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Landmark pancreatic cancer treatment paves way for targeting other tricky tumors

Landmark pancreatic cancer treatment paves way for targeting other tricky tumors Unprecedented results against a stubbornly hard-to-treat cancer are boosting optimism that other challenging tumors will be next The landmark success of a drug against an โ€˜undruggableโ€™ cancer is sp

Landmark pancreatic cancer treatment paves way for targeting other tricky tumors
Scientific American โ€” 3 June 2026
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Landmark pancreatic cancer treatment paves way for targeting other tricky tumors

Unprecedented results against a stubbornly hard-to-treat cancer are boosting optimism that other challenging tumors will be next

The landmark success of a drug against an โ€˜undruggableโ€™ cancer is spurring fresh optimism in the quest to treat seemingly untouchable tumour targets.

The experimental drug, daraxonrasib , disarms all three members of the RAS family of proteins, which are linked to some of the deadliest cancers. Designing drugs that target the RAS proteins has been notoriously challenging . But a large clinical trial has found that daraxonrasib nearly doubled survival โ€” from 6.7 months to 13.2 months โ€” in people with a form of advanced pancreatic cancer.

The results were presented to a packed room at the American Society of Clinical Oncology annual meeting in Chicago, Illinois, on 31 May, and published in the New England Journal of Medicine . At the conference, the talk was met with a long standing ovation, says Ecaterina Dumbrava, an oncologist at the University of Texas MD Anderson Cancer Center in Houston. โ€œAfter more than a decade without major advances in treatment for pancreatic cancer, seeing this is really emotional,โ€ she says.

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That success is raising hopes that other challenging targets might also soon fall. Nature talked to researchers about progress in targeting RAS and other โ€œundruggableโ€ cancer proteins that canโ€™t be bested with conventional approaches.

RAS proteins are molecular onโ€“off switches that help to control cell growth and division. But some mutations leave RAS proteins stuck in the โ€˜onโ€™ position, which drives tumour growth.

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