heme101
跨領域 › 支持療護

G-CSF 與 pegfilgrastim

G-CSF / Pegfilgrastim
跨領域 未策展 更新 2026-08-02

概覽

Buzzwords → Dx

Concept Detail
Filgrastim rhG-CSF; daily SC 5 µg/kg/d; short-acting
Pegfilgrastim Long-acting; 6 mg SC once per cycle (24 h post-chemo, ≥24 h before next chemo)
Tbo-filgrastim, eflapegrastim Biosimilars / next-generation
Sargramostim (GM-CSF) Different agent; approved for AML post-induction (less common)
FN risk >20 % Indication for primary G-CSF prophylaxis (e.g., regimens with high myelosuppression)
FN risk 10-20 % + risk factors Consider primary prophylaxis (age >65, prior chemo, CHF, CKD, mucositis, baseline neutropenia, comorbid)
Secondary prophylaxis After FN with prior cycle
Stem cell mobilization G-CSF 10 µg/kg/d × 5 d (autologous); + plerixafor for hard-to-mobilize
Allogeneic donor mobilization G-CSF 10 µg/kg/d × 5 d → apheresis day 5
Bone pain Most common AE; treat with NSAIDs / loratadine (NSAIDs ASCO recommended)
Spleen rupture Rare but serious AE — esp. mobilization
G-CSF + bleomycin Synergistic pulmonary toxicity — avoid concurrent
Adjunct in FN with sepsis / pneumonia / fungal Limited indication; reduces FN duration but not survival

分類與診斷

Workup before initiation

  • Cancer + chemo regimen FN risk assessment.
  • Risk factors: age >65, prior chemo / RT, baseline cytopenia, mucositis, CHF, CKD, infection.
  • Schedule: start 24–72 h post-chemo; pegfilgrastim ≥24 h before next chemo cycle.

治療

Indications

  1. Primary prophylaxis for chemo with FN risk ≥20 %.
  2. Secondary prophylaxis for previously febrile cycle.
  3. Stem cell mobilization (autologous / allogeneic).
  4. Severe neutropenia in MDS / AA / cyclic neutropenia / chronic idiopathic neutropenia.
  5. Adjunct in serious FN with infection-related complications (high-risk pts; per ASCO 2015).
  6. Marrow transplant to accelerate engraftment.

Treatment Algorithm

flowchart TD
  A[Chemotherapy planned] --> B[Calculate FN risk per regimen]
  B --> C{FN risk?}
  C -- ≥20% --> D[Primary G-CSF prophylaxis<br>filgrastim daily or pegfilgrastim per cycle]
  C -- 10-20% with risk factors --> D
  C -- <10% --> E[No primary ppx<br>monitor; secondary if FN occurs]
  E -- FN occurs --> F[Add secondary G-CSF prophylaxis next cycle]
  D --> G{Concurrent radiation to mediastinum / chest?}
  G -- yes --> H[Avoid G-CSF during RT; reactive pneumonitis risk<br>esp. with bleomycin]
  G -- no --> I[Standard G-CSF dosing]
  D --> J{Stem cell mobilization}
  J -- autologous --> K[G-CSF 10 µg/kg/d × 5 d<br>± plerixafor for hard-to-mobilize]
  J -- allogeneic donor --> L[G-CSF 10 µg/kg/d × 5 d]

陷阱與考點

Pearls / Pitfalls

  • G-CSF + bleomycin → synergistic pulmonary toxicity — avoid concurrent. Modern HL regimens often omit bleomycin if PET-2 negative (RATHL).
  • Pegfilgrastim must be given ≥24 h post-chemo AND ≥14 d before next chemo — premature dosing risks myelosuppression accumulation.
  • Bone pain is most common AE — treat with loratadine or NSAIDs (often more effective than opioids; ASCO recommends).
  • G-CSF for AML / MDS in remission: avoided in active disease (theoretical leukemia stimulation); used post-induction once recovery starts.
  • Avoid in CML / aggressive MDS (theoretical risk of myeloid clone stimulation).
  • Spleen rupture is rare but reported with mobilization — counsel about LUQ pain.
  • Mobilization failure (<2 × 10⁶ CD34+/kg) — plerixafor (CXCR4 antagonist) added to G-CSF rescues most.
  • Severe chronic neutropenia (Kostmann syndrome, cyclic, CIN) — chronic low-dose G-CSF effective; monitor for MDS/AML evolution.
  • G-CSF in FN sepsis — adjunctive role per ASCO 2015 in high-risk FN with serious complications; not routine.
  • Pegfilgrastim on-body injector (Onpro) — automated 27 h post-chemo delivery; alternative to clinic visits.

延伸

Cross-references

相關題目

  • Q-196 — G-CSF — primary prophylaxis indication
  • Q-197 — G-CSF + bleomycin combination
  • Q-198 — G-CSF — bone pain management

來源

Sources

Footnotes

  1. Smith TJ, Bohlke K, Lyman GH, et al. Recommendations for the Use of WBC Growth Factors: ASCO Clinical Practice Guideline Update. Journal of Clinical Oncology 2015;33(28):3199–3212. doi:10.1200/JCO.2015.62.3488.