The Pretreatment Controlling Nutritional Status Score in Ovarian Cancer: Influence on Prognosis, Surgical Outcome, and Postoperative Complication Rate.

Introduction The Controlling Nutritional (CONUT) Status score is an established predictor of impaired prognosis in patients with solid tumors. The aim of this study was to investigate the prognostic value of the CONUT score for overall survival and perioperative complication rates in patients with epithelial ovarian cancer. Patients In this retrospective study we assessed the data of 337 consecutive patients with ovarian cancer. The CONUT score was associated with surgical outcome, postoperative complications and clinicopathological parameters. We used univariate log-rank test and multivariable Cox regression models to evaluate the association between pretreatment CONUT scores and survival. Results A low CONUT score (0 - 2) was associated with an early FIGO stage (p = 0.004), complete tumor resection (p < 0.001), less neoadjuvant chemotherapy (p = 0.017) and other histologies than serous cystadenocarcinoma (p = 0.006). Postoperative complications were observed in 51.4% and 60.5% of patients with a CONUT score of 0 - 2 and a score > 2, respectively (p = 0.161). A shorter overall survival was observed in patients with a CONUT score > 2 compared to patients with a low CONUT score, with 5-year overall survival rates of 31.5% and 58.7%, respectively (p < 0.001). In multivariable analysis, both advanced age (p < 0.001) and FIGO stage (p < 0.001), residual disease (p < 0.001) and a high CONUT score (p = 0.048) were independently associated with unfavorable overall survival. Conclusion Pretreatment CONUT score is an independent prognostic marker for overall survival and associated with successful surgery. Patients with a high CONUT score might benefit from pretreatment nutritional intervention. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ).

Introduction

Ovarian cancer is a rare disease but still represents the fifth most common malignancy in women 1 . Moreover, the five-year survival prognosis is poor, due to late diagnosis at advanced stages. Because of the absence of early symptoms and lack of an effective screening option, the majority of epithelial ovarian cancer (EOC) cases are diagnosed at an advanced stage. Various prognostic parameters have been evaluated for ovarian cancer, but none of them have entered clinical practice to date 2 ,  3 ,  4 ,  5 .

There is accumulating evidence on the impact of nutrition and inflammation status on mortality and morbidity in ovarian cancer 6 ,  7 ,  8 . Several biomarkers reflecting nutrition and inflammation status such as prognostic nutritional index 9 , neutrophil-to-lymphocyte ratio 10 , lymphocyte-to-monocyte ratio 11 , platelet-to-lymphocyte ratio 12 and the Glasgow prognostic score 13 have been identified as independent predictors of survival in patients with ovarian cancer.

The Controlling Nutritional Status (CONUT) score is a novel tool which evaluates nutritional and immunologic status. It is calculated using serum albumin concentration, total lymphocyte count and cholesterol concentration 14 . A high CONUT score reflects malnutrition and immunoactivation and is associated with a poor prognosis 14 .

The CONUT score has been reported to be a prognostic survival marker for several cancers 15 ,  16 ,  17 ,  18 . To our knowledge, only one study has investigated the significance of the CONUT score in ovarian cancer patients 19 . In 2020, Li et al. demonstrated in a small cohort that the CONUT score is an independent prognostic factor for overall survival. Although malnutrition has been linked to postoperative complications in ovarian cancer patients 2 , the above-mentioned study failed to evaluate the impact of a preoperative CONUT score on postoperative complications.

The aim of this study was to investigate the value of the CONUT score as an indicator for a poor prognosis and the association between CONUT score and postoperative complications in a large cohort of epithelial ovarian cancer patients treated at a cancer center.

Materials and Methods

Three hundred and thirty-seven consecutive patients treated for epithelial ovarian cancer between 2000 and 2015 at the Comprehensive Cancer Center Vienna at the Medical University of Vienna were enrolled. Data were retrospectively extracted from paper-based and electronic medical records. As suggested in the current guidelines 20 , tubal and primary peritoneal carcinomas were included in this patient cohort.

Patients were treated according to the standards of our institution, with upfront surgery and adjuvant platinum-based chemotherapy. Surgical staging according to FIGO guidelines was performed, including hysterectomy, bilateral salpingo-oophorectomy, pelvic and/or para-aortic lymphadenectomy, appendectomy, omentectomy, and a cytoreductive procedure to resect all gross tumor masses. Residual tumor load was defined as negative if macroscopically absent. Experienced gynecologic oncologists and an experienced pathologist performed the clinical and histopathologic evaluation.

Fertility-sparing surgery was performed in accordance with the patientʼs choice in young patients with ovarian tumors of low malignant potential or nonepithelial ovarian cancers and patients with stage IA EOC. If unilateral salpingo-oophorectomy was considered, full surgical staging, including washings, omentectomy, pelvic and paraaortic lymphadenectomy, and peritoneal biopsies were performed. Thorough abdominal exploration with biopsy of any abnormal areas was done. Endometrial biopsy to exclude synchronous endometrial cancer was completed.

NACT was given to patients with advanced EOC and unresectable disease who were unlikely to achieve complete cytoreduction if operated on at the time of presentation or patients with EOC who were initially poor candidates for surgery but were likely to tolerate surgery after chemotherapy.

For those who were unlikely to tolerate surgery at any point due to poor functional status, chemotherapy alone was administered for tumor control.

We assessed treatment response using computed tomography after three cycles of NACT. All patients were also seen by our interdisciplinary tumor board to determine whether to proceed with surgery. We proceeded with surgical cytoreduction in patients who did not progress during NACT and in whom there was a chance of resecting all residual disease or achieving optimal cytoreduction. After surgery, another three to six more cycles of chemotherapy were administered.

Patients with disease progression at any point, as well as those who showed an insufficient response after three cycles of therapy for optimal cytoreduction to be feasible, represent a group with chemoresistant disease. These patients were treated similarly to women with platinum-resistant EOC and typically did not pursue surgical options. However, in some patients, especially those with incomplete response, further rounds of neoadjuvant treatment were administered followed by re-evaluation for surgery of those who showed some response to NACT.

All treatment decisions were based on the conclusions of our weekly tumor board, which consisted of experienced gynecologic oncologists, a radiologist, a radiotherapist, an internal oncologist and an experienced pathologist.

Prior to treatment, a daily routine physical examination of patients was done by a specialist in internal medicine.

Patients with signs of active inflammation or chronic liver disease were excluded from the study.

Overall survival was the interval between diagnosis and cancer-associated death.

Laboratory measurements

Fasting blood collection for the evaluation of serum albumin, total lymphocyte count and total cholesterol concentration was performed by peripheral venous puncture during routinely performed blood tests prior to treatment.

CONUT scores were calculated using data for serum albumin, total cholesterol concentrations, and total peripheral lymphocyte counts 14 : (1) albumin concentrations ≥ 35, 30 – 34.9, 25 – 29.9, and < 25 g/L were scored as 0, 2, 4, and 6 points, respectively; (2) total lymphocyte counts ≥ 1600, 1200 – 1599, 800 – 1199, and < 800/mm 3 were scored as 0, 1, 2, and 3 points, respectively; and (3) total cholesterol concentrations ≥ 180, 140 – 179, 100 – 139, and < 100 mg/dL were scored as 0, 1, 2, and 3 points, respectively. The CONUT score was defined as the sum of (1), (2), and (3). The cut-off for the CONUT score was 0 – 2 and > 2 as reported before 21 .

Patient follow-up

Postoperative complications were graded according to the Clavien-Dindo classification 22 .

The continuous follow-up of patients was documented until hospital discharge. Thereafter, patients were followed up every three months in the first year, every 6 months until the fifth year and annually up to 10 years. If patients missed scheduled follow-up visits, they were contacted by administrative personnel or nurses for follow-up data.

Complications which arose after hospital discharge were assessed in our outpatient clinic.

Residual tumor load was defined as negative if macroscopically absent. Overall survival was the interval between diagnosis and cancer-associated death. Patients without recurrence, cancer progression, or death were censored at the time of last follow-up.

Management of disease relapse depended on various criteria such as tumor biology, the patientʼs general condition (ECOG), toxicity, previous chemotherapy, and response to chemotherapy 23 .

Statistical analysis

Values are presented as mean values with standard deviation. Studentʼs t-test was performed to compare mean serum albumin levels with clinicopathological parameters. P-values of < 0.05 were considered statistically significant. With respect to overall survival, differences between groups were evaluated using log-rank test and presented as Kaplan-Meier survival curves. Multivariable analysis was performed using a Cox regression model and included the CONUT score (> 2 vs. 0 – 2), patient age (dichotomized at the median value of 59.5 years), tumor stage (FIGO IV. vs. FIGO III vs. FIGO II vs. FIGO I), tumor grade (G3 vs. G1/2) histology (serous adenocarcinoma vs. other) and residual disease (no residual disease vs. residual disease) as independent variables. Statistical analyses were performed using the statistical software SPSS version 25.0.

Results

Patient characteristics

Patient demographics are shown in Table 1 .

Table 1  Patient characteristics of 337 patients with epithelial ovarian cancer.

Parameter	n (%) or median (IR)
IR = interquartile range; FIGO = International Federation of Gynecology and Obstetrics
Total number of patients enrolled	337
Age at diagnosis, years	59.54 (range: 13.40)
BMI	25.84 (range: 9.66)
Eastern Cooperative Oncology Group (ECOG) status
0	266 (78.9%)
1	31 (9.2%)
2	6 (1.8%)
3	1 (0.3%)
4	0
unknown	33 (9.8%)
Histological type
serous adenocarcinoma	212 (62.9%)
endometroid adenocarcinoma	55 (16.3%)
mucinous adenocarcinoma	16 (4.7%)
clear cell carcinoma	16 (4.7%)
other	38 (11.3%)
Histological grade
G1	48 (14.2%)
G2	83 (24.6%)
G3	189 (56.1%)
unknown	11 (3.3%)
Tumor stage
FIGO I	70 (20.8%)
FIGO II	23 (6.8%)
FIGO III	194 (57.6%)
FIGO IV	49 (14.5%)
unknown	1 (0.3%)
Neoadjuvant chemotherapy
yes	47 (13.9%)
no	290 (86.1%)
Residual disease
no residual disease	207 (61.4%)
residual disease	123 (36.5%)
unknown	7 (2.1%)
Recurrence status
No. of patients with recurrent disease	202 (59.9%)
Median time to recurrent disease (months)	17.0 (8.0 – 34.75)
Status at last observation
alive with no evidence of disease or stable disease	143 (42.4%)
progressive disease	41 (12.2%)
tumor-related death	138 (40.9%)
death from other causes	15 (4.5%)
Median time of follow-up (months)	28.0 (14.0 – 71.0)

67.1% of patients were treated with upfront surgery and adjuvant platinum-based chemotherapy. Surgical staging according to FIGO guidelines was performed, including hysterectomy, bilateral salpingo-oophorectomy, pelvic and/or para-aortic lymphadenectomy, appendectomy, omentectomy, and cytoreductive procedure to resect all gross tumor masses. Surgical resection without adjuvant treatment was performed in 16.0%. Neoadjuvant chemotherapy with intervention debulking surgery was performed in 10.4%. Neoadjuvant chemotherapy with intervention debulking surgery and adjuvant chemotherapy was performed in 3.0%. Neoadjuvant chemotherapy was administered in 0.6%. Other standard forms of treatment were performed in 3% of patients.

BRCA status was available for 45 patients. Fifteen patients had a pathogenic BRCA1 mutation and 4 patients a pathogenic BRCA2 mutation. One patient had a somatic BRCA1 mutation and 3 patients a BRCA2 variant of unknown significance. Twenty-two out of 45 were BRCA1/2 wildtype patients.

CONUT score and postoperative complications

In the present study, 256 (76.0%) patients had a CONUT score of 0 – 2 and 81 (24.0%) patients had a CONUT score of > 2. Calculated Controlling Nutritional Status scores broken down by clinicopathological parameters are provided in Table 2 .

Table 2  Relationship between clinicopathological variables and Controlling Nutritional Status score in 337 patients with epithelial ovarian cancer.

	Controlling Nutritional Status score 0 – 2 (n = 256)	Controlling Nutritional Status score > 2 (n = 81)	p-value 1
1 χ 2 test; FIGO = International Federation of Gynecology and Obstetrics; n = number; bold = p-values < 0.05
Tumor stage			0.004
FIGO I	62 (24.3%)	8 (9.9%)
FIGO II	21 (8.2%)	2 (2.5%)
FIGO III	135 (52.9%)	59 (72.8%)
FIGO IV	37 (14.5%)	12 (14.8%)
Residual disease			< 0.001
no residual disease	172 (68.8%)	37 (46.3%)
residual disease	78 (31.2%)	43 (53.8%)
Neoadjuvant chemotherapy			0.017
yes	29 (11.3%)	18 (22.2%)
no	227 (88.7%)	63 (77.8%)
Age at first diagnosis			0.315
≤ 59.5 years	127 (49.6%)	35 (43.2%)
> 59.6 years	129 (50.4%)	46 (56.8%)
Histological grade			0.117
G1	42 (16.7%)	6 (7.5%)
G2	65 (25.9%)	18 (22.5%)
G3	137 (54.6%)	52 (27.5%)
unknown	7 (2.8%)	4 (5.0%)
Histological type			0.006
serous cystadenocarcinoma	153 (59.8%)	59 (72.8%)
other	103 (40.2%)	22 (27.2%)

Advanced tumor stage, higher rate of residual disease after surgery, more serous cancers and more patients receiving neoadjuvant chemotherapy were observed in the group of patients with a CONUT score of > 2.

Postoperative complications (mainly mild complications) were observed in 51.4% and 60.5% of patients with a CONUT score of 0 – 2 and > 2, respectively (p = 0.161). Severe complications (Clavien-Dindo classification 3 – 5) were observed in 10.5% and 14.8% of patients with a CONUT score of 0 – 2 and > 2, respectively. Any type of postoperative complication was observed in 176/337 (53.7%) patients. Numbers of postoperative complications broken down by CONUT score are provided in Table 3 .

Table 3  Numbers of postoperative complications classified according to the Clavien-Dindo classification and broken down according to the preoperative Controlling Nutritional Status score in 337 patients with epithelial ovarian cancer.

Postoperative complications	Controlling Nutritional Status score 0 – 2 (n = 256)	Controlling Nutritional Status score > 2 (n = 81)	Complete cohort
n = number
None	120 (46.9%)	32 (39.5%)	152 (45.1%)
Grade 1	34 (13.3%)	13 (16.0%)	47 (13.9%)
Grade 2	64 (29.7%)	24 (29.6%)	88 (26.1%)
Grade 3a	5 (2.0%)	1 (1.2%)	6 (1.8%)
Grade 3b	12 (4.7%)	9 (11.1%)	21 (6.2%)
Grade 4	8 (3.1%)	0 (0.0%)	8 (2.4%)
Grade 5	4 (1.6%)	2 (2.5%)	6 (1.8%)
Unknown	9 (3.5%)	0 (0.0%)	9 (2.8%)
Total	256	81	337

CONUT score and overall survival analysis

The 5-year overall survival rate of patients with a CONUT score of > 2 was 24.9% compared to 52.5% for patients with a CONUT score of 0 – 2, (p < 0.001). The Kaplan-Meier survival curves in Fig. 1 demonstrate the association between CONUT score and overall survival.

Fig. 1

 Kaplan-Meier curves for overall survival broken down according to pretreatment CONUT scores (n = 337).

In univariate survival analysis, a high CONUT score (p < 0.001), advanced FIGO stage (p < 0.001), advanced patient age (p < 0.001), high tumor grade (p = 0.012), residual disease (p < 0.001), and serous histology (p = 0.022) were associated with poor overall survival. In multivariable analysis, a high CONUT score (p = 0.048), advanced FIGO stage (p < 0.001), advanced patient age (p < 0.001), and residual disease (p < 0.001) were associated with poor overall survival. Univariate and multivariate overall survival analyses are shown in Table 4 .

Table 4  Univariate and multivariate overall survival analyses in 337 patients with epithelial ovarian cancer.

	Overall survival
	Univariate 1 analysis		Multivariate 2 analysis
	p-value	5-year overall survival rate	p-value	HR (95% CI)
1 log rank test; 2 multivariate Cox regression analysis; HR = hazard ratio; 95% CI = 95% confidence interval; bold = p-values < 0.05
Controlling Nutritional Status score (> 2 vs. 0 – 2)	< 0.001	31.5% vs. 58.7%	0.048	1.4 (1.0 – 2.1)
FIGO stage (IV vs. III vs. II vs. I)	< 0.001	28.9% vs. 42.3% vs. 66.8% vs. 92.0%	< 0.001	1.5 (1.2 – 1.9)
Patient age (> 59.6 vs. ≤ 59.5 years)	< 0.001	42.2% vs. 64.0%	< 0.001	2.0 (1.4 – 2.9)
Histological grade (high-grade vs. low-grade)	0.012	42.3% vs. 62.8%	0.890	1.0 (0.7 – 1.5)
Residual disease (residual disease vs. no residual disease)	< 0.001	23.8% vs. 66.7%	< 0.001	2.5 (1.7 – 3.6)
Type of histology (serous adenocarcinoma vs. other)	0.022	45.0% vs. 64.1%	0.936	1.0 (0.7 – 1.4)

CONUT score and progression-free survival

The 5-year progression-free survival rate of patients with a CONUT score > 2 was 23.9% compared to 34.2% for patients with a CONUT score of 0 – 2 (p = 0.004).

The Kaplan-Meier survival curves in Fig. 2 demonstrate the association between CONUT score and progression-free survival.

Fig. 2

 Kaplan-Meier curves for progression-free survival broken down according to pretreatment CONUT scores (n = 337).

In univariate survival analysis, a high CONUT score (p = 0.004), advanced FIGO stage (p < 0.001), advanced patient age (p = 0.005), high tumor grade (p < 0.001), residual disease (p < 0.001), and serous histology (p = 0.002) were associated with poor progression-free survival. In multivariable analysis, advanced FIGO stage (p < 0.001), advanced patient age (p = 0.002), and residual disease (p < 0.001) were associated with poor progression-free survival. Univariate and multivariate overall survival analyses are shown in Table 5 .

Table 5  Univariate and multivariate progression-free survival analyses in 337 patients with epithelial ovarian cancer.

	Progression-free survival
	Univariate 1 analysis		Multivariate 2 analysis
	p-value	5-year progression-free survival rate	p-value	HR (95% CI)
1 log rank test; 2 multivariate Cox regression analysis; HR = hazard ratio; 95% CI = 95% confidence interval; bold = p-values < 0.05
Controlling Nutritional Status score (> 2 vs. 0 – 2)	0.004	21.5% vs. 34.2%	0.119	1.3 (0.9 – 1.8)
FIGO stage (IV vs. III vs. II vs. I)	< 0.001	4.5% vs. 19.7% vs. 37.1% vs. 79.7%	< 0.001	2.0 (1.6 – 2.4)
Patient age (> 59.6 vs. ≤ 59.5 years)	0.005	25.0% vs. 39.3%	0.002	1.6 (1.2 – 2.1)
Histological grade (high-grade vs. low-grade)	< 0.001	27.4% vs. 59.7%	0.290	0.8 (0.6 – 1.2)
Residual disease (residual disease vs. no residual disease)	< 0.001	9.3% vs. 44.5%	< 0.001	2.0 (1.4 – 2.7)
Type of histology (serous adenocarcinoma vs. other)	0.002	22.6% vs. 47.0%	0.808	1.0 (0.7 – 1.5)

Discussion

In the present study, we analyzed the predictive and prognostic value of preoperative CONUT scores on postoperative complications and survival in a large cohort of consecutive patients with epithelial ovarian cancer. Our results demonstrate that pretreatment CONUT scores can be used as an independent prognostic factor for overall survival.

This observation has also been reported for various other cancer types, e.g., prostate cancer 18 , esophageal carcinoma 21 , and soft tissue sarcomas 24 . Our findings seem biologically plausible and are supported by the results of other studies 19 . Several preoperative assessment tools have been developed to evaluate nutritional risk, postoperative complications, and long-term outcomes, such as the prognostic nutritional index, subjective global assessment, and nutritional risk index 8 ,  25 ,  26 . Obesity is an independent risk factor which considerably increases the probability of developing various cancer types, but its relevance for disease risk and risk of cancer-specific mortality in epithelial ovarian cancer is clinically negligible 27 . The CONUT score summarizes measurements of serum albumin, total cholesterol, and total lymphocyte count.

The combination of the three components may provide a better reflection of the balance of nutritional status and enhance the ability to accurately predict the patientʼs general condition. In a study of 697 patients with gastric cancer, the CONUT score was superior as an independent predictor of outcome compared to body mass index, prognostic nutritional index and performance status 28 . Furthermore, the CONUT score is an easy-to-use, cost-effective method of objectively and comprehensively evaluating patients in hospital settings.

Serum albumin is used as the standard parameter to evaluate a patientʼs nutritional status and has been shown to be closely associated with the prognosis of ovarian cancer 29 . Cholesterol is known to be an indicator of a patientʼs caloric reserves 30 , and an important component of the cell membrane has been linked to proliferation, metastasis, and the immune response of tumor cells 31 . Several studies have demonstrated that lipid metabolism plays a substantial role in the pathology of malignancies and correlates with the prognosis of various solid tumors 32 .

Total lymphocyte count is an established indicator of cell-mediated immune status, including both acquired and adaptive immunities. The lymphocyte subsets CD4+ and CD8+ T cells, natural killer cells and B cells are closely associated with tumor immunity. Several studies have demonstrated that a reduced number of these cells are associated with impaired tumor immunity, resulting in cancer progression 33 .

Taken together, a higher pretreatment CONUT score is not only an indicator of malnutrition but also of systemic inflammatory activity and might be a useful tool which could help us recognize a broader high-risk population and provide optimized therapy such as pretreatment nutrition intervention or physical therapy intervention. Poor preoperative physical fitness and nutritional status are linked to poor postoperative outcomes 34 . 50 – 80% of cancer patients suffer from cancer cachexia due to catabolic effects of the tumor, abnormal metabolism of nutrients, physical obstruction of the gastrointestinal tract, reduced food intake due to pain, anxiety, and depression 35 . Malnutrition in cancer patients has been associated with negative outcomes, altering the immunological response and increasing the risk of infection while decreasing functional capacity, tolerance to treatment, and chances of survival 36 ,  37 . Furthermore, malnourished patients tend to experience prolonged hospitalization which negatively affects their prognosis 38 . Therefore, identifying interventions to optimize preoperative nutritional status and fitness prior to major surgery is a priority.

A randomized controlled study compared immune-enhancing enteral nutrition with standard enteral feeding in oncologic gynecologic patients (32% of ovarian cancer patients) after surgery and found decreased postoperative complications and reduced length of hospital stay but no significant differences in mortality rates 39 . The length of hospital stay of patients receiving early oral feeding was shorter than the hospital stay of patients receiving traditional oral feeding 40 . Furthermore, patients who received traditional oral feeding presented with significantly more postoperative complications than patients who received early oral feeding 40 .

According to the Enhanced Recovery After Surgery (ERAS) guidelines for perioperative care in gynecologic oncology, maintenance of a regular diet within the first 24 hours after gynecologic oncology surgery is recommended 41 . A higher postoperative protein intake is also associated with earlier discharge 42 . Currently, there are no definitive guidelines for surgical patients with regard to protein needs; however, in the acute care setting, guidelines have recommended up to 2.0 g of protein/kg/day and 25 – 30 kcal/kg/day 43 .

High-quality studies on prehabilitation including exercise and dietary interventions in gynecologic oncology patients are still lacking. A number of publications on colorectal surgery have shown that nutrition prehabilitation with and without exercise shortened the length of hospital stay by 2 days in a largely traditional surgical care setting 44 . A meta-analysis of prehabilitation interventions consisting of inspiratory muscle training, aerobic exercise, and/or resistance training found that prehabilitation decreased postoperative complications after intraabdominal operations in a traditional surgical care setting 45 . These results for colorectal surgery show that certain patients will benefit clinically from prehabilitation, but further work in the field of gynecologic oncology is needed.

We found that advanced tumor stage, residual disease after surgery, serous histology and neoadjuvant treatment regimens were associated with a CONUT score of > 2. These findings appear biologically plausible as a high tumor burden fosters tumor necrosis factor, transforming growth factor and interleukin-6 secretion, which are related to cancer cachexia through direct interference with protein homeostasis in muscle cells. These cytokines promote proteasome-mediated protein catabolism in differentiated muscle cells 46 , suppress muscle-cell differentiation 47 and induce excessive fatty acid oxidation in muscle cells 48 .

Other reports on breast cancer and ovarian cancer patients also showed an association between advanced tumor stage and high CONUT score 15 ,  19 . It remains unclear whether a high CONUT score is directly caused by tumor load and cytokine secretion or whether it is a secondary result of increased vascular permeability contributing to a shift of albumin from the intravascular sector towards the interstitium 49 , and of comorbidities associated with cancer, such as sepsis, chronic liver or renal disease and gastrointestinal bleeding, which contribute to malnutrition and inflammation through various mechanisms 50 .

Our data support the findings of Li et al. 19 that a high pretreatment CONUT score is associated with a poor prognosis in ovarian cancer patients. Their investigation included 206 ovarian cancer patients, and a high CONUT score was found be associated with high FIGO stage, high volumes of ascites on imaging, high concentrations of CA 125, and chemoresistance.

For other tumor entities, the benefit of using the CONUT score to evaluate postoperative complications remains controversial 16 ,  17 ,  28 . In our study cohort, we observed no differences in the incidence of postoperative complications between patients with a preoperative CONUT score of > 2 compared to patients with a low CONUT score. We observed a total postoperative complication rate of 53.7%, with severe complications (Clavien-Dindo classification 3 – 5) occurring in 11.6%.

In a retrospective study by Ataseven et al. investigating a cohort of 309 patients with epithelial ovarian cancer, a total complication rate of 83.5% and severe complication rate of 25.2% were observed after cytoreductive surgery 2 . Although the patient cohort and clinicopathological parameters are comparable between both studies, differences in postoperative management such as following the ERAS protocol 51 , prophylactic antibiotics, offering chewing gum, coffee or an early oral diet may explain the different results. Due to the retrospective design, the rate of postoperative complications may also have been underestimated in our cohort.

The strengths of the present study include the uniform single-institution approach to care and the completeness of clinical data. The main potential limitation of this study – which is typical for retrospective studies – is the lack of random patient assignment and patient selection. However, our data are in line with several series published so far regarding the prognostic impact of CONUT scores in epithelial ovarian cancer and other tumor types.

Conclusion

In conclusion, this study suggests that CONUT scores might be a useful prognostic biomarker of overall survival in women with ovarian cancer that is low cost and broadly available. Future prospective investigations are warranted to investigate the clinical applications of CONUT scores in ovarian cancer patients. The impact of preoperative nutrition on patients suffering from malnutrition and the influence on prognosis in patients with ovarian cancer undergoing cytoreductive surgery need to be further elucidated.

Declarations

Funding: Not applicable.

Ethics approval: The study was approved by the Ethics Committee of the Medical University of Vienna (1696/2017) before the study was initiated.

Consent to participate: Due to its retrospective design, the Ethics Committee waived the requirement to obtain specific informed consent from patients.

Consent for publication: not applicable.

Availability of data and material (data transparency): In accordance with the journalʼs guidelines, we will provide our data for the reproducibility of this study in other centers if requested.

Code availability: not applicable.

Authorsʼ contributions: All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by Lisa Gensthaler, Thomas Bartl, Richard Schwameis and Alexander Reinthaller. The first draft of the manuscript was written by Christine Bekos, Christoph Grimm and Stephan Polterauer; all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.