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G-CSF 與 pegfilgrastim
G-CSF / Pegfilgrastim
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
- Primary prophylaxis for chemo with FN risk ≥20 %.
- Secondary prophylaxis for previously febrile cycle.
- Stem cell mobilization (autologous / allogeneic).
- Severe neutropenia in MDS / AA / cyclic neutropenia / chronic idiopathic neutropenia.
- Adjunct in serious FN with infection-related complications (high-risk pts; per ASCO 2015).
- 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
- Febrile Neutropenia — primary use
- Hematopoiesis + mobilization
- Auto-HCT — G-CSF mobilization
- HL — bleomycin avoidance
- Drug Regimens — filgrastim, pegfilgrastim, plerixafor
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
-
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. ↩