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DOI 10.1002/bcp.70118

Медицинская библиотека · British journal of clinical pharmacology · 2025

Exposure-response relationship of fedratinib in patients with intermediate-2 or high-risk myelofibrosis.

Chen Yizhe, Li Yan, Xue Yongjun, Brown Patrick, Hernandez Christopher, Rose Shelonitda, Pilot Richard, Krishna Gopal, Ogasawara Ken

Клиническое исследование II фазыКлиническое исследование III фазыСтатьяПеревод пока не подготовлен

Аннотация

AIMS: Fedratinib is a potent, oral, Janus kinase inhibitor for the treatment of myelofibrosis (MF). This report describes exposure-response (E-R) analyses of fedratinib based on pooled data from phase 2/3 studies in patients with intermediate-2 or high-risk MF, with or without prior ruxolitinib exposure.

METHODS

Pharmacokinetic (PK) exposures were derived from the population PK analysis. Efficacy endpoints included spleen volume reduction ≥35% (SVR35) and total symptom score reduction ≥50% (TSS response). Safety endpoints included grade ≥3 anaemia or thrombocytopenia, any-grade nausea/vomiting and diarrhoea. The E-R models were developed using logistic regression analyses.

RESULTS

Fedratinib exposure was positively associated with SVR35 (odds ratio [OR], 38.2; 95% confidence interval [CI], 12.4-118; P < 0.001) and TSS response (OR, 20.8; 95% CI, 6.27-69.2; P < 0.001), after adjusting for covariates. Baseline spleen volume was inversely associated with SVR35 (P = 0.029). Prior ruxolitinib exposure was not associated with SVR35 (P = 0.090) or TSS response (P = 0.326). Although numerically higher incidence of adverse events was observed in patients with higher fedratinib exposure, there was no statistically significant association between fedratinib exposure and any safety related endpoints. Prior ruxolitinib exposure was associated with experiencing grade ≥3 thrombocytopenia (P = 0.004). Lower baseline haemoglobin level (<10 g/dL) and platelet count (<100 × 109/L) were associated with experiencing grade ≥3 anaemia (P < 0.001) and thrombocytopenia (P < 0.001), respectively. Antiemetic prophylaxis was associated with lower rates of nausea/vomiting (P < 0.001).

CONCLUSIONS

Fedratinib exposure was positively associated with spleen volume reduction and TSS responses, without having significant impact on safety. Fedratinib 400 mg once daily is an appropriate dose for patients with MF regardless of ruxolitinib exposure.

Для цитирования: Chen Yizhe, Li Yan, Xue Yongjun, Brown Patrick, Hernandez Christopher, Rose Shelonitda, Pilot Richard, Krishna Gopal, Ogasawara Ken. Exposure-response relationship of fedratinib in patients with intermediate-2 or high-risk myelofibrosis.. British journal of clinical pharmacology. 2025. DOI: 10.1002/bcp.70118.

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