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Adverse Events in 1406 Patients Receiving 13,780 Cycles of Azacitidine within the Austrian Registry of Hypomethylating Agents-A Prospective Cohort Study of the AGMT Study-Group.
Leisch, Michael; Pfeilstöcker, Michael; Stauder, Reinhard; Heibl, Sonja; Sill, Heinz; Girschikofsky, Michael; Stampfl-Mattersberger, Margarete; Tinchon, Christoph; Hartmann, Bernd; Petzer, Andreas; Schreder, Martin; Kiesl, David; Vallet, Sonia; Egle, Alexander; Melchardt, Thomas; Piringer, Gudrun; Zebisch, Armin; Machherndl-Spandl, Sigrid; Wolf, Dominik; Keil, Felix; Drost, Manuel; Greil, Richard; Pleyer, Lisa.
Afiliação
  • Leisch M; 3rd Medical Department with Hematology, Medical Oncology, Rheumatology and Infectiology, Paracelsus Medical University, 5020 Salzburg, Austria.
  • Pfeilstöcker M; Salzburg Cancer Research Institute (SCRI) Center for Clinical Cancer and Immunology Trials (CCCIT), Cancer Cluster Salzburg (CCS), 5020 Salzburg, Austria.
  • Stauder R; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Heibl S; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Sill H; 3rd Medical Department for Haematology and Oncology, Hanusch Hospital, 1140 Vienna, Austria.
  • Girschikofsky M; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Stampfl-Mattersberger M; Department of Internal Medicine V, Innsbruck Medical University, 6020 Innsbruck, Austria.
  • Tinchon C; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Hartmann B; 4th Medical Department of Internal Medicine, Hematology, Internistic Oncology and Palliative Medicine, Klinikum Wels-Grieskirchen GmbH, 4600 Wels, Austria.
  • Petzer A; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Schreder M; Division of Hematology, Medical University of Graz, 8036 Graz, Austria.
  • Kiesl D; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Vallet S; 1st Medical Department, Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz GmbH Elisabethinen, 4020 Linz, Austria.
  • Egle A; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Melchardt T; Department of Internal Medicine 2, Klinik Donaustadt, 1220 Vienna, Austria.
  • Piringer G; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Zebisch A; Department for Hemato-Oncology, LKH Hochsteiermark, 8700 Leoben, Austria.
  • Machherndl-Spandl S; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Wolf D; Department of Internal Medicine, Landeskrankenhaus Feldkirch, 6800 Feldkirch, Austria.
  • Keil F; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Drost M; Medical Oncology and Hematology, Internal Medicine I, Ordensklinikum Linz GmbH Barmherzige Schwestern, 4020 Linz, Austria.
  • Greil R; Austrian Group of Medical Tumor Therapy (AGMT) Study Group, 1140 Vienna, Austria.
  • Pleyer L; 1st Department of Internal Medicine, Center for Oncology and Hematology, Klinik Ottakring, 1160 Vienna, Austria.
Cancers (Basel) ; 14(10)2022 May 17.
Article em En | MEDLINE | ID: mdl-35626063
Background: Azacitidine is the treatment backbone for patients with acute myeloid leukemia, myelodysplastic syndromes and chronic myelomonocytic leukemia who are considered unfit for intensive chemotherapy. Detailed reports on adverse events in a real-world setting are lacking. Aims: To analyze the frequency of adverse events in the Austrian Registry of Hypomethylating agents. To compare real-world data with that of published randomized clinical trials. Results: A total of 1406 patients uniformly treated with a total of 13,780 cycles of azacitidine were analyzed. Hematologic adverse events were the most common adverse events (grade 3-4 anemia 43.4%, grade 3-4 thrombopenia 36.8%, grade 3-4 neutropenia 36.1%). Grade 3-4 anemia was significantly more common in the Registry compared to published trials. Febrile neutropenia occurred in 33.4% of patients and was also more common in the Registry than in published reports. Other commonly reported adverse events included fatigue (33.4%), pain (29.2%), pyrexia (23.5%), and injection site reactions (23.2%). Treatment termination due to an adverse event was rare (5.1%). Conclusion: The safety profile of azacitidine in clinical trials is reproducible in a real-world setting. With the use of prophylactic and concomitant medications, adverse events can be mitigated and azacitidine can be safely administered to almost all patients with few treatment discontinuations.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article