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Hematology

Cost-efficiency and expanded access of prophylaxis for chemotherapy-induced (febrile) neutropenia: economic simulation analysis for the US of conversion from reference pegfilgrastim to biosimilar pegfilgrastim-cbqv

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Pages 1466-1476 | Received 31 Aug 2020, Accepted 28 Sep 2020, Published online: 24 Oct 2020

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Read on this site (5)

Hala H. Halawah, Nimer S. Alkhatib, Abdulaali R. Almutairi, Mohammad Saleh, Shiraz S. Halloush, Omar Rashdan, Lama Masadh, Osama H. Abusara & Ivo Abraham. (2023) Cost-efficiency analysis and expanded treatment access modeling of conversion to rituximab biosimilars from reference rituximab in Jordan. Journal of Medical Economics 26:1, pages 835-842.
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Consuela Cheriece Yousef, Mansoor Ahmed Khan, Hind Almodaimegh, Majed Alshamrani, Meteb Al-Foheidi, Hana AlAbdalkarim, Ahmed AlJedai, Anjum Naeem & Ivo Abraham. (2023) Cost-efficiency analysis of conversion to biosimilar filgrastim for supportive cancer care and resultant expanded access analysis to supportive care and early-stage HER2+ breast cancer treatment in Saudi Arabia: simulation study. Journal of Medical Economics 26:1, pages 394-402.
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Nimer S Alkhatib, Shiraz Halloush & Ivo Abraham. (2023) The status and preparation for the next decade of biosimilars in the Middle Eastern and North African region. Expert Opinion on Biological Therapy 23:8, pages 671-677.
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Ali McBride, Karen MacDonald, Adolfo Fuentes-Alburo & Ivo Abraham. (2021) Cost-efficiency and expanded access modeling of conversion to biosimilar trastuzumab-dkst with or without pertuzumab in metastatic breast cancer. Journal of Medical Economics 24:1, pages 743-756.
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Ali McBride, Karen MacDonald, Adolfo Fuentes-Alburo & Ivo Abraham. (2021) Conversion from pegfilgrastim with on-body injector to pegfilgrastim-jmdb: cost-efficiency analysis and budget-neutral expanded access to prophylaxis and treatment. Journal of Medical Economics 24:1, pages 598-606.
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Articles from other publishers (8)

Sherin Ismail, Laila Abu Esba, Mansoor Khan, Hana Al-Abdulkarim, Hind Modimagh & Consuela Yousef. (2022) An Institutional Guide for Formulary Decisions of Biosimilars. Hospital Pharmacy 58:1, pages 38-48.
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Sophia Z. Humphreys, Robert B. Geller & Paul Walden. (2022) Pegfilgrastim Biosimilars in US Supportive Oncology: A Narrative Review of Administration Options and Economic Considerations to Maximize Patient Benefit. Oncology and Therapy 10:2, pages 351-361.
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Seenu M. Hariprasad, Richard P. Gale, Christina Y. Weng, Hans C. Ebbers, Mourad F. Rezk & Ramin Tadayoni. (2022) An Introduction to Biosimilars for the Treatment of Retinal Diseases: A Narrative Review. Ophthalmology and Therapy 11:3, pages 959-982.
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Paul Cornes, John Kelton, Rongzhe Liu, Omer Zaidi, Jennifer Stephens & Jingyan Yang. (2022) Real-world cost–effectiveness of primary prophylaxis with G-CSF biosimilars in patients at intermediate/high risk of febrile neutropenia. Future Oncology 18:16.
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Ali McBride, Neda Alrawashdh, Karen MacDonald & Ivo Abraham. (2022) Expanded access to anticancer treatments from conversion to biosimilar pegfilgrastim-cbqv in US breast cancer patients. Future Oncology 18:3, pages 363-373.
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Karen MacDonald, Neda Alrawashdh, Ali McBride & Ivo Abraham. (2021) Conversion to biosimilar pegfilgrastim-cbqv enables budget-neutral access to FOLFIRINOX treatment for metastatic pancreatic cancer. Future Oncology 17:33, pages 4561-4570.
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Florian Scotte, Hélène Simon, Philippe Laplaige, Eric-Charles Antoine, Caroline Spasojevic, Nathalie Texier, Karine Gouhier & Christos Chouaid. (2021) Febrile neutropenia prophylaxis, G-CSF physician preferences: discrete-choice experiment. BMJ Supportive & Palliative Care, pages bmjspcare-2021-003082.
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Barbara Finck, Robert B. Geller & Paul Walden. (2021) Letter to the Editor Regarding “The Challenges of Switching Therapies in an Evolving Multiple Biosimilars Landscape: A Narrative Review of Current Evidence”. Advances in Therapy 38:6, pages 3483-3486.
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