TY - JOUR
T1 - Time from diagnosis to treatment has no impact on survival in newly diagnosed acute myeloid leukemia treated with venetoclax-based regimens
AU - Baden, David
AU - Zukunft, Sven
AU - Hernandez, Gema
AU - Wolgast, Nadine
AU - Steinhaeuser, Sophie
AU - Pohlmann, Alexander
AU - Schliemann, Christoph
AU - Mikesch, Jan-Henrik
AU - Steffen, Bjoern
AU - Sauer, Tim
AU - Hanoun, Maher
AU - Schaefer-Eckart, Kerstin
AU - Krause, Stefan W.
AU - Haenel, Mathias
AU - Einsele, Hermann
AU - Jost, Edgar
AU - Bruemmendorf, Tim H.
AU - Scholl, Sebastian
AU - Hochhaus, Andreas
AU - Neubauer, Andreas
AU - Burchert, Andreas
AU - Kaufmann, Martin
AU - Niemann, Dirk
AU - Schaich, Markus
AU - Blau, Wolfgang
AU - Kiani, Alexander
AU - Goerner, Martin
AU - Kaiser, Ulrich
AU - Kullmer, Johannes
AU - Weber, Thomas
AU - Berdel, Wolfgang E.
AU - Ehninger, Gerhard
AU - Mueller-Tidow, Carsten
AU - Platzbecker, Uwe
AU - Serve, Hubert
AU - Bornhaeuser, Martin
AU - Roellig, Christoph
AU - Baldus, Claudia D.
AU - Fransecky, Lars
N1 - Schäfer-Eckart: Medical Department 5, University Hospital of Paracelsus Medical
University Nuremberg, Nuremberg, Germany
PY - 2024/8
Y1 - 2024/8
N2 - In newly diagnosed acute myeloid leukemia (AML), immediate initiation of treatment is standard of care. However, deferral of antileukemic therapy may be indicated to assess comorbidities or pretherapeutic risk factors. We explored the impact of time from diagnosis to treatment on outcomes in newly diagnosed AML undergoing venetoclax-based therapy in two distinct cohorts. By querying the Study Alliance Leukemia database and the global health network TriNetX, we identified 138 and 717 patients respectively with an average age of 76 and 72 years who received venetoclax-based first-line therapy. When comparing patients who started treatment earlier or later than 10 days after initial diagnosis, no significant difference in median overall survival was observed- neither in the SAL cohort (7.7 vs . 9.6 months; P =0.42) nor in the TriNetX cohort (7.5 vs . 7.2 months; P =0.41). Similarly, severe infections, bleeding, and thromboembolic events were equally observed between early and later treatments, both in the overall patient groups and specific subgroups (age >= 75 years or leukocytes >= 20x109/L). 9 /L). This retrospective analysis indicates that delaying the start of venetoclax-based therapy in newly diagnosed AML might be a safe option for selected patients, provided that close clinical monitoring is performed.
AB - In newly diagnosed acute myeloid leukemia (AML), immediate initiation of treatment is standard of care. However, deferral of antileukemic therapy may be indicated to assess comorbidities or pretherapeutic risk factors. We explored the impact of time from diagnosis to treatment on outcomes in newly diagnosed AML undergoing venetoclax-based therapy in two distinct cohorts. By querying the Study Alliance Leukemia database and the global health network TriNetX, we identified 138 and 717 patients respectively with an average age of 76 and 72 years who received venetoclax-based first-line therapy. When comparing patients who started treatment earlier or later than 10 days after initial diagnosis, no significant difference in median overall survival was observed- neither in the SAL cohort (7.7 vs . 9.6 months; P =0.42) nor in the TriNetX cohort (7.5 vs . 7.2 months; P =0.41). Similarly, severe infections, bleeding, and thromboembolic events were equally observed between early and later treatments, both in the overall patient groups and specific subgroups (age >= 75 years or leukocytes >= 20x109/L). 9 /L). This retrospective analysis indicates that delaying the start of venetoclax-based therapy in newly diagnosed AML might be a safe option for selected patients, provided that close clinical monitoring is performed.
KW - Chemotherapy
KW - Azacitidine
KW - Initiation
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pmu_pure&SrcAuth=WosAPI&KeyUT=WOS:001381323000012&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.3324/haematol.2024.285225
DO - 10.3324/haematol.2024.285225
M3 - Original Article
C2 - 38654660
SN - 0390-6078
VL - 109
SP - 2469
EP - 2477
JO - HAEMATOLOGICA
JF - HAEMATOLOGICA
IS - 8
ER -