A New subtype of prostate cancer identified

Researchers have identified a new subtype of prostate cancer that occurs in about seven percent of patients with advanced disease.

A New subtype of prostate cancer identified

New York: Researchers have identified a new subtype of prostate cancer that occurs in about seven percent of patients with advanced disease.

The subtype is characterized by loss of the gene CDK12. It was found to be more common in metastatic prostate cancer compared to early-stage tumors that had not spread, said the study published in the journal Cell.

"Because prostate cancer is so common, seven percent is a significant number," said senior study author Arul Chinnaiyan from the University of Michigan in the US. 

Tumors in which CDK12 was inactivated were responsive to immune checkpoint inhibitors, a type of immunotherapy treatment that has overall had limited success in prostate cancer, the study said.

"The fact that immune checkpoint inhibitors may be effective against this sub-type of prostate cancer makes it even more significant. This is an exciting prospect for patients who have CDK12 alterations and may benefit from immunotherapy," Chinnaiyan added. 

The researchers said they will lead a multisite clinical trial to assess checkpoint inhibitors as a treatment for metastatic prostate cancer with the CDK12 loss.

In this study, the researchers looked at DNA and RNA sequencing data from 360 tumor samples from patients with metastatic castration-resistant prostate cancer. 

This is an aggressive, advanced form of the disease in which cancer has spread throughout the body and no longer responds to traditional hormone-based treatments.

The researchers found the loss of CDK12 in only about one percent of early prostate cancer samples. That jumped to 7 percent for metastatic cancer, which indicates a more aggressive form of the disease.

By following the mechanism of how CDK12 loss impacts the cell, the researchers found a process in which cells create neoantigens that are foreign to the immune system. 

This boosts immune-fighting T-cells, which may explain why these patients benefit from immune checkpoint blockade.
 

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