Prognostic Value of the Neutrophil-to-Lymphocyte Ratio before and after Radiotherapy for Anaplastic Thyroid Carcinoma

The neutrophil-lymphocyte ratio (NLR) is a marker of systemic inflammation, and its elevation has recently been associated with poor survival in many solid cancers. Leukocyte elevation and lymphocyte reduction are associated with a poor response to radiotherapy (RT). This study aimed to assess the p...

Full description

Saved in:
Bibliographic Details
Published inCancers Vol. 13; no. 8; p. 1913
Main Authors Park, Jiyun, Park, Jun, Shin, Jung-Hee, Oh, Young-Lyun, Jung, Hyun-Ae, Chung, Man-Ki, Choe, Jun-Ho, Ahn, Yong-Chan, Kim, Sun-Wook, Chung, Jae-Hoon, Kim, Tae-Hyuk, Noh, Jae-Myoung
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 15.04.2021
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The neutrophil-lymphocyte ratio (NLR) is a marker of systemic inflammation, and its elevation has recently been associated with poor survival in many solid cancers. Leukocyte elevation and lymphocyte reduction are associated with a poor response to radiotherapy (RT). This study aimed to assess the prognostic value of NLR before and after RT for anaplastic thyroid carcinoma (ATC). This retrospective study analyzed 40 patients with ATC who received RT with available complete blood cell count data from November 1995 through May 2020 at Samsung Medical Center (Seoul, Korea). Patients were classified into two groups according to the NLR before and after RT. The median overall survival (OS) was 8.9 months (range, 3.5-18.2) in the low NLR group (<3.47) and 5.2 months (range, 2.7-7.5) months in the high NLR group (≥3.47). The association between NLR and OS was also observed in multivariable Cox regression analysis (hazard ratio, 3.18; 95% confidence interval, 1.15-8.85; = 0.026). The OS curves differed significantly according to post-RT NLR ( = 0.036). A high NLR before and after RT may be significantly associated with poor OS in patients with ATC who receive RT.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These two authors contributed equally to this work.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers13081913