PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Disaster Med Public Health Prep. Author manuscript; available in PMC May 3, 2013.
Published in final edited form as:
Disaster Med Public Health Prep. Oct 2011; 5(3): 202–212.
Published online Oct 10, 2011. doi:  10.1001/dmp.2011.68
PMCID: PMC3643115
NIHMSID: NIHMS458613
First Global Consensus for Evidence-Based Management of the Hematopoietic Syndrome Resulting From Exposure to Ionizing Radiation
Dr Nicholas Dainiak, MD, FACP, Dr Robert Nicolas Gent, MB, ChB, FFPH, Dr Zhanat Carr, MD, PhD, Dr Rita Schneider, MD, Dr Judith Bader, MD, Dr Elena Buglova, MD, PhD, DrSci, Dr Nelson Chao, MD, MBA, Dr C. Norman Coleman, MD, Dr Arnold Ganser, MD, Dr Claude Gorin, MD, Dr Martin Hauer-Jensen, MD, PhD, FACS, Dr L. Andrew Huff, MD, Dr Patricia Lillis-Hearne, MD, Dr Kazuhiko Maekawa, MD, PhD, Dr Jeffrey Nemhauser, MD, Dr Ray Powles, CBE, MD, BSc, FRCP, FRCPath, Dr Holger Schünemann, MD, PhD, Dr Alla Shapiro, MD, PhD, Dr Leif Stenke, MD, PhD, Dr Nelson Valverde, MD, Dr David Weinstock, MD, Dr Douglas White, MD, MAS, Dr Joseph Albanese, PhD, and Dr Viktor Meineke, MD
Dr Dainiak is with the Yale University School of Medicine and Yale-New Haven Health-Bridgeport Hospital; Dr Gent is with the Health Protection Agency (Porton Down); Dr Carr is with the World Health Organization; Dr Schneider is with the Department of Nuclear Medicine, University of Würzburg; Drs Bader and Coleman are with the National Cancer Institute; Dr Buglova is with the International Atomic Energy Agency; Dr Chao is with Duke University; Dr Gansler is with the Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School; Dr Gorin is with Hospital Saint-Antoine; Dr Hauer-Jensen is with the University of Arkansas for Medical Science; Drs Huff and Lillis-Hearne are with the Armed Forces Radiobiology Research Institute; Dr Maekawa is with the Kanto Central Hospital; Dr Nemhauser is with the Centers for Disease Control and Prevention; Dr Powles is with the Parkside Oncology Clinic; Dr Schünemann is with McMaster University; Dr Shapiro is with the US Food and Drug Administration; Dr Stenke is with the Karolinska Institute; Dr Valverde is with the JLVF Consultants for Hospital & Health Management; Dr Weinstock is with the Dana-Farber Cancer Institute; Dr White is with the University of Pittsburgh Program on Ethics and Critical Care Medicine; Dr Albanese is with the Yale-New Haven Health Center for Emergency Preparedness and Disaster Response; and Dr Meineke is with the Bundeswehr Institute of Radiobiology
Correspondence: Address correspondence and reprint requests to Dr Viktor Meineke, Bundeswehr Institute of Radiobiology, Neuherbergstrasse 11, D-80937, Munich, Germany. ViktorMeineke/at/bundeswehr.org
Objective
Hematopoietic syndrome (HS) is a clinical diagnosis assigned to people who present with ≥1 new-onset cytopenias in the setting of acute radiation exposure. The World Health Organization convened a panel of experts to evaluate the evidence and develop recommendations for medical countermeasures for the management of HS in a hypothetical scenario involving the hospitalization of 100 to 200 individuals exposed to radiation. The objective of this consultancy was to develop recommendations for treatment of the HS based upon the quality of evidence.
Methods
English-language articles were identified in MEDLINE and PubMed. Reference lists of retrieved articles were distributed to panel members before the meeting and updated during the meeting. Published case series and case reports of individuals with HS, published randomized controlled trials of relevant interventions used to treat nonirradiated individuals, reports of studies in irradiated animals, and prior recommendations of subject matter experts were selected. Studies were extracted using the Grading of Recommendations Assessment Development and Evaluation (GRADE) system. In cases in which data were limited or incomplete, a narrative review of the observations was made. No randomized controlled trials of medical countermeasures have been completed for individuals with radiation-associated HS. The use of GRADE analysis of countermeasures for injury to hematopoietic tissue was restricted by the lack of comparator groups in humans. Reliance on data generated in nonirradiated humans and experimental animals was necessary.
Results
Based upon GRADE analysis and narrative review, a strong recommendation was made for the administration of granulocyte colony-stimulating factor or granulocyte macrophage colony-stimulating factor and a weak recommendation was made for the use of erythropoiesis-stimulating agents or hematopoietic stem cell transplantation.
Conclusions
Assessment of therapeutic interventions for HS in humans exposed to nontherapeutic radiation is difficult because of the limits of the evidence.
Keywords: countermeasures for ARS, cytokines and radiation injury, transplantation for ARS, acute radiation syndrome management, hematopoietic syndrome management
Hematopoietic syndrome (HS) is a clinical diagnosis assigned to individuals who present with ≥1 new-onset cytopenias in the setting of whole-body or significant partial-body acute radiation exposure. The severity of lymphopenia and thrombocytopenia correlate in general with cumulative radiation dose and dose rate.1 The rate of decline in absolute lymphocyte count correlates closely with dose and dose rate, and has been used as a surrogate marker for whole-body dose.2,3 The primary causes of HS are radiation-induced suppression of mitosis in hematopoietic stem/progenitor cells and their progeny, resulting in hypocellularity and aplasia of the bone marrow and apoptosis in lymphocytes and other hematopoietic cells.
Although guidelines have been proposed to aid clinicians in the evaluation, triage, and/or medical management of victims of acute radiation injury,4,5 the level of evidence supporting the current recommendations has not been evaluated. The World Health Organization (WHO) convened a panel of experts in Geneva, Switzerland, from March 16 to 18, 2009, to develop a harmonized approach to the medical management of acute radiation exposure. Among their considerations was the evidence supporting the clinical management of HS.6,7 Using the Grading of Recommendations Assessment Development and Evaluation (GRADE) system for evaluating evidence supporting clinical guidelines,8 the consultation group weighted the available evidence supporting the use of cytokines, hematopoietic stem cell transplantation, or both in the management of HS.
Participants in the consultancy were selected based upon their established expertise in the field. They were asked to consider and respond to a virtual scenario in which 100 to 200 victims required hospitalization. English language references were identified by each consultant before the meeting. All of the references were provided to the WHO and were made available to conferees. At the time of the meeting, additional English-language articles were identified in MEDLINE and PubMed from inception to the time of the consultancy. Search terms included radiation or radiation toxicity or ionizing radiation and therapy or treatment or cytokines or transplantation or hematopoietic system. Publications included case series, individual case reports of humans who were accidentally exposed to ionizing radiation, randomized control trials and cohort studies of humans who received therapeutic radiation or who may not have been exposed to radiation but who received the indicated treatment, reports of experimental studies in irradiated animals, and prior publications of recommendations of other consensus groups. Reference lists and references were distributed periodically throughout the meeting, as specific topics were raised for discussion.
Questions on the clinical management of HS were framed in the PICO format (patient problem, intervention, comparison, and outcome).9 To assess the quality of the evidence objectively, drafts of GRADE evidence profiles were prepared, according to WHO recommendations for guideline development.8 Letter assignments (A, B, C, and D) were made based upon the level of certainty that the magnitudes of benefits and harms of an intervention are known (Table 1 of the accompanying article by the same authors). Ranking the evidence with this tool was discussed and clarified by an expert (H.S.) on the GRADE approach.10,11 Criteria included study design, study limitations, consistency rate across studies, directness or generalizability of study results, bias, dose-response gradient, and confounding variables. A single individual (R.N.G.) entered all of the data, and the subsequent findings were reviewed for accuracy by a subgroup of conferees (N.D., Z.C., R.S., J.A., and V.M.) in advance of consideration by the entire consultation group. All of the consultants were asked to make final comments before scoring the strength of each recommendation. A final consensus ranking of recommendations was made by e-mail to all of the conferees.
TABLE 1
TABLE 1
Among Individuals With Refractory Bone Marrow Failure After Exposure to Ionizing Radiation, Do Cytokines (G-CSF or GM-CSF) vs No Such Therapy Affect Overall Survival?12,2026
Strong or weak recommendations for the use of hematopoietic cytokines/growth factors or stem cell transplantation were made based upon the balance between desirable and undesirable consequences of alternative treatment strategies, the quality of the evidence, uncertainty about or variability in values and preferences, and impact on resource utilization. A numerical score was used to gauge the strength of recommendations (see the accompanying article by the same authors). These recommendations included one favoring a practice having a high certainty of substantial net benefit (1a) or a practice having a moderate certainty of moderate net benefit (1b). A recommendation against a practice was made when the practice was believed to have a moderate or high certainty of no net benefit (2a) or to have a moderate or high certainty of a small net benefit (2b).
Rationale for Cytokine Administration
Hematopoietic cytokines such as granulocyte colony-stimulating factor (G-CSF) and granulocyte macrophage colony-stimulating factor (GM-CSF) have been used since the 1980s to treat radiation-associated cytopenias.12 Although their use in radiation accident victims has been recommended by 2 expert groups,4,5 the quality of the evidence supporting this recommendation is highly variable.
Clinical trial data supporting the use of cytokine efficacy in the treatment of humans with accidental radiation-induced hematopoietic stem/progenitor cell injury is not robust; additional evidence comes from studies in experimental animals. The administration of G-CSF, GM-CSF, erythropoiesis-stimulating agents (ESAs), and/or thrombopoietin-receptor agonists after exposure to ionizing radiation appears to significantly increase circulating blood counts in humans or nonhuman primates1215; however, the lack of a human control group (eg, patients not receiving cytokine treatment) limits interpretation of these results.16 Spontaneous recovery of blood counts occurred several weeks after the appearance of severe cytopenias in humans with HS, even in the absence of cytokine therapy.17
In an effort to justify the use and efficacy of cytokines in treating HS, researchers have used animal models. Based on the scientific literature suggesting a beneficial effect in the treatment of HS and the evidence of efficacy of cytokines in chemotherapy, a consensus has emerged that it is not ethically justifiable to conduct a placebo-controlled trial of cytokines in human victims of radiation sickness. In light of this lack of clinical equipoise, the best-available scientific evidence comes (and may continue to come) from animal-based experiments. Survival benefits observed in irradiated rhesus macaques and canines receiving G-CSF, GM-CSF, pegylated G-CSF thrombo-poietin13,18,19 support continued use of cytokines in humans exposed to high-dose ionizing radiation.
Analysis of Cytokine Effects Using GRADE
In reviewing the evidence of hematological system injury, we found 5 reported accidents (Goiãnia, Brazil; Tokai-mura, Japan; Henan Province, China; Istanbul, Turkey; and Gilan, Iran), that enabled the establishment of bone marrow failure, the documentation of cytokine use, and the demonstration of effect on the hematological system. Table 1 provides a summary of an analysis of the evidence. Table 2 is a complete GRADE analysis of the effects of cytokines on overall survival among individuals with cytopenias after exposure to ionizing radiation. Among these accidents, 18 cases of cytokine use were reported.12,2024 Eight patients received G-CSF and 10 received GM-CSF (Table 1).
TABLE 2
TABLE 2
Analysis of Studies Included in the GRADE Profile Question: Among Individuals With Cytopenias After Exposure to Ionizing Radiation, Do Cytokines (G-CSF or GM-CSF) vs No Such Therapy Affect Overall Survival?
Among the data reported from the Goiãnia accident, 2 patients experienced spontaneous reversal of leukopenia by 35 days postexposure to 6.2 or 7.1 Gy, and 8 individuals demonstrated persistent leukopenia for 24 to 47 days, and GM-CSF therapy was initiated at this time. Four of the individuals treated with cytokines (radiation doses of 2.5–4.4 Gy) survived and recovered from leukopenias. Four of the treated individuals (doses of 4.0–6.0 Gy received) died of Gram-negative sepsis and/or hemorrhagic complications, 3 of whom experienced minimal increase in their white blood cell count (Table 2). Four of the 6 patients from the Tokai-mura accident (1 patient) and the Henan Province accident (3 patients) were evaluable by GRADE, and all of them demonstrated improvement in absolute neutrophil count (Table 2).
In the 5 nuclear accidents, among the patients whose exposure dose was >5 Gy, 1 of 3 patients treated with cytokines survived. At exposures <5 Gy, 14 of 15 patients survived. The consultation group interpreted this observational finding as suggesting a possible benefit to myelopoiesis used in patients with exposure doses <5 Gy, when the only likely organ-critical failure is the hematopoietic system.
In assessing the effectiveness of cytokines, the GRADE analysis was severely restricted by our failure to identify any true control or comparator groups. Descriptive studies like these that do not have an appropriate, contemporaneous comparison group allow assessment of hypotheses for possible associations but not robust assessments of causality.25 Randomized, appropriately designed, and powered studies are much more useful in studying causality.25 In this case, a temporal association of cytokine administration followed by myeloid recovery should not be inferred as strong evidence of causality.26
Rationale for Stem Cell Transplantation
Hematopoietic stem/progenitor cells of the bone marrow undergo mitotic death after exposure to ionizing radiation, with a Do (the radiation dose that reduces survival to e−1 or 0.37 of its previous value on the exponential portion of the survival curve) for human marrow colony-forming units granulocyte-macrophage of 1.02 ± 0.05 at a dose rate of 2 Gy/min27 and for human peripheral blood total colony-forming cells of 1.18 ± 0.24 at a dose rate of 0.8 Gy/min.28 This particular in vitro measure of sensitivity to radiation correlates with the appearance of the HS that occurs in individuals whose partial-body or whole-body radiation exposure exceeds approximately 1 Gy.7,29 The clinical correlate of this laboratory observation is the significantly diminished capacity of hematopoietic stem/progenitor cells to proliferate in vivo after a whole-body dose exceeding 2 to 3 Gy.
Depending on the dose, dose rate, and radiation quality factor, various degrees of pancytopenia develop over several weeks after whole-body or significant partial-body exposure.4,6,30 Hypo-cellularity and aplasia of the bone marrow may occur at doses >3 Gy.4,6,30,31 Factors that may exacerbate the effects of radiation include a patient’s age, underlying state of health, and overall nutritional status.
Hematopoietic stem/progenitor cell therapy has been recommended for patients with complete aplasia of the bone marrow, as assessed by bone marrow biopsies taken from 2 non-contiguous sites.4,5 Such individuals would be expected to have third- or fourth-degree hematopoietic toxicity (Table 3).
TABLE 3
TABLE 3
Levels of Hematopoietic Toxicity1
Analysis of the Effects of Bone Marrow Transplantation Using GRADE
A crude meta-analysis of 3 reported incidents in which bone marrow transplantation was used to treat radiation-induced marrow failure was performed. Table 4 provides a summary of this analysis. Table 5 presents a complete GRADE analysis of the question of the impact of bone marrow transplantation on overall survival among individuals with bone marrow failure after exposure to ionizing radiation. In these reports,3235 some of which predate the use of cytokines, survival appeared not to rely on transplantation, and may have been affected adversely by transplantation.
TABLE 4
TABLE 4
Among Individuals With Bone Marrow Failure After Exposure to Ionizing Radiation, Does Bone Marrow Transplantation vs No Transplantation Affect Overall Survival?3235
TABLE 5
TABLE 5
Analysis of Studies Included in the GRADE Profile Question: Among Individuals With Bone Marrow Failure After Exposure to Ionizing Radiation, Does Bone Marrow Transplantation vs No Transplantation Affect Overall Survival?
Stratification of the results from the Chernobyl study33 suggests that survival is more likely among individuals receiving <9 Gy and no bone marrow transplant. Nevertheless, the data are too restrictive to allow definitive statistical analysis. Survival in 2 additional patients (one receiving a peripheral blood transplant and the other receiving a cord blood transplant) from the Tokai-mura accident was possibly longer than predicted by the estimated whole-body radiation dose.36 These individuals also received concurrent cytokine therapy, and comparators were not available. Data are insufficient to determine the impact of genetically identical bone marrow transplantation on outcomes. In summary, the data available from these reports strongly suggest that the effect of hematopoietic stem/progenitor cell transplantation is unproven as initial therapy for HS after irradiation.
The consultation group strongly considered the GRADE evidence profiles for cytokine administration and bone marrow transplantation in developing recommendations for the management of HS. The group also derived recommendations in part from results of these therapies in controlled animal trials. During the deliberation process, guidelines provided by expert consensus groups and by national and international societies also were considered, reviewed, and discussed.
Although the evidence for cytokine administration from radiation incident reports alone is weak, results are remarkably consistent from controlled animal trials13,18,37,38 and reports recommending the use of CSF in nonirradiated (eg, chemotherapy treated) patients with malignancy, as recommended by the American Society of Clinical Oncology,39 by the European Society of Medical Oncology,40 and by consensus groups.4,5,29 The consistency of the observation that cytokines successfully treat hematological injury in animal models and in humans with hematological deficits of nonradiation origin, together with the relatively limited drug-related toxicity reported for certain cytokines, leads to a strong recommendation that these cytokines should be used in the management of radiation-induced hematotopoietic system injury (Table 6).
TABLE 6
TABLE 6
Summary of Recommendations for Treating Hematopoietic Syndrome in Hospitalized Patients With Whole-Body Exposure to Ionizing Radiation
Health care providers should consider initiating cytokine therapy for exposures of ≥2 Gy and/or a significant decrease in the absolute lymphocyte count, or when it is anticipated that neutropenia of <.5 × 109 cells per liter will persist for ≥7 days. It is recommended that cytokine therapy with G-CSF or GM-CSF be initiated within 24 hours of exposure. Pegylated G-CSF may be used as an alternative to G-CSF. Patients should continue to receive treatment until their absolute neutrophil count reaches and maintains a level >1.0×109 cells per liter in the absence of active infection. Those with infection should be treated with cytokines, according to the guidelines published by infectious disease societies, including the Infectious Diseases Society of America.41
Individuals with prolonged anemia, a significant decline in hemoglobin concentration, or both may be candidates for treatment with erythropoietin. In contrast to the relatively short life span of myeloid cells and platelets (<10 days), the life span of erythrocytes is approximately 120 days. Experiencing a response to erythropoietin will take weeks rather than days. Consideration should be given to the administration of oral iron supplementation in individuals receiving ESAs. ESAs may be considered in the lowest dosage that induces a sufficiently high hemoglobin level to render blood transfusion unnecessary (ie, 9–10 g/dL), although a higher level of hemoglobin may be reasonably targeted on a case-by-case basis. Strong caveats recommending specific indications for the use of ESAs are incorporated in a “black box” warning by the US Food and Drug Administration (FDA).42 The initial dose of ESAs should follow the recommendations of the FDA, the the European Medicines Agency, or other relevant regulatory authorities, as provided in the manufacturer’s labeling. Dosing is based on a patient’s hemoglobin level at the initiation of therapy, his or her target hemoglobin level, the observed rate of increase in hemoglobin level, and individual clinical circumstances. Finding few published reports in humans with nonimmunological thrombocytopenia or exposure to radiation, the consultancy group makes no recommendation regarding the use of second-generation thrombopoietic growth factors.
Because patients with severe hematopoietic injury may recover, either spontaneously or after G-CSF treatment alone, clinicians considering bone marrow transplantation are advised to adopt a wait-and-see approach with careful surveillance. Stem/progenitor cell replacement therapy should not be administered until there is a documented lack of spontaneous recovery and/or lack of response following 2 to 3 weeks of cytokine treatment. Survival outcomes have been poor among patients who have received transplants who also have radiation burns, gastrointestinal syndrome, infection, adult respiratory distress syndrome, and/or renal insufficiency3236; therefore, it has been recommended that hematopoietic stem/progenitor cell therapy not be used for patients with aplasia and significant injury to another organ system.4,7,29,43,44 With these caveats in mind, the consulting group makes a weak recommendation for the administration of allogeneic hematopoietic stem/progenitor cells from the bone marrow, peripheral blood, or cord blood of patients who are unresponsive to cytokine therapy and in whom there is no significant injury to a nonhemopoietic organ system (Table 6).
CONCLUSIONS
The WHO panel of experts used the GRADE tool to extract and analyze data from reports of cytokine administration and/or bone marrow transplantation in individuals with HS after exposure to ionizing radiation. The lack of comparator groups in humans restricts these analyses. Nevertheless, together with results of controlled trials in large animals and clinical trials in nonirradiated humans, these analyses support the strong recommendation for G-CSF or GM-CSF administration and the weak recommendation for ESA or hematopoietic stem cell administration in humans with HS.
Acknowledgments
Owing to their seminal contributions in the field of radiation biology and their pioneering approaches to treatment of victims of radiation injury, this consultancy report is dedicated to Theodor M. Fliedner and Angelina Guskova. The authors thank Makoto Akashi, Axel Bottger, Thierry de Revel, Patrick Gourmelon, Richard Hatchett, Mikhail Konchalovski, Ying Liu, Maria Julia Marinissen, Hilary Walker, Helmut Walerius, and Wei Zhang for participating in the consultancy and contributing to consensus building. The authors are grateful to the National Institute of Allergy and Infectious Diseases for providing financial support for this consultancy.
Footnotes
Disclaimer: The opinions or assertions contained herein are the private views of the authors and are not necessarily those of the World Health Organization, the International Atomic Energy Agency, the Centers for Disease Control and Prevention, the Bundeswehr Institute of Radiobiology, the Health Protection Agency, the National Institutes of Health, the Department of Health and Human Services, the US Army, or the US Department of Defense. The mention of specific commercial equipment or therapeutic agents does not constitute endorsement by the Bundeswehr Institute of Radiobiology, the Health Protection Agency, the US Department of Defense, or the Centers for Disease Control and Prevention. Trade names are used only for the purpose of clarification.
Author Disclosures: Dr Weinstock has been a consultant to Genzyme and Novartis.
The other authors report no conflicts of interest.
1. Fliedner TM, Friesecke I, Beyrer K. Medical Management of Radiation Accidents: Manual on Acute Radiation Syndrome. Oxford, UK: British Institute of Radiobiology; 2001.
2. Goans RE, Holloway EC, Berger ME, Ricks RC. Early dose assessment following severe radiation accidents. Health Phys. 1997;72(4):513–518. [PubMed]
3. Parker DD, Parker JC. Estimating radiation dose from time to emesis and lymphocyte depletion. Health Phys. 2007;93(6):701–704. [PubMed]
4. Waselenko JK, MacVittie TJ, Blakely WF, et al. Strategic National Stockpile Radiation Working Group. Medical management of the acute radiation syndrome: recommendations of the Strategic National Stockpile Radiation Working Group. Ann Intern Med. 2004;140(12):1037–1051. [PubMed]
5. Gorin NC, Fliedner TM, Gourmelon P, et al. Consensus conference on European preparedness for haematological and other medical management of mass radiation accidents. Ann Hematol. 2006;85(10):671–679. [PubMed]
6. Mettler FA, Upton AC. Deterministic effects of ionizing radiation. In: Mettler FA, Upton AC, editors. Medical Effects of Radiation. 3. Philadelphia: Saunders Elsevier; 2008.
7. Dainiak N, Waselenko JK, Armitage JO, MacVittie TJ, Farese AM. The hematologist and radiation casualties. Hematol Am Soc Hematol Educ Program. 2003:473–496. [PubMed]
8. Schünemann HJ, Oxman AD, Brozek J, et al. GRADE Working Group. Grading quality of evidence and strength of recommendations for diagnostic tests and strategies. BMJ. 2008;336:1106–1110. [PMC free article] [PubMed]
9. Richardson WS, Wilson MC, Nishikawa J, Hayward RS. The well-built clinical question: a key to evidence-based decisions. ACP J Club. 1995;123(3):A12–A13. [PubMed]
10. Guyatt GH, Oxman AD, Kunz R, et al. GRADE Working Group. Going from evidence to recommendations. BMJ. 2008;336:1049–1051. [PMC free article] [PubMed]
11. Guyatt GH, Oxman AD, Vist GE, et al. GRADE Working Group. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336:924–926. [PMC free article] [PubMed]
12. Butturini A, De Souza PC, Gale RP, et al. Use of recombinant granulocyte-macrophage colony stimulating factor in the Brazil radiation accident. Lancet. 1988;2:471–475. [PubMed]
13. Neelis KJ, Dubbelman YD, Qingliang L, Thomas GR, Eaton DL, Wagemaker G. Simultaneous administration of TPO and G-CSF after cytoreductive treatment of rhesus monkeys prevents thrombocytopenia, accelerates platelet and red cell reconstitution, alleviates neutropenia, and promotes the recovery of immature bone marrow cells. Exp Hematol. 1997;25(10):1084–1093. [PubMed]
14. Asano S. Multi-organ involvement: lessons from the experience of one victim of the Tokai-mura criticality accident. BJR Suppl. 2005;27(Suppl):9–12. [PubMed]
15. Liu Q, Jiang B, Jiang LP, et al. Clinical report of three cases of acute radiation sickness from a (60)Co radiation accident in Henan Province in China. J Radiat Res (Tokyo) 2008;49(1):63–69. [PubMed]
16. Dainiak N. Rationale and recommendations for treatment of radiation injury with cytokines. Health Phys. 2010;98(6):838–842. [PubMed]
17. Baranov AE, Guskova AK, Nadejina NM, Nugis VYu. Chernobyl experience: biological indicators of exposure to ionizing radiation. Stem Cells. 1995;13(Suppl 1):69–77. [PubMed]
18. Patchen ML, MacVittie TJ, Solberg BD, Souza LM. Therapeutic administration of recombinant human granulocyte colony-stimulating factor accelerates hemopoietic regeneration and enhances survival in a murine model of radiation-induced myelosuppression. Int J Cell Cloning. 1990;8(2):107–122. [PubMed]
19. Neelis KJ, Hartong SC, Egeland T, Thomas GR, Eaton DL, Wagemaker G. The efficacy of single-dose administration of thrombopoietin with coadministration of either granulocyte/macrophage or granulocyte colony-stimulating factor in myelosuppressed rhesus monkeys. Blood. 1997;90 (7):2565–2573. [PubMed]
20. Brandao-Mello CE, Oliveira AR, Valverde NJ, Farina R, Cordeiro JM. Clinical and hematological aspects of 137Cs: the Goiãnia radiation accident. Health Phys. 1991;60(1):31–39. [PubMed]
21. International Atomic Energy Agency. The Radiological Accident in Goiãnia. Vienna: IAEA; 1998.
22. Hirama T, Tanosaki S, Kandatsu S, et al. Initial medical management of patients severely irradiated in the Tokai-mura criticality accident. Br J Radiol. 2003;76(904):246–253. [PubMed]
23. International Atomic Energy Agency. The Radiological Accident in Gilan. Vienna: IAEA; 2002.
24. International Atomic Energy Agency. The Radiological Accident in Istanbul. Vienna: IAEA; 2000.
25. Grimes DA, Schulz KF. An overview of clinical research: the lay of the land. Lancet. 2002;359(9300):57–61. [PubMed]
26. Grimes DA, Schulz KF. Descriptive studies: what they can and cannot do. Lancet. 2002;359(9301):145–149. [PubMed]
27. FitzGerald TJ, McKenna M, Rothstein L, Daugherty C, Kase K, Greenberger JS. Radiosensitivity of human bone marrow granulocyte-macrophage progenitor cells and stromal colony-forming cells: effect of dose rate. Radiat Res. 1986;107(2):205–215. [PubMed]
28. Oriya A, Takahashi K, Inanami O, et al. Individual differences in the radiosensitivity of hematopoietic progenitor cells detected in steady-state human peripheral blood. J Radiat Res (Tokyo) 2008;49(2):113–121. [PubMed]
29. International Atomic Energy Agency. Safety Reports Series No 2. Vienna: IAEA; 1998. Diagnosis and Treatment of Radiation Injuries.
30. Alexander GA, Swartz HM, Amundson SA, et al. BiodosEPR-2006 Meeting: acute dosimetry consensus committee recommendations on biodosimetry applications in events involving uses of radiation by terrorists and accidents. Radiat Meas. 2007;42(Suppl):972–996.
31. Fliedner TM, Meineke V, Akashi M, Dainiak N, Gourmelon P, editors. Proceedings of the Advanced Research Workshop on Radiation-Induced Multi-Organ Involvement and Failure: A Challenge for Pathogenetic, Diagnostic, and Therapeutic Approaches and Research. London: British Institute of Radiology; 2003.
32. Jammet H, Mathe G, Pendic B, et al. Study of six cases of accidental acute total irradiation. Rev Fr Etud Clin Biol. 1959;4(3):210–225. [PubMed]
33. Baranov A, Gale RP, Guskova A, et al. Bone marrow transplantation after the Chernobyl nuclear accident. N Engl J Med. 1989;321(4):205–212. [PubMed]
34. International Atomic Energy Agency. The Vinca Dosimetry Experiment, Tech Rep Ser No 6. Vienna: IAEA; 1962.
35. Gilbert MV. The 1967 radiation accident near Pittsburgh, Pennsylvania, and a follow up report. In: Hubner KF, Fry SA, editors. The Medical Basis for Radiation Accident Preparedness. Amsterdam: Elsevier-North Holland; 1980. pp. 131–140.
36. Maekawa K. Overview of medical care for highly exposed victims in Tokaimura accident. In: Ricks RC, Berger ME, O’Hara FM, editors. The Medical Basis for Radiation-Accident Preparedness: The Clinical Care of Victims. Boca Raton, FL: Partheon Publishing Group; 2002. pp. 313–318.
37. Drouet M, Mourcin F, Grenier N, et al. Single administration of stem cell factor, FLT-3 ligand, megakaryocyte growth and development factor, and interleukin-3 in combination soon after irradiation prevents nonhuman primates from myelosuppression: long-term follow-up of hematopoiesis. Blood. 2004;103(3):878–885. [PubMed]
38. Hérodin F, Grenier N, Drouet M. Revisiting therapeutic strategies in radiation casualties. Exp Hematol. 2007;35(4 Suppl 1):28–33. [PubMed]
39. Smith TJ, Khatcheressian J, Lyman GH, et al. 2006 update of recommendations for the use of white blood cell growth factors: an evidence-based clinical practice guideline. J Clin Oncol. 2006;24(19):3187–3205. [PubMed]
40. Greil R, Thödtman R, Roila F. ESMO Guidelines Working Group. Erythropoietins in cancer patients: ESMO recommendations for use. Ann Oncol. 2008;19(Suppl 2):ii113–ii115. [PubMed]
41. Hughes WT, Armstrong D, Bodey GP, et al. 2002 guidelines for the use of antimicrobial agents in neutropenic patients with cancer. Clin Infect Dis. 2002;34(6):730–751. [PubMed]
42. Food and Drug Administration. [Accessed August 29, 2011];Information on erythropoiesis-stimulating agents (ESAs) epoetin alfa (marketed as Procrit, Epogen) darbepoetin alfa (marketed as Aranesp) http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/UCM109375.
43. Dainiak N, Ricks RC. The evolving role of haematopoietic cell transplantation in radiation injury: potentials and limitations. BJR Suppl. 2005;27(Suppl):169–174. [PubMed]
44. Densow D, Kindler H, Baranov AE, Tibken B, Hofer EP, Fliedner TM. Criteria for the selection of radiation accident victims for stem cell transplantation. Stem Cells. 1997;15(Suppl 2):287–297. [PubMed]