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Conference/Presentation Title: | Assure- interim results: a phase 3b safety study of acalabrutinib (a) in patients with chronic lymphocytic leukemia (CLL). | Authors: | Von Tresckow J.;Opat S. ;Awan F.T.;Fogliatto L.;Nikitin E.;Czerwinski J.;Santucci Alves da Silva R.;Jujjavarapu S.;Samoilova O.;Dartigeas C.;Tran H. ;De Laserna J.;Banerji V.;Magnano Mayer L.M.M.;Hart J.;Poulsen C.B.;Seong Eom K.;Merli M.;John E.;Munley J.;Hakre S.;Hermann R.;Niemann C.U. | Monash Health Department(s): | Monash University - School of Clinical Sciences at Monash Health | Institution: | (Von Tresckow) Universitatsklinikum Essen, Klinik fur Hamatologie und Stammzelltransplantation, Essem, Germany (Opat) Monash University and Monash Health, Melbourne, Australia (Awan) University of Texas Southwestern Medical Center, Dallas, TX, United States (Fogliatto) Hospital de Clinicas de Porte Alegre, Porte Alegre, Brazil (Nikitin) S.P Botkin's City Hospital, Moskau, Russian Federation (Czerwinski) Flinders Medical Centre, Bedford Park, Australia (Santucci Alves da Silva) Instituto Hemomed, Sao Paulo, Brazil (Jujjavarapu) Illinois Cancer Care, Peoria, IL, United States (Samoilova) Regional Clinical Hospital, Nizhny Novgorod, Russian Federation (Dartigeas) CHU Tours, Tours, France (Tran) Akershus University Hospital, Lorenskog, Norway (De Laserna) De Octubre, Madrid, Spain (Banerji) University of Manitoba, CancerCare Manitoba Research Institute, Manitoba, Canada (Magnano Mayer) Hospital Clinic-IDIBAPS, University of Barcelona, Barcelona, Spain (Hart) BC Cancer-Victoria, Victoria, BC, Canada (Poulsen) Zealand University Hospital, Roskilde, Denmark (Seong Eom) Catholic University of Korea, Seoul, South Korea (Merli) Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Mailand, Italy (John) AstraZeneca, Cambridge, United Kingdom (Munley) AstraZeneca, Wilmington, United States (Hakre, Hermann) AstraZeneca, Gaithersburg, United States (Niemann) Rigshospitalet Copenhagen University Hospital, Kopenhagen, Denmark |
Presentation/Conference Date: | 13-Nov-2024 | Copyright year: | 2024 | Publication information: | Oncology Research and Treatment. Conference: Jahrestagung der Deutschen, Osterreichischen und Schweizerischen Gesellschaften fur Hamatologie und Medizinische Onkologie. Basel Switzerland. 47(Supplement 2) (pp 272-273), 2024. Date of Publication: October 2024. | Journal: | Oncology Research and Treatment | Abstract: | Introduction: Here, we report interim results from ASSURE, a global, phase 3b safety study evaluating A monotherapy in pts with CLL in real-world clinical practice. Method(s): Pts >=18y with CLL and ECOG-PS <=2 were divided into 3 cohorts (TN, R/R, ibrutinib intolerant [IbrI]). Pts receive A 100mg twice daily for 48 cycles or until progression, toxicity, withdrawal of consent, loss to follow-up, death, or study termination. The primary objective is the frequency of treatment-emergent adverse events (TEAEs). Result(s): 552 pts had received treatment and were analyzed. Median age was 69.5y; 20% had del(17p)/TP53m and 68% uIGHV. Median number of prior lines of therapy was 1 in the R/R and 2 in the IbrI cohort. At data cutoff, 64% of pts remained on treatment; reasons for discontinuation are in the Table. Median duration of exposure was 32.1 (TN), 32.3 (R/R), and 20.5 (IbrI) months (mo). The estimated proportion of pts remaining on treatment at 30mo was 71% (TN), 62% (R/R), and 45% (IbrI). The most common TEAEs are shown in the Table. Serious TEAEs were reported in 42% of pts (TN, 38%; R/R, 50%; IbrI, 25%), including COVID-19 (COV19) (12%), pneumonia (6%), and COV19 pneumonia (5%). TEAEs led to treatment discontinuation in 19% of pts, including COV19 (n=22), COV19 pneumonia (n=9), hepatitis B reactivation (n=5), myalgia (n=3), and pneumonia (n=3). Events of clinical interest are in the Table. Deaths were reported in 65 pts (TN, 7%; R/R, 19%; IbrI, 8%) including TEAE-related deaths (n=56). Most TEAE-related deaths were in pts with COV19 (n=41). Other TEAE-related deaths in pts without COV19 (n=15) included infections/infestations (n=4) and neoplasms (n=4). No new safety risks were identified based on TEAEs or laboratory data. Conclusion(s): In this ASSURE interim analysis, the safety profile of A in pts with CLL (TN, R/R, IbrI) in a real-world setting was consistent with former studies. COV19 TEAEs, including fatal ones, occurred as study enrollment spanned the COV19 pandemic (Niemann CU, et al. Hemasphere. 2022;6(10):e780); rates of cardiac events were low, rates of infection high but manageable with low mortality excluding COV19 deaths; no new safety signals were reported. | Conference Name: | Jahrestagung der Deutschen, Osterreichischen und Schweizerischen Gesellschaften fur Hamatologie und Medizinische Onkologie | Conference Start Date: | 2024-10-11 | Conference End Date: | 2024-10-27 | Conference Location: | Basel, Switzerland | DOI: | http://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1159/000540557 | URI: | https://repository.monashhealth.org/monashhealthjspui/handle/1/52844 | Type: | Conference Abstract | Subjects: | cardiovascular disease chronic lymphatic leukemia coronavirus disease 2019 hepatitis B monotherapy myalgia pandemic pneumonia |
Type of Clinical Study or Trial: | Clinical trial |
Appears in Collections: | Conferences |
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