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Association of Systemic Inflammation and Overall Survival in Elderly Patients with Cancer Cachexia – Results from a Multicenter Study
Authors Ruan GT, Yang M, Zhang XW, Song MM, Hu CL, Ge YZ, Xie HL, Liu T, Tang M, Zhang Q, Zhang X, Zhang KP, Li XR, Li QQ, Chen YB, Yu KY, Cong MH, Wang KH, Shi HP
Received 4 August 2021
Accepted for publication 9 October 2021
Published 27 October 2021 Volume 2021:14 Pages 5527—5540
DOI https://doi.org/10.2147/JIR.S332408
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Professor Ning Quan
Guo-Tian Ruan,1– 3,* Ming Yang,1– 3,* Xiao-Wei Zhang,1– 3,* Meng-Meng Song,1– 3 Chun-Lei Hu,1– 3 Yi-Zhong Ge,1– 3 Hai-Lun Xie,1– 3 Tong Liu,1– 3 Meng Tang,1– 3 Qi Zhang,1– 3 Xi Zhang,1– 3 Kang-Ping Zhang,1– 3 Xiang-Rui Li,1– 3 Qin-Qin Li,1– 3 Yong-Bing Chen,1– 3 Kai-Ying Yu,1– 3 Ming-Hua Cong,4 Kun-Hua Wang,5 Han-Ping Shi1– 3
1Department of Gastrointestinal Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, 100038, People’s Republic of China; 2Department of Clinical Nutrition, Beijing Shijitan Hospital, Capital Medical University, Beijing, 100038, People’s Republic of China; 3Beijing International Science and Technology Cooperation Base for Cancer Metabolism and Nutrition, Beijing, 100038, People’s Republic of China; 4Comprehensive Oncology Department, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100038, People’s Republic of China; 5Department of Surgery, The First Affiliated Hospital of Kunming Medical University, Kunming, 650000, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Han-Ping Shi
Department of Gastrointestinal Surgery and Beijing Shijitan Hospital, Capital Medical University, 10 Tie Yi Road, Beijing, 100038, People’s Republic of China
Tel +86-10- 6392 6985
Fax +86-10 -6392 6325
Email [email protected]
Background: Systemic inflammation and cachexia are associated with adverse clinical outcomes in elderly patients with cancer. The survival outcomes of elderly patients with cancer cachexia (EPCC) with high inflammation and a high risk of mortality are unknown. This study aimed to investigate the impact of high inflammation on the prognosis of EPCC patients with high mortality.
Patients and Methods: This multicenter cohort study included 746 EPCC (age > 65 years) with a mean age of 72.00 ± 5.24 years, of whom 489 (65.5%) were male. The cut-off value for the inflammation index was obtained using the optimal survival curve. The different inflammatory indicators were assessed using the concordance index (C-index), decision curve analysis (DCA), and prognostic receiver operating characteristic (ROC). The high mortality risk group of EPCC was defined by the 2011 Fearon Cancer Diagnostic Consensus. EPCC were divided into the high-risk group, which satisfies three diagnostic criteria, and a low-risk group, which satisfies only one or two diagnostic criteria.
Results: The C-index, DCA, and prognostic ROC indicated the superiority of advanced lung cancer inflammation index (ALI) compared with other indicators, including neutrophil–lymphocyte ratio (NLR), prognostic nutritional index (PNI), systemic immune-inflammation index (SII), and platelet–lymphocyte ratio (PLR). Whether ALI was used as a continuous or a categorical variable, ALI had a better prognostic value in EPCC compared with other inflammatory indicators. In particular, patients with low ALI (< 25.03) had a worse overall survival (OS) than patients with high ALI (≥ 25.03) (P < 0.001, HR [95% CI] = 2.092 [1.590– 2.751]). The combination effect analysis showed that the risk of mortality of the patients in the low-ALI and high-risk groups was 3.095-fold higher than that of patients in the high-ALI and low-risk groups.
Conclusion: The prognostic and discriminative value of the inflammatory indicator ALI was better than that of NLR, PNI, SII, and PLR in EPCC. The high-risk group of EPCC with a low ALI would increase the death risk of OS.
Keywords: ALI, systemic inflammation, cancer cachexia, elderly, overall survival
Introduction
Cancer cachexia is a complex and debilitating disease resulting from cancer progression. It is estimated that approximately 2 million people worldwide die from cancer-related cachexia each year.1 Although cachexia may affect all cancer patients, it is most often associated with malignancies involving the gastrointestinal tract and lungs.2 Patients with pancreatic or gastric cancer suffer from the highest frequency of unintended weight loss, wherein patients can lose up to 30% of their pre-morbid body weight.2 The elderly are one of the most heterogeneous and vulnerable groups, and are at higher risk for nutritional problems and sarcopenia. Sarcopenia, also known as age-related muscle atrophy and weakness, can aggravate the defects associated with cancer cachexia in the elderly and complicate the conditions in this population.3
Cancer cachexia is characterized by fat and skeletal muscle catabolism, leading to significant weight loss, decreased mobility and muscle function, fatigue, impaired quality of life, poor survival, and death in cases of a 25–30% weight loss.4,5 Cancer cachexia results from a combination of reduced food intake, increased inflammation, and abnormal metabolism, including increased energy expenditure and excessive catabolism.6 Reduced food intake due to anorexia and physical inactivity promotes the degradation of muscle protein and induces fatigue.7 This vicious cycle may be exacerbated by an increase in inflammation, thereby further limiting quality of life and increasing mortality in patients.8
Systemic inflammation is considered a key mediator of cachexia.9 The systemic inflammation in cachexia is caused by the interaction between the tumor and the peripheral tissue, and significantly participates in immune cell infiltration of the peripheral tissue and the tumor.10 Inflammation is usually associated with negative nitrogen balance and increased resting energy expenditure, leading to increased protein and energy requirements.11 Increasing evidence shows that the host inflammatory response is an important element in the occurrence and development of cancer,12 and is a main driving force behind changes in cancer metabolism.8 Indeed, systemic inflammation is a hallmark of cancer and is the main driving force for changes in cancer cachexia metabolism.13 The systemic inflammation of cancer is caused by a multitude of factors including cytokines and other inflammatory mediators released by tumors, cytokines and chemokines released by activated immune cells,14 and increased levels of circulating inflammatory components. These changes can be observed in the elderly as increased levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), IL-1 receptor antagonists, soluble TNF receptor, C-reactive protein (CRP), serum amyloid A, and neutrophil counts.15 Elderly have other conditions that favour weight loss and changes of body composition, in particular they typically present sarcopenia, that is independent from cancer, and can aggravate and further precipitate cachexia.15 For instance, IL-1β and TNF-α can act on glucose-sensitive neurons in the ventromedial nucleus (satisfaction area) and lateral hypothalamus (starvation area) to cause anorexia.16 The negative energy balance caused by anorexia leads to the aggravation of cancer cachexia. Decreased muscle mass and muscle strength are also common in the elderly.15 An inevitable result of aging, the continuous loss of skeletal muscle mass in patients with cancer cachexia causes further deterioration to the patient’s function. An increase in the concentration of inflammatory markers, such as cytokines, is related to a decrease in lean muscle mass.15 Some cytokines, including TNF-α, IL-6, IL-1β, and INF-, reproduce cachexia symptoms in animal models.17 In a previous study, IL-6 was injected directly into the muscle of mice, and 14 days later, a 17% decrease in myofibrillar protein was observed, indicating a direct effect on the muscles.18 The combination of age-related muscle loss and sustained muscle wasting caused by cancer cachexia may be a metabolic challenge that skeletal muscles in elderly patients cannot handle. The resulting metabolic abnormalities include increased glucose turnover, increased lipolysis, disarrayed hormone balance (such as in hypogonadism), increased insulin resistance, decreased net muscle protein balance, increased cytokine levels, and increased acute phase protein synthesis.19
At the time of writing, due to the increase in the aging population and the heterogeneity of the physical conditions of the elderly, simple and accurate prognostic indicators for elderly patients with cancer cachexia (EPCC) are urgently needed. Some currently available clinical prognostic indicators related to inflammation include advanced lung cancer inflammation index (ALI), neutrophil–lymphocyte ratio (NLR), prognostic nutritional index (PNI), systemic immune-inflammation index (SII), and platelet–lymphocyte ratio (PLR). However, the optimal prognostic inflammatory indicator in EPCC population still needs to be determined. This study aimed to identify the optimal inflammatory indicator for EPCC and to distinguish the EPCC population with high inflammation and high mortality risk.
Materials and Methods
Patient Selection and Study Design
This was a retrospective study of cancer data collected from multiple clinical centers in China from June 2012 to December 2019. Data included were strictly selected according to the inclusion and exclusion criteria. The inclusion criteria were age of 18 years and older, hospitalization time of 2 days or longer, diagnosis of cancer, and existence of signed consent form. The exclusion criteria were age of less than 18 years, hospitalization of less than 2 days, refusal to sign the consent form, and admitted to Intensive Care Unit at the beginning of recruitment. A total of 9727 patients with cancer were initially included in the cohort, and a total of 2560 patients were diagnosed with cancer cachexia. Finally, 746 EPCC (age > 65 years) were included in this study. The details are presented in the flowchart (Figure S1).This retrospective study followed the Declaration of Helsinki. All participating units or institutions were approved by the ethics committee (registration number: ChiCTR1800020329), and all participants signed an informed consent form (Table S1).
Patient Evaluation
This study collected comprehensive patient information, including demographics, clinical parameters, anthropometric measurements, and laboratory tests. Age, sex, height, weight, and body mass index (BMI) of patients were obtained. In addition, tumor types (lung cancer, gastric cancer, colorectal cancer, esophageal cancer, hepatobiliary cancer, pancreatic cancer, breast cancer, uterine ovarian cancer, nasopharyngeal cancer, urological cancer, and other cancer subtypes), comorbidities (diabetes, hypertension, and coronary heart disease), daily habits (smoking, yes vs no; alcohol consumption, yes vs no; and tea consumption, yes vs no), tumor-node-metastasis (TNM) stage, radical resection, postoperative chemoradiotherapy, Eastern Cooperative Oncology Group Performance Status (ECOG PS), and Karnofsky Performance Status (KPS) were retrieved as clinical parameters. Clinical laboratory indicators (serum total protein, serum albumin, aspartate aminotransferase [AST], alanine transaminase [ALT], hemoglobin, white blood cells [WBC], lymphocytes, neutrophils, and platelets), nutrition-related information (weight loss, food intake, daily activity and function, and nutritional interventions), and 30-day mortality were also identified.BMI was calculated as follows: BMI (kg/m2) = weight/height2. The BMI classification was based on Chinese classification standards. Systemic inflammation indices were obtained according to the following formulas: NLR = neutrophil (count/mm3)/lymphocyte (count/mm3);20 ALI = BMI (kg/m2) × albumin (g/dl)/NLR;21 PNI = 10 × albumin (g/dl) + 0.005×lymphocyte (count/mm3);22 SII = platelet (count/mm3) × neutrophil (count/mm3)/lymphocyte (count/mm3);20 PLR= platelet (count/mm3)/lymphocyte (count/mm3).20 The best survival cutoffs for different inflammatory indicators were obtained using R software: ALI (25.03), NLR (3.47), PNI (42.40), SII (819.71), and PLR (129.80) (Figure S2).23 Patient-generated subjective global assessment (PGSGA) criteria were obtained through patient’s self-assessment and professional assessment. The PGSGA was divided into three groups according to the scores: well-nourished group (0–3), moderately malnourished group,4–8 and severely malnourished group (≥9).24
Assessment of Cancer Cachexia
The diagnostic criteria for cancer cachexia in this study adopted the 2011 Fearon Cancer Diagnostic Consensus,4 which utilizes the following criteria: 1) weight loss greater than 5% of starting body weight in the past 6 months, unconsciousness and 2) BMI less than 20 kg/m2 (or sarcopenia) and any degree of weight loss greater than 2%. Skeletal muscle depletion was estimated by the mid upper-arm muscle area (men: <32 cm2, women: <18 cm2).
We performed a survival curve analysis for the three different diagnostic conditions for cancer cachexia: 1) weight loss greater than 5%, 2) BMI less than 20 kg/m2 and weight loss greater than 2%, and 3) sarcopenia and weight loss greater than 2%. The OS of EPCC who satisfied all three diagnostic criteria at the same time was significantly worse than those who satisfied only one or two criteria (P<0.001). However, there was no difference in OS between patients who satisfied one and those who satisfied two diagnostic criteria (P>0.05) (Figure S3). Therefore, we divided EPCC into the high-risk group (satisfying three diagnostic criteria at the same time) and low-risk group (satisfying only one or two diagnostic criteria) (Figure 1A).
Outcome Evaluation
The follow-up records of all patients were obtained in strict accordance with the established content from telephone consultation or follow-up in the outpatient clinic. The observed outcome was the overall survival (OS) of the patient, that is, from the time of the first diagnosis of cancer to the time of death, the time of withdrawal from the study, or the time of the last follow-up.
Statistical Analysis
In this study, continuous variables in the baseline data were calculated as mean ± standard deviation (SD) or median (interquartile range, IQR: quartile 1 to quartile 3), while categorical variables were calculated as absolute numbers or proportions. The independent Student’s t-test for continuous variables or the χ2 test for categorical data were used for comparison between the two groups. The Kaplan–Meier method was used to estimate survival curves. Hazard ratios (HRs) and their 95% confidence intervals (CIs) were calculated to assess the mortality risk and reliability of values. In the multivariate Cox regression model for risk of mortality, model 0 was an unadjusted model, model 1 was adjusted for age, sex, and TNM staging, and model 2 was adjusted for all variables. All statistical analyses were performed through the R platform. Two-sided P-values < 0.05 were considered statistically significant.
Results
Baseline Characteristics
In this study, the average age of the 746 EPCC was 72.00±5.24 years, of which 489 (65.50%) were male, and the average survival time was 25.4 months. Additionally, a total of 343 deaths were observed during the study period and the median survival time was 44.3 months. Based on the diagnostic criteria for cancer cachexia, there were 655 (87.80%) elderly patients with a weight loss greater than 5%, 371 (49.70%) elderly patients with a BMI of less than 20 kg/m2 and a weight loss greater than 2%, and 319 (42.80%) elderly patients with sarcopenia and a weight loss greater than 2% (Table 1). We also observed the overall mortality rate of EPCC from 1 to 5 years: at 12 months, 34.3% (95% CI: 62.3–69.2%); at 24 months, 49.5% (95% CI: 46.8–54.4%); at 36 months, 55.3% (95% CI: 40.9–48.7%); at 48 months, 59.4% (95% CI: 36.8–44.9%); and at 60 months, 59.8% (95% CI: 36.4–44.5%), which resulted in a rate of 278 events per 1000 patient-years.
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Table 1 Demographic and Clinical Characteristics |
Comparison of Inflammatory Indicators
We compared the prognostic predictive and discriminative ability of different inflammatory indicators (ALI, NLR, PNI, SII, and PLR) in EPCC. The concordance index (C-index) and 95% CIs of different indicators was as follows: ALI = 0.634 (0.604–0.664), NLR = 0.624 (0.594–0.654), PNI = 0.595 (0.563–0.626), SII = 0.594 (0.564–0.624), and PLR = 0.541 (0.510–0.573). Additionally, a decision curve analysis (DCA) was performed to assess the discriminative ability and clinical utility of the prognostic markers, and the results showed that ALI was superior to other inflammatory indicators (Figure 2A).
For the prognostic predictive ability of different inflammatory indicators in EPCC, we conducted a prognostic receiver operating characteristic (ROC) curve analysis, and the results showed that the area under the curve (AUC) of ALI was greater than that of other indicators (Figure 2B). The survival curve results showed that the prognosis of patients with low ALI (<25.03) and low PNI (<42.40) were worse than that of patients with high ALI (≥25.03) and high PNI (≥42.40), respectively, while patients with high NLR (≥3.47), high SII (≥819.71), and high PLR (≥129.80) had a worse prognosis than those with low NLR (<3.47), low SII (<819.71), and low PLR (<129.80), respectively (Figure S4).
Multivariate Cox regression survival analysis found that compared with other inflammation indices, ALI showed a good prognostic predictive ability in EPCC as a continuous variable or a categorical variable (Table 2, Figure S5). When ALI was used as a continuous variable, the risk of mortality in EPCC decreased with an increase in ALI (model 2: adjusted P<0.001, HR [95% CI] = 0.743 [0.623–0.885]). When ALI was used as a binary variable, compared with patients in the high-ALI (≥25.03) group, patients with low ALI (<25.03) had an increased risk of mortality (model 2: adjusted P<0.001, HR [95% CI] = 2.092 [1.590–2.751]). When ALI was treated as a quartile variable, compared with patients in the first quartile (ALI>38.04) group, the risk of mortality in EPCC in the third and fourth quartile groups was significantly increased (model 2: P<0.001; quartile 3, adjusted P<0.001, HR [95% CI] = 2.108 [1.477–3.007]); quartile 4, adjusted P<0.001, HR [95% CI] = 2.296 [1.476–3.570]).
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Table 2 Univariate and Multivariate Analysis of the OS in EPCC |
However, we also excluded patients who died within 6 months and performed a sensitivity analysis. The results showed that compared with other inflammatory indicators, ALI showed a good prognostic ability whether it was a continuous variable or a categorical variable. These results are similar to those of previous multivariate survival analyses (Table S2).
Analysis of the Distribution, Correlation, and Prognosis of ALI
Based on the ALI cut-off value, patients were divided into high- (≥25.03, n=339) and low-ALI groups (<25.03, n=407). Comparison of baseline clinical characteristics between the two groups showed that age, tumor type, BMI, TNM stage, KPS, serum total protein, serum albumin, hemoglobin, WBC, lymphocytes, neutrophils, platelets, 30-day mortality, and PGSGA were significantly different (all P<0.05) (Table S3).
In the EPCC cohort, we investigated the distribution of ALI in different TNM stages and cancer types based on different age and sex subgroups. The results showed that there was a significant difference in the distribution of patients with gastric cancer (P<0.05) (Figure 3).
Pearson correlation analysis showed that ALI was significantly correlated with serum albumin (R=0.40), neutrophils (R=−0.48), and lymphocytes (R=0.41) (all P<0.05). Correlation analyses of different sex subgroups and age subgroups showed consistent significant correlation results (R>0.3 or R<-0.3, P<0.05) (Figure S6).
To compare the prognostic accuracy of ALI in EPCC, the calibration curves showed that ALI showed good consistency for 1-, 3-, and 5-year prognosis predictions. The risk model we constructed further showed that the lower the ALI score, the higher the risk of mortality, and the worse the prognosis in EPCC (Figure S7).
Combined Risk Effect Analysis
Compared with patients in the low-risk group, the risk of mortality in the high-risk group was significantly increased (model 2: adjusted P = 0.017, HR [95% CI] = 1.400 [1.078–1.819]) (Table 3). We performed a combined-effect analysis of the high- and low-ALI groups and the high- and low-risk groups. The results showed that the mortality risk of patients in the low-ALI and high-risk groups reached 3.095-fold compared with patients in the high-ALI and low-risk groups, respectively (adjusted P<0.001, 95% CI = 2.085–4.592) (Table 3, Figure 1B).
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Table 3 Survival Analysis of Different Risk Groups and Combination Analysis |
Stratified Analysis
The stratified analysis showed a significant interaction between ALI (high ALI, ≥ 25.03 vs low ALI, <25.03) and the EPCC mortality risk in BMI (kg/m2; <18.5, 18.5–23.9, and >23.9; P for interaction < 0.001). However, no significant interaction was observed in the other subgroup parameters (P for interaction > 0.05) (Figure 4).
Discussion
Our understanding of cancer progression has evolved from emphasizing the internal changes in cancer cells to emphasizing the key interactions between cancer and non-cancerous cells in the primary tumor microenvironment.25 In fact, non-tumor cells in the tumor microenvironment, including immune cells, fibroblasts, and endothelial cells, play an important role in regulating the secretion of cachexia-inducing factors from tumors.10 In the resistance phase, immune cells (such as macrophages, dendritic cells, T cells, and B cells) are activated and accompanied by the release of pro-inflammatory factors (IL-6, IL-1, TNF-α), hypoxia-inducible factor-1, and reactive oxygen species(ROS), which determine the specific changes in energy metabolism. In the absence of specific immunity, patients often have general non-specific immune responses mediated by macrophages (such as cytokine storm), and the body’s continuous inflammatory response further leads to the phenomena of tolerance and the symptoms of cancer cachexia (such as anorexia and muscle wasting).26
Elderly might be inflamed as consequence of inflammaging. One of the main features of aging is the increase in pro-inflammatory mediators in the blood, and the parallel reduction in the ability to produce effective inflammatory responses to sufficient immunogenic stimulations.27 In this study, the optimal inflammation index was investigated in EPCC. Both the distinguishing ability and prognostic value of ALI were superior to those of NLR, PNI, SII, and PLR. For the prognostic prediction of EPCC, the ALI showed consistent discrimination. Notably, ALI had a good prognostic value, whether as a continuous or a categorical variable. For every SD increase in ALI, the patient’s risk of mortality decreased by 0.733-fold. The prognosis of EPCC with low ALI (< 25.03) was worse than those with high ALI (≥25.03). Thus, ALI could be used as an independent prognostic factor in EPCC.
In recent years, a growing number of studies have suggested that ALI, a new inflammation index, can be used to assess the survival of patients with a variety of malignant tumors. ALI was originally used to assess the prognosis of lung cancer patients, such as non-small cell lung cancer28 and small cell lung cancer.29 Soon after, researchers found that ALI is also a good independent prognostic indicator in nasopharyngeal carcinoma,30 head and neck squamous cell carcinoma,31 thymic epithelial tumors,32 esophageal cancer,32 gastric cancer,21,33 colorectal cancer,34,35 melanoma,36 and diffuse large B-cell lymphoma.37 ALI is an index related to inflammation and nutritional status.21 The difference between ALI and other previously reported indicators is that ALI not only includes inflammation related NLR and albumin, but also includes BMI, which is used to assess nutritional status.21 BMI has always been considered a diagnostic criterion for nutrition.38 Among elderly community residents, a BMI of less than 22 was associated with a high 1-year mortality rate and poor functional status.39 Interestingly, previous studies have reported that BMI is associated with skeletal muscle reduction.32,40 For instance, Shibutani et al found a significant correlation between BMI and psoas muscle mass index (PMI).35 Albumin has been proven to predict the survival of patients with cancer cachexia and has been shown to indicate the severity of the disease.41,42 Systemic inflammation affects liver metabolism, stimulating an increase in acute phase protein production, while reducing albumin synthesis and increasing degradation.43 Therefore, hypoalbuminemia reflects a systemic inflammatory state and is influenced by systemic inflammatory response (SIR).44,45 SIR is deeply involved in various carcinogenesis and tumorigenesis through host-tumor interactions. The potential of SIR status as a prognostic marker of various cancers has also been confirmed, with NLR as a reliable SIR marker.46,47 NLR can explain the role of neutrophils in promoting inflammation and providing an appropriate environment for tumor growth by activating a variety of inflammatory markers.46 The lymphocyte count can also reflect the activation of the immune system and its inhibitory effect on tumor proliferation and migration.43 Since cancer cachexia is the result of chronic systemic inflammation, the combination of BMI and inflammatory markers can more accurately assess the prognosis of cancer cachexia and evaluate the degree of systemic inflammation.
In our study, we found that patients who satisfied the three diagnostic conditions of the 2011 Fearon Cancer Cachexia Diagnosis Consensus4 at the same time, namely 1) weight loss greater than 5%, 2) BMI less than 20 kg/m2 and weight loss greater than 2%, and 3) sarcopenia and weight loss greater than 2%, had a significantly higher risk of mortality than those who did not. When these high-risk patients had low ALI, the risk of mortality increased 3.028-fold. Unintended weight loss, low BMI, skeletal muscle reduction, and systemic inflammation are inevitable in elderly patients with cancer and are precursors of adverse consequences. If these conditions exist in EPCC at the same time, it will have an unfavorable additive effect on the prognosis of patients, which means that the treatment of these patients requires a more comprehensive strategy. On the contrary, another part of patients seems to be more likely to benefit from treatment. These factors pose a major challenge for healthcare providers in caring for elderly patients with cancer in the coming years. Given the multifaceted nature of these diseases, multimodal interventions are often associated with the best outcome.48
For the first time, the combined effects of inflammation in different EPCC populations was investigated, but the current research still has several limitations. First, this study aimed to explore the impact of systemic inflammation in EPCC, but it did not include other inflammatory indicators, such as CRP and IL-6. Compared with the indicators such as albumin used at this stage, the medical costs of CRP and IL-6 are relatively high in China, but considering the value of these indicators, more inflammatory indicators need to be further included in this study in the future. Second, appropriate physical activity can improve sarcopenia and muscle atrophy typical of cachexia. Considering the particularity of EPCC, targeted physical activity measurement and evaluation tools and methods need to be developed. Third, this study did not involve a large study population. While increasing the number of samples, we need to pay more attention to homogeneous groups of patients, such as different stages and types of tumor. Fourth, some of the exclusion criteria in this study may cause some missing data on cachexia and cause selection bias. The cohort design should be further improved in the future. Finally, cancer cachexia is not entirely sarcopenia, distinguishing the difference between cachexia and sarcopenia is important for judging the patient’s disease state. Additionally, to distinguish if the results reported are due to cancer or cachexia, a control/comparator group without cachexia should be added.
Conclusions
In summary, the prognostic and discriminative value of the inflammatory indicator ALI was better than that of NLR, PNI, SII, and PLR in EPCC. Whether ALI was used as a continuous variable or a categorical variable (binary and quarter), ALI had a better prognostic value in EPCC. Particularly, patients with low ALI (<25.03) had a worse OS than patients with high ALI (≥25.03). ALI might be an independent prognostic factor for EPCC. Notably, the high-risk group of EPCC with low ALI would significantly increase the mortality risk and OS. Effectively distinguish EPCCs with different prognostic statuses, so that different and targeted treatment strategies could be adopted more effectively.
Data Sharing Statement
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
Ethics Approval and Informed Consent
This study followed the Helsinki declaration. All participants signed an informed consent form and this study was approved by the Institutional Review Board of each hospital (Registration number: ChiCTR1800020329).
Acknowledgments
We would like to thank Editage (www.editage.cn) for English language editing. We are grateful to all the participants who have been part of the project and to the many members of the study teams at different study centers who have enabled this research.
Author Contributions
All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.
Funding
This work was supported by the National Key Research and Development Program [grant number 2017YFC1309200].
Disclosure
The authors report no competing interests in this work.
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