Immune thrombocytopenia in patients with chronic lymphocytic leukemia treated with cladribine-based regiments or chlorambucil - follow-up of PALG-CLL randomized trials
Objectives The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2‐CdA) or chlorambucil and immune thrombocytopenia (IT) has not been yet determined. Methods The records of 777 patients in two randomized Polish Adult Leukemia Group (PALG)‐CLL programs treated wit...
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Published in: | European journal of haematology Vol. 91; no. 1; pp. 1 - 9 |
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01-07-2013
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Abstract | Objectives
The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2‐CdA) or chlorambucil and immune thrombocytopenia (IT) has not been yet determined.
Methods
The records of 777 patients in two randomized Polish Adult Leukemia Group (PALG)‐CLL programs treated with these agents were retrospectively analyzed.
Results
Immune thrombocytopenia occurred in 55 of 777 (7.1%) patients. No significant differences in IT prevalence were seen between patients on chlorambucil or 2‐CdA‐based regiments (P = 0.33). IT developed at a median time of 0.499 yr (0.06–4.8) from the start of CLL therapy. This time was significantly longer in patients treated with chlorambucil (2.03 yr, 95%CI: 0.06–4.22) in relation to patients treated with 2‐CdA‐based regiments (0.52 yr, 95%CI: 0.34–0.69, P = 0.049). Overall survival (OS) of patients with IT and those without IT were similar (2.65 yr vs. 3.2 yr P = 0.23) but the severity of bleeding was more pronounced in the 2‐CdA group. The responses to IT therapy were 35%, 54% and 75% for steroids, chemotherapy and splenectomy, respectively.
Conclusions
In this study, an unexpectedly high percentage of IT incidence was demonstrated in patients with CLL requiring chemotherapy. Although no marked differences were seen in IT frequency in patients treated with 2‐CdA‐based regiments compared to chlorambucil regimen, the clinical course of hemorrhagic diathesis was more severe in 2‐CdA group. Also, the time elapsed from study screening to IT diagnosis was significantly shorter in the 2‐CdA group than in the chlorambucil group suggesting a causative relationship. The appearance of IT did not influence the median time of OS. |
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AbstractList | The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2-CdA) or chlorambucil and immune thrombocytopenia (IT) has not been yet determined. The records of 777 patients in two randomized Polish Adult Leukemia Group (PALG)-CLL programs treated with these agents were retrospectively analyzed. Immune thrombocytopenia occurred in 55 of 777 (7.1%) patients. No significant differences in IT prevalence were seen between patients on chlorambucil or 2-CdA-based regiments (P = 0.33). IT developed at a median time of 0.499 yr (0.06-4.8) from the start of CLL therapy. This time was significantly longer in patients treated with chlorambucil (2.03 yr, 95%CI: 0.06-4.22) in relation to patients treated with 2-CdA-based regiments (0.52 yr, 95%CI: 0.34-0.69, P = 0.049). Overall survival (OS) of patients with IT and those without IT were similar (2.65 yr vs. 3.2 yr P = 0.23) but the severity of bleeding was more pronounced in the 2-CdA group. The responses to IT therapy were 35%, 54% and 75% for steroids, chemotherapy and splenectomy, respectively. In this study, an unexpectedly high percentage of IT incidence was demonstrated in patients with CLL requiring chemotherapy. Although no marked differences were seen in IT frequency in patients treated with 2-CdA-based regiments compared to chlorambucil regimen, the clinical course of hemorrhagic diathesis was more severe in 2-CdA group. Also, the time elapsed from study screening to IT diagnosis was significantly shorter in the 2-CdA group than in the chlorambucil group suggesting a causative relationship. The appearance of IT did not influence the median time of OS. The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2-CdA) or chlorambucil and immune thrombocytopenia (IT) has not been yet determined. The records of 777 patients in two randomized Polish Adult Leukemia Group (PALG)-CLL programs treated with these agents were retrospectively analyzed. Immune thrombocytopenia occurred in 55 of 777 (7.1%) patients. No significant differences in IT prevalence were seen between patients on chlorambucil or 2-CdA-based regiments (P = 0.33). IT developed at a median time of 0.499 yr (0.06-4.8) from the start of CLL therapy. This time was significantly longer in patients treated with chlorambucil (2.03 yr, 95% CI: 0.06-4.22) in relation to patients treated with 2-CdA-based regiments (0.52 yr, 95%CI: 0.34-0.69, P = 0.049). Overall survival (OS) of patients with IT and those without IT were similar (2.65 yr vs. 3.2 yr P = 0.23) but the severity of bleeding was more pronounced in the 2-CdA group. The responses to IT therapy were 35%, 54% and 75% for steroids, chemotherapy and splenectomy, respectively. In this study, an unexpectedly high percentage of IT incidence was demonstrated in patients with CLL requiring chemotherapy. Although no marked differences were seen in IT frequency in patients treated with 2-CdA-based regiments compared to chlorambucil regimen, the clinical course of hemorrhagic diathesis was more severe in 2-CdA group. Also, the time elapsed from study screening to IT diagnosis was significantly shorter in the 2-CdA group than in the chlorambucil group suggesting a causative relationship. The appearance of IT did not influence the median time of OS. Objectives The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2‐CdA) or chlorambucil and immune thrombocytopenia (IT) has not been yet determined. Methods The records of 777 patients in two randomized Polish Adult Leukemia Group (PALG)‐CLL programs treated with these agents were retrospectively analyzed. Results Immune thrombocytopenia occurred in 55 of 777 (7.1%) patients. No significant differences in IT prevalence were seen between patients on chlorambucil or 2‐CdA‐based regiments (P = 0.33). IT developed at a median time of 0.499 yr (0.06–4.8) from the start of CLL therapy. This time was significantly longer in patients treated with chlorambucil (2.03 yr, 95%CI: 0.06–4.22) in relation to patients treated with 2‐CdA‐based regiments (0.52 yr, 95%CI: 0.34–0.69, P = 0.049). Overall survival (OS) of patients with IT and those without IT were similar (2.65 yr vs. 3.2 yr P = 0.23) but the severity of bleeding was more pronounced in the 2‐CdA group. The responses to IT therapy were 35%, 54% and 75% for steroids, chemotherapy and splenectomy, respectively. Conclusions In this study, an unexpectedly high percentage of IT incidence was demonstrated in patients with CLL requiring chemotherapy. Although no marked differences were seen in IT frequency in patients treated with 2‐CdA‐based regiments compared to chlorambucil regimen, the clinical course of hemorrhagic diathesis was more severe in 2‐CdA group. Also, the time elapsed from study screening to IT diagnosis was significantly shorter in the 2‐CdA group than in the chlorambucil group suggesting a causative relationship. The appearance of IT did not influence the median time of OS. OBJECTIVESThe relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2-CdA) or chlorambucil and immune thrombocytopenia (IT) has not been yet determined.METHODSThe records of 777 patients in two randomized Polish Adult Leukemia Group (PALG)-CLL programs treated with these agents were retrospectively analyzed.RESULTSImmune thrombocytopenia occurred in 55 of 777 (7.1%) patients. No significant differences in IT prevalence were seen between patients on chlorambucil or 2-CdA-based regiments (P = 0.33). IT developed at a median time of 0.499 yr (0.06-4.8) from the start of CLL therapy. This time was significantly longer in patients treated with chlorambucil (2.03 yr, 95% CI: 0.06-4.22) in relation to patients treated with 2-CdA-based regiments (0.52 yr, 95%CI: 0.34-0.69, P = 0.049). Overall survival (OS) of patients with IT and those without IT were similar (2.65 yr vs. 3.2 yr P = 0.23) but the severity of bleeding was more pronounced in the 2-CdA group. The responses to IT therapy were 35%, 54% and 75% for steroids, chemotherapy and splenectomy, respectively.CONCLUSIONSIn this study, an unexpectedly high percentage of IT incidence was demonstrated in patients with CLL requiring chemotherapy. Although no marked differences were seen in IT frequency in patients treated with 2-CdA-based regiments compared to chlorambucil regimen, the clinical course of hemorrhagic diathesis was more severe in 2-CdA group. Also, the time elapsed from study screening to IT diagnosis was significantly shorter in the 2-CdA group than in the chlorambucil group suggesting a causative relationship. The appearance of IT did not influence the median time of OS. |
Author | Kowal, Malgorzata Nowak, Wieslaw Robak, Tadeusz Dmoszynska, Anna Trelinski, Jacek Sulek, Kazimierz Wiater, Elzbieta Chojnowski, Krzysztof Kuliczkowski, Kazimierz Kostyra, Aleksandra Kloczko, Janusz Blonski, Jerzy Z. Stella-Holowiecka, Beata Dwilewicz-Trojaczek, Jadwiga Potoczek, Stanislaw Seferynska, Ilona Calbecka, Malgorzata Skotnicki, Aleksander Mital, Andrzej Gora-Tybor, Joanna Warzocha, Krzysztof Hellmann, Andrzej Lewandowski, Krzysztof Ceglarek, Bernadetta Zawilska, Krystyna |
Author_xml | – sequence: 1 givenname: Jerzy Z. surname: Blonski fullname: Blonski, Jerzy Z. organization: Department of Hematology, Medical University of Lodz, Lodz, Poland – sequence: 2 givenname: Tadeusz surname: Robak fullname: Robak, Tadeusz email: robaktad@csk.umed.lodz.pl organization: Department of Hematology, Medical University of Lodz, Lodz, Poland – sequence: 3 givenname: Krzysztof surname: Chojnowski fullname: Chojnowski, Krzysztof organization: Department of Hematology, Medical University of Lodz, Lodz, Poland – sequence: 4 givenname: Joanna surname: Gora-Tybor fullname: Gora-Tybor, Joanna organization: Department of Hematology, Medical University of Lodz, Lodz, Poland – sequence: 5 givenname: Krzysztof surname: Warzocha fullname: Warzocha, Krzysztof organization: Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland – sequence: 6 givenname: Bernadetta surname: Ceglarek fullname: Ceglarek, Bernadetta organization: Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland – sequence: 7 givenname: Ilona surname: Seferynska fullname: Seferynska, Ilona organization: Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland – sequence: 8 givenname: Malgorzata surname: Calbecka fullname: Calbecka, Malgorzata organization: Department of Hematology, City Hospital, Torun, Poland – sequence: 9 givenname: Aleksandra surname: Kostyra fullname: Kostyra, Aleksandra organization: Department of Hematology, City Hospital, Torun, Poland – sequence: 10 givenname: Beata surname: Stella-Holowiecka fullname: Stella-Holowiecka, Beata organization: Department of Hematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland – sequence: 11 givenname: Janusz surname: Kloczko fullname: Kloczko, Janusz organization: Department of Hematology, Medical University, Bialystok, Poland – sequence: 12 givenname: Anna surname: Dmoszynska fullname: Dmoszynska, Anna organization: Department of Hematooncology and Bone Marrow Transplantation, Medical University, Lublin, Poland – sequence: 13 givenname: Malgorzata surname: Kowal fullname: Kowal, Malgorzata organization: Department of Hematooncology and Bone Marrow Transplantation, Medical University, Lublin, Poland – sequence: 14 givenname: Krzysztof surname: Lewandowski fullname: Lewandowski, Krzysztof organization: Department of Hematology, University of Medical Sciences, Poznan, Poland – sequence: 15 givenname: Jadwiga surname: Dwilewicz-Trojaczek fullname: Dwilewicz-Trojaczek, Jadwiga organization: Department of Hematology, Oncology and Internal Diseases, Warsaw Medical University, Warsaw, Poland – sequence: 16 givenname: Elzbieta surname: Wiater fullname: Wiater, Elzbieta organization: Department of Hematology, Oncology and Internal Diseases, Warsaw Medical University, Warsaw, Poland – sequence: 17 givenname: Kazimierz surname: Kuliczkowski fullname: Kuliczkowski, Kazimierz organization: Department of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw, Poland – sequence: 18 givenname: Stanislaw surname: Potoczek fullname: Potoczek, Stanislaw organization: Department of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw, Poland – sequence: 19 givenname: Andrzej surname: Hellmann fullname: Hellmann, Andrzej organization: Department of Hematology and Transplantology, Medical University of Gdansk, Gdansk, Poland – sequence: 20 givenname: Andrzej surname: Mital fullname: Mital, Andrzej organization: Department of Hematology and Transplantology, Medical University of Gdansk, Gdansk, Poland – sequence: 21 givenname: Aleksander surname: Skotnicki fullname: Skotnicki, Aleksander organization: Department of Hematology, Jagiellonian University, Krakow, Poland – sequence: 22 givenname: Wieslaw surname: Nowak fullname: Nowak, Wieslaw organization: Department of Hematology, Jagiellonian University, Krakow, Poland – sequence: 23 givenname: Kazimierz surname: Sulek fullname: Sulek, Kazimierz organization: Department of Internal Medicine, Military Institute of Medicine, Warsaw, Poland – sequence: 24 givenname: Krystyna surname: Zawilska fullname: Zawilska, Krystyna organization: Department of Hematology and Internal Diseases, Strus Hospital, Poznan, Poland – sequence: 25 givenname: Jacek surname: Trelinski fullname: Trelinski, Jacek organization: Department of Hematology, Medical University of Lodz, Lodz, Poland |
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The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2‐CdA) or chlorambucil and immune thrombocytopenia (IT)... The relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2-CdA) or chlorambucil and immune thrombocytopenia (IT) has not been... OBJECTIVESThe relationship between treatments of chronic lymphocytic leukemia (CLL) with cladribine (2-CdA) or chlorambucil and immune thrombocytopenia (IT)... |
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Title | Immune thrombocytopenia in patients with chronic lymphocytic leukemia treated with cladribine-based regiments or chlorambucil - follow-up of PALG-CLL randomized trials |
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