Proportional weight loss in six months as a risk factor for mortality in stage IV non-small cell lung cancer.

OBJECTIVE: To evaluate different weight loss (WL) cut-off points as prognostic markers of 3-month survival after diagnosis of stage IV non-small cell lung cancer (NSCLC).
METHODS: This was a prospective study involving 104 patients with metastatic (stage IV) NSCLC who were admitted to a cancer treatment center in southern Brazil between January of 2014 and November of 2016. We evaluated total WL and WL per month, as well as WL and WL per month in the 6 months preceding the diagnosis. The patients were followed for 3 months after diagnosis. A Cox proportional hazards regression model and Kaplan-Meier curves were used in order to evaluate 3-month survival.
RESULTS: The median WL in the 6 months preceding the diagnosis was 6% (interquartile range, 0.0-12.9%). Patients with WL ≥ 5% had a median survival of 78 days, compared with 85 days for those with WL < 5% (p = 0.047). Survival at 3 months was 72% for the patients with WL ≥ 5% (p = 0.047), 61% for those with WL ≥ 10% (p < 0.001), and 45% for those with WL ≥ 15% (p < 0.001). In the multivariate analysis, the hazard ratio for risk of death was 4.51 (95% CI: 1.32-15.39) for the patients with WL ≥ 5%, 6.34 (95% CI: 2.31-17.40) for those with WL ≥ 10%, and 14.17 (95% CI: 5.06-39.65) for those with WL ≥ 15%.
CONCLUSIONS: WL in the 6 months preceding the diagnosis of NSCLC is a relevant prognostic factor and appears to be directly proportional to the rate of survival at 3 months.

INTRODUCTION

Weight loss (WL) is a common complaint of patients with lung cancer and a common reason for patient referral to a specialist. - Cancer cachexia, resulting from an imbalance between energy intake and consumption, is associated with a combination of poor caloric intake and increased resting energy expenditure, probably due to a cytokine-induced systemic inflammatory response. - Some studies have demonstrated that this increase in resting energy expenditure can also vary depending on the type of tumor. , Other factors that contribute to cancer cachexia include nausea, vomiting, constipation, diarrhea, pain, altered taste perception, and depression.

Despite its potential benefit for the clinical evaluation of patients with non-small cell lung cancer (NSCLC), the definition of cachexia varies significantly across studies and many WL cut-off points have been proposed in the attempt to classify the syndrome in an objective manner. - A recent consensus suggested that WL be defined as any decrease greater than 5% in relation to the usual weight or greater than 2% in individuals with a body mass index < 20 kg/m2. However, setting up a single cut-off point to classify cachexia can underestimate its real prognostic value. Different levels of cachexia severity can have various effects on the prognosis of cancer and could serve as a valuable clinical indicator.

The objective of this study was to evaluate 3-month survival in a population of patients with stage IV NSCLC. We also tested the prognostic value of different WL cut-off points.

METHODS

Study population

This prospective cohort study was conducted at Santa Rita Hospital, an oncology referral center and part of the Santa Casa de Misericórdia de Porto Alegre Hospital Complex, in the city of Porto Alegre, located in southern Brazil. We included consecutive patients newly diagnosed with metastatic (stage IV) NSCLC and admitted to Santa Rita Hospital between January of 2014 and November of 2016. Patients were treated at the discretion of the attending physician. All patients received a nutritional consultation at admission, regularly received high-calorie meals, and were instructed to rest before meals. However, they did not receive any type of nutritional supplementation as part of the palliative care or during chemotherapy. The follow-up period was ≤ 3 months after the diagnosis of cancer, as confirmed by reviews of medical records, hospital records, and phone calls. All diagnoses required clinical, radiological, and histological confirmation. Patients who had previously undergone antineoplastic treatment were excluded, as were those who were under 18 years of age. Survival and mortality rates were calculated from the time of the histological diagnosis until death or until the end of the third month of follow-up. Patient charts were reviewed, and tumor-node-metastasis variables were upgraded in accordance with the revised stage groupings established by the International Association for the Study of Lung Cancer. Performance status was assessed with the Eastern Cooperative Oncology Group scale. ) The study was approved by the local institutional review board. All participating patients gave written informed consent.

WL classification

Each patient was prospectively evaluated following the standards established in previous reports. Definitions of WL-related variables were also based on those established in other studies : total WL-the difference between weight at the time of diagnosis and usual weight; WL per month-total WL divided by the number of months of WL; and WL per month in 6 months-total difference between weight at the time of diagnosis and weight in the preceding 6 months. Patients were also subjectively evaluated in terms of their self-awareness of WL at the time of NSCLC diagnosis in relation to their usual weight. Different WL cut-off points (5%, 10%, and 15%) were tested in order to classify cachexia and to correlate the different degrees of cachexia with the survival rates.

Statistical analysis

Continuous variables are expressed as medians and interquartile range (IQR). Univariate analyses of survival were based on the Kaplan-Meier method. Survival was calculated by Cox proportional hazards regression model in a multivariate analysis. The Wald test was used in order to calculate significance for each factor. All parameters associated with mortality (p < 0.1) in the univariate analysis were included in a multivariate model, in which values of p < 0.05 were considered statistically significant. All tests were two-tailed, with the level of significance set at 0.05. All results were analyzed with the SPSS Statistics software package, version 20.0 (IBM Corporation, Armonk, NY, USA).

RESULTS

Patient characteristics are summarized in Table 1. The median age was 63 years (IQR, 52.5-69.0 years). Of a total of 104 patients evaluated, 63 (60.6%) were male. The most prevalent histological type of NSCLC was adenocarcinoma, which was seen in 57 (54.7%) of the patients, followed by squamous cell carcinoma, seen in 36 (34.6%), and mixed/undefined, seen in 11 (10.6%). The median Eastern Cooperative Oncology Group performance status was 2 (IQR, 1-3). Most (60.6%) of the patients underwent chemotherapy after diagnosis. Of the 104 patients, 44 (42.3%) underwent radiation therapy and 10 (9.6%) received supportive care exclusively. The 3-month mortality rate was 20.1% (95% CI: 12.9-29.1), 21 patients dying within the first 3 months after being diagnosed with cancer. The median WL in 6 months was 6% (IQR, 0.0-12.9%).

Table 1

Baseline anthropometric and clinical characteristics of the study sample.

Characteristic	N = 104
Male gender, n (%)	63 (60.6)
Age (years), median (IQR)	63 (52.5 to 69.0)
Body weight at diagnosis (kg), median (IQR)	63 (53.0 to 70.7)
Patient awareness of WL, n (%)	67 (64.4)
Smoking status, n (%)
Non-smoker	18 (17.3)
Former smoker	51 (49.0)
Current smoker	35 (33.7)
Total WL, median (IQR)	−6.0% (−12.9% to 0%)
WL per month, median (IQR)	−1.0% (−2.1% to 0%)
WL in 6 months, median (IQR)	−6.0% (−12.4% to 0%)
WL in 6 months ≥ 5%, n (%)	59 (56.7)
WL in 6 months ≥ 10%, n (%)	36 (34.6)
WL in 6 months ≥ 15%, n (%)	22 (21.2)
ECOG PS, median (IQR)	2 (1 to 3)
Tumor cell type, n (%)
Adenocarcinoma	57 (54.8)
Squamous cell carcinoma	36 (34.6)
Mixed or undefined histology	11 (10.6)
Main treatment, n (%)
Chemotherapy	63 (60.6)
Supportive care only	10 (9.6)
Radiation therapy	44 (42.3)

IQR: interquartile range; WL: weight loss; and ECOG-PS: Eastern Cooperative Oncology Group performance status.

Patient outcomes, stratified by WL cut-off points, are summarized in Table 2. All cut-off points for WL in 6 months were statistically associated with a poorer prognosis as assessed by mean days of survival in 3 months. Patients with WL ≥ 5% had a mean survival of 78 days, compared with 85 days for those with WL < 5% (p = 0.047). When the WL cut-off points of ≥ 10% and ≥ 15% were applied, the mean survival decreased to 73 days and 66 days, respectively (p < 0.001 for both). However, there was no statistically significant difference between the patients who were aware of their WL and those who were not in terms of the 3-month survival rate (p = 0.081).

Table 2

Kaplan-Meier survival analysis, by weight loss-related variable.

Variable	Mean survival	χ2	p*
	Days (95% CI)
WL, self-awareness
Yes	85 (80-89)	3.05	0.080
No	78 (73-84)
Proportional WL in 6 months
< 5%	85 (80-89)	3.94	0.047
≥ 5%	78 (72-84)
< 10%	85 (81-89)	11.58	< 0.001
≥ 10%	73 (64-82)
< 15%	85 (81-88)	23.78	< 0.001
≥ 15%	66 (53-78)

WL: weight loss. *Log-rank test.

Kaplan-Meier survival curves for the first 3 months after diagnosis are shown in Figure 1. We observed a direct linear trend between the proportional WL and mortality. Event-free survival at 3 months was 88% for the patients with WL < 5%, compared with 72% for those with WL ≥ 5% (p = 0.047), 61% for those with WL ≥ 10% (p < 0.001), and 45% for those with WL ≥ 15% (p < 0.001).

Figure 1

Kaplan-Meier curves of cumulative survival probability, by weight loss cut-off point.

The outcomes of the Cox proportional hazards regression model are summarized in Table 3. The univariate and multivariate (adjusted) analyses both demonstrated that the risk of death during the 3-month follow-up period was higher when the higher WL cut-off points were applied. The adjusted multivariate analysis showed that the risk of death increases exponentially as the cut-off points of WL increase, the hazard ratios for the 5%, 10%, and 15% cut-off points being 4.51 (95% CI: 1.32-15.39), 6.34 (95% CI: 2.31-17.40), and 14.17 (95% CI: 5.06-39.65), respectively.

Table 3

Crude and adjusted hazard ratios for weight-loss related prognostic factors.

Variable	Crude HR (95% CI)	p	Adjusted HR* (95% CI)	p
WL, self-awareness	2.54 (0.86-7.49)	0.089	3.59 (1.03-12.48)	0.044
WL in 6 months ≥ 5%	2.65 (0.97-7.21)	0.055	4.51 (1.32-15.39)	0.016
WL in 6 months ≥ 10%	4.45 (1.80-10.99)	0.001	6.34 (2.31-17.40)	< 0.001
WL in 6 months ≥ 15%	6.53 (2.76-15.44)	< 0.001	14.17 (5.06-39.65)	< 0.001

HR: hazard ratio; and WL: weight loss. *Cox proportional hazards regression model analysis, adjusted for gender, age, Eastern Cooperative Oncology Group performance status, and tumor cell type.

DISCUSSION

In the present study, our aim was to determine the value of WL as a prognostic factor in patients with NSCLC, as well as whether that association differs among four WL cut-off points. We have shown that greater WL translates to shorter overall survival for patients with NSCLC. We found that, among patients with advanced NSCLC, the 3-month mortality rate was almost two times higher for those with WL ≥ 15% than for those with WL < 5%. Our results suggest that pre-treatment WL is an important clinical parameter with relevant prognostic value in patients with advanced NSCLC.

Our findings are consistent with those of previous studies that evaluated survival and WL in populations of lung cancer patients that were more heterogeneous, including patients in different stages of the disease. - , - , - The prognostic significance of WL in stage IV NSCLC could be attributed to the potential link to cachexia. Defined as a multifactorial syndrome of progressive loss of skeletal muscle mass that cannot be completely reversed, cachexia has a heterogeneous clinical presentation that varies according to tumor type, site, and stage. , Lung cancer is often accompanied by malnutrition, sarcopenia, and cachexia. Following the cancer-specific cachexia classifications, van der Meij et al. demonstrated that, at the time of diagnosis, approximately 18% and 23% of stage III NSCLC patients had cachexia or were in a state of pre-cachexia, respectively. However, the exact basis of these prognostic differences remains unknown.

Several hypotheses have been proposed to explain the association between cachexia and poorer prognosis. Some authors have suggested that the survival advantage associated with obesity is due to the relatively large energy stores. - Conversely, when the stores are depleted, the energy balance is negative. - Cachexia and a loss of skeletal muscle mass are associated with poor prognosis in patients with advanced NSCLC who are receiving chemotherapy. , Another hypothesis is that individuals with sarcopenia are susceptible to infections during hospitalization and residence in nursing homes, where such infections and premature termination of treatment are both possible contributors to shortened survival. Accordingly, the well-recognized poor prognosis in advanced lung cancer masks some heterogeneity that could be partially explained by WL stratification and other, as yet unconfirmed, biological factors.

Cachexia is a multifactorial syndrome with a complex pathogenesis. Therefore, multimodal interventions should be used in order to prevent WL among patients with cachexia. Frequent high-calorie meals and rest before meals are recommended. Currently, there is little evidence that nutritional supplementation is efficacious. Physical activity has an anti-inflammatory effect and is effective in reducing muscle catabolism, increasing protein synthesis, and reversing protein degradation. Pharmacological treatment can also be used to prevent cachexia. Corticosteroids and progesterone analogs have been shown to increase appetite, thus resulting in modest weight gain. However, such drugs do not improve survival or quality of life.

Our study has some limitations, not the least of which is the small sample size. In addition, there are many confounding variables that could influence the analysis of 3-month survival of patients with advanced NSCLC. One such variable is the main treatment adopted, which, in our sample. was quite heterogeneous, therefore potentially affecting the prognosis. However, we believe that using a Cox proportional hazards regression model was an effective strategy to reduce the influence of those confounders, and the associations detected retained their significance even after the multivariate analyses. Studies including larger patient samples are needed in order to corroborate our findings. Further studies should also include biomarkers linked to aggressive behavior of lung cancer, such as circulating tumor cells and circulating cell-free nucleic acids, which could also affect survival rates, and patients who have such biomarkers might show different rates of WL.

Although increased efforts have been directed toward the identification of biological markers as prognostic indicators of lung cancer, there are some important clinical indices that should be also considered more thoroughly. In conclusion, our results indicate that proportional WL is an important prognostic factor for 3-month survival after diagnosis in patients with stage IV NSCLC.