Abstract
Background
Soft tissue sarcomas are a heterogenous group of neoplasms without well-validated
biomarkers. Cancer-related inflammation is a known driver of tumor growth and progression.
Recent studies have implicated a high circulating neutrophil-lymphocyte ratio as a
surrogate marker for the inflammatory tumor microenvironment and a poor prognosticator
in multiple solid tumors, including colorectal and pancreatic cancers. The impact
of circulating neutrophil-lymphocyte ratio in soft tissue sarcomas has yet to be elucidated.
Methods
We performed a retrospective analysis of patients undergoing curative resection for
primary or recurrent extremity soft tissue sarcomas at academic centers within the
US Sarcoma Collaborative. Neutrophil-lymphocyte ratio was calculated retrospectively
in treatment-naïve patients using blood counts at or near diagnosis.
Results
A high neutrophil-lymphocyte ratio (≥4.5) was associated with worse survival on univariable
analysis in patients with extremity soft tissue sarcomas (hazard ratio 2.07; 95% confidence
interval, 1.54–2.8; P < .001). On multivariable analysis, increasing age (hazard ratio 1.03; 95% confidence
interval, 1.02–1.04; P < .001), American Joint Committee on Cancer T3 (hazard ratio 1.89; 95% confidence
interval, 1.16–3.09; P = .011), American Joint Committee on Cancer T4 (hazard ratio 2.36; 95% confidence
interval, 1.42–3.92; P = .001), high tumor grade (hazard ratio 4.56; 95% confidence interval, 2.2–9.45;
P < .001), and radiotherapy (hazard ratio 0.58; 95% confidence interval, 0.41–0.82;
P = .002) were independently predictive of overall survival, but a high neutrophil-lymphocyte
ratio was not predictive of survival (hazard ratio 1.26; 95% confidence interval,
0.87–1.82; P = .22).
Conclusion
Tumor inflammation as measured by high pretreatment neutrophil-lymphocyte ratio was
not independently associated with overall survival in patients undergoing resection
for extremity soft tissue sarcomas.
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Article info
Publication history
Published online: July 28, 2020
Accepted:
June 10,
2020
Identification
Copyright
© 2020 Elsevier Inc. All rights reserved.