The Impact of Tirabrutinib Monotherapy for the Treatment of Bing-Neel Syndrome: A Multicenter Retrospective Study
- PMID: 40751704
- PMCID: PMC12417752
- DOI: 10.1002/ajh.70029
The Impact of Tirabrutinib Monotherapy for the Treatment of Bing-Neel Syndrome: A Multicenter Retrospective Study
Keywords: Bing‐Neel syndrome; Waldenström macroglobulinemia; tirabrutinib.
Conflict of interest statement
M.S. has received honoraria from Janssen and Ono. N.F. has received research grants from Abbvie, Chugai, Chordia Therapeutics, Genmab, Haihe, Incyte, Kyowa Kirin, Loxo Oncology, Ono, and Takeda, and honoraria from Abbvie, AstraZeneca, BMS, Chugai, CSL Behring, Eisai, Eli Lilly, Genmab, Janssen, Kyowa Kirin, Nippon Shinyaku, Novartis, Ono, Sanofi, Symbio, and Takeda. Y.I. has received honoraria from Kyowa Kirin, Sanofi, BMS, Jansen, Pharmaessensia, and Novartis. K.M. has received research grants or contracts from Takeda, Otsuka, Chugai, Kyowa Kirin, Sumitomo, and Zenyaku Kogyo, and honoraria from Chugai, Janssen, AstraZeneca, Novartis, Incyte, Asahi Kasei, Abbvie, SymBio, Ono, Genmab, Meiji Seika, BMS, Kyowa Kirin, Daiichi Sankyo, Gilead Sciences, and Nippon Shinyaku. Y.H. has been involved in advisory board participation with Janssen and received honoraria from Janssen, Sanofi, Ono, BMS, Takeda, CSL Behring, Novartis, and Chugai. N.S. has received honoraria from Janssen, Ono, and BeiGene, and research funding from Incyte Biosciences Japan, Janssen, Mitsubishi Tanabe Pharma Corporation, MSD, and Ono.
Figures
References
-
- Simon L., Fitsiori A., Lemal R., et al., “Bing‐Neel Syndrome, a Rare Complication of Waldenström Macroglobulinemia: Analysis of 44 Cases and Review of the Literature. A Study on Behalf of the French Innovative Leukemia Organization (FILO),” Haematologica 100, no. 12 (2015): 1587–1594. - PMC - PubMed
-
- Castillo J. J., Itchaki G., Paludo J., et al., “Ibrutinib for the Treatment of Bing‐Neel Syndrome: A Multicenter Study,” Blood 133, no. 4 (2019): 299–305. - PubMed
Publication types
LinkOut - more resources
Full Text Sources
