Filgrastim improves survival in lethally irradiated nonhuman primates
Open accessAbstract
Leukocyte growth factors (LGF), such as filgrastim, pegfilgrastim and sargramostim, have been used to mitigate the hematologic symptoms of acute radiation syndrome (ARS) after radiation accidents. Although these pharmaceuticals are currently approved for treatment of chemotherapy-induced myelosuppression, such approval has not been granted for myelosuppression resulting from acute radiation exposure. Regulatory approval of drugs used to treat radiological or nuclear exposure injuries requires their development and testing in accordance with the Animal Efficacy Rule, set forth by the U.S. Food and Drug Administration. To date, filgrastim is the only LGF that has undergone efficacy assessment conducted under the Animal Efficacy Rule. To confirm the efficacy of another LGF with a shorter dosing regimen compared to filgrastim, we evaluated the use of pegfilgrastim (Neulasta(®)) in a lethal nonhuman primate (NHP) model of hematopoietic acute radiation syndrome (H-ARS). Rhesus macaques were exposed to 7.50 Gy total-body irradiation (the LD(50/60)), delivered at 0.80 Gy/min using linear accelerator 6 MV photons. Pegfilgrastim (300 μg/kg, n = 23) or 5% dextrose in water (n = 23) was administered on day 1 and 8 postirradiation and all animals received medical management. Hematologic and physiologic parameters were evaluated for 60 days postirradiation. The primary, clinically relevant end point was survival to day 60; secondary end points included hematologic-related parameters. Pegfilgrastim significantly (P = 0.0014) increased 60 day survival to 91.3% (21/23) from 47.8% (11/23) in the control. Relative to the controls, pegfilgrastim also significantly: 1. decreased the median duration of neutropenia and thrombocytopenia; 2. improved the median time to recovery of absolute neutrophil count (ANC) ≥500/μL, ANC ≥1,000/μL and platelet (PLT) count ≥20,000/μL; 3. increased the mean ANC at nadir; and 4. decreased the incidence of Gram-negative bacteremia. These data demonstrate that pegfilgrastim is an additional medical countermeasure capable of increasing survival and neutrophil-related parameters when administered in an abbreviated schedule to a NHP model of lethal H-ARS.
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The observed improvement in survival with Neupogen was associated with a significantly shortened duration of neutropenia (approximately 19.7 days versus 25.8 days in Neupogen versus vehicle arms, p < 0.0001).
“The observed improvement in survival was associated with significantly shortened duration of neutropenia (~19.7 days versus 25.8 days in Neupogen vs. vehicle arms respectively, p < 0.0001), and no significant effect on the onset, severity, or duration of thrombocytopenia (Farese et al., 2013).”
From Medical countermeasures for the hematopoietic-subsyndrome of acute radiation syndrome in space (2022) · cites this paper as Farese et al., 2013
The Results, under Neutrophil-Related Parameters, report that Neupogen significantly shortened neutropenia, but its duration was 14.3 versus 18.6 days at ANC <500 cells/μL. The cited 19.7 versus 25.8 days (P < 0.0001) measure time to recovery above ANC 1,000 cells/μL, not duration of neutropenia. The Platelet-Related Parameters results also support the sentence’s statement that the measured thrombocytopenia differences were not significant. (LLM, conf=0.92)
Experimental — accuracy not yet measuredTreatment with Neupogen led to a 38.3% reduction in mortality (from 59.1% to 20.8%) compared to the control arm.
“Treatment with Neupogen®led to a 38.3% reduction in mortality (59.1% to 20.8%) when compared to the control arm (Farese et al., 2013).”
From Medical countermeasures for the hematopoietic-subsyndrome of acute radiation syndrome in space (2022) · cites this paper as Farese et al., 2013
Neupogen had no significant effect on the onset, severity, or duration of thrombocytopenia.
“The observed improvement in survival was associated with significantly shortened duration of neutropenia (~19.7 days versus 25.8 days in Neupogen vs. vehicle arms respectively, p < 0.0001), and no significant effect on the onset, severity, or duration of thrombocytopenia (Farese et al., 2013).”
From Medical countermeasures for the hematopoietic-subsyndrome of acute radiation syndrome in space (2022) · cites this paper as Farese et al., 2013
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References 110 · Cited by 187
Research works printed but not linked: 4
- [1]Biological effects of radiation injury Miamisburg (OH) AlphaMed Press 1997
- [2]Ricks RC Fry SA The medical basis for radiation accident preparedness II: Clinical experience and follow-up since 1979 New York Elsevier Science Inc. 1990
- [15]MacVittie TJ Monroy RL Potential improvement in the management of seriously irradiated person Ricks RC Fry SA The medical basis for radiation accident preparedness II: Clinical experience and follow-up since 1979 New York Elsevier 1990 121 147
- [54]Dalrymple GV Lindsay IR Ghidoni JJ The effect of 2-Mev whole-body x-irradiation on primates Radiat Res 1965 25 377 400 14295128
- Authors
- Farese, A. M., Cohen, M. V., Katz, B. P., Smith, C. P., Gibbs, A., Cohen, D. M., & MacVittie, T. J.
- Affiliations
- University of Maryland, Baltimore (US)
- Indiana University School of Medicine (US)
- Corresponding author
- Farese, Ann M.
- Venue
- Radiation Research
- Publisher
- Radiation Research Society
- Published
- 2013-01
- Volume
- 179
- Issue
- 1
- Pages
- 89-100
- ISSN
- 0033-7587 (ISSN-L)
- 1938-5404
- PMC
- PMC4562422
- OpenAlex
- W2152600399
- Semantic Scholar
- 604de41aaa5355d736267f4a3f2e58a8e058b113
- Cited by
- 187
- References
- 110
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 11 · 2023: 15 · 2022: 14 · 2021: 20 · 2020: 16 · 2019: 16 · 2018: 16 · 2017: 14 · 2016: 11 · 2015: 14 · 2014: 13 · 2013: 7
- FWCI
- 8.21
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Radiation Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- BioOne Complete (BioOne) (submittedVersion)
- Funders
- American Society of Clinical Oncology
- National Institutes of Health (n01ai50043-8-0-1)
- National Institute of Allergy and Infectious Diseases (HHSN272201000046C, N01 AI050043)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Health Sciences › Medicine › Oncology › Neutropenia and Cancer Infections
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Keywords
- pegfilgrastim, filgrastim, hematopoietic acute radiation syndrome, total body irradiation, survival, neutropenia, thrombocytopenia, neutrophil recovery, platelet recovery, gram-negative bacteremia, nonhuman primate model, rhesus monkeys
- MeSH terms
- Filgrastim, Animals, Anti-Bacterial Agents, Blood Platelets, Blood Transfusion, Diarrhea, Female, Macaca mulatta, Male, Neutropenia, Neutrophils, Radiation-Protective Agents, Recombinant Proteins, Survival Analysis, Granulocyte Colony-Stimulating Factor
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