TY - JOUR
T1 - Pretreatment monocyte counts and neutrophil counts predict the risk for febrile neutropenia in patients undergoing TPF chemotherapy for head and neck squamous cell carcinoma
AU - Shimanuki, Marie
AU - Imanishi, Yorihisa
AU - Sato, Yoichiro
AU - Nakahara, Nana
AU - Totsuka, Daisuke
AU - Sato, Emiri
AU - Iguchi, Sena
AU - Sato, Yasuo
AU - Soma, Keiko
AU - Araki, Yasutomo
AU - Shigetomi, Seiji
AU - Yoshida, Satoko
AU - Uno, Kosuke
AU - Ogawa, Yusuke
AU - Tominaga, Takehiro
AU - Ikari, Yuichi
AU - Nagayama, Junko
AU - Endo, Ayako
AU - Miura, Koshiro
AU - Tomioka, Takuya
AU - Ozawa, Hiroyuki
AU - Ogawa, Kaoru
N1 - Funding Information:
The authors thank Editage (www.editage.jp) for English language editing. This work was supported in part by the Grants-in-Aid for Scientific Research (C) from The Japan Society for the Promotion of Science (No.16K11245).
Publisher Copyright:
© Shimanuki et al.
PY - 2018/4/10
Y1 - 2018/4/10
N2 - Background: Febrile neutropenia (FN) is the most serious hematologic toxicity of systemic chemotherapy. However, accurate prediction of FN development has been difficult because the risk varies largely depending on the chemotherapy regimen and various individual factors. Methods: We retrospectively analyzed diverse clinical factors including pretreatment hematological parameters to clarify the reliable predictors of FN development during chemotherapy with a docetaxel, cisplatin, and fluorouracil (TPF) regimen in patients with head and neck squamous cell carcinoma. Results: Among the 50 patients, grade ≥3 neutropenia, grade 4 neutropenia, and FN developed in 36 (72%), 21 (42%), and 12 (24%) patients, respectively. Multivariate logistic regression revealed that a pretreatment absolute monocyte count (AMC) < 370/mm3 is an independent predictor of TPF chemotherapy-induced FN (odds ratio=6.000, p=0.017). The predictive performance of the model combining AMC and absolute neutrophil count (ANC), in which the high-risk group was defined as having an AMC < 370/mm3 and/or ANC < 3500/mm3, was superior (area under the curve [AUC]=0.745) to that of the model with a cutoff for AMC alone (AUC=0.679). Conclusions: On the basis of our results, we recommend primary prophylactic use of granulocyte colony-stimulating factor and/or antibiotics selectively for patients predicted to be at high risk for TPF chemotherapy-induced FN.
AB - Background: Febrile neutropenia (FN) is the most serious hematologic toxicity of systemic chemotherapy. However, accurate prediction of FN development has been difficult because the risk varies largely depending on the chemotherapy regimen and various individual factors. Methods: We retrospectively analyzed diverse clinical factors including pretreatment hematological parameters to clarify the reliable predictors of FN development during chemotherapy with a docetaxel, cisplatin, and fluorouracil (TPF) regimen in patients with head and neck squamous cell carcinoma. Results: Among the 50 patients, grade ≥3 neutropenia, grade 4 neutropenia, and FN developed in 36 (72%), 21 (42%), and 12 (24%) patients, respectively. Multivariate logistic regression revealed that a pretreatment absolute monocyte count (AMC) < 370/mm3 is an independent predictor of TPF chemotherapy-induced FN (odds ratio=6.000, p=0.017). The predictive performance of the model combining AMC and absolute neutrophil count (ANC), in which the high-risk group was defined as having an AMC < 370/mm3 and/or ANC < 3500/mm3, was superior (area under the curve [AUC]=0.745) to that of the model with a cutoff for AMC alone (AUC=0.679). Conclusions: On the basis of our results, we recommend primary prophylactic use of granulocyte colony-stimulating factor and/or antibiotics selectively for patients predicted to be at high risk for TPF chemotherapy-induced FN.
KW - Febrile neutropenia
KW - Head and neck squamous cell carcinoma
KW - Monocyte count
KW - Neutrophil count
KW - TPF
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U2 - 10.18632/oncotarget.24863
DO - 10.18632/oncotarget.24863
M3 - Article
C2 - 29721176
AN - SCOPUS:85045193544
SN - 1949-2553
VL - 9
SP - 18970
EP - 18984
JO - Oncotarget
JF - Oncotarget
IS - 27
ER -