An anti-cancer drug used to fight leukemia shows promise against a rare and aggressive type of ovarian cancer
— small cell carcinoma of the ovary hypercalcemic type (SCCOHT) — which strikes young women and girls, according to a study led by the Translational Genomics Research Institute (TGen)
, an affiliate of City of Hope.
Ponatinib was found in TGen-led preclinical studies to significantly delay tumor growth and reduce tumor volume in SCCOHT, according to a study published online in the scientific journal Clinical Cancer Research. The findings suggest that ponatinib should be tested for use in SCCOHT patients in clinical trials.
The statistics for SCCOHT are bleak. This rare and aggressive form of ovarian cancer has been diagnosed in women as old as 47, and as young as 14 months, with a median diagnosis of 24 years of age. It has a dismal two-year survival rate of less than 35 percent.
“Current treatment for this devastating cancer has such poor response rates and extreme toxicity that we must find better therapeutics,” said Jeffrey Trent, Ph.D.
, TGen president and research director, and the senior author of the study. “Our work identifies a new treatment strategy that could provide these young women with improved patient benefit.”
An international research team led by TGen first discovered that a mutation in the gene SMARCA4
was the genetic cause of SCCOHT, according to a 2014 study published in Nature Genetics
. The SMARCA4
gene — previously associated with lung
and pancreatic cancer
— was the only recurrently mutated gene in the study's samples.
In the most recent study, TGen laboratory researchers found that SCCOHT tumors, driven by the inactivation of the SMARCA4 gene, are reliant on receptor tyrosine kinase (RTK) cellular pathways. Researchers identified these pathways from screens of drugs already approved by the Food and Drug Administration (FDA) that might be effective against this cancer.
“We identified ponatinib as the most effective clinically approved RTK inhibitor,” said Jessica Lang, Ph.D., a TGen postdoctoral fellow and co-lead author of the study. “It holds the potential for rapidly improving outcomes for these young patients.”
In laboratory models, ponatinib delayed tumor-doubling time four-fold, while reducing tumor volumes in models by as much as 58.6 percent, the study said.
“Evaluation of a panel of selective RTK inhibitors highlighted ponatinib as the most potent tested agent in SCCOHT cell lines,” said William Hendricks, Ph.D., assistant professor in TGen’s Integrated Cancer Genomics Division, and the other co-lead author of the study. “Clinical investigation of this FDA-approved oncology drug is warranted in SCCOHT.”
Much of the work in this study was inspired by the memory of Taryn Ritchey, a 22-year-old TGen patient who in 2007 lost her battle with ovarian cancer. More than 14,000 patients in the U.S. will die this year from ovarian cancer, making it the fifth leading cause of cancer death among American women.
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