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Malignant mesothelioma patients likely to benefit from drug pemetrexed identified, study suggests

Date:
August 29, 2012
Source:
University of Colorado Denver
Summary:
Previous studies have hypothesized that low levels of the enzyme thymidylate synthase (TS) likely mark patients who will benefit from the drug pemetrexed – but results have been inconclusive at best and at times contradictory. A new study provides an explanation why: Only in combination with high levels of a second enzyme, FPGS, does low TS predict response to pemetrexed in patients with malignant pleural mesothelioma.

Previous studies have hypothesized that low levels of the enzyme thymidylate synthase (TS) likely mark patients who will benefit from the drug pemetrexed -- but results have been inconclusive at best and at times contradictory.

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A University of Colorado Cancer Center study recently published in the Journal of Thoracic Oncology provides an explanation of why: only in combination with high levels of a second enzyme, FPGS, does low TS predict response to pemetrexed in patients with malignant pleural mesothelioma.

"The hope is that oncologists could test a patient for TS and FPGS levels and so discover if the patient should be treated with pemetrexed or if another therapy might be more appropriate," says the paper's first author, Daniel C. Christoph, MD, PhD, medical oncologist at the West German Cancer Center, working as an international postdoctoral researcher in the lab of CU Cancer Center investigator, Fred Hirsch, MD, PhD.

Pemetrexed works by inhibiting the enzyme TS, which cancer cells need in order to replicate their DNA. So it stands to reason that tumors already low in TS would be most affected by the drug -- blocking the remaining TS would effectively stop the ability of cancer cells to synthesize new DNA.

However, Christoph and colleagues tested 84 samples of mesothelioma in which patients had been treated with pemetrexed and found that low levels of TS only in combination with concurrently high levels of FPGS predicted patients' response to the drug.

The study also explained the mechanism by which FPGS increases the clinical effectiveness of pemetrexed: "High levels of FPGS allow pemetrexed to stay longer inside cells, giving the drug longer to work against TS," Christoph says. Of the samples tested, patients with low TS and high FPGS had more response to pemetrexed and longer durations of survival.

According to Christoph, the current study provides the preclinical work needed to justify exploring the predictive power of TS and FPGS in mesothelioma patients. A prospective observational study of these biomarkers could lead to their wide use in predicting patients' response to pemetrexed.


Story Source:

The above story is based on materials provided by University of Colorado Denver. The original article was written by Garth Sundem. Note: Materials may be edited for content and length.


Journal Reference:

  1. Daniel C. Christoph, Bernadette Reyna Asuncion, Celine Mascaux, Cindy Tran, Xian Lu, Murry W. Wynes, Thomas C. Gauler, Jeremias Wohlschlaeger, Dirk Theegarten, Volker Neumann, Rodrigo Hepp, Stefan Welter, Georgios Stamatis, Andrea Tannapfel, Martin Schuler, Wilfried E. Eberhardt, Fred R. Hirsch. Folylpoly-Glutamate Synthetase Expression Is Associated with Tumor Response and Outcome from Pemetrexed-Based Chemotherapy in Malignant Pleural Mesothelioma. Journal of Thoracic Oncology, 2012; 7 (9): 1440 DOI: 10.1097/JTO.0b013e318260deaa

Cite This Page:

University of Colorado Denver. "Malignant mesothelioma patients likely to benefit from drug pemetrexed identified, study suggests." ScienceDaily. ScienceDaily, 29 August 2012. <www.sciencedaily.com/releases/2012/08/120829141809.htm>.
University of Colorado Denver. (2012, August 29). Malignant mesothelioma patients likely to benefit from drug pemetrexed identified, study suggests. ScienceDaily. Retrieved January 26, 2015 from www.sciencedaily.com/releases/2012/08/120829141809.htm
University of Colorado Denver. "Malignant mesothelioma patients likely to benefit from drug pemetrexed identified, study suggests." ScienceDaily. www.sciencedaily.com/releases/2012/08/120829141809.htm (accessed January 26, 2015).

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