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Optimal timing of prophylactic pegylated G-CSF after chemotherapy administration for patients with cancer: a systematic review and meta-analysis from Clinical Practice Guidelines for the use of G-CSF 2022.
Ozaki, Yukinori; Yokoe, Takamichi; Yoshinami, Tetsuhiro; Nozawa, Kazuki; Nishio, Hiroshi; Tsuchihashi, Kenji; Ichihara, Eiki; Miura, Yuji; Endo, Makoto; Yano, Shingo; Maruyama, Dai; Susumu, Nobuyuki; Takekuma, Munetaka; Motohashi, Takashi; Ito, Mamoru; Baba, Eishi; Ochi, Nobuaki; Kubo, Toshio; Uchino, Keita; Kimura, Takahiro; Kamiyama, Yutaro; Nakao, Shinji; Tamura, Shinobu; Nishimoto, Hitomi; Kato, Yasuhisa; Sato, Atsushi; Takano, Toshimi.
Afiliação
  • Ozaki Y; Department of Breast Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, 3-8-31, Araike, Kotou-Ku, Tokyo, Japan. yukinori.ozaki@jfcr.or.jp.
  • Yokoe T; Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
  • Yoshinami T; Department of Breast and Endocrine Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.
  • Nozawa K; Department of Center for Cancer Genomics and Advanced Therapeutics, Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Nishio H; Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
  • Tsuchihashi K; Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Ichihara E; Center for Clinical Oncology, Okayama University Hospital, Okayama, Japan.
  • Miura Y; Department of Medical Oncology, Toranomon Hospital, Tokyo, Japan.
  • Endo M; Department of Orthopaedic Surgery, Kyushu University, Fukuoka, Japan.
  • Yano S; Division of Clinical Oncology/Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
  • Maruyama D; Department of Hematology Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Susumu N; Department of Obstetrics and Gynecology, International University of Health and Welfare Narita Hospital, Chiba, Japan.
  • Takekuma M; Department of Gynecology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Motohashi T; Department of Obstetrics and Gynecology, Tokyo Women's Medical University Hospital, Tokyo, Japan.
  • Ito M; Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Baba E; Department of Oncology and Social Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Ochi N; Department of General Internal Medicine 4, Kawasaki Medical School, Okayama, Japan.
  • Kubo T; Department of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
  • Uchino K; Department of Medical Oncology, NTT Medical Center Tokyo, Tokyo, Japan.
  • Kimura T; Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
  • Kamiyama Y; Department of Clinical Oncology/Hematology, The Jikei University School of Medicine, Tokyo, Japan.
  • Nakao S; Department of Hematology, Faculty of Medicine, Institute of Medical Pharmaceutical and Health Sciences, Kanazawa University, Ishikawa, Japan.
  • Tamura S; Department of Hematology/Oncology, Wakayama Medical University, Wakayama, Japan.
  • Nishimoto H; Department of Nursing, Okayama University Hospital, Okayama, Japan.
  • Kato Y; Department of Drug Information, Faculty of Pharmaceutical Sciences, Shonan University of Medical Sciences, Kanagawa, Japan.
  • Sato A; Department of Medical Oncology, Hirosaki University Graduate School of Medicine, Aomori, Japan.
  • Takano T; Department of Breast Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, 3-8-31, Araike, Kotou-Ku, Tokyo, Japan.
Int J Clin Oncol ; 29(5): 551-558, 2024 May.
Article em En | MEDLINE | ID: mdl-38526621
ABSTRACT

INTRODUCTION:

The timing of prophylactic pegylated granulocyte colony-stimulating factor (G-CSF) administration during cancer chemotherapy varies, with Day 2 and Days 3-5 being the most common schedules. Optimal timing remains uncertain, affecting efficacy and adverse events. This systematic review sought to evaluate the available evidence on the timing of prophylactic pegylated G-CSF administration.

METHODS:

Based on the Minds Handbook for Clinical Practice Guideline Development, we searched the PubMed, Ichushi-Web, and Cochrane Library databases for literature published from January 1990 to December 2019. The inclusion criteria included studies among the adult population using pegfilgrastim. The search strategy focused on timing-related keywords. Two reviewers independently extracted and assessed the data.

RESULTS:

Among 300 initial search results, only four articles met the inclusion criteria. A meta-analysis for febrile neutropenia incidence suggested a potential higher incidence when pegylated G-CSF was administered on Days 3-5 than on Day 2 (odds ratio 1.27, 95% CI 0.66-2.46, p = 0.47), with a moderate certainty of evidence. No significant difference in overall survival or mortality due to infections was observed. The trend of severe adverse events was lower on Days 3-5, without statistical significance (odds ratio 0.72, 95% CI 0.14-3.67, p = 0.69) and with a moderate certainty of evidence. Data on pain were inconclusive.

CONCLUSIONS:

Both Day 2 and Days 3-5 were weakly recommended for pegylated G-CSF administration post-chemotherapy in patients with cancer. The limited evidence highlights the need for further research to refine recommendations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator Estimulador de Colônias de Granulócitos / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator Estimulador de Colônias de Granulócitos / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article