Real-World Experience with Isavuconazole in Allogeneic Stem Cell Transplantation in Spain.
СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Kwon Mi, Gómez-Centurión Ignacio, Oarbeascoa Gillen, Torres Melissa, Martinez Ariadna Perez, Suarez-Lledó Maria, Chinea Anabelle, Cascón Maria Jesus Pascual, Vazquez Lourdes, Espigado Ildefonso, Izquierdo Isabel, Parody Rocio, Cadenas Irene Garcia, Calbacho Maria, Sierra Pedro Gonzalez, Heras Inmaculada, Yañez Lucrecia, Torrent Anna, Bautista Guiomar, Gonzalez Soledad, Roldan Elisa, Vallejo Juan Carlos, Bailen Rebeca, Borrero Asunción, Lopez-Jiménez Javier, Casas Maria Angeles Cuesta, Solano Carlos, Spanish Group of Hematopoietic Stem Cell Transplantation and Cell Therapy (GETH-TC)
Аннотация
Invasive fungal infections (IFI) pose a significant complication after hematopoietic stem cell transplantation (HSCT). Isavuconazole (ISV) is a new generation azole with a favourable adverse effect and interaction profile approved for the treatment of invasive aspergillosis and mucormycosis. We analyzed the indications, effectiveness, adverse event profile and drug interaction management of ISV in the real-world setting in adults who received allogeneic-HSCT (allo-HSCT) within the Spanish Group of HSCT and Cell Therapy (GETH-TC). We conducted a multicenter retrospective study of all consecutive adult allo-HSCT recipients (≥18 years) who received ISV either for IFI treatment or prophylaxis, from December 2017 to August 2021, in 20 centers within the Spanish Group of Hematopoietic Stem Cell Transplantation and Cell Therapy (GETH-TC). A total of 166 adult allografted patients who received ISV from 2017 to 2021 were included. Median age was 48 years with 43% females. In 81 (49%) patients, ISV was used for treatment of IFI, and in 85 (51%) for prophylaxis. Median duration of ISV administration for IFI treatment was 57 days (range 31-126) and 86 days (range 33-196) for prophylaxis. Most frequent indication for treatment was invasive aspergillosis (78%), followed by mucormycosis (6%). Therapeutic success (45%) was the most frequent reason for ISV withdrawal. In the prophylaxis group, the resolution of IFI risk factors was the most frequent reason for withdrawal (62%). Six (7%) breakthrough IFI were reported. The majority of patients (80%) presented pharmacologic interactions. Twenty-one patients (13%) reported adverse events related to ISV, mainly liver biochemistry abnormalities, which led to ISV withdrawal in 7 patients (4%). ISV was effective and well tolerated for IFI treatment and prophylaxis, with a manageable interaction profile.