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‘Breakthrough therapy’: a new Chinese drug shows record treatment success against one of the deadliest lung cancers

  • Phase 2 clinical trial of sunvozertinib shows 61 per cent anti-tumour activity response, higher than any previous candidates: paper
  • It aims to combat a specific type of lung cancer in which tumour harbours ‘EGFR exon 20 insertions’ mutation

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Sunvozertinib was granted breakthrough therapy designations from China’s National Medical Products Administration in 2020 and the US Food and Drug Administration in 2022. Photo: Shutterstock
Dannie Peng

For patients wrestling with an uncommon and recalcitrant subtype of lung cancer that will not ease with conventional therapies, such as platinum-based chemotherapy, a Chinese targeted antitumour drug shows encouraging outcomes and offers a beacon of hope.

In a phase 2 clinical trial that enrolled 104 advanced patients and analysed 97 cases, a new drug called sunvozertinib could reportedly achieve a 61 per cent anti-tumour activity response, higher than any previous candidates, according to a team of Chinese scientists who published their results in a paper.

The initial results of this trial were presented at the American Society of Clinical Oncology (ASCO) annual meeting in Chicago in mid-June, and were peer reviewed and published by The Lancet Respiratory Medicine journal on December 12.

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This new drug was developed by Dizal, a biopharmaceutical company based in eastern China’s Jiangsu province. It aims to combat a specific type of lung cancer in which the tumour harbours a mutation known as “EGFR exon 20 insertions”.

“It’s an impressive outcome because previously other potential candidates could only achieve a response rate below 50 per cent for this lung cancer subgroup, ” said one chief scientist from a major biotech company surnamed Tang, who declined to be identified by his full name.

06:10

China’s new cancer drug gets US approval at huge price mark-up

China’s new cancer drug gets US approval at huge price mark-up

In 2020 and 2022 respectively, the drug was granted breakthrough therapy designations from China’s National Medical Products Administration and the US Food and Drug Administration.

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