Effectiveness and safety of primary prophylaxis with G-CSF after induction therapy for acute myeloid leukemia : a systematic review and meta-analysis of the clinical practice guidelines for the use of G-CSF 2022 from the Japan society of clinical oncology
© 2024. The Author(s)..
Although granulocyte colony-stimulating factor (G-CSF) reduces the incidence, duration, and severity of neutropenia, its prophylactic use for acute myeloid leukemia (AML) remains controversial due to a theoretically increased risk of relapse. The present study investigated the effects of G-CSF as primary prophylaxis for AML with remission induction therapy. A detailed literature search for related studies was performed using PubMed, Ichushi-Web, and the Cochrane Library. Data were independently extracted and assessed by two reviewers. A qualitative analysis of pooled data was conducted, and the risk ratio with corresponding confidence intervals was calculated in the meta-analysis and summarized. Sixteen studies were included in the qualitative analysis, nine of which were examined in the meta-analysis. Although G-CSF significantly shortened the duration of neutropenia, primary prophylaxis with G-CSF did not correlate with infection-related mortality. Moreover, primary prophylaxis with G-CSF did not affect disease progression/recurrence, overall survival, or adverse events, such as musculoskeletal pain. However, evidence to support or discourage the use of G-CSF as primary prophylaxis for adult AML patients with induction therapy remains limited. Therefore, the use of G-CSF as primary prophylaxis can be considered for adult AML patients with remission induction therapy who are at a high risk of infectious complications.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:29 |
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Enthalten in: |
International journal of clinical oncology - 29(2024), 5 vom: 15. Apr., Seite 535-544 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Maeda, Tomoya [VerfasserIn] |
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Links: |
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Themen: |
143011-72-7 |
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Anmerkungen: |
Date Completed 24.04.2024 Date Revised 27.04.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1007/s10147-023-02465-0 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM369842642 |
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245 | 1 | 0 | |a Effectiveness and safety of primary prophylaxis with G-CSF after induction therapy for acute myeloid leukemia |b a systematic review and meta-analysis of the clinical practice guidelines for the use of G-CSF 2022 from the Japan society of clinical oncology |
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500 | |a Citation Status MEDLINE | ||
520 | |a © 2024. The Author(s). | ||
520 | |a Although granulocyte colony-stimulating factor (G-CSF) reduces the incidence, duration, and severity of neutropenia, its prophylactic use for acute myeloid leukemia (AML) remains controversial due to a theoretically increased risk of relapse. The present study investigated the effects of G-CSF as primary prophylaxis for AML with remission induction therapy. A detailed literature search for related studies was performed using PubMed, Ichushi-Web, and the Cochrane Library. Data were independently extracted and assessed by two reviewers. A qualitative analysis of pooled data was conducted, and the risk ratio with corresponding confidence intervals was calculated in the meta-analysis and summarized. Sixteen studies were included in the qualitative analysis, nine of which were examined in the meta-analysis. Although G-CSF significantly shortened the duration of neutropenia, primary prophylaxis with G-CSF did not correlate with infection-related mortality. Moreover, primary prophylaxis with G-CSF did not affect disease progression/recurrence, overall survival, or adverse events, such as musculoskeletal pain. However, evidence to support or discourage the use of G-CSF as primary prophylaxis for adult AML patients with induction therapy remains limited. Therefore, the use of G-CSF as primary prophylaxis can be considered for adult AML patients with remission induction therapy who are at a high risk of infectious complications | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Najima, Yuho |e verfasserin |4 aut | |
700 | 1 | |a Kamiyama, Yutaro |e verfasserin |4 aut | |
700 | 1 | |a Nakao, Shinji |e verfasserin |4 aut | |
700 | 1 | |a Ozaki, Yukinori |e verfasserin |4 aut | |
700 | 1 | |a Nishio, Hiroshi |e verfasserin |4 aut | |
700 | 1 | |a Tsuchihashi, Kenji |e verfasserin |4 aut | |
700 | 1 | |a Ichihara, Eiki |e verfasserin |4 aut | |
700 | 1 | |a Miumra, Yuji |e verfasserin |4 aut | |
700 | 1 | |a Endo, Makoto |e verfasserin |4 aut | |
700 | 1 | |a Maruyama, Dai |e verfasserin |4 aut | |
700 | 1 | |a Yoshinami, Tatsuhiro |e verfasserin |4 aut | |
700 | 1 | |a Susumu, Nobuyuki |e verfasserin |4 aut | |
700 | 1 | |a Takekuma, Munetaka |e verfasserin |4 aut | |
700 | 1 | |a Motohashi, Takashi |e verfasserin |4 aut | |
700 | 1 | |a Ito, Mamoru |e verfasserin |4 aut | |
700 | 1 | |a Baba, Eishi |e verfasserin |4 aut | |
700 | 1 | |a Ochi, Nobuaki |e verfasserin |4 aut | |
700 | 1 | |a Kubo, Toshio |e verfasserin |4 aut | |
700 | 1 | |a Uchino, Keita |e verfasserin |4 aut | |
700 | 1 | |a Kimura, Takahiro |e verfasserin |4 aut | |
700 | 1 | |a Tamura, Shinobu |e verfasserin |4 aut | |
700 | 1 | |a Nishimoto, Hitomi |e verfasserin |4 aut | |
700 | 1 | |a Kato, Yasuhisa |e verfasserin |4 aut | |
700 | 1 | |a Sato, Atsushi |e verfasserin |4 aut | |
700 | 1 | |a Takano, Toshimi |e verfasserin |4 aut | |
700 | 1 | |a Yano, Shingo |e verfasserin |4 aut | |
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