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Makale detayı · 2025

Perioperative Management With Efanesoctocog Alfa in Patients With Haemophilia A in the Phase 3 XTEND‐1 and XTEND‐Kids Studies

Haemophilia

YÖKSİS OpenAlex ISSN 1351-8216 DOI 10.1111/hae.70017 Atıf 8 Açık erişim · green SJR Q1 JCR Q2

10.1111/hae.70017

YÖKSİS YÖKSİS makale kaydı

OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

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İngilizce (OpenAlex)

INTRODUCTION: The Phase 3 studies, XTEND-1 (NCT04161495) and XTEND-Kids (NCT04759131), showed once-weekly efanesoctocog alfa provided high-sustained factor VIII (FVIII) activity levels that translated into highly effective bleed prevention in patients with severe haemophilia A. AIM: This analysis evaluated the efficacy and safety of efanesoctocog alfa for perioperative management during XTEND-1 and XTEND-Kids. METHODS: Patients undergoing major or minor surgery were to receive a single preoperative 50 IU/kg dose, with additional 30 or 50 IU/kg doses every 2-3 days as needed following major surgery. Outcomes assessed included FVIII activity levels, number and dose of efanesoctocog alfa injections, surgeon's/investigator's assessment of haemostatic response, total factor consumption, estimated blood loss, number and type of blood transfusions, and safety. RESULTS: In XTEND-1, 11 adults/adolescents underwent 12 evaluable major surgeries (6 orthopaedic). Eleven surgeries had one preoperative dose (median [range]: 49.9 [13-52] IU/kg); one had no preoperative dose. Median (range) total consumption from Day -1 to 14 was 163.3 (45-361) IU/kg. In XTEND-Kids, two children underwent major surgery with a single preoperative loading dose (60.4 and 61.9 IU/kg). Across trials, 15 adults/adolescents underwent 18 minor surgeries and 8 children underwent 9 minor surgeries, with a single preoperative dose or no preoperative dose (5 surgeries in adults/adolescents). Haemostatic response was rated excellent for all surgeries. No surgeries required blood transfusion. No safety concerns or inhibitor development was reported. CONCLUSION: Efanesoctocog alfa provided highly effective perioperative protection in patients with severe haemophilia A. TRIAL REGISTRATION: XTEND-1: NCT04161495 https://clinicaltrials.gov/study/NCT04161495; XTEND-Kids: NCT04759131 https://clinicaltrials.gov/study/NCT04759131.

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Konular

  • Hemophilia Treatment and Research
  • Blood transfusion and management
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema

Tür: article Hemophilia Treatment and Research

İndeks bilgisi

WoS (JCR) ve Scopus (SJR) çeyrekleri ISSN ve yayın yılına göre. · 2025

Scopus (SJR) / WoS (JCR)

Haemophilia

Scopus (SJR) Q1 0,961 2025 yılı
WoS (JCR) Q2 JIF 3 2025 yılı

Üniversiteler

  • AKDENİZ ÜNİVERSİTESİ

Yazarlar

  1. Robert Klamroth
  2. Annette von Drygalski
  3. cedric hermans
  4. Young-Shil Park
  5. Anthony K C Chan
  6. OSMAN ALPHAN KÜPESİZ AKDENİZ ÜNİVERSİTESİ
  7. María Teresa Alvarez-Román
  8. Lynn Malec
  9. Elena Santagostino
  10. Graham Neill
  11. Linda Bystrická
  12. Jennifer Dumont
  13. Lydia Abad-Franch
  14. Lila-Sabrina Fetita
  15. Liane Khoo