Observational study demonstrates reduced febrile neutropenia in hormone-sensitive prostate cancer, suggesting safer treatment options.
Older age and high-volume disease were independent risk factors for FN in patients with mHSPC receiving triplet therapy. A longer interval from ADT initiation to docetaxel (≥40 days) was associated with a significantly lower risk of FN, suggesting that extending the pre-docetaxel castration period is a practical, adjustable scheduling strategy to improve treatment safety. These findings may support treatment selection and proactive prevention of FN.
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Yamada et al. (2026) studied this question.
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