Applicability of modified Glasgow Prognostic Score in the assessment of elderly patients with cancer: A pilot study

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Abstract

Objectives

To evaluate the relationship between inflammatory parameters through the modified Glasgow Prognostic Score (mGPS) and other clinical characteristics of elderly patients with cancer, including frailty evaluated by the Edmonton Frailty Scale (EFS).

Materials and Methods

We included patients from the oncology service at Faculdade de Medicina do ABC with a confirmed diagnosis of solid tumor aged 65 years or more at diagnosis. Patients were assessed by applying the translated and validated to Portuguese version of the EFS and also had blood sample collection for the evaluation of C-reactive protein (CRP) and albumin for calculation of the mGPS.

Results

We included 52 patients of both sexes, with median age of 72.5 years, of these 67.3% had localized disease and 32.7% metastatic disease. The mGPS presented 17.3% of high-risk patients. The frailty evaluated by EFS occurred in 57.6% of patients. Patients with both abnormal parameters (CRP and albumin) in the mGPS had significantly higher scores on EFS when compared to those with no change (6 vs. 9.56 points, p = 0.021). The mGPS correlated also with clinical staging (p = 0.019) and performance status (p = 0.039).

Conclusions

Inflammatory parameters correlate significantly with frailty, more advanced clinical stage and poor functional status.

Introduction

About 60% of new cases of cancer and 70% of mortality related to this disease occur in patients over 65 years of age [1], [2], [3]. Therefore, the oncologist should determine the best treatment for this clinically heterogeneous age group, ranging from those with multiple comorbidities that limit their quality of life and functional status to those with good health. Furthermore, elderly patients included in clinical studies often represent a carefully selected subset that usually does not include frail elderly and more debilitated subjects.

Frailty is defined as the loss of the ability to adapt to stress due to reduced functional reserves. Frail individuals have a higher risk of complications such as hospitalizations, falls, functional decline, difficulties in recovering from acute insults, greater risk of adverse events and mortality [4], [5]. There are several methods in the literature designed to evaluate for the presence of frailty in the elderly [6], [7]. Among them, the Edmonton Frail Scale (EFS) [7], already translated and validated into Portuguese [6], allows for the detection of frailty in the elderly population in an easy and expedient way.

Frailty is a multifactorial syndrome which has neuroendocrine and inflammatory components in its pathophysiology. Many authors proposed potential biological markers for this syndrome, but no typical laboratory profile associated with frailty has so far emerged. Interestingly, however, increased values of interleukin-6 (IL-6) and C-reactive protein (CRP) correlate with low body mass index (BMI) and frailty [8], [9]. Additionally, there is evidence that the host's inflammatory response plays a significant role in the development and progression of cancer [10], [11], [12], [13], [14].

The assessment of systemic inflammatory response was refined using a selective combination of CRP and albumin called the modified Glasgow Prognostic Score (mGPS) [15], [16], [17], [18]. Recently, it has been shown in a large study group with more than 200,000 patients (Glasgow Outcome Inflammation Study), that the mGPS is elevated in patients with cancer, when compared with those without cancer [17]. Furthermore, mGPS is an independent prognostic factor for several types of cancer including lung, gastrointestinal, and renal neoplasms [17].

Since mGPS is easy to measure and relates to inflammation, which is one of the mechanisms underlying frailty, the objective of this study was to evaluate whether mGPS is associated with frailty and other clinical characteristics of elderly patients with cancer at initial presentation.

Section snippets

Patients and Methods

This study was approved by the Ethics and Research Committee of the Faculdade de Medicina do ABC and all patients who agreed to participate signed the required informed consent forms. In this study cross-sectional study, we included patients with malignant solid tumors, aged 65 years or more, at the first Medical Oncology evaluation at Faculdade de Medicina do ABC. We included patients treated at Hospital Mário Covas in Santo André and the Hospital Padre Anchieta in São Bernardo do Campo, in the

General Characteristics

Between October and December 2014, 52 patients were included. Clinical and demographic characteristics of the patients included in the study are shown in Table 1. The median age was 72.5, most patients where male (55%), had localized disease (67%) and had an ECOG Performance Status of 0 (68%).

Laboratory and Clinical Parameters

The values of CRP and albumin are described in Table 2. Approximately 17% of all the patients presented a high-risk mGPS, and 57.6% of them had some degree of frailty by EFS. The median EFS score was of 7

Discussion

mGPS is a widely-studied prognostic factor based on the presence of an inflammatory response. Interestingly, McMillan [18] reviewing more than 60 papers, including more than 30,000 patients with cancer, reported that the mGPS correlated with the presence of a chronic inflammatory state. The characteristics of this inflammatory state were decreased muscle mass, lower functional level and by increased levels of inflammatory and angiogenic cytokines [18].

We observed in this study that the mGPS was

Disclosures and Conflict of Interest Statements

The authors have no conflicts of interest to disclose.

Author Contributions

Study concept: V Lealdini, A Del Giglio

Study design: V Lealdini, A Del Giglio, PX Santi

Data acquisition: V Lealdini, FBF da Silva, SRC Normando, EW Camargo

Quality control of data and algorithms: V Lealdini, DC Trufelli, EW Camargo

Data analysis and interpretation: DC Trufelli, LL de Matos, FLA Fonseca, FBF da Silva

Statistical analysis: DC Trufelli, LL de Matos, FLA Fonseca, SRC Normando

Manuscript preparation: V Lealdini, DC Trufelli, PX Santi

Manuscript editing: V Lealdini, DC Trufelli, PX Santi

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