From Bench to Bedside: February 1, 2010
Combination therapy may benefit patients with specific genetic subtype of non-small cell lung cancer Even when their tumors are shrinking in response to medical therapy, some non-small cell lung cancer (NSCLC) patients have a scattering of cancer cells that are undeterred by the drug, causing the tumor to resume its growth, Massachusetts General Hospital (MGH) Cancer Center and Dana-Farber Cancer Institute scientists report in the January issue of Cancer Cell. The findings suggest that identifying such patients and treating them with a combination of drugs from the very start of therapy can produce longer remissions.
The study involves NSCLC tumors which are driven by a mutation in the gene EGFR. Such tumors, which account for about 12 percent of all NSCLC cases in the United States, often recede when treated with a tyrosine kinase inhibitor such as Tarceva or Iressa, which targets the faulty EGFR protein.
A few years ago, this same group of investigators showed that NSCLCs being held in check by Tarceva can switch on an alternate growth circuit if they have too many copies of a gene called MET. Such tumors are considered Tarceva- and Iressa-resistant.
In the new paper, investigators led by Jeffrey Engelman, MD, PhD, of Mass General, and Pasi Jänne, MD, PhD, of Dana-Farber, found that some patients with EGFR-mutant lung cancers harbor a small number of tumor cells with an overabundance, or "amplification," of MET even before treatment with a tyrosine kinase inhibitor, and that those few cells are enough to spark drug resistance. One of the triggers for resistance, the researchers found, is HGF, a ligand or "hook" that activates the MET protein.
When activated, HGF works through two entirely different channels to produce drug resistance. First, it can generate cell-growth signals through a protein called GAB1. Second, it expands the number of MET-amplified cancer cells, ensuring they will become the dominant type in the lung tumors.
HGF can spur cell growth on its own as well as speed up the process by which MET-amplified cells emerge and take over the composition of the tumor. In about 20 percent of NSCLC patients who are resistant to Tarceva, the mechanism is amplification of MET, and in another 20 percent it may involve HGF.
The findings suggest that patients whose NSCLC tumors harbor even a few MET-amplified cells prior to treatment would benefit from drugs that specifically target those cells, in combination with a tyrosine kinase inhibitor. Such drugs are already being studied in clinical trials.
These findings provide a strong rationale for combination treatment strategies as initial therapies for some patients, especially those with evidence of pre-existing MET amplifications.
According to Dr. Engelman, "thorough analysis of a patient's cancer prior to treatment can establish how it would ultimately develop resistance to therapy, allowing physicians to tailor treatment with greater precision to prevent resistance. For example, cancers found to harbor a small population of cells with pre-existing MET amplification will likely benefit from adding MET inhibitors to initial treatment. Those without such cells may not benefit, and these patients can avoid the added toxicity of MET inhibitors and instead focus on other strategies to prevent their cancers from becoming resistant."
The study was supported by grants from the National Institutes of Health, American Association for Cancer Research, the V Foundation, American Cancer Society, Hazel and Samuel Bellin Research Fund, and the Ellison Foundation.
The study's co-lead authors were Alexa Turke of MGH, and Kreshnik Zejnullahu, of Dana-Farber. Co-authors include Yi-Long Wu, of Guangdong General Hospital, Guangzhou, China; Youngchul Song, Dora Dias-Santagata, PhD, Eugene Lifshits, Lecia Sequist, MD, MPH, Sara Akhavanfard, MD, Beow Yeap, and A. John Iafrate, MD, PhD, of MGH; Luca Toschi, MD, Andrew Rogers, and Marzia Capelletti of Dana-Farber; Tony Mok, MD, of the Chinese University of Hong Kong; Neal Lindeman, MD, Carly Murphy, Yun Xiao, and Charles Lee, PhD, of Brigham and Women's Hospital; and James Christensen, of Pfizer Global Research and Development, La Jolla, Calif.
