participants who share the latest discoveries and developments in the field. Special conferences throughout the year present novel data across a wide variety of topics in cancer research, treatment and patient care. The AACR publishes six major peer-reviewed journals: Cancer Research; Clinical Cancer Research; Molecular Cancer Therapeutics; Molecular Cancer Research; Cancer Epidemiology, Biomarkers & Prevention; and Cancer Prevention Research. The AACR also publishes CR, a magazine for cancer survivors and their families, patient advocates, physicians and scientists. CR provides a forum for sharing essential, evidence-based information and perspectives on progress in cancer research, survivorship and advocacy.

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