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Abstract

Background: Pancreatic ductal adenocarcinoma (PDAC) is known to have a poor prognosis, early local invasion, and distant metastasis. Surgical resection is the most effective treatment, and tumor recurrence can be the key factor affecting the surgical outcome. Serum carbohydrate antigen 19-9 (CA19-9) is a tumor marker with high sensitivity to pancreatic cancer; elevated CA19-9 levels often indicate poor biological behavior. Tumor size is also a crucial factor that affects the prognosis. Therefore, we developed a program to evaluate the effect of the ratio of CA19-9 to total tumor volume (CA19-9/TTV) as a prognostic marker on tumor recurrence and long-term survival in patients with PDAC following pancreaticoduodenectomy (PD). Methods: Data from 200 patients who underwent PD for PDAC were retrospectively analyzed. CA19-9/TTV was calculated according to preoperative CA19-9 and TTV, and patients were divided into two groups according to the optimal cut-off value. Univariate and multivariate analyses were performed on the clinicopathological data to screen the risk factors affecting postoperative recurrence and long-term prognosis of patients with PDAC undergoing PD. Results: The receiver operating characteristic curve showed that the best cut-off value was 5.62 (area under curve [AUC], 0.633; 95% CI: 0.548-0.718). Multivariate analysis showed that tumor differentiation and CA19-9/TTV were independent risk factors for the long-term prognosis of PDAC (P = 0.004, P = 0.007), as well as for tumor recurrence (P = 0.008, P = 0.008). Conclusion: CA19-9/TTV is an independent risk factor for the prognosis of PDAC and may be a new marker for lower survival benefits.

Keywords

Pancreatic carcinoma pancreaticoduodenectomy carbohydrate antigen 19-9 total tumor volume prognosis‌

Introduction

Due to the high degree of malignancy, the easy occurrence of local vascular invasion,e distant metastasis, and other reasons, the overall resection rate of pancreatic cancer is less than 20%, and the 5-year survival rate is less than 10%.e¹ Data from the National Comprehensive Cancer Network (NCCN) in 2019 shows that pancreatic cancer is the 10th leading cause of cancer-related death worldwide. Adenocarcinomas represent 85% of the pancreatic cancers originating from exocrine pancreatic ductal epithelial cells. The rest include acinar cell carcinoma derived from pancreatic exocrine acini and pancreatic neuroendocrine tumors derived from neuroendocrine cells.² Although the specific mechanism of its pathogenesis is not clear, a large number of epidemiological studies have shown that smoking, obesity, history of diabetes, and chronic pancreatitis are high-risk factors for pancreatic cancer.

At present, curative resection is the only way to cure pancreatic cancer.³ Patients with unresectable tumors can be treated with therapies such as chemotherapy, radiotherapy, immunotherapy, and molecular targeted therapy. With the development in surgical techniques and the progress of anesthesia and monitoring, the postoperative complications of the pancreas showed an overall downward trend, and the perioperative mortality rate was less than 2%.⁴ However, the onset of pancreatic cancer is insidious, and most patients have no specific symptoms. As a result, 80% of the patients have lost the chance of surgical resection at the time of diagnosis.⁵ Even after R0 resection, the median survival time of patients eeremains only 12–20 months.⁶ Hishinuma and others conducted autopsies on 27 patients with pancreatic cancer and found that 85% to 90% of the patients died due to tumor recurrence.⁷ Pancreatic cancer usually relapses within 2 years after the operation;⁸ therefore, there is an urgent need for potential markers that can predict postoperative prognosis and recurrence of pancreatic ductal adenocarcinoma (PDAC).

Serum carbohydrate antigen 19-9 (CA19-9) is a tumor marker with a high sensitivity to pancreatic cancer. Studies have found that distant metastasis of pancreatic cancer increases serum CA19-9 levels, and the degree of increase is closely related to the degree of metastasis.⁹ The size of the tumor has always been considered to be an independent risk factor for prognosis after a surgical treatment because tumor size is related to invasiveness. Larger tumors are more likely to have local invasion and lymph node metastasis, and it is challenging to achieve R0 resection. The purpose of this study was to combine CA19-9 with total tumor volume (TTV) to investigate the effect of the CA19-9/TTV ratio on the long-term prognosis and tumor recurrence of PDAC in patients undergoing pancreaticoduodenectomy (PD).

Methods

This study has been reported using the STROBE checklist for cohort studies.¹⁰

Ethics approval and consent to participate: The conduct of the study complied with the Declaration of Helsinki and was approved by the Ethics Committee of Beijing Chaoyang Hospital (Acceptance No.: 2020-5-20-4;Number: 2020-CO-302).It's a project with waived informed consent.

Inclusion and Exclusion Criteria

The data of patients with PDAC who underwent PD in the Department of Hepatobiliary Surgery of Beijing Chaoyang Hospital from January 2013 to December 2019 were analyzed retrospectively (n = 333). After implementing the relevant inclusion/exclusion criteria and NCCN guidelines,² 200 patients with PDAC were enrolled (Figure 1).

Figure 1.

Flow chart of patients with PDAC.

The inclusion criteria were as follows: (1) Patients with PDAC who underwent PD between January 2013 and December 2019; (2) 20–85 years old; (3) assessed as resectable PDAC or borderline resectable PDAC according to the NCCN guidelines; (4) en bloc resection of the tumor during surgery; (5) postoperative pathology confirmed pancreatic ductal adenocarcinoma; (6) informed consent from the patients and their families regarding the mode of operation and treatment strategy.

The exclusion criteria were as follows: (1) unresectable condition or metastasis found during surgery; (2) surgical rule violations; (3) pathologic diagnosis other than conventional ductal adenocarcinoma; (4) postoperative follow-up data were incomplete or lost to follow-up; (5) perioperative deaths.

The Optimal Cut-Off of CA19-9/TTV and Grouping Basis

When available, the tumor volume was measured by volumetric computed tomography (CT) scan or magnetic resonance imaging or calculated using the following formula: 4/3 × 3.14 × (maximum tumor radius in cm).³ The distribution of TTV is shown in Supplemental Figure 1. Chemiluminescence microparticle immunoassay was used to detect serum CA19-9 in tumor diagnosis, and its normal value was less than or equal to 37 U/mL. The receiver operating characteristic curve was drawn based on CA19-9/TTV and 1-year survival, and the best cut-off value was 5.62 (area under the curve [AUC]: 0.633, 95% CI: 0.548-0.718) (Figure 2). Patients with CA19-9/TTV ≤ 5.62 were labeled as group 1, and patients with CA19-9/TTV > 5.62 were group 2. There were 61 patients in group 1 and 139 patients in group 2.

Figure 2.

ROC curve of CA199/TTV and 1-year survival.

Index Analysis and Follow-up Strategy

The clinical and pathological data were extracted from the medical records, and perioperative data of the different groups were compared. The results of the CA19-9 test were taken from the patient's last blood sample before surgery. In the cases of patients treated for reducing jaundice, we rechecked CA19-9 the day before surgery; the frequency of postoperative follow-up was 1 and 3 months after the operation, once every 3 months within 2 years, and once every half a year for more than 2 years. The endpoints of follow-up were tumor recurrence and death. The contents of follow-up mainly included blood examination (including routine blood analysis, blood biochemistry, and tumor markers), imaging examination (including abdominal enhanced CT, pulmonary CT, and ECT), follow-up treatment, tumor recurrence and survival, and comparison of the long-term prognosis of the patients in different groups.

Statistical Analysis

The results are presented as mean ± standard error of the mean. Nominal data were compared using the χ² tests, and continuous variables were compared using the Student's t-test. Survival outcomes were calculated using the Kaplan–Meier method and compared using the log-rank test. Only variables statistically significant by univariate analysis were included in the multivariate analysis performed using a Cox proportional hazards regression model. All statistical analyses were performed using SPSS, version 22.0 (IBM), and two-sided P < 0.05 was considered to be statistically significant.

Results

Clinicopathological Data of Perioperative Period

The 200 enrolled patients included 111 males and 89 females aged between 29 and 83 (62.8 ± 10.7) years. The initial symptoms were jaundice in 80 patients, abdominal pain in 83, atypical gastrointestinal symptoms in 10, and physical examination in 27 cases; 65 (32.5%) patients had a history of smoking and 67 (33.5%) had a history of diabetes. Among the 80 patients with jaundice symptoms, 37 patients were treated with jaundice reduction before the operation, including nine cases of ERCP and 28 cases of PTBD. Six patients received neoadjuvant therapy in group one (mFOLFIRINOX four cases, gemcitabine hydrochloride + nab-paclitaxel therapy two cases), and four patients in group two (mFOLFIRINOX three cases, gemcitabine hydrochloride + nab-paclitaxel therapy one case). All patients completed the operation, and the intraoperative blood loss was 500 (quartile, 400, 800) mL (range, 100-2000 mL). Blood transfusion was performed in 83 patients (39.5%). The operation time was (10.0 ± 3.0) h (range 4-18 h). Twenty-seven patients received postoperative chemotherapy in group one (mFOLFIRINOX 15 cases, combined gemcitabine hydrochloride + nab-paclitaxel therapy 12 cases), and 30 patients in group two (mFOLFIRINOX 17 cases, gemcitabine plus albumin-bound paclitaxel 13 cases). The comparison of clinicopathological data between Group 1 and Group 2 in Table 1 shows that there was no significant difference in clinicopathological data between the two groups.

Table 1.

The Data of Clinicopathological in Patients with Pancreatic Carcinoma.

Variable	Goup1（n = 61）	Grou2（n = 139）	P
Gender(Male/Female)	32/29	80/59	0.429
Age (Year)	63.7 ± 9.23	61.0.0 ± 11.0	0.087
Smoking(Yes/No)	20/31	45/94	0.378
Diabetes(Yes/No)	18/43	49/90	0.430
Jaundice reduction（Yes/No）	13/48	27/112	0.800
Total bilirubin（umol/L）	16.8 (9.1,80.8)	20.0 (11.9，88.9)	0.237
CEA（ng/ml）	3.0 (1.6,5.0)	3.2 (1.7,4.9)	0.911
CA19-9（U/mL）	299.5 (117.6,1180.5)	152.7 (37.7,548.0)	0.014
Tumor differentiation(poor/moderate/high)	19/42	41/98	0.800
Operative blood loss（ml）	500.0（300.0，500.0）	500.0 (400.0,800.0)	0.242
Blood transfusion（Yes/No）	23/38	50/89	0.808
Operative time（h）	9 (7,11)	10 (8,12)	0.971
Lymph node metastasis（Yes/No）	40/21	86/53	0.561
Type of resection（R0/R1）	58/3	129/10	0.466
Postoperative chemotherapy（Yes/No）	20/41	42/97	0.734
Nerve invasion（Yes/No）	57/4	134/5	0.482
Tumor size（cm）	4.0 （3.5，5.0）	3.0 （2.4，4.0）	0.544
Tumor recurrence(Yes/No)	37/24	106/33	0.024
Patterns of recurrence
Local region	7	18	0.965
Hepatic and lung	22	57
Other distant	10	29

Overall Prognosis

The median follow-up time was 45 months up to June 2020. By the date of follow-up, a total of 143 cases recurred after surgery, including 37 cases in group 1 and 106 cases in group 2. The recurrence rate in group 2 was significantly higher than that in group 1(76.3% vs 60.7%, P = 0.024), but there were no differences in the recurrence patterns (local, hepatic, lung, and other distant, P = 0.965). The overall median disease-free survival (DFS) was 14 months. The 1-, 3-, and 5-year DFS rates were 53.9%, 22.1%, and 16.7%, respectively (Figure 3A). The median overall survival (OS) of the patients was 18 months, and the overall 1-, 3-, and 5-year survival rates were 65.1%, 26.0%, and 15.5%, respectively (Figure 3B).

Figure 3.

A Kaplan-Meier curve for disease-free survival. B Kaplan-Meier curve for overall survival.

Comparison of Long-Term Prognosis Between Two Groups

The median DFS of patients in groups 1 and 2 was 24 months and 12 months, respectively, and the 1-, 3-, and 5-year DFS rates were 69.5%, 38.7%, 25.6%, and 46.8%, 14.8%, and 12.7%, respectively (P = 0.002, Figure 4A). The median OS of patients in Group 1 and Group 2 was 26 months and 15 months, respectively, and the 1-, 3-, and 5-year OS rates were 81.6%, 42.8%, 26.0% and 57.5%, 19.0%, 11.2%, respectively (P = 0.002, Figure 4B).

Figure 4.

A Kaplan-Meier curve for disease-free survival in patients with different groups. B Kaplan-Meier curve for overall survival in patients with different groups.

Univariate Analysis of Postoperative Long-Term Prognosis and Tumor Recurrence

Sex, age, diabetes, preoperative serum bilirubin, preoperative serum CEA, R0 resection, nerve invasion, lymph node metastasis, tumor diameter, pathological differentiation, TNM stage, postoperative chemotherapy, CA19-9/TTV, postoperative CA19-9 value, intraoperative hemorrhage, and blood transfusion were included in the univariate analysis. The log-rank test showed that lymph node metastasis, nerve invasion, pathological differentiation, CA19-9/TTV level, postoperative CA19-9, and TNM stage were risk factors that might affect long-term prognosis and tumor recurrence (P < 0.05, Tables 2 and 3).

Table 2.

Univariate Analysis of Postoperative Long-term Prognosis.

Variables	Patients	1-year OS (%)	3-year OS (%)	5-year OS (%)	P
Gender					0.962
Male	112	63.5	28.5	17.6
Female	88	67.2	22.1	11.8
Age (Year)
>65	83	60.5	28.7	15.2	0.413
≤65	117	68.3	23.1	15.2
Diabetes
Yes	67	62.6	22.1	11.7	0.328
No	133	66.4	27.9	17.9
TB（umol/L)
≤21	92	65.4	32.1	22.1	0.370
>21	108	65.1	20.3	9.1
CEA（ng/ml）
<5	149	64.6	25.7	16.5	0.751
≥5	51	66.5	26.2	14.8
Resection type					0.920
R0	187	66.2	25.7	15.6
R1	13	50.0	25.0	12.5
Nerve invasion					0.020
Yes	191	63.5	23.9	13.4
No	9	100.0	68.6	68.6
Lymph node metastasis					0.006
Yes	126	57.2	20.6	11.3
No	74	78.7	36.6	23.8
Tumor size(cm)					0.195
≤2	38	75.5	27.1	21.7
>2	162	62.8	26.0	15.1
Tumor differentiation					0.000
Low	50	47.6	10.8	7.2
Medium-high	150	71.1	31.2	18.3
Postoperative chemotherapy					0.802
Yes	62	70.2	18.6	12.8
No	138	62.8	29.8	16.6
TNM staging					0.039
I	56	81.2	37.2	19.5
II	93	61.2	22.7	18.2
III	51	55.3	20.1	9.1
CA19-9/TTV					0.000
≤5.62	61	81.6	42.8	26.0
>5.62	139	57.5	19.0	11.2
Postoperative CA19-9					0.035
Elevation	106	60.0	17.6	10.6
No elevation	94	70.7	34.3	20.0
Blood transfusion					0.570
Yes	73	57.8	36.0	18.0
No	127	69.3	18.7	13.1
Blood loss					0.816
≤800	85	66.2	33.8	18.0
>800	115	64.2	20.2	13.8

Table 3.

Univariate Analysis of Postoperative Tumor Recurrence

Variables	Patients	1-year DFS (%)	3-year DFS (%)	5-year DFS (%)	P
Gender					0.854
Male	112	51.5	27.3	19.8
Female	88	57.0	15.0	12.0
Age (Year)
>65	83	47.7	22.1	16.4	0.339
≤65	117	58.2	21.3	16.6
Diabetes
Yes	67	48.5	19.0	13.3	0.347
No	133	56.7	23.3	18.7
TB（umol/L)
≤21	92	53.1	31.0	23.6	0.468
>21	108	54.6	13.3	10.0
CEA（ng/ml）
<5	151	54.1	21.7	17.1	0.732
≥5	49	53.4	21.9	16.0
Resection type					0.858
R0	187	54.6	21.2	17.0
R1	13	44.9	26.9	13.5
Nerve invasion					0.016
Yes	191	51.8	19.7	14.4
No	9	100	72.9	72.9
Lymph node metastasis					0.006
Yes	126	46.9	16.6	11.7
No	74	65.9	32.9	27.4
Tumor size(cm)					0.201
≤2	38	71.9	22.1	22.1
>2	162	50.2	22.2	16.2
Tumor differentiation					0.000
Low	50	40.1	12.2	8.1
Medium-high	150	58.5	25.4	19.6
Chemotherapy					0.734
Yes	62	59.1	17.6	14.7
No	138	51.7	24.0	17.3
TNM staging					0.021
I	56	67.3	31.8	23.9
II	93	50.8	21.3	18.9
III	51	45.3	35.0	8.80
CA199/TTV					0.000
≤5.62	61	69.5	38.7	30.7
>5.62	139	46.8	14.8	12.7
Postoperative CA19-9（U/mL）					0.033
Elevation	106	47.9	14.9	12.4
No elevation	94	60.7	29.4	21.4
Blood transfusion					0.562
Yes	73	51.5	28.7	18.5
No	127	55.2	17.4	15.4
Blood loss(ml)					0.860
≥800	110	58.4	21.3	16.5
<800	90	48.2	23.3	16.9

Multifactor Analysis of Postoperative Long-Term Prognosis and Tumor Recurrence

The Cox proportional hazard model included lymph node metastasis, nerve invasion, pathological differentiation, CA19-9/TTV level, postoperative CA19-9, and TNM stage, all of which are factors that may affect the long-term prognosis and tumor recurrence. The results showed that tumor differentiation and CA19-9/TTV were independent risk factors for the long-term prognosis of PDAC (P = 0.004, P = 0.007) (Table 4), as well as for tumor recurrence (P = 0.008, P = 0.008) (Table 5).

Table 4.

Multifactor Analysis of Postoperative Long-term Prognosis.

Variables	P	RR	95%CI
Lymph node metastasis	0.836	0.939	0.519−1.699
Nerve invasion	0.173	0.438	0.134−1.437
TNM staging	0.157	1.296	0.905−1.856
Tumor differentiation	0.004	1.744	1.199−2.536
CA19-9/TTV	0.007	1.720	1.157−2.557
Postoperative CA19-9	0.072	0.729	0.517−1.028

Table 5.

Multifactor Analysis of Postoperative Tumor Recurrence.

Variables	P	RR	95%CI
Lymph node metastasis	0.993	0.998	0.554−1.795
Nerve invasion	0.144	0.413	0.126−1.351
TNM staging	0.104	1.342	0.942−1.912
Tumor differentiation	0.008	1.657	1.141−2.405
CA19-9/TTV	0.008	1.698	1.151−2.506
Postoperative CA19-9	0.107	0.755	0.537−1.062

Discussion

Based on the NCCN guidelines, pancreatic carcinoma can be divided into resectable, borderline resectable, and non-resectable pancreatic cancer.² Curative resection is considered to be the only effective way to cure this type of disease. However, resectable pancreatic cancer often relapses after surgical treatment. Previous studies have found that the median disease-free time of patients with resectable pancreatic cancer was 7.0–21.0 months,^11–14 the median survival time was 20.1–22.8 months, and the 5-year survival rate was only 20.7–22.5%.¹⁵ In view of the poor prognosis and high recurrence rate after the diagnosis, we hope to implement early intervention for high-risk patients. It is essential to identify markers that can indicate postoperative patients’ long-term prognosis and recurrence risk with PDAC.

During tumorigenesis, abnormal glycosylation often occurs on the cell surface. CA19-9 is an oligosaccharide antigen secreted by adenocarcinoma cells into the blood through the thoracic duct. It is abnormally elevated in the serum of patients with pancreatic cancer, gallbladder cancer, and cholangiocarcinoma.¹⁶ Magnani JL¹⁷ found that CA19-9 was expressed regularly in cells of the pancreaticobiliary system and was initially detected by monoclonal antibody 19-9¹⁸ at a very low level in the serum of normal individuals (< 37 U/mL). Expression of CA19-9 in many cancers, such as colorectal, gastric, ovarian, cholangiocarcinoma, and pancreatic carcinoma, has been determined since.

A retrospective analysis by O’Brien et al.¹⁹ showed that within 2 years of diagnosis of pancreatic cancer, CA19-9 levels were significantly upregulated with a specificity of 95% and a sensitivity of 53%. CA19-9 is being used as a common auxiliary diagnosis and prognostic index for pancreatic cancer. Some studies have shown that with an increase in the degree of malignancy of pancreatic cancer, the level of serum CA19-9 increases. This is of great value for condition monitoring and evaluation.²⁰ The study by Liu²¹ asserted that the positive rate of CA19-9 in the serum of patients with pancreatic cancer was 84.54%. In addition to indicating the occurrence and progression of pancreatic cancer, CA19-9 levels can also predict tumor recurrence. Nishio et al. reported that preoperative serum CA19-9 ≥ 529 U/mL is an independent risk factor for pancreatic cancer recurrence after radical resection.²² Studies by Asaoka et al.²³ showed that the overall 2-year survival rate of patients with high CA19-9 (≥ 230 U/mL) was 37.5%, while that of the low-level group was 89.9%, with the difference being significant. Nevertheless, serum CA19-9 levels are elevated in pancreatic cancer and other cancers, and some inflammatory diseases. It has been reported that high CA19-9 levels as diagnostic criteria may lead to false-negative diagnoses in patients with a negative Lewis blood group phenotype.²⁴ Therefore, the sensitivity and specificity of CA19-9 as a diagnostic and prognostic tool are low. Hence, the sensitivity and specificity of CA19-9 as a diagnostic and prognostic tool are limited, and it is difficult to determine the level of CA19-9 that should be considered as a diagnostic criterion for pancreatic cancer.^25–27

A small tumor size indicates that the tumor is at an early stage of differentiation; tumor size has long been considered an independent risk factor for pancreatic cancer surgery prognosis. Satake et al.²⁸ pointed out that a 4 mm pancreatic tumor is micro-pancreatic cancer, and early detection of micro-pancreatic cancer can improve the overall prognosis of pancreatic cancer. However, micro-pancreatic cancer is not an early pancreatic cancer that can be cured by surgery alone. Benassai et al.²⁹ believed that a tumor diameter of > 3 cm would lead to a poor prognosis. This might be related to the fact that the larger the tumor, the more likely it is to invade surrounding tissues, nerves, and extra-pancreatic tissues.

Hazem et al.³⁰ have discussed the relationship between serum alpha-fetoprotein/TTV and tumor recurrence after hepatectomy for liver cancer. A total of 286 patients were included in the study, and the patients were divided into AFP/TTV ≤ 2 and AFP/TTV > 2 groups. The 1-, 3-, and 5-year DFS rates of the two groups were 79.3%, 65.8%, 48.1%, and 69.6%, 41.1%, and 32.1%, respectively, suggesting that AFP/TTV > 2 can indicate the recurrence of liver cancer after hepatectomy. The study led us toward the question of whether the concentration of CA19-9 per unit volume of the tumor could better predict postoperative recurrence and prognosis in patients with pancreatic cancer than the reference serum level of CA19-9 and tumor volume alone. In our study, the multivariate analysis showed that tumor differentiation and CA19-9/TTV were independent risk factors for tumor recurrence and poor prognosis of patients with PDAC after PD. The long-term prognosis of group 2 was significantly worse than that of group 1, and the recurrence rate was considerably higher. We believe that the lower the level of tumor differentiation, the higher is the degree of malignancy of the tumor, and the worse would be the prognosis; Furthermore, there are limitations in determining the prognosis of PDAC patients by tumor size or serum CA19-9 alone. Tumor volume cannot fully account for the tumor'sits biological characteristics; serum CA19-9 levels are often affected by other factors such as bile duct obstruction. It is of great significance that the combination of the two can eliminate many confounding factors. CA19-9/TTV is also of great value in the postoperative prognosis of patients with pancreatic cancer. Based on our study, patients with a higher ratio of CA19-9/TTV should receive preoperative treatment, strengthened postoperative follow-up, and appropriate adjuvant therapy to improve the long-term prognosis of PDAC following PD.

The limitation of this study is that it was a retrospective study conducted at a single center. The sample size of patients with pancreatic cancer is insufficient, the time span is long, and the experience level of surgeons is different. The above limitations may lead to a bias in the results; hence, more data from multiple centers are required for further verification of our results.

In conclusion, CA19-9/TTV and tumor differentiation are independent risk factors for the prognosis of PDAC. CA19-9/TTV > 5.62 predicts a poor prognosis and may be a new marker for lower survival benefits.

Supplemental Material

sj-png-1-tct-10.1177_15330338221078438 - Supplemental material for Ratio of CA19-9 Level to Total Tumor Volume as a Prognostic Predictor of Pancreatic Carcinoma After Curative Resection

Supplemental material, sj-png-1-tct-10.1177_15330338221078438 for Ratio of CA19-9 Level to Total Tumor Volume as a Prognostic Predictor of Pancreatic Carcinoma After Curative Resection by Junming Xu, Shaocheng Lyu, Yang Zhao, Xinxue Zhang, Zhe Liu, Xin Zhao and Qiang He in Technology in Cancer Research & Treatment

Footnotes

Abbreviations

Acknowledgements

We will thank the patients for their great help in this report. This paper is supported by Dr HQ.

Ethics Approval

The conduct of the study complied with the Declaration of Helsinki and was approved by the Ethics Committee of Beijing Chaoyang Hospital (Acceptance No.: 2020-5-20-4; Number: 2020-CO-302). It's a project with waived informed consent.

Availability of Data and Materials

The data used and analyzed in this study is included in the article or are available from the corresponding and first authors on reasonable request.

Authors’ Contributions

Contributions: (I) Conception and design: Junming Xu,Shaocheng Lyu and Yang zhao; (II) Administrative support: Qiang He; (III) Provision of study materials or patients: Xinxue Zhang, Zhe Liu; (IV) Collection and assembly of data: Junming Xu and Zhe Liu; (V) Data analysis and interpretation: Xinzhao and Shaocheng Lyu; (VI) Manuscript writing: All authors.

ORCID iD

Qiang He

Supplemental Material

Supplemental material for this article is available online.

References

Bray

Ferlay

Soerjomataram

, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394-424.

Tempero

. NCCN Guidelines updates: pancreatic cancer. J Natl Compr Canc Netw. 2019;17(5.5):603-605.

Siegel

Miller

Jemal

. Cancer statistics, 2018. CA Cancer J Clin. 2018;68(1):7-30.

Wolf

Lavu

Pancreaticoduodenectomy and its variants. Cancer J. 2012;18(6):55-61.

Rawla

Sunkara

Gaduputi

. Epidemiology of pancreatic cancer: global trends, etiology and risk factors. World J Oncol. 2019;10(1):10-27.

Fischer

Breidert

Keck

Makowiec

Lohrmann

Harder

. Early recurrence of pancreatic cancer after resection and during adjuvant chemotherapy. Saudi J Gastroenterol. 2012;18(2):118-121.

Hishinuma

Ogata

Tomikawa

Ozawa

Hirabayashi

Igarashi

. Patterns of recurrence after curative resection of pancreatic cancer, based on autopsy findings. J Gastrointest Surg. 2006;10(4):511-518.

Van den Broeck

Sergeant

Ectors

Van Steenbergen

Aerts

Topal

. Patterns of recurrence after curative resection of pancreatic ductal adenocarcinoma. Eur J Surg Oncol. 2009;35(6):600-604.

Cui

Wei

Dong

Liu

. Association of serum tumor markers with interstitial lung disease in patients with or without connective tissue disease: a cross-sectional study. Traditional Medicine & Modern Medicine. 2018; 01(02):1-7.

10.

von Elm

Altman

Egger

, et al. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Ann Intern Med. 2007;147(8):573-577.

11.

Zhang

Frampton

Kyriakides

Bong

Jiao

. Loco-recurrence after resection for ductal adenocarcinoma of the pancreas: predictors and implications for adjuvant chemoradiotherapy. Journal of Cancer Research & Clinical Oncology. 2012; 138(6):1063-1071.

12.

Sperti

Pasquali

Piccoli

Pedrazzoli

. Recurrence after resection for ductal adenocarcinoma of the pancreas. World J Surg. 1997;21(2):195-200.

13.

Morita

Oshiro

Mito

, et al. Prognostic significance of the degree of lymphatic vessel invasion in locally advanced, surgically resectable pancreatic head cancer: a single center experience. Medicine (Baltimore). 2018;97(49):e13466.

14.

Cao

Gao

, et al. Evaluation of serum D-dimer, fibrinogen, and CA19-9 for postoperative monitoring and survival prediction in resectable pancreatic carcinoma. World J Surg Oncol. 2017;15(1):48.

15.

Oettle, Helmut, Post, et al. Adjuvant chemotherapy With gemcitabine vs observation in patients undergoing curative-intent resection of pancreatic cancer. JAMA. 2007;297(3):267–77.

16.

Teng

Sun

, et al. Significant increased CA199 levels in acute pancreatitis patients predicts the presence of pancreatic cancer. Oncotarget. 2018;9(16):12745-12753.

17.

Magnani

Nilsson

Brockhaus

, et al. A monoclonal antibody-defined antigen associated with gastrointestinal cancer is a ganglioside containing sialylated lacto-N-fucopentaose II. J Biol Chem. 1982;257(23):14365-9.

18.

Magnani

Steplewski

Koprowski

Ginsburg

. Identification of the gastrointestinal and pancreatic cancer-associated antigen detected by monoclonal antibody 19-9 in the sera of patients as a mucin. Cancer Res. 1983;43(11):5489-5492.

19.

O’Brien

Sandanayake

Jenkinson

, et al. Serum CA19-9 is significantly upregulated up to 2 years before diagnosis with pancreatic cancer: implications for early disease detection. Clin Cancer Res. 2015;21(3):622-631.

20.

Wang

Sun

Wang

, et al. Predictive value of CONUT score combined with serum CA199 levels in postoperative survival of patients with pancreatic ductal adenocarcinoma: a retrospective study. PeerJ. 2020;8:e8811.

21.

Liu

Wang

, et al. A preoperative serum signature of CEA + /CA125 + /CA19-9 ≥ 1000 U/mL indicates poor outcome to pancreatectomy for pancreatic cancer. Int J Cancer. 2015;36(9):2216-2227.

22.

Nishio

Yamazoe

Ohira

,et al. Preoperative predictors for early recurrence of resectable pancreatic cancer. 2017,15(1):16.

23.

Asaoka

Miyamoto

Maeda

, et al. Prognostic impact of preoperative NLR and CA19-9 in pancreatic cancer. Pancreatology. 2016;16(3):434-440.

24.

Hirano

Kawa

Oguchi

, et al. Loss of Lewis antigen expression on erythrocytes in some cancer patients with high serum CA19-9 levels. J Natl Cancer Inst. 1987;79(6):1261-1268.

25.

Matsumoto

Murakami

Shinzeki

, et al. Proposed preoperative risk factors for early recurrence in patients with resectable pancreatic ductal adenocarcinoma after surgical resection: a multi-center retrospective study. Pancreatology. 2015;15(6):674-680.

26.

Kang

Kim

Choi

, et al. The use of adjusted preoperative CA 19-9 to predict the recurrence of resectable pancreatic cancer. J Surg Res. 2007;140(1):31-35.

27.

Rieser

Zenati

Hamad

, et al. CA19-9 On postoperative surveillance in pancreatic ductal adenocarcinoma: predicting recurrence and changing prognosis over time. Ann Surg Oncol. 2018;25(12):3483-3491.

28.

Satake

Chung

Umeyama

Takeuchi

Kim

. The possibility of diagnosing small pancreatic cancer (less than 4.0 cm) by measuring various serum tumor markers. A retrospective study. Cancer. 1991;68(1):149-152.

29.

Long-term survival after curative resection for pancreatic ductal adenocarcinoma – surgical treatment. Int J Surg. 2015; 21 Suppl 1: S1.

30.

Zakaria

Mohamed

Omar

Gaballa

. Alpha-fetoprotein level to total tumor volume as a predictor of hepatocellular carcinoma recurrence after resection. A retrospective cohort study. Ann Med Surg (Lond). 2020:109-113.

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