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KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ

Year 2025, Volume: 26 Issue: 4, 286 - 294, 13.10.2025
https://doi.org/10.18229/kocatepetip.1477957

Abstract

AMAÇ: Febril nötropeni (FN), miyelosüpresif kemoterapinin en
yaygın görülen komplikasyonlarından biridir ve önemli oranda
hospitalizasyon ve mortalite nedenidir. Çalışmada kemoterapi
alan pediatrik onkoloji hastalarında görülen FN atağında nötrofil/
lenfosit oranı (NLR), platelet/lenfosit oranı (PLR), sistemik
immün-inflamasyon indeksi (SII) ve ortalama trombosit hacmiyle
(MPV) ilişkili hematolojik indekslerin değerlendirilmesi
amaçlandı.
GEREÇ VE YÖNTEM: Tek merkezli, retrospektif kohort çalışmada,
0-16 yaş aralığında kanser nedeniyle kemoterapi alan
hastalar (n = 98), kemoterapiden sonraki bir ay içinde FN atağı
olanlar (n = 40) ve olmayanlar (n = 58) şeklinde iki gruba ayrıldı.
Hastaların sosyodemografik özellikleri (yaş, cinsiyet), temel
klinik özellikleri (geliş nedeni, öykü, tanı, antibiyotik kullanımı,
komorbidite vb) ve hematolojik bulgularına ait veriler kaydedildi.
Hastaların mevcut hemogram verileri kullanılarak NLR, PLR,
SII, MPV/platelet oranı (MPV/PLT), MPV/C-reaktif protein oranı
(MPV/CRP) ve MPV/prokalsitonin oranı (MPV/PCT) hesaplandı.
Grupları karşılaştırmak için ki-kare, bağımsız örneklem t testi
veya Mann-Whitney U testi kullanıldı. Ayrıca lojistik regresyon
ve alıcı çalışma karakteristikleri (ROC) analizleri yapıldı. P < 0,05
düzeyi istatistiksel olarak anlamlı kabul edildi.
BULGULAR: FN grubunda NLR ve SII anlamlı olarak düşük, PLR
ise yüksek bulundu. MPV ilişkili indekslerden MPV/PLT, FN grubunda
anlamlı olarak yüksek iken MPV/CRP ve MPV/PCT ise düşüktü.
FN için potansiyel prediktif faktörler olarak tespit edilen
yaş, CRP, PLR ve MPV/PCT ile oluşturulan çok değişkenli lojistik
regresyon modelinde sadece MPV/PCT’nin FN için bağımsız
prediktif faktör olduğu bulundu. Ayrıca 57,33 optimal kesme
değeri için MPV/PCT’nin % 89,7 duyarlılık ve %100 özgüllüğe
sahip olduğu görüldü.
SONUÇ: Araştırdığımız indeksler arasında MPV/PCT’nin, pediatrik
onkoloji hastalarında kemoterapi sonrasında görülebilen FN
atağını yordayan başlıca değişken olduğu söylenebilir.

Ethical Statement

Çalışmaya Afyonkarahisar Sağlık Bilimleri Üniversitesi Klinik Araştırmalar Etik Kurulu onayını takiben başlanmıştır (Tarih: 01.12.2023, Toplantı-Karar No: 2023/12-513).

Supporting Institution

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Thanks

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References

  • 1. 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):730–51.
  • 2. Freifeld AG, Bow EJ, Sepkowitz KA, et al. Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2011;52(4):e56–93.
  • 3. Masaoka T. Evidence-based recommendations for antimicrobial use in febrile neutropenia in Japan: Executive summary. Clin Infect Dis. 2004;39(1):49–52.
  • 4. Rosa RG, Goldani LZ. Factors associated with hospital length of stay among cancer patients with febrile Neutropenia. PLoS One. 2014;9(10):e108969.
  • 5. Kebudi R, DEvecioğlu Ö, Gürler N. Tanımlar ve tanı yöntemleri (Definitions and diagnostic approach in childhood febrile neutropenia). Flora. 2004;2:73–105.
  • 6. Özdemir ZC, Düzenli-Kar Y, Canik A, Küskü-Kiraz Z, Özen H, Bör Ö. The predictive value of procalcitonin, C- reactive protein, presepsin, and soluble-triggering receptor expressed on myeloid cell levels in bloodstream infections in pediatric patients with febrile neutropenia. Turk J Pediatr. 2019;61(3):359–67.
  • 7. Boeriu E, Borda A, Vulcanescu DD, et al. Diagnosis and management of febrile neutropenia in pediatric oncology patients - a systematic review. Diagnostics. 2022;12(8):1800.
  • 8. Mendes AVA, Sapolnik R, Mendonça N. New guidelines for the clinical management of febrile neutropenia and sepsis in pediatric oncology patients. J Pediatr (Rio J). 2007;83:54–63.
  • 9. Thangthong J, Anugulruengkitt S, Lauhasurayotin S, et al. Predictive factors of severe adverse events in pediatric oncologic patients with febrile neutropenia. Asian Pacific J Cancer Prev. 2020;21(12):3487–92.
  • 10. Cennamo F, Masetti R, Largo P, Argentiero A, Pession A, Esposito S. Update on febrile neutropenia in pediatric oncological patients undergoing chemotherapy. Children. 2021;8(12):1086.
  • 11. Llamas R, Acosta M, Silva J. Management of febrile neutropenia in pediatric cancer patients. J Pediatr Neonatal Care. 2019;9(1):22–6.
  • 12. Alali M, David MZ, Danziger-Isakov LA, Elmuti L, Bhagat PH, Bartlett AH. Pediatric febrile neutropenia: Change in etiology of bacteremia, empiric choice of therapy and clinical outcomes. J Pediatr Hematol Oncol. 2020;42(6):e445–51.
  • 13. Basu SK, Fernandez ID, Fisher SG, Asselin BL, Lyman GH. Length of stay and mortality associated with febrile neutropenia among children with cancer. J Clin Oncol. 2005;23(31):7958–66.
  • 14. Das A, Trehan A, Bansal D. Risk factors for microbiologically-documented infections, mortality and prolonged hospital stay in children with febrile neutropenia. Indian Pediatr. 2018;55(10):859–64.
  • 15. Markanday A. Acute phase reactants in infections: evidence-based review and a guide for clinicians. Open forum Infect Dis Oxford Univ Press. 2015;2(3):ofv098.
  • 16. Niehues T. C-reactive protein and other biomarkers the sense and non-sense of using inflammation biomarkers for the diagnosis of severe bacterial infection. LymphoSign J. 2018;5(2):35–47.
  • 17. Kim DY, Lee YS, Ahn S, Chun YH, Lim KS. The usefulness of procalcitonin and C-reactive protein as early diagnostic markers of bacteremia in cancer patients with febrile neutropenia. Cancer Res Treat. 2011;43(3):176– 80.
  • 18. Lin SG, Hou TY, Huang DH, et al. Role of procalcitonin in the diagnosis of severe infection in pediatric patients with fever and neutropenia-a systemic review and meta-analysis. Pediatr Infect Dis J. 2012;31(10):e182–8.
  • 19. Durnaś B, Wątek M, Wollny T, et al. Utility of blood procalcitonin concentration in the management of cancer patients with infections. Onco Targets Ther. 2016;9:469–75.
  • 20. Christ-Crain M, Schuetz P, Huber AR, Müller B. Procalcitonin: Importance for the diagnosis of bacterial infections. Laboratoriums Medizin. 2008;65(9):559-68.
  • 21. Leader A, Pereg D, Lishner M. Are platelet volume indices of clinical use? A multidisciplinary review. Ann Med. 2012;44(8):805–16.
  • 22. Choi A, Park I, Lee HS, Chung J, Kim MJ, et al. Usefulness of complete blood count parameters to predict poor outcomes in cancer patients with febrile neutropenia presenting to the emergency department. Ann Med. 2022;54(1):599–609.
  • 23. Detopoulou P, Panoutsopoulos GI, Mantoglou M, et al. Relation of mean platelet volume (MPV) with cancer: A systematic review with a focus on disease outcome on twelve types of cancer. Curr Oncol. 2023;30(3):3391–420
  • 24. Korniluk A, Koper-Lenkiewicz OM, Kamińska J, Kemona H, Dymicka-Piekarska V. Mean platelet volume (MPV): New perspectives for an old marker in the course and prognosis of inflammatory conditions. Mediators Inflamm. 2019;17:9213074.
  • 25. Kim CH, Kim SJ, Lee MJ, et al. An increase in mean platelet volume from baseline is associated with mortality in patients with severe sepsis or septic shock. PLoS One. 2015;10(3):1–13.
  • 26. Halalsheh OM, Al Zu’bi YO, Al Sharie AH, et al. The prognostic utility of lymphocyte-based measures and ratios in chemotherapy-ınduced febrile neutropenia patients following granulocyte colony-stimulating factor therapy. Med. 2022;58(11):1508.
  • 27. Ma K, Zhang Y, Hao J, Zhao J, Qi Y, Liu C. Correlation analysis of systemic immune inflammatory index, serum IL-35 and HMGB-1 with the severity and prognosis of sepsis. Pakistan J Med Sci. 2023;39(2):497–501.
  • 28. Wang H, Huang Z, Xu B, et al. The predictive value of systemic immune-inflammatory markers before and after treatment for pathological complete response in patients undergoing neoadjuvant therapy for breast cancer: a retrospective study of 1994 patients. Clin Transl Oncol. 2024;1–13(0123456789).
  • 29. Boccia R, Glaspy J, Crawford J, Aapro M. Chemotherapy-induced neutropenia and febrile neutropenia in the US: A beast of burden that needs to be tamed? Oncologist. 2022;27(8):625–36.
  • 30. Nessle CN, Njuguna F, Dettinger J, et al. Barriers to and facilitators of effective management of fever episodes in hospitalised Kenyan children with cancer: protocol for convergent mixed methods study. BMJ Open. 2023;13(11):e078124.
  • 31. Cullen M, Baijal S. Prevention of febrile neutropenia: Use of prophylactic antibiotics. Br J Cancer. 2009;101:11–4.
  • 32. Mohammed HB, Yismaw MB, Fentie AM, Tadesse TA. Febrile neutropenia management in pediatric cancer patients at Ethiopian Tertiary Care Teaching Hospital. BMC Res Notes. 2019;12(1):1–6.
  • 33. Gonzalez ML, Aristizabal P, Loera-Reyna A, et al. The golden hour: Sustainability and clinical outcomes of adequate time to antibiotic administration in children with cancer and febrile neutropenia in Northwestern Mexico. JCO Glob Oncol. 2021;(7):659–70.
  • 34. Green LL, Goussard P, Van Zyl A, Kidd M, Kruger M. Predictive indicators to identify high-risk paediatric febrile neutropenia in paediatric oncology patients in a middle-income country. J Trop Pediatr. 2018;64(5):395–402.
  • 35. Mikoshiba T, Saito S, Ikari Y, et al. Usefulness of hematological inflammatory markers in predicting severe side-effects from induction chemotherapy in head and neck cancer patients. Anticancer Res. 2019;39(6):3059– 65.
  • 36. Kim YJ, Kang J, Ryoo SM, Ahn S, Huh JW, Kim WY. Platelet-lymphocyte ratio after granulocyte colony stimulating factor administration: An early prognostic marker in septic shock patients with chemotherapy- ınduced febrile neutropenia. Shock. 2019;52(2):160–5.
  • 37. Kumazawa S, Mizuno T, Muramatsu N, et al. Neutrophil-lymphocyte ratio is associated with occurrence of febrile neutropenia in patients treated with 5-fluorouracil and cisplatin. In Vivo. 2022;36(5):2319–83.
  • 38. Secmeer G, Devrim I, Kara A, et al. Role of procalcitonin and CRP in differentiating a stable from a deteriorating clinical course in pediatric febrile neutropenia. J Pediatr Hematol Oncol. 2007;29(2):107–11.
  • 39. Becker KL, Snider R, Nylen ES. Procalcitonin in sepsis and systemic inflammation: A harmful biomarker and a therapeutic target. Br J Pharmacol. 2010;159(2):253–64.
  • 40. Chambliss AB, Patel K, Colón-Franco JM, et al. AACC guidance document on the clinical use of procalcitonin. J Appl Lab Med. 2023;8(3):598–634.

PROGNOSTIC VALUE OF NEUTROPHIL/LYMPHOCYTE RATIO, PLATELET/LYMPHOCYTE RATIO, SYSTEMIC IMMUNE-INFLAMMATION INDEX, AND MEAN PLATELET VOLUME-RELATED INDICES IN PEDIATRIC ONCOLOGY PATIENTS EXPERIENCING FEBRILE NEUTROPENIA EPISODES AFTER CHEMOTHERAPY

Year 2025, Volume: 26 Issue: 4, 286 - 294, 13.10.2025
https://doi.org/10.18229/kocatepetip.1477957

Abstract

OBJECTIVE: Febrile neutropenia (FN) is one of the most common
complications of myelosuppressive chemotherapy and
a significant cause of hospitalization and mortality. The study
aimed to evaluate hematological indices, including neutrophil/
lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR), systemic
immune-inflammation index (SII), and mean platelet volume
(MPV) related indices in the FN episodes in pediatric oncology
patients receiving chemotherapy.
MATERIAL AND METHODS: In a single-center, retrospective
cohort study, patients aged 0-16 years receiving chemotherapy
for cancer (n = 98) were divided into two groups: those who
experienced an FN episode within one month following chemotherapy
(n = 40) and those who did not (n = 58). Socio-demographic
characteristics (age, gender), basic clinical features
(reason for admission, history, diagnosis, antibiotic use, comorbidities,
etc.), and hematologic findings data were recorded. Based
on the patients' current hemogram data, NLR, PLR, SII, MPV/
platelet ratio (MPV/PLT), MPV/C-reactive protein ratio (MPV/
CRP), and MPV/procalcitonin ratio (MPV/PCT) were calculated.
Chi-square, independent sample t-test, or Mann-Whitney U-test
were used to compare groups. Logistic regression and receiver
operating characteristics (ROC) analyses were also conducted.
A level of P < 0.05 was considered statistically significant.
RESULTS: In the FN group, NLR and SII were significantly lower
whereas PLR was significantly higher. Among the MPV related
indices, MPV/PLT was significantly higher in the FN group, whereas
MPV/CRP and MPV/PCT were significantly lower. In the
multivariate logistic regression model constructed with age,
CRP, PLR, and MPV/PCT as potential predictive factors for FN,
only MPV/PCT was identified as an independent predictive factor
for FN. Additionally, it was observed that MPV/PCT had a
sensitivity of 89.7% and a specificity of 100% for FN at the optimal
cut-off value of 57.33.
CONCLUSIONS: It can be said that among the indices we investigated,
the MPV/PCT is the primary variable predicting FN episodes
that may occur in pediatric oncology patients following
chemotherapy.

References

  • 1. 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):730–51.
  • 2. Freifeld AG, Bow EJ, Sepkowitz KA, et al. Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2011;52(4):e56–93.
  • 3. Masaoka T. Evidence-based recommendations for antimicrobial use in febrile neutropenia in Japan: Executive summary. Clin Infect Dis. 2004;39(1):49–52.
  • 4. Rosa RG, Goldani LZ. Factors associated with hospital length of stay among cancer patients with febrile Neutropenia. PLoS One. 2014;9(10):e108969.
  • 5. Kebudi R, DEvecioğlu Ö, Gürler N. Tanımlar ve tanı yöntemleri (Definitions and diagnostic approach in childhood febrile neutropenia). Flora. 2004;2:73–105.
  • 6. Özdemir ZC, Düzenli-Kar Y, Canik A, Küskü-Kiraz Z, Özen H, Bör Ö. The predictive value of procalcitonin, C- reactive protein, presepsin, and soluble-triggering receptor expressed on myeloid cell levels in bloodstream infections in pediatric patients with febrile neutropenia. Turk J Pediatr. 2019;61(3):359–67.
  • 7. Boeriu E, Borda A, Vulcanescu DD, et al. Diagnosis and management of febrile neutropenia in pediatric oncology patients - a systematic review. Diagnostics. 2022;12(8):1800.
  • 8. Mendes AVA, Sapolnik R, Mendonça N. New guidelines for the clinical management of febrile neutropenia and sepsis in pediatric oncology patients. J Pediatr (Rio J). 2007;83:54–63.
  • 9. Thangthong J, Anugulruengkitt S, Lauhasurayotin S, et al. Predictive factors of severe adverse events in pediatric oncologic patients with febrile neutropenia. Asian Pacific J Cancer Prev. 2020;21(12):3487–92.
  • 10. Cennamo F, Masetti R, Largo P, Argentiero A, Pession A, Esposito S. Update on febrile neutropenia in pediatric oncological patients undergoing chemotherapy. Children. 2021;8(12):1086.
  • 11. Llamas R, Acosta M, Silva J. Management of febrile neutropenia in pediatric cancer patients. J Pediatr Neonatal Care. 2019;9(1):22–6.
  • 12. Alali M, David MZ, Danziger-Isakov LA, Elmuti L, Bhagat PH, Bartlett AH. Pediatric febrile neutropenia: Change in etiology of bacteremia, empiric choice of therapy and clinical outcomes. J Pediatr Hematol Oncol. 2020;42(6):e445–51.
  • 13. Basu SK, Fernandez ID, Fisher SG, Asselin BL, Lyman GH. Length of stay and mortality associated with febrile neutropenia among children with cancer. J Clin Oncol. 2005;23(31):7958–66.
  • 14. Das A, Trehan A, Bansal D. Risk factors for microbiologically-documented infections, mortality and prolonged hospital stay in children with febrile neutropenia. Indian Pediatr. 2018;55(10):859–64.
  • 15. Markanday A. Acute phase reactants in infections: evidence-based review and a guide for clinicians. Open forum Infect Dis Oxford Univ Press. 2015;2(3):ofv098.
  • 16. Niehues T. C-reactive protein and other biomarkers the sense and non-sense of using inflammation biomarkers for the diagnosis of severe bacterial infection. LymphoSign J. 2018;5(2):35–47.
  • 17. Kim DY, Lee YS, Ahn S, Chun YH, Lim KS. The usefulness of procalcitonin and C-reactive protein as early diagnostic markers of bacteremia in cancer patients with febrile neutropenia. Cancer Res Treat. 2011;43(3):176– 80.
  • 18. Lin SG, Hou TY, Huang DH, et al. Role of procalcitonin in the diagnosis of severe infection in pediatric patients with fever and neutropenia-a systemic review and meta-analysis. Pediatr Infect Dis J. 2012;31(10):e182–8.
  • 19. Durnaś B, Wątek M, Wollny T, et al. Utility of blood procalcitonin concentration in the management of cancer patients with infections. Onco Targets Ther. 2016;9:469–75.
  • 20. Christ-Crain M, Schuetz P, Huber AR, Müller B. Procalcitonin: Importance for the diagnosis of bacterial infections. Laboratoriums Medizin. 2008;65(9):559-68.
  • 21. Leader A, Pereg D, Lishner M. Are platelet volume indices of clinical use? A multidisciplinary review. Ann Med. 2012;44(8):805–16.
  • 22. Choi A, Park I, Lee HS, Chung J, Kim MJ, et al. Usefulness of complete blood count parameters to predict poor outcomes in cancer patients with febrile neutropenia presenting to the emergency department. Ann Med. 2022;54(1):599–609.
  • 23. Detopoulou P, Panoutsopoulos GI, Mantoglou M, et al. Relation of mean platelet volume (MPV) with cancer: A systematic review with a focus on disease outcome on twelve types of cancer. Curr Oncol. 2023;30(3):3391–420
  • 24. Korniluk A, Koper-Lenkiewicz OM, Kamińska J, Kemona H, Dymicka-Piekarska V. Mean platelet volume (MPV): New perspectives for an old marker in the course and prognosis of inflammatory conditions. Mediators Inflamm. 2019;17:9213074.
  • 25. Kim CH, Kim SJ, Lee MJ, et al. An increase in mean platelet volume from baseline is associated with mortality in patients with severe sepsis or septic shock. PLoS One. 2015;10(3):1–13.
  • 26. Halalsheh OM, Al Zu’bi YO, Al Sharie AH, et al. The prognostic utility of lymphocyte-based measures and ratios in chemotherapy-ınduced febrile neutropenia patients following granulocyte colony-stimulating factor therapy. Med. 2022;58(11):1508.
  • 27. Ma K, Zhang Y, Hao J, Zhao J, Qi Y, Liu C. Correlation analysis of systemic immune inflammatory index, serum IL-35 and HMGB-1 with the severity and prognosis of sepsis. Pakistan J Med Sci. 2023;39(2):497–501.
  • 28. Wang H, Huang Z, Xu B, et al. The predictive value of systemic immune-inflammatory markers before and after treatment for pathological complete response in patients undergoing neoadjuvant therapy for breast cancer: a retrospective study of 1994 patients. Clin Transl Oncol. 2024;1–13(0123456789).
  • 29. Boccia R, Glaspy J, Crawford J, Aapro M. Chemotherapy-induced neutropenia and febrile neutropenia in the US: A beast of burden that needs to be tamed? Oncologist. 2022;27(8):625–36.
  • 30. Nessle CN, Njuguna F, Dettinger J, et al. Barriers to and facilitators of effective management of fever episodes in hospitalised Kenyan children with cancer: protocol for convergent mixed methods study. BMJ Open. 2023;13(11):e078124.
  • 31. Cullen M, Baijal S. Prevention of febrile neutropenia: Use of prophylactic antibiotics. Br J Cancer. 2009;101:11–4.
  • 32. Mohammed HB, Yismaw MB, Fentie AM, Tadesse TA. Febrile neutropenia management in pediatric cancer patients at Ethiopian Tertiary Care Teaching Hospital. BMC Res Notes. 2019;12(1):1–6.
  • 33. Gonzalez ML, Aristizabal P, Loera-Reyna A, et al. The golden hour: Sustainability and clinical outcomes of adequate time to antibiotic administration in children with cancer and febrile neutropenia in Northwestern Mexico. JCO Glob Oncol. 2021;(7):659–70.
  • 34. Green LL, Goussard P, Van Zyl A, Kidd M, Kruger M. Predictive indicators to identify high-risk paediatric febrile neutropenia in paediatric oncology patients in a middle-income country. J Trop Pediatr. 2018;64(5):395–402.
  • 35. Mikoshiba T, Saito S, Ikari Y, et al. Usefulness of hematological inflammatory markers in predicting severe side-effects from induction chemotherapy in head and neck cancer patients. Anticancer Res. 2019;39(6):3059– 65.
  • 36. Kim YJ, Kang J, Ryoo SM, Ahn S, Huh JW, Kim WY. Platelet-lymphocyte ratio after granulocyte colony stimulating factor administration: An early prognostic marker in septic shock patients with chemotherapy- ınduced febrile neutropenia. Shock. 2019;52(2):160–5.
  • 37. Kumazawa S, Mizuno T, Muramatsu N, et al. Neutrophil-lymphocyte ratio is associated with occurrence of febrile neutropenia in patients treated with 5-fluorouracil and cisplatin. In Vivo. 2022;36(5):2319–83.
  • 38. Secmeer G, Devrim I, Kara A, et al. Role of procalcitonin and CRP in differentiating a stable from a deteriorating clinical course in pediatric febrile neutropenia. J Pediatr Hematol Oncol. 2007;29(2):107–11.
  • 39. Becker KL, Snider R, Nylen ES. Procalcitonin in sepsis and systemic inflammation: A harmful biomarker and a therapeutic target. Br J Pharmacol. 2010;159(2):253–64.
  • 40. Chambliss AB, Patel K, Colón-Franco JM, et al. AACC guidance document on the clinical use of procalcitonin. J Appl Lab Med. 2023;8(3):598–634.
There are 40 citations in total.

Details

Primary Language Turkish
Subjects Pediatric Hematology and Oncology
Journal Section Articles
Authors

Arzu Keskin Aktan 0000-0002-2878-0841

İbrahim Eker 0000-0002-1880-546X

Fatma Nur Üstün 0009-0009-0839-3439

Ali İhsan Karaman 0009-0001-7089-8739

Ahmet Eren Çağıl 0009-0008-0987-7286

Buket Çam 0009-0000-8986-4830

Ece Merve Sökmen 0009-0007-5825-9081

Nilüfer Bağcı 0009-0007-9299-9059

Tuana Kepel 0009-0009-4317-9569

Publication Date October 13, 2025
Submission Date May 8, 2024
Acceptance Date February 24, 2025
Published in Issue Year 2025 Volume: 26 Issue: 4

Cite

APA Keskin Aktan, A., Eker, İ., Üstün, F. N., … Karaman, A. İ. (2025). KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ. Kocatepe Tıp Dergisi, 26(4), 286-294. https://doi.org/10.18229/kocatepetip.1477957
AMA Keskin Aktan A, Eker İ, Üstün FN, et al. KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ. Kocatepe Tıp Dergisi. October 2025;26(4):286-294. doi:10.18229/kocatepetip.1477957
Chicago Keskin Aktan, Arzu, İbrahim Eker, Fatma Nur Üstün, Ali İhsan Karaman, Ahmet Eren Çağıl, Buket Çam, Ece Merve Sökmen, Nilüfer Bağcı, and Tuana Kepel. “KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL LENFOSİT ORANI, PLATELET LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ”. Kocatepe Tıp Dergisi 26, no. 4 (October 2025): 286-94. https://doi.org/10.18229/kocatepetip.1477957.
EndNote Keskin Aktan A, Eker İ, Üstün FN, Karaman Aİ, Çağıl AE, Çam B, Sökmen EM, Bağcı N, Kepel T (October 1, 2025) KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ. Kocatepe Tıp Dergisi 26 4 286–294.
IEEE A. Keskin Aktan, İ. Eker, F. N. Üstün, A. İ. Karaman, A. E. Çağıl, B. Çam, E. M. Sökmen, N. Bağcı, and T. Kepel, “KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ”, Kocatepe Tıp Dergisi, vol. 26, no. 4, pp. 286–294, 2025, doi: 10.18229/kocatepetip.1477957.
ISNAD Keskin Aktan, Arzu et al. “KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL LENFOSİT ORANI, PLATELET LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ”. Kocatepe Tıp Dergisi 26/4 (October2025), 286-294. https://doi.org/10.18229/kocatepetip.1477957.
JAMA Keskin Aktan A, Eker İ, Üstün FN, Karaman Aİ, Çağıl AE, Çam B, Sökmen EM, Bağcı N, Kepel T. KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ. Kocatepe Tıp Dergisi. 2025;26:286–294.
MLA Keskin Aktan, Arzu et al. “KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL LENFOSİT ORANI, PLATELET LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ”. Kocatepe Tıp Dergisi, vol. 26, no. 4, 2025, pp. 286-94, doi:10.18229/kocatepetip.1477957.
Vancouver Keskin Aktan A, Eker İ, Üstün FN, Karaman Aİ, Çağıl AE, Çam B, et al. KEMOTERAPİ SONRASI FEBRİL NÖTROPENİ ATAĞI GEÇİREN PEDİATRİK ONKOLOJİ HASTALARINDA NÖTROFİL/LENFOSİT ORANI, PLATELET/LENFOSİT ORANI, SİSTEMİK İMMÜN-İNFLAMASYON İNDEKSİ VE ORTALAMA TROMBOSİT HACMİYLE İLİŞKİLİ İNDEKSLERİN DEĞERLENDİRİLMESİ. Kocatepe Tıp Dergisi. 2025;26(4):286-94.