Prognostic value of neutrophil-to-lymphocyte ratio and other inflammatory markers in patients with high-risk soft tissue sarcomas.


Journal

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
ISSN: 1699-3055
Titre abrégé: Clin Transl Oncol
Pays: Italy
ID NLM: 101247119

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 28 01 2020
accepted: 12 02 2020
pubmed: 4 3 2020
medline: 4 6 2021
entrez: 4 3 2020
Statut: ppublish

Résumé

Soft tissue sarcomas (STS) have a high risk of relapse in spite of the use of (neo)adjuvant chemotherapy. In this context, looking for new prognostic biomarkers is an interesting field of research. Our aim is to analyze the prognostic impact of neutrophil-to-lymphocyte ratio (NLR) and other serum markers in patients with STS who received chemotherapy with curative intent. This is a retrospective observational study. We included all patients with STS (primary tumor, local recurrence or resected metastatic disease) treated with high-dose ifosfamide and epirubicin with curative intent from January 2007 to December 2018. The pretreatment NLR and other serum markers were calculated, selecting the median as the cut-off value for the survival and multivariate analysis. Seventy-nine patients were included. Median NLR, platelet-to-lymphocyte ratio (PLR) and lymphocyte-to-monocyte ratio (LMR) were 2.83, 174.05 and 3.25, respectively. Median progression-free survival (PFS) was significantly longer in patients with low NLR [not reached (NR) vs 21, 92 months, P < 0.01]. No significant differences were found for PFS regarding PLR or LMR. For overall survival (OS), a significant survival advantage was also found for patients with low NLR (NR vs 65.45 months, P = 0.01), without differences for PLR or LMR. In multivariate analysis, NLR remains an independent prognostic factor for PFS. In our cohort, low NLR was significantly associated with a longer PFS and OS, and is consolidated as an independent prognostic factor.

Sections du résumé

BACKGROUND BACKGROUND
Soft tissue sarcomas (STS) have a high risk of relapse in spite of the use of (neo)adjuvant chemotherapy. In this context, looking for new prognostic biomarkers is an interesting field of research. Our aim is to analyze the prognostic impact of neutrophil-to-lymphocyte ratio (NLR) and other serum markers in patients with STS who received chemotherapy with curative intent.
MATERIALS AND METHODS METHODS
This is a retrospective observational study. We included all patients with STS (primary tumor, local recurrence or resected metastatic disease) treated with high-dose ifosfamide and epirubicin with curative intent from January 2007 to December 2018. The pretreatment NLR and other serum markers were calculated, selecting the median as the cut-off value for the survival and multivariate analysis.
RESULTS RESULTS
Seventy-nine patients were included. Median NLR, platelet-to-lymphocyte ratio (PLR) and lymphocyte-to-monocyte ratio (LMR) were 2.83, 174.05 and 3.25, respectively. Median progression-free survival (PFS) was significantly longer in patients with low NLR [not reached (NR) vs 21, 92 months, P < 0.01]. No significant differences were found for PFS regarding PLR or LMR. For overall survival (OS), a significant survival advantage was also found for patients with low NLR (NR vs 65.45 months, P = 0.01), without differences for PLR or LMR. In multivariate analysis, NLR remains an independent prognostic factor for PFS.
CONCLUSION CONCLUSIONS
In our cohort, low NLR was significantly associated with a longer PFS and OS, and is consolidated as an independent prognostic factor.

Identifiants

pubmed: 32125644
doi: 10.1007/s12094-020-02324-8
pii: 10.1007/s12094-020-02324-8
doi:

Substances chimiques

L-Lactate Dehydrogenase EC 1.1.1.27

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1849-1856

Auteurs

D Viñal (D)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

D Martinez (D)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

J A Garcia-Cuesta (JA)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

L Gutierrez-Sainz (L)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

S Martinez-Recio (S)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

J Villamayor (J)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

V Martinez-Marin (V)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.
Translational Oncology Group, IdiPAZ, Madrid, Spain.

A Gallego (A)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.

E Ortiz-Cruz (E)

Department of Orthopaedic Surgery, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046, Madrid, Spain.

M Mendiola (M)

Molecular Pathology and Therapeutic Targets Group, IdiPAZ, Madrid, Spain.
CIBERONC, Madrid, Spain.

J J Pozo-Kreilinger (JJ)

Molecular Pathology and Therapeutic Targets Group, IdiPAZ, Madrid, Spain.
Department of Pathology, Hospital Universitario La Paz, Madrid, Spain.
Faculty of Medicine, Universidad Autonoma de Madrid, Madrid, Spain.

A Berjon (A)

Department of Pathology, Hospital Universitario La Paz, Madrid, Spain.

B Belinchon (B)

Department of Radiation Oncology, Hospital Universitario La Paz, Madrid, Spain.

D Bernabeu (D)

Department of Radiology, Hospital Universitario La Paz, Madrid, Spain.

E Espinosa (E)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.
Faculty of Medicine, Universidad Autonoma de Madrid, Madrid, Spain.
Translational Oncology Group, IdiPAZ, Madrid, Spain.
CIBERONC, Madrid, Spain.
Cátedra UAM-AMGEN, Madrid, Spain.

J Feliu (J)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.
Faculty of Medicine, Universidad Autonoma de Madrid, Madrid, Spain.
Translational Oncology Group, IdiPAZ, Madrid, Spain.
CIBERONC, Madrid, Spain.
Cátedra UAM-AMGEN, Madrid, Spain.

A Redondo (A)

Department of Medical Oncology, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain. andres.redondos@uam.es.
Faculty of Medicine, Universidad Autonoma de Madrid, Madrid, Spain. andres.redondos@uam.es.
Translational Oncology Group, IdiPAZ, Madrid, Spain. andres.redondos@uam.es.
Cátedra UAM-AMGEN, Madrid, Spain. andres.redondos@uam.es.

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Classifications MeSH