# Factors Influencing the Use of G-CSF in Drug-Induced Agranulocytosis

**Authors:** Emmanuel Andrès, Jean-Edouard Terrade, Xavier Jannot, Noel Lorenzo-Villalba

PMC · DOI: 10.3390/hematolrep18010014 · Hematology Reports · 2026-02-03

## TL;DR

This review discusses factors affecting the use of G-CSF in treating drug-induced agranulocytosis, a rare but dangerous condition.

## Contribution

The paper provides a comprehensive review of factors influencing G-CSF use and highlights gaps in clinical trial evidence.

## Key findings

- G-CSF reduces neutropenia duration and hospitalization in drug-induced agranulocytosis.
- Mortality impact of G-CSF remains uncertain despite observational evidence.
- Treatment decisions should consider neutrophil count, infection severity, age, and comorbidities.

## Abstract

Drug-induced agranulocytosis is a rare but life-threatening adverse reaction associated with numerous non-chemotherapy drugs. Management relies on immediate drug withdrawal, infection control, and, in selected patients, administration of granulocyte-colony stimulating factor (G-CSF). This review summarizes current knowledge on the determinants of epidemiology, clinical presentation, hematologic and biologic features, comorbidities, and outcomes influencing the decision to introduce G-CSF in drug-induced agranulocytosis. Evidence from observational studies and meta-analyses suggests that G-CSF shortens neutropenia duration and hospitalization, although its impact on mortality remains uncertain. The decision to use G-CSF should consider initial neutrophil count, presence of severe infection or sepsis, age, and comorbidities. Despite the accumulated experience, randomized controlled trials are still lacking, and treatment algorithms remain empirical.

## Full-text entities

- **Genes:** CYP2C19 (cytochrome P450 family 2 subfamily C member 19) [NCBI Gene 1557] {aka CPCJ, CYP2C, CYPIIC17, CYPIIC19, P450C2C, P450IIC19}, CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119] {aka CELIAC1, HLA-DQB, IDDM1}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, MPO (myeloperoxidase) [NCBI Gene 4353], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, CSF3R (colony stimulating factor 3 receptor) [NCBI Gene 1441] {aka CD114, GCSFR, SCN7}
- **Diseases:** acute lung injury (MESH:D055371), pancytopenia (MESH:D010198), diabetes (MESH:D003920), psychiatric (MESH:D001523), mitochondrial dysfunction (MESH:D028361), bone pain (MESH:D010146), injury to (MESH:D014947), inflammatory (MESH:D007249), Agranulocytosis (MESH:D000380), hepatic dysfunction (MESH:D008107), fever (MESH:D005334), MDS (MESH:D009190), AML (MESH:D015470), pneumonia (MESH:D011014), multi-organ failure (MESH:D009102), ulcerations (MESH:D014456), capillary leak syndrome (MESH:D019559), cytotoxic (MESH:D064420), Bacteremia (MESH:D016470), thrombocytopenia (MESH:D013921), cardiovascular disease (MESH:D002318), infection (MESH:D007239), sore throat (MESH:D010612), neutropenia (MESH:D009503), Mortality (MESH:D003643), toxic suppression of myelopoiesis (MESH:C563551), sepsis (MESH:D018805), infectious (MESH:D003141), febrile neutropenia (MESH:D064147), septic (MESH:D001170), erythema (MESH:D004890), septic shock (MESH:D012772), Anaemia (MESH:D000743), splenic enlargement (MESH:D013158), Renal impairment (MESH:D007674), mucositis (MESH:D052016), DIA (MESH:D000081015)
- **Chemicals:** sulfonamides (MESH:D013449), oxygen (MESH:D010100), Clozapine (MESH:D003024), methimazole (MESH:D008713), cefepime (MESH:D000077723), propylthiouracil (MESH:D011441), carbapenems (MESH:D015780), vancomycin (MESH:D014640), piperacillin-tazobactam (MESH:D000077725), Metamizole (MESH:D004177), DIA (-), beta-lactams (MESH:D047090), cotrimoxazole (MESH:D015662)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280]

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921758/full.md

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Source: https://tomesphere.com/paper/PMC12921758