
Pfizer's combination therapy improves survival in bladder cancer trial
The interim results from an ongoing late-stage trial of the combination therapy showed significant improvement in event-free survival – which measures how long a patient remains free from disease recurrence – and overall survival when compared to surgery alone, the company said.
"These latest results underscore the practice-changing potential of this combination in earlier stages of bladder cancer, where it has the potential to improve outcomes for even more patients," said Johanna Bendell, Pfizer's oncology chief development officer.
In muscle-invasive bladder cancer, the tumor extends beyond the inner lining and penetrates the muscular wall of the organ. It accounts for about 25% of all newly diagnosed bladder cancers and is a particularly aggressive form with a high risk of spreading, according to the National Institutes of Health.
Pfizer said it plans to discuss the trial results with global health authorities for potential regulatory filings.
The combination therapy leverages anti-PD-1 treatments that block the PD-1 protein to help the immune system combat cancer, where Padcev, an antibody-drug conjugate, targets specific cancer cells without damaging healthy ones.
Padcev, co-developed with Japan's Astellas (4503.T), opens new tab, was approved by the U.S. Food and Drug Administration in 2019 to treat patients with a form of bladder cancer called metastatic urothelial cancer.
The drug brought $1.59 billion in sales last year, contributing about 2% of Pfizer's total revenue.

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The Independent
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- The Independent
AI could soon detect early voice box cancer from the sound of your voice
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BBC News
31 minutes ago
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Medical News Today
37 minutes ago
- Medical News Today
Subtle signs of multiple sclerosis may appear years before onset
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Burcu Zeydan, MD, an assistant professor of neurology at Mayo Clinic, who was not involved in this research noted the following cautions to Medical News Today: 'We see that healthcare visits in the 'pre-MS diagnosis' period are mainly for rather nonspecific and/or common causes such as headaches, fatigue, and mental health issues. Since most of these individuals will never develop MS, identification of individuals in a possible MS prodrome carries the risk for overdiagnosis and overtreatment as well as a concern for causing unnecessary distress for individuals and families. There is also a possibility of missed opportunities for earlier recognition of MS by clinicians, which is supported by the rise in ophthalmology and neurology visits in the current study as pointed out by the authors. 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