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Comparison between a single dose of PEG G-CSF and multiple doses of non-PEG G-CSF: a systematic review and meta-analysis from Clinical Practice Guidelines for the use of G-CSF 2022

  • Tetsuhiro Yoshinami,
  • Kazuki Nozawa,
  • Takamichi Yokoe,
  • Yukinori Ozaki,
  • Hiroshi Nishio,
  • Kenji Tsuchihashi,
  • Eiki Ichihara,
  • Yuji Miura,
  • Makoto Endo,
  • Shingo Yano,
  • Dai Maruyama,
  • Nobuyuki Susumu,
  • Munetaka Takekuma,
  • Takashi Motohashi,
  • Mamoru Ito,
  • Eishi Baba,
  • Nobuaki Ochi,
  • Toshio Kubo,
  • Keita Uchino,
  • Takahiro Kimura,
  • Yutaro Kamiyama,
  • Shinji Nakao,
  • Shinobu Tamura,
  • Hitomi Nishimoto,
  • Yasuhisa Kato,
  • Atsushi Sato,
  • Toshimi Takano

摘要

Backgroud

Granulocyte colony-stimulating factor (G-CSF) is widely used for the primary prophylaxis of febrile neutropenia (FN). Two types of G-CSF are available in Japan, namely G-CSF chemically bound to polyethylene glycol (PEG G-CSF), which provides long-lasting effects with a single dose, and non-polyethylene glycol-bound G-CSF (non-PEG G-CSF), which must be sequentially administrated for several days.

Methods

This current study investigated the utility of these treatments for the primary prophylaxis of FN through a systematic review of the literature. 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 or meta-analysis was conducted to evaluate six outcomes.

Results

Through the first and second screenings, 23 and 18 articles were extracted for qualitative synthesis and meta-analysis, respectively. The incidence of FN was significantly lower in the PEG G-CSF group than in the non-PEG G-CSF group with a strong quality/certainty of evidence. The differences in other outcomes, such as overall survival, infection-related mortality, the duration of neutropenia (less than 500/μL), quality of life, and pain, were not apparent.

Conclusions

A single dose of PEG G-CSF is strongly recommended over multiple-dose non-PEG G-CSF therapy for the primary prophylaxis of FN.