Comparison of Survival Outcomes between Radical Antegrade Modular Pancreatosplenectomy and Conventional Distal Pancreatosplenectomy for Pancreatic Body and Tail Cancer: Korean Multicenter Propensity Score Match Analysis
by
, , ,
Jaewoo Kwon
1,†
,
Huisong Lee
2,†,
Hongbeom Kim
3,
Sung Hyun Kim
4,
Jae Do Yang
5,
Woohyung Lee
6,
Jun Suh Lee
7,
Sang Hyun Shin
3,* and
Hee Joon Kim
8,* 1
Department of Surgery, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 06351, Republic of Korea
2
Department of Surgery, Ewha Womans University Mokdong Hospital, Seoul 07985, Republic of Korea
3
Division of Hepatobiliary-Pancreatic Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Republic of Korea
4
Department of Hepatobiliary and Pancreatic Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Republic of Korea
5
Department of Surgery, Jeonbuk National University Hospital, Jeonbuk National University Medical School, Jeonju 54896, Republic of Korea
6
Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea
7
Department of Surgery, College of Medicine, Incheon St. Mary’s Hospital, Catholic University of Korea, Seoul 06591, Republic of Korea
8
Division of Hepato-Pancreato-Biliary Surgery, Department of Surgery, Chonnam National University Medical School, Chonnam National University Hospital, Gwangju 61469, Republic of Korea
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work as first authors.
Cancers 2024, 16(8), 1546; https://doi.org/10.3390/cancers16081546
Submission received: 12 March 2024
/
Revised: 10 April 2024
/
Accepted: 16 April 2024
/
Published: 18 April 2024
(This article belongs to the Special Issue The Progress of Pancreatectomy for Pancreatic Cancer Treatment)
Abstract
:Simple Summary
Our study aimed to compare the operative and survival outcomes between radical antegrade modular pancreatosplenectomy (RAMPS) and conventional distal pancreatosplenctomy (cDPS), and identify prognostic factors for left-sided pancreatic cancer. We performed a retrospective propensity score match (PSM) analysis from 333 patients who underwent RAMPS or cDPS for left-sided pancreatic cancer. After PSM, 99 cohorts were matched in each group. We compared survival and operative outcomes and assessed prognostic factors. R0 resection rate was similar between both groups, and R1 resection rate was a significant prognostic factor. RAMPS was found to be safe, feasible, and to improve the number of retrieved lymph nodes. However, when R0 resection was similar in both groups, RAMPS was not associated with improved survival. Adjuvant treatment was a significant independent prognostic factor for overall and disease-free survival, but operation type was not.
Abstract
(1) Background: The aim of this study was to compare the survival benefit of radical antegrade modular pancreatosplenectomy (RAMPS) with conventional distal pancreatosplenectomy (cDPS) in left-sided pancreatic cancer. (2) Methods: A retrospective propensity score matching (PSM) analysis was conducted on 333 patients who underwent RAMPS or cDPS for left-sided pancreatic cancer at four tertiary cancer centers. The study assessed prognostic factors and compared survival and operative outcomes. (3) Results: After PSM, 99 patients were matched in each group. RAMPS resulted in a higher retrieved lymph node count than cDPS (15.0 vs. 10.0, p < 0.001). No significant differences were observed between the two groups in terms of R0 resection rate, blood loss, hospital stay, or morbidity. The 5-year overall survival rate was similar in both groups (cDPS vs. RAMPS, 44.4% vs. 45.2%, p = 0.853), and disease-free survival was also comparable. Multivariate analysis revealed that ASA score, preoperative CA19-9, histologic differentiation, R1 resection, adjuvant treatment, and lymphovascular invasion were significant prognostic factors for overall survival. Preoperative CA19-9, histologic differentiation, T-stage, adjuvant treatment, and lymphovascular invasion were independent significant prognostic factors for disease-free survival. (4) Conclusions: Although RAMPS resulted in a higher retrieved lymph node count, survival outcomes were not different between the two groups. RAMPS was a surgical option to achieve R0 resection rather than a standard procedure.
1. Introduction
Pancreatic ductal adenocarcinoma (PDAC) has a poor prognosis, with margin status and lymph node metastasis being recognized as unfavorable prognostic factors [1,2,3,4,5,6]. To address this issue, Strasberg et al. developed the concept of radical antegrade modular pancreatosplenectomy (RAMPS) [7]. RAMPS is a modified type of distal pancreatectomy to facilitate complete dissection of the N1 and N2 lymph nodes and obtaining negative posterior margins. RAMPS has been shown to be effective in achieving a higher lymph node yield and a negative posterior tangential margin in advanced left-sided PDAC when the tumor involves the peripancreatic soft tissue or peripancreatic lymph node metastases are suspected. However, it remains unclear whether RAMPS should be considered a standard operation for all left-sided PDACs, including non-advanced cases, or if it should be reserved as one of the surgical options only for advanced PDACs. Reports have shown that RAMPS has a 91% success rate in achieving negative tangential margins in patients [8]. However, the benefits of RAMPS over conventional distal pancreatosplenectomy (cDPS) in terms of survival outcomes have not been clearly established in previous studies [3,9,10,11]. This study aims to compare the operative and survival outcomes of RAMPS and cDPS to evaluate the value of RAMPS as a standard procedure in left-sided PDACs, as well as identify prognostic factors for left-sided pancreatic cancer.
2. Materials and Methods
2.1. Data Collection
We conducted a retrospective study of patients with PDAC who underwent RAMPS or cDPS at four tertiary hospitals between January 2010 and December 2020. RAMPS was defined according to the method described by Strasberg et al. [7]. The resection level at the pancreatic neck was reviewed from a postoperative CT scan and the extent of retropancreatic dissection and lymph node dissection was confirmed from the operation record. cDPS was defined as a distal pancreatectomy that does not fulfil the criteria for RAMPS (neck level transection, N1 and N2 lymph node dissection, and posterior dissection plane including the Gerota’s fascia). Cases in which the pancreatic resection was performed more distal than the pancreatic neck, depending on the location of the tumor, or a reduced lymph node dissection was performed according to the surgeon’s decision, or the posterior dissection plane did not follow the RAMPS plane were classified as cDPS. For patients with metastatic lesions, non-curative resection was excluded. Patients who underwent extended surgery such as combined organ resection or celiac axis resection that could not be classified in routine RAMPS nor cDPS were also excluded. We collected demographic and operative data, including age, sex, American Society of Anesthesiologist (ASA) score, body mass index (BMI), preoperative carcinoembryonic antigen (CEA) level, preoperative carbohydrate antigen 19-9 (CA19-9) level, neoadjuvant treatment, adjuvant treatment, operation type (RAMPS vs. cDPS), operation time, estimated blood loss, and hospital stay. Pathological data included tumor size, histologic differentiation, retrieved lymph node count, metastatic lymph node count, perineural invasion (PNI), lymphovascular invasion (LVI), and margin status. R1 resection was defined as the safety margin from the tumor to the resection margin being less than 1 mm. All postoperative morbidities were recorded and graded according to the Clavien–Dindo classification, and postoperative pancreatic fistula (POPF), post-pancreatectomy hemorrhage (PPH), and delayed gastric emptying (DGE) were graded according to the International Study Group of Pancreatic Surgery.
2.2. Statistical Analysis
A retrospective 1:1 propensity score matching analysis was conducted to compare the clinical and pathological outcomes of patients who underwent RAMPS or cDPS for PDAC. Six preoperative covariates, including age, sex, ASA score, tumor location, tumor size, and preoperative serum CA19-9 level, were used for propensity score matching. Because the tumor location influenced the decision regarding the pancreatic resection level and extent of lymph node dissection, tumor location was included in the propensity score matching. The matching was performed using a nearest neighborhood method with 0.01 of caliper. Continuous variables were compared using either the independent samples t-test or Mann–Whitney U test based on the normality test results, and categorical variables were compared using the chi-square test or Fisher’s exact test. The Kaplan–Meier method was used to estimate overall survival (OS) and disease-free survival (DFS), and the log-rank test was used to identify risk factors. Multivariate analysis was conducted using a Cox regression hazard model. Statistical significance was set at p < 0.05, and all statistical analyses were performed using SPSS version 26.0 (IBM SPSS Statistics for Windows, IBM Corp., Armonk, NY, USA).
3. Results
3.1. Baseline Characteristics before and after Propensity Score Matching
In this study, 333 patients with pancreatic ductal adenocarcinoma were initially enrolled. To balance the baseline characteristics between the two groups, 1:1 propensity score matching was performed, resulting in 99 patients included in both the RAMPS and cDPS groups. Table 1 demonstrates the baseline characteristics of the patients before and after PSM. After matching, both groups were found to be well balanced in terms of their preoperative characteristics.
3.2. Operative Outcomes
The results revealed a significantly higher retrieved lymph node count in the RAMPS group than in the cDPS group. However, the R0 resection rate was comparable between the two groups. Moreover, no significant differences were observed in the length of hospital stay, operation time, estimated blood loss, transfusion rate, and morbidity between the two groups. There was no mortality within 30 and 90 days. The recurrence rate and recurrence pattern were also found to be comparable between both groups. The detailed operative outcomes are presented in Table 2.
3.3. Comparison of Pathologic Results
No significant differences were found in terms of histologic differentiation, T-stage, perineural invasion, and lymphovascular invasion between the two groups. However, there was a significant difference in the number of positive lymph nodes and N-stage, with higher counts observed in the RAMPS group compared to the cDPS group. This observation raises the possibility of under-staging in the cDPS group. The detailed pathologic results can be found in Table 3.
3.4. Comparison of Survival Outcomes
The study included a mean and median follow-up time of 30.84 and 22.5 months (range 3–133 months) for all matched patients, with no significant differences in the mean and median follow-up times between the cDPS and RAMPS groups (32.81 vs. 28.88 months, p = 0.281; 26.0 vs. 20.0 months, p = 0.576, respectively). The 2-year and 5-year overall survival rates for all matched cohorts were 68.5% and 44.8%, respectively, with a median survival time of 48.0 months. Although the median survival time was slightly longer in the cDPS group than in the RAMPS group, the difference was not significant (50.0 vs. 41.0 months, p = 0.853). The 2-year and 5-year overall survival rates were comparable between the cDPS and RAMPS groups (71.9% and 44.4% vs. 64.5% and 45.2%, respectively) (Figure 1A). The overall recurrence rate was 73.2%, with no significant difference between both groups (cDPS vs. RAMPS, 75.8% vs. 70.7%, p = 0.422). The 2-year and 5-year disease-free survival rates for all matched cohorts were 35.1% and 21.9%, respectively, with no significant difference between the cDPS and RAMPS groups (34.5% and 21.2% vs. 35.4% and 22.3%, respectively). The median DFS time was also similar between the groups (RAMPS: 14.0 months; cDPS: 10.0 months, p = 0.929) (Figure 1B).
3.5. Prognostic Factor Analysis
In the univariate analysis, several prognostic factors for overall survival (OS) were found to be significant, including age, ASA score, preoperative serum CA19-9, histologic differentiation, lymph node ratio, margin status, adjuvant treatment, PNI, and LVI. However, in the multivariate analysis, only ASA score, preoperative CA19-9, histologic differentiation, margin status, adjuvant treatment, and lymphovascular invasion were identified as independent significant prognostic factors for OS, as shown in Table 4.
Regarding disease-free survival (DFS), in the univariate analysis, preoperative CA19-9, histologic differentiation, T-stage, N-stage, lymph node ratio, adjuvant treatment, PNI, and LVI were identified as significant prognostic factors. However, in the multivariate analysis, only preoperative CA19-9, histologic differentiation, T-stage, adjuvant treatment, and LVI were found to be independent significant prognostic factors for DFS (Table 5).
3.6. Subgroup Analysis of Patients who underwent Resection at the Pancreatic Neck
Subgroup analysis was conducted on patients who underwent RAMPS and cDPS at the level of the pancreatic neck. In the univariate analysis, age, sex, histologic differentiation, margin status, and adjuvant treatment were significant prognostic factors for OS. In the multivariate analysis, histologic differentiation, margin statue, and adjuvant treatment were identified as independent significant prognostic factors for OS (Table 6).
Regarding disease-free survival (DFS), in the multivariate analysis, histologic differentiation, T-stage, and adjuvant treatment were found to be independent significant prognostic factors for DFS (Table 7).
4. Discussion
RAMPS involves resection of the pancreatic body and tail, as well as an extensive lymph node dissection. Several studies have reported that RAMPS does not increase morbidity and mortality rates [2,9,10,11,12,13]. In our study, the operative outcomes in terms of EBL, transfusion, hospital stay, and the incidence of morbidity, including POPF, PPH, and DGE, were comparable between the groups. In our study, we found that the short-term operative outcomes, including estimated blood loss, transfusion requirements, hospital stay, and the incidence of complications such as postoperative pancreatic fistula, post-pancreatectomy hemorrhage, and delayed gastric emptying, were similar between the RAMPS and cDPS groups. However, the removal of a significant portion of the pancreas during RAMPS can increase the risk of developing diabetes or pancreatic exocrine insufficiency, which may require lifelong enzyme replacement therapy [14,15,16]. The operative time was not significantly different after PSM (Table 2).
Previous studies have demonstrated that RAMPS is associated with a higher number of retrieved lymph nodes and R0 resection rate compared to cDPS [2,3,4,9,11,12,13,17,18]. In contrast, Sham et al. reported lower rates for these parameters in the RAMPS group compared to the cDPS group [10]. In our study, we also observed a significantly higher median number of retrieved lymph nodes in the RAMPS group compared to the cDPS group (15.0 vs. 10.0, p = 0.001), but no significant difference in R0 resection rates between the two groups (94.9% in RAMPS vs. 93.9% in cDPS, p = 0.756). Although the retrieved LN count was significantly higher in the RAMPS group, there was no evidence that extensive LN dissection can improve survival in patients with pancreatic ductal adenocarcinoma [19]. Several researchers suggested a tailored lymph node dissection extent according to the location of the tumor, based on the results of their research on lymph node metastasis pattern according to the tumor location [20,21]. The N-stage was significantly higher in the RAMPS group, but it was not a significant risk factor in the prognostic factor analysis. In the cDPS group, the number of retrieved lymph nodes (LN) was small, which may have led to downstaging, and this could have influenced the result of the analysis of N-stage as a prognostic factor. Even considering the possibility of downstaging, extensive lymph node resection did not affect survival rate, and adjuvant chemotherapy was a significant prognostic factor. This suggests that adjuvant chemotherapy is more important for improving survival rate than the extent of surgery.
Although RAMPS has been shown to improve retrieved lymph node counts and R0 resection rates, the evidence for its survival benefit remains unclear. Dai et al. reported that the RAMPS group had a higher number of retrieved lymph nodes, longer OS time, and longer DFS time compared to cDPS [3]. However, other studies, including that of Kim et al., Park et al., and Sham et al., found no significant differences in OS and DFS rates between the RAMPS and cDPS groups [4,10,11]. The meta-analysis also showed mixed results, with some authors reporting no significant survival benefit [12,17,18,22], while others reported higher 1-year survival rates in the RAMPS group. In our study, we found no significant difference in OS and DFS between the two groups. By contrast, Dragomir et al. and Zhou et al. reported that the 1-year survival rate was significantly higher in the RAMPS group than in the cDPS group [9,13]. In our study, There was also no significant difference in OS and DFS between the two groups. Translation: In our study, the R0 resection rate, a significant prognostic factor, was similar between the two groups, and there was no difference in survival rate. There was a significant difference in the resection level depending on the location of the tumor, and there was a significant difference in the retrieved LN count, but it did not affect the survival rate. This suggests that if a negative resection margin is obtained, the resection level and retrieved LN count do not affect the survival rate.
Previous studies have demonstrated that margin status, histological grade, lymph node involvement, tumor size, LNR, and CEA are independent prognostic factors in pancreatic ductal adenocarcinoma [1,2,6,23,24,25,26,27]. In the present study, higher ASA score, preoperative CA19-9 > 37 U/mL, poorly/undifferentiated carcinoma, R1 resection, no adjuvant treatment, and lymphovascular invasion were independent poor prognostic factors for OS, and preoperative serum CA19-9 > 37 U/mL, poorly/undifferentiated carcinoma, T3 stage, no adjuvant treatment, and lymphovascular invasion were independent poor prognostic factors for DFS. OS and DFS were not affected by the operation type. Old age and higher ASA scores did not affect DFS. However, they were significant prognostic factors in the univariate analysis for OS, because the patients with old age or poor physical status often could not receive adjuvant chemotherapy.
Our study has limitations, including potential selection bias in this retrospective analysis. To evaluate the value of RAMPS as a standard procedure, the tumor size was included in the covariates for PSM. Therefore large, advanced cases requiring RAMPS to achieve R0 resection could be excluded. R0 resection rate was not significantly different between both groups. Another limitation of this study is that the annual number of cases varies by center, which may result in differences in surgical and pathological expertise. A larger prospective study with longer follow-up is necessary to accurately assess the survival benefit of RAMPS.
5. Conclusions
In conclusion, our study demonstrates that RAMPS is a safe and feasible procedure that increases the number of retrieved lymph nodes; however, a significant survival benefit was not observed. Margin status was a significant prognostic factor. Therefore, RAMPS is a treatment option for advanced cases to achieve negative tangential margin rather than a standard procedure for all left-sided pancreatic cancer. Adjuvant treatment remains a significant independent prognostic factor for OS and DFS.
Author Contributions
Conceptualization, H.J.K. and S.H.S.; methodology, J.K. and H.L.; validation, H.K. and S.H.K.; formal analysis, J.D.Y. and W.L.; investigation, J.S.L.; data curation, H.J.K., S.H.S., J.K. and H.L.; writing—original draft preparation, J.K. and H.L.; writing—review and editing, H.J.K. and S.H.S.; visualization, J.D.Y.; supervision, H.J.K.; project administration, H.J.K. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
The study was conducted in accordance with the Declaration of Helsinki, and approved by the Institutional Review Board of Chonnam National University Hospital (Gwangju, Republic of Korea, IRB No. CNUH-2022-298, date of approval: 16 August 2022).
Informed Consent Statement
Our Institutional Review Board of Chonnam National University Hospital waived the need for written informed consent from the participants since the research involved no more than minimal risk to subjects, and there was no reason to assume rejection of agreement.
Data Availability Statement
Data are contained within the article.
Conflicts of Interest
The authors declare no conflicts of interest.
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Figure 1.
(A) Overall survival curve according to the operation type. (B) Disease-free survival curve according to the operation type. There were no differences in overall survival or disease-free survival between the conventional DPS and the RAMPS groups.
Figure 1.
(A) Overall survival curve according to the operation type. (B) Disease-free survival curve according to the operation type. There were no differences in overall survival or disease-free survival between the conventional DPS and the RAMPS groups.
Table 1.
Basal characteristics of total and matched cohorts.
| Pre-PSM | Post-PSM | |||||
|---|---|---|---|---|---|---|
| cDPS (n = 130) | RAMPS (n = 203) | p-Value | cDPS (n = 99) | RAMPS (n = 99) | p-Value | |
| Age [median (range)] (y) | 66.0 (39–86) | 64.0 (41–84) | 0.503 * | 65.0 (39–80) | 66.0 (43–81) | 0.301 * |
| Sex [n (%)] | 0.262 | 1.000 | ||||
| Male | 72 (55.4) | 125 (61.6) | 53 (53.5) | 53 (53.5) | ||
| Female | 58 (44.6) | 78 (38.4) | 46 (46.5) | 46 (46.5) | ||
| Approach [n (%)] | 0.031 † | 0.747 † | ||||
| Open | 120 (92.3) | 198 (97.5) | 93 (93.9) | 95 (96.0) | ||
| Laparoscopic | 10 (7.7) | 5 (2.5) | 6 (6.1) | 4 (4.0) | ||
| Tumor location [n (%)] | <0.001 | 1.000 | ||||
| Confined to neck/body | 58 (44.6) | 159 (78.3) | 56 (56.6) | 56 (56.6) | ||
| Body to tail | 19 (14.6) | 11 (5.4) | 10 (10.1) | 10 (10.1) | ||
| Confined to tail | 53 (40.8) | 33 (16.3) | 33 (33.3) | 33 (33.3) | ||
| Resection level [n (%)] | <0.001 | <0.001 | ||||
| At neck | 56 (43.1) | 203 (100) | 42 (42.4) | 99 (100) | ||
| Neck~aorta left border | 49 (37.7) | 0 (0.0) | 42 (42.4) | 0 (0.0) | ||
| Lateral to aorta left border | 25 (19.2) | 0 (0.0) | 15 (15.1) | 0 (0.0) | ||
| BMI (mean ± SD) | 23.70 ± 3.288 | 23.29 ± 2.937 | 0.234 | 23.71 ± 3.459 | 23.41 ± 2.781 | 0.513 |
| ASA score [n (%)] | 0.503 | 0.571 | ||||
| I | 14 (10.8) | 31 (15.3) | 12 (12.1) | 14 (14.1) | ||
| II | 102 (78.5) | 151 (74.4) | 78 (78.8) | 72 (72.7) | ||
| III | 14 (10.8) | 21 (10.3) | 9 (9.1) | 13 (13.1) | ||
| CEA, ng/mL [median (range)] | 2.52 (0.20–165.10) | 2.20 (0.44–56.92) | 0.126 * | 2.49 (0.20–165.10) | 2.51 (0.44–56.92) | 0.734 * |
| CA19-9, U/mL [median (range)] | 59.93 (1.00–11,387.00) | 75.01 (1.20–10,028.49) | 0.436 * | 168.13 (1.80–11,387.00) | 244.32 (2.00–6808.37) | 0.101 * |
| Tumor size, cm [median (range)] | 3.0 (0.5–9.5) | 2.5 (0.3–10.0) | 0.282 * | 3.0 (1.0–8.0) | 3.2 (1.2–8.5) | 0.132 * |
| Neoadjuvant treatment [n (%)] | 0.606 † | 0.246 † | ||||
| No | 125 (96.2) | 192 (94.6) | 96 (97.0) | 99 (100) | ||
| Yes | 5 (3.8) | 11 (5.4) | 3 (3.0) | 0 (0.0) | ||
| Adjuvant treatment [n (%)] | 0.164 | 0.66 | ||||
| No | 54 (41.5) | 69 (34.0) | 36 (36.4) | 39 (39.4) | ||
| Yes | 76 (58.5) | 134 (66.0) | 63 (63.6) | 60 (60.6) | ||
PSM, propensity score matching; DPS, distal pancreatosplenectomy; RAMPS, radical antegrade-modular pancreatosplenctomy; BMI, body mass index; SD, standard deviation; ASA, American Society of Anesthesiologists; CEA, carcinoembryonic antigen; CA, carbohydrate antigen; * Mann–Whitney U test; † Fisher’s exact test.
Table 2.
Comparison of operative outcomes.
| Pre-PSM | Post-PSM | |||||
|---|---|---|---|---|---|---|
| cDPS (n = 130) | RAMPS (n = 203) | p-Value | cDPS (n = 99) | RAMPS (n = 99) | p-Value | |
| LOS [median (range)] (days) | 10.0 (5–52) | 9.0 (6–152) | 0.065 * | 10.0 (5–52) | 10.0 (7–35) | 0.806 * |
| Approach [n (%)] | 0.031 | 0.747 | ||||
| Open | 120 (92.3) | 198 (97.5) | 93 (93.9) | 95 (96.0) | ||
| Laparoscopic | 10 (7.7) | 5 (2.5) | 6 (6.1) | 4 (4.0) | ||
| Op. time [median (range)] (min) | 195 (93–420) | 204 (117–494) | 0.045 * | 195 (98–420) | 210 (118–458) | 0.305 * |
| EBL [median (range)] (mL) | 250 (30–1600) | 300 (50–3000) | 0.488 * | 250 (50–1600) | 250 (50–3000) | 0.934 * |
| Retrieved LN count [median (range)] | 10 (0–39) | 15 (4–51) | <0.001 * | 10.0 (0–36) | 15.0 (5–51) | 0.001 * |
| R0 resection [n (%)] | 120/130 (92.3) | 198/203 (97.5) | 0.031 | 93/99 (93.9) | 94/99 (94.9) | 0.756 |
| Transfusion [n (%)] | 0.692 | >0.99 | ||||
| No | 123 (94.6) | 194 (95.6) | 94 (94.9) | 94 (94.9) | ||
| Yes | 7 (5.4) | 9 (4.4) | 5 (5.1) | 5 (5.1) | ||
| POPF [n (%)] | 0.045 † | 0.165 † | ||||
| No or BCL | 110 (84.6) | 187 (92.1) | 85 (85.9) | 92 (92.9) | ||
| CR-POPF | 20 (15.4) | 16 (7.9) | 14 (14.1) | 7 (7.1) | ||
| DGE [n (%)] | 0.262 | 0.261 | ||||
| No | 127 (97.7) | 199 (98.0) | 96 (97.0) | 96 (97.0) | ||
| Grade A | 0 (0.0) | 3 (1.5) | 0 (0.0) | 2 (2.0) | ||
| Grade B | 1 (0.8) | 1 (0.5) | 1 (1.0) | 1 (1.0) | ||
| Grade C | 2 (1.5) | 0 (0.0) | 2 (2.0) | 0 (0.0) | ||
| PPH [n (%)] | 0.22 | 0.384 | ||||
| No | 125 (96.2) | 201 (99.0) | 95 (96.0) | 98 (99.0) | ||
| Grade A | 1 (0.8) | 0 (0.0) | 1 (1.0) | 0 (0.0) | ||
| Grade B | 3 (2.3) | 0 (0.0) | 2 (2.0) | 0 (0.0) | ||
| Grade C | 1 (0.8) | 2 (1.0) | 1 (1.0) | 1 (1.05) | ||
| Chyle leak [n (%)] | 0.300 | 0.251 | ||||
| No | 126 (96.9) | 191 (94.1) | 95 (96.0) | 90 (90.9) | ||
| Yes | 4 (3.1) | 12 (5.9) | 4 (4.0) | 9 (9.1) | ||
| SSI [n (%)] | 0.966 | 0.884 | ||||
| No | 128 (98.5) | 199 (98.0) | 97 (98.0) | 96 (97.0) | ||
| Superficial | 1 (0.8) | 3 (1.5) | 1 (1.0) | 2 (2.0) | ||
| Organ/space | 1 (0.8) | 1 (0.5) | 1 (1.0) | 1 (1.0) | ||
| Severe complication [n (%)] | 0.998 | 0.663 | ||||
| No | 114 (87.7) | 178 (87.7) | 86 (86.9) | 88 (88.9) | ||
| Yes | 16 (12.3) | 25 (12.3) | 13 (13.1) | 11 (11.1) | ||
| Recurrence [n (%)] | 0.251 | >0.99 | ||||
| No | 37 (28.5) | 70 (34.5) | 24 (24.2) | 24 (24.2) | ||
| Yes | 93 (71.5) | 133 (65.5) | 75 (75.8) | 75 (75.8) | ||
| Recurrence pattern [n (%)] | 0.177 | 0.507 | ||||
| No | 37 (28.5) | 70 (34.5) | 24 (24.2) | 24 (24.2) | ||
| Locoregional | 20 (15.4) | 17 (8.4) | 16 (16.2) | 11 (11.1) | ||
| Systemic | 61 (46.9) | 92 (45.3) | 49 (49.5) | 51 (51.5) | ||
| Both | 12 (9.2) | 24 (11.8) | 10 (10.1) | 13 (13.1) | ||
PSM, propensity score match; DPS, distal pancreatosplenectomy; RAMPS, radical antegrade modular pancreatosplenectomy; LOS, length of stay; Op, operation; EBL, estimated blood loss; LN, lymph node; POPF, postoperative pancreatic fistula; BCL, biochemical leak; CR-POPF, clinically relevant POPF; DGE, delayed gastric emptying; PPH, post-pancreatectomy hemorrhage; SSI, surgical site infection; * Mann–Whitney U test; † Fisher’s exact test.
Table 3.
Histopathologic results before and after propensity score matching.
| Pre-PSM | Post-PSM | |||||
|---|---|---|---|---|---|---|
| cDPS (n = 130) | RAMPS (n = 203) | p-Value | cDPS (n = 99) | RAMPS (n = 99) | p-Value | |
| Differentiation [n (%)] | 0.472 | 0.677 | ||||
| Well | 18 (13.8) | 20 (9.9) | 13 (13.4) | 12 (12.1) | ||
| Moderate | 82 (63.1) | 129 (63.5) | 61 (62.9) | 68 (68.7) | ||
| Poorly/undifferentiated | 30 (23.1) | 54 (26.6) | 23 (23.7) | 19 (19.2) | ||
| T-stage [n (%)] | 0.208 | 0.216 | ||||
| T1 | 30 (23.1) | 65 (32.0) | 23 (23.2) | 19 (45.2) | ||
| T2 | 72 (55.4) | 98 (48.3) | 54 (54.5) | 47 (47.5) | ||
| T3 | 28 (21.5) | 40 (19.7) | 22 (22.2) | 33 (33.3) | ||
| Involved LN count [median (range)] | 0.0 (0–15) | 1.0 (0–22) | 0.028 | 1.0 (0–15) | 1.0 (0–17) | 0.006 |
| LNR [median (range)] | 0.048 (0.0–1.00) | 0.057 (0–0.71) | 0.383 | 0.042 (0–1.0) | 0.090 (0–0.71) | 0.059 |
| N-stage [n (%)] | 0.083 * | 0.024 | ||||
| N0 | 62 (47.7) | 83 (40.9) | 44 (44.4) | 31 (41.3) | ||
| N1 | 48 (36.9) | 84 (41.4) | 38 (38.4) | 42 (42.4) | ||
| N2 | 12 (9.2) | 36 (17.7) | 12 (12.1) | 26 (26.3) | ||
| Nx | 8 (6.2) | 0 (0.0) | 5 (5.1) | 0 (0.0) | ||
| Perineural invasion [n (%)] | 0.360 | 0.290 | ||||
| PNI− | 17 (13.1) | 21 (10.3) | 13 (13.5) | 8 (8.2) | ||
| PNI+ | 106 (81.5) | 180 (88.7) | 83 (86.5) | 90 (91.8) | ||
| Unknown | 7 (5.4) | 2 (1.0) | 3 (3.0) | 1 (1.0) | ||
| Lymphovascular invasion [n (%)] | 0.376 | 0.281 | ||||
| LVI− | 64 (49.2) | 95 (46.8) | 44 (44.4) | 37 (37.4) | ||
| LVI+ | 46 (35.4) | 85 (41.9) | 39 (39.4) | 50 (50.5) | ||
| Unknown | 20 (15.4) | 23 (11.3) | 16 (16.2) | 12 (42.9) | ||
PSM, propensity score matching; cDPS, conventional distal pancreatosplenectomy; RAMPS, radical antegrade modular pancreatosplenectomy; LN, lymph node; LNR, lymph node ratio; PNI, perineural invasion; LVI, lymphovascular invasion. * Nx was excluded from the analysis of N-stage.
Table 4.
Risk factor analysis for overall survival after propensity score matching.
| Univariate | Multivariate | ||||||
|---|---|---|---|---|---|---|---|
| n | 2YSR (%) | 5YSR (%) | MST (Months) | p-Value | HR (95% CI) | p-Value | |
| Age (years) | 0.008 | ||||||
| <65 | 95 | 75.5 | 56.1 | 85.62 | 1 (Reference) | ||
| 65–75 | 75 | 66.1 | 34.3 | 51.77 | 1.663 (0.899–3.079) | 0.105 | |
| >75 | 28 | 47.5 | 34.6 | 46.71 | 1.328 (0.511–3.453) | 0.561 | |
| Sex | 0.060 | ||||||
| Male | 106 | 64.2 | 33.7 | 61.72 | |||
| Female | 92 | 73.4 | 55.5 | 80.35 | |||
| Operation type | 0.853 | ||||||
| Conventional DPS | 99 | 71.9 | 44.4 | 72.90 | 1 (Reference) | ||
| RAMPS | 99 | 64.5 | 45.2 | 69.82 | 1.014 (0.568–1.811) | 0.962 | |
| ASA physical status | 0.047 | ||||||
| 1 | 26 | 87.6 | 74.9 | 105.04 | 1 (Reference) | ||
| 2 | 150 | 66.0 | 41.9 | 66.87 | 4.553 (1.081–19.172) | 0.039 | |
| 3 | 22 | 63.6 | 31.9 | 51.69 | 5.494 (1.148–26.298) | 0.033 | |
| CEA | 0.079 | ||||||
| ≤6 ng/mL | 147 | 69.0 | 45.9 | 74.40 | |||
| >6 ng/mL | 24 | 65.4 | 29.3 | 36.86 | |||
| CA19-9 | 0.039 | ||||||
| ≤37 U/mL | 49 | 75.9 | 57.9 | 84.98 | 1 (Reference) | ||
| >37 U/mL | 149 | 65.9 | 39.6 | 66.59 | 2.155 (1.112–4.174) | 0.023 | |
| Differentiation | <0.001 | ||||||
| Well/moderate | 25 | 74.0 | 49.8 | 79.24 | 1 (Reference) | ||
| Poorly/undifferentiated | 42 | 46.8 | 25.3 | 40.58 | 2.299 (1.290–4.096) | 0.005 | |
| T-stage | 0.143 | ||||||
| T1 | 42 | 74.4 | 58.8 | 79.15 | |||
| T2 | 101 | 68.0 | 37.0 | 64.39 | |||
| T3 | 55 | 64.7 | 42.9 | 59.61 | |||
| N-stage (Nx excluded) | 0.254 | ||||||
| N0 | 75 | 74.4 | 53.0 | 72.89 | |||
| N1 | 80 | 65.0 | 37.6 | 65.97 | |||
| N2 | 38 | 58.9 | 26.9 | 45.57 | |||
| Nx | 5 | 80.0 | 80.0 | 45.40 | |||
| Lymph node ratio | 0.016 | ||||||
| <0.2 | 143 | 72.1 | 49.6 | 78.24 | 1 (Reference) | ||
| ≥0.2 | 50 | 55.8 | 26.0 | 44.81 | 1.758 (0.718–4.305) | 0.217 | |
| Margin status | <0.001 | ||||||
| R0 | 187 | 70.9 | 47.5 | 75.93 | 1 (Reference) | ||
| R1 | 11 | 31.8 | 0.0 | 21.06 | 4.583 (2.034–10.325) | <0.001 | |
| Adjuvant treatment | 0.005 | ||||||
| Yes | 118 | 74.8 | 50.2 | 79.90 | 1 (Reference) | ||
| No | 80 | 56.6 | 35.3 | 54.20 | 1.915 (1.112–3.298) | 0.019 | |
| Perineural invasion | 0.032 | ||||||
| No | 21 | 80.7 | 74.9 | 99.32 | 1 (Reference) | ||
| Yes | 173 | 65.9 | 39.4 | 67.08 | 3.423 (0.813–14.415) | 0.093 | |
| Lymphovascular invasion | 0.003 | ||||||
| No | 81 | 80.5 | 55.8 | 83.83 | 1 (Reference) | ||
| Yes | 89 | 63.6 | 31.7 | 50.78 | 2.054 (1.196–3.528) | 0.009 | |
YSR, year survival rate; MST, mean survival time; HR, hazard ratio; CI, confidence interval; DPS, distal pancreatosplenectomy; RAMPS, radical antegrade modular pancreatosplenectomy; ASA, American Society of Anesthesiologists; CEA, carcinoembryonic antigen; CA19-9, cancer antigen 19-9.
Table 5.
Risk factor analysis for disease-free survival after propensity score matching.
| Univariate | Multivariate | ||||||
|---|---|---|---|---|---|---|---|
| n | 2YSR (%) | 5YSR (%) | MST (Months) | p-Value | HR (95% CI) | p-Value | |
| Age (years) | 0.290 | ||||||
| <65 | 95 | 38.5 | 28.1 | 40.71 | |||
| 65–75 | 75 | 32.1 | 14.5 | 26.58 | |||
| >75 | 28 | 29.7 | 14.8 | 25.32 | |||
| Sex | 0.341 | ||||||
| Male | 106 | 32.7 | 17.1 | 33.14 | |||
| Female | 92 | 37.7 | 26.7 | 38.46 | |||
| Operation type | 0.929 | ||||||
| Conventional DPS | 99 | 34.5 | 21.2 | 36.25 | |||
| RAMPS | 99 | 35.4 | 22.3 | 34.19 | |||
| ASA physical status | 0.665 | ||||||
| 1 | 26 | 38.1 | 29.6 | 43.63 | |||
| 2 | 150 | 34.8 | 20.4 | 33.09 | |||
| 3 | 22 | 33.8 | 21.1 | 32.15 | |||
| CEA | 0.580 | ||||||
| ≤6 ng/mL | 147 | 37.0 | 22.3 | 37.56 | |||
| >6 ng/mL | 24 | 32.5 | 17.3 | 23.77 | |||
| CA19-9 | 0.003 | ||||||
| ≤37 U/mL | 49 | 48.8 | 28.4 | 49.56 | 1 (Reference) | ||
| >37 U/mL | 149 | 30.6 | 20.0 | 30.65 | 1.808 (1.182–2.767) | 0.006 | |
| Differentiation | 0.002 | ||||||
| Well/moderate | 25 | 39.9 | 25.0 | 39.62 | 1 (Reference) | ||
| Poorly/undifferentiated | 42 | 16.0 | 0.0 | 18.48 | 1.729 (1.122–2.664) | 0.013 | |
| T-stage | <0.001 | ||||||
| T1 | 42 | 57.9 | 36.5 | 48.88 | 1 (Reference) | ||
| T2 | 101 | 34.9 | 20.6 | 35.52 | 1.627 (0.975–2.718) | 0.063 | |
| T3 | 55 | 18.0 | 12.8 | 20.52 | 2.611 (1.504–4.532) | 0.001 | |
| N-stage (Nx excluded) | 0.039 | ||||||
| N0 | 75 | 41.8 | 29.2 | 41.74 | 1 (Reference) | ||
| N1 | 80 | 33.1 | 16.6 | 30.07 | 1.030 (0.621–1.630) | 0.899 | |
| N2 | 38 | 21.3 | 15.9 | 21.59 | 1.255 (0.599–2.627) | 0.548 | |
| Nx | 5 | 60.0 | 0.0 | 24.40 | 1.905 (0.565–6.420) | 0.299 | |
| Lymph node ratio | 0.012 | ||||||
| <0.2 | 143 | 38.4 | 23.9 | 40.35 | 1 (Reference) | ||
| ≥0.2 | 50 | 24.9 | 15.6 | 21.18 | 0.963 (0.629–1.474) | 0.864 | |
| Margin status | 0.563 | ||||||
| R0 | 187 | 34.9 | 22.1 | 35.88 | |||
| R1 | 11 | 36.4 | 0.0 | 17.46 | |||
| Adjuvant treatment | 0.018 | ||||||
| Yes | 114 | 36.7 | 23.1 | 37.20 | 1 (Reference) | ||
| No | 75 | 27.9 | 17.6 | 28.40 | 1.848 (1.257–2.717) | 0.002 | |
| Perineural invasion | 0.013 | ||||||
| No | 21 | 52.4 | 46.6 | 58.40 | 1 (Reference) | ||
| Yes | 173 | 31.8 | 17.0 | 30.80 | 1.740 (0.831–3.647) | 0.142 | |
| Lymphovascular invasion | 0.001 | ||||||
| No | 81 | 46.2 | 26.8 | 42.50 | 1 (Reference) | ||
| Yes | 89 | 22.6 | 13.4 | 22.20 | 1.846 (1.256–2.714) | 0.002 | |
YSR, year survival rate; MST, mean survival time; HR, hazard ratio; CI, confidence interval; DPS, distal pancreatosplenectomy; RAMPS, radical antegrade modular pancreatosplenectomy; ASA, American society of anesthesiologists; CEA, carcinoembryonic antigen; CA19-9, cancer antigen 19-9.
Table 6.
Subgroup analysis: risk factor for overall survival of the patients who underwent RAMPS and cDPS at the level of the pancreatic neck.
Table 6.
Subgroup analysis: risk factor for overall survival of the patients who underwent RAMPS and cDPS at the level of the pancreatic neck.
| Univariate | Multivariate | ||||||
|---|---|---|---|---|---|---|---|
| n | 2YSR (%) | 5YSR (%) | MST (Months) | p-Value | HR (95% CI) | p-Value | |
| Age (years) | 0.003 | ||||||
| <65 | 52 | 79.9 | 63.6 | 89.93 | 1 (Reference) | ||
| 65–75 | 40 | 68.4 | 26.9 | 48.49 | 1.359 (0.606–3.046) | 0.457 | |
| >75 | 14 | 43.0 | 21.5 | 35.89 | 3.153 (0.872–11.395) | 0.080 | |
| Sex | 0.044 | ||||||
| Male | 58 | 65.2 | 31.5 | 50.67 | 1 (Reference) | ||
| Female | 48 | 79.7 | 58.9 | 85.39 | 0.434 (0.181–1.041) | 0.062 | |
| Operation type | 0.351 | ||||||
| Conventional DPS | 35 | 69.7 | 38.0 | 60.64 | 1 (Reference) | ||
| RAMPS | 71 | 73.2 | 49.5 | 76.02 | 0.704 (0.333–1.491) | 0.360 | |
| ASA physical status | 0.158 | ||||||
| 1 | 13 | 83.9 | 73.4 | 91.17 | |||
| 2 | 77 | 72.3 | 43.4 | 70.60 | |||
| 3 | 16 | 62.5 | 30.4 | 49.15 | |||
| CEA | 0.070 | ||||||
| ≤6 ng/mL | 79 | 71.9 | 47.3 | 74.04 | |||
| >6 ng/mL | 12 | 64.3 | 25.7 | 35.09 | |||
| CA19-9 | 0.403 | ||||||
| ≤37 U/mL | 27 | 71.2 | 53.4 | 80.42 | |||
| >37 U/mL | 79 | 72.5 | 41.8 | 59.29 | |||
| Differentiation | <0.001 | ||||||
| Well/moderate | 83 | 77.0 | 52.7 | 80.10 | 1 (Reference) | ||
| Poorly/undifferentiated | 21 | 46.4 | 15.5 | 34.21 | 3.437 (1.525–7.744) | 0.003 | |
| T-stage | 0.061 | ||||||
| T1 | 24 | 85.7 | 65.6 | 87.79 | |||
| T2 | 52 | 68.3 | 36.8 | 61.96 | |||
| T3 | 30 | 65.0 | 33.0 | 54.17 | |||
| N-stage (Nx excluded) | 0.984 | ||||||
| N0 | 43 | 72.0 | 48.1 | 67.96 | |||
| N1 | 39 | 73.2 | 37.6 | 67.43 | |||
| N2 | 21 | 70.0 | 43.8 | 60.58 | |||
| Nx | 3 | N/A | N/A | N/A | |||
| Lymph node ratio | 0.312 | ||||||
| <0.2 | 78 | 73.7 | 48.2 | 74.58 | |||
| ≥0.2 | 25 | 65.4 | 28.6 | 50.64 | |||
| Margin status | 0.002 | ||||||
| R0 | 97 | 75.3 | 49.0 | 75.95 | 1 (Reference) | ||
| R1 | 9 | 40.0 | 0.0 | 22.98 | 8.547 (3.160–23.116) | <0.001 | |
| Adjuvant treatment | 0.023 | ||||||
| Yes | 62 | 77.7 | 53.5 | 80.66 | 1 (Reference) | ||
| No | 44 | 62.1 | 32.2 | 53.71 | 2.493 (1.162–5.346) | 0.019 | |
| Perineural invasion | 0.117 | ||||||
| No | 10 | 88.9 | 38.9 | 62.78 | |||
| Yes | 93 | 67.1 | 37.4 | 56.85 | |||
| Lymphovascular invasion | 0.514 | ||||||
| No | 44 | 79.6 | 47.0 | 75.63 | |||
| Yes | 51 | 65.1 | 44.8 | 62.18 | |||
YSR, year survival rate; MST, mean survival time; HR, hazard ratio; CI, confidence interval; DPS, distal pancreatosplenectomy; RAMPS, radical antegrade modular pancreatosplenectomy; ASA, American Society of Anesthesiologists; CEA, carcinoembryonic antigen; CA19-9, cancer antigen 19-9.
Table 7.
Subgroup analysis: risk factor for disease-free survival of the patients who underwent RAMPS and cDPS at the level of the pancreatic neck.
Table 7.
Subgroup analysis: risk factor for disease-free survival of the patients who underwent RAMPS and cDPS at the level of the pancreatic neck.
| Univariate | Multivariate | ||||||
|---|---|---|---|---|---|---|---|
| n | 2YSR (%) | 5YSR (%) | MST (Months) | p-Value | HR (95% CI) | p-Value | |
| Age (years) | 0.136 | ||||||
| <65 | 52 | 41.9 | 29.3 | 43.03 | |||
| 65–75 | 40 | 31.2 | 9.4 | 23.67 | |||
| >75 | 14 | 17.9 | 17.9 | 24.48 | |||
| Sex | 0.203 | ||||||
| Male | 58 | 31.5 | 13.6 | 25.24 | |||
| Female | 48 | 39.1 | 27.4 | 41.49 | |||
| Operation type | 0.930 | ||||||
| Conventional DPS | 35 | 31.0 | 18.1 | 32.21 | 1 (Reference) | ||
| RAMPS | 71 | 36.8 | 21.2 | 34.77 | 0.696 (0.425–1.142) | 0.151 | |
| ASA physical status | 0.540 | ||||||
| 1 | 13 | 46.2 | 30.8 | 45.31 | |||
| 2 | 77 | 34.9 | 19.7 | 33.21 | |||
| 3 | 16 | 25.0 | 12.5 | 24.50 | |||
| CEA | 0.432 | ||||||
| ≤6 ng/mL | 79 | 37.0 | 21.9 | 36.72 | |||
| >6 ng/mL | 12 | 30.0 | 10.0 | 19.65 | |||
| CA19-9 | 0.052 | ||||||
| ≤37 U/mL | 27 | 39.1 | 27.4 | 47.41 | |||
| >37 U/mL | 79 | 33.7 | 17.6 | 26.84 | |||
| Differentiation | 0.001 | ||||||
| Well/moderate | 83 | 41.1 | 24.7 | 40.13 | 1 (Reference) | ||
| Poorly/undifferentiated | 21 | 9.5 | 4.8 | 13.24 | 1.958 (1.161–3.303) | 0.012 | |
| T-stage | <0.001 | ||||||
| T1 | 24 | 66.0 | 44.0 | 56.76 | 1 (Reference) | ||
| T2 | 52 | 31.5 | 15.0 | 31.21 | 2.193 (1.159–4.152) | 0.016 | |
| T3 | 30 | 15.2 | 7.6 | 16.14 | 3.837 (1.107–2.776) | <0.001 | |
| N-stage (Nx excluded) | 0.208 | ||||||
| N0 | 43 | 37.9 | 29.5 | 43.21 | |||
| N1 | 39 | 35.9 | 11.3 | 27.64 | |||
| N2 | 21 | 27.2 | 20.4 | 25.37 | |||
| Nx | 3 | N/A | N/A | N/A | |||
| Lymph node ratio | 0.170 | ||||||
| <0.2 | 78 | 34.9 | 22.4 | 38.87 | |||
| ≥0.2 | 25 | 31.1 | 15.6 | 23.51 | |||
| Margin status | 0.708 | ||||||
| R0 | 97 | 35.4 | 21.8 | 35.83 | |||
| R1 | 9 | 29.6 | 0.0 | 19.22 | |||
| Adjuvant treatment | 0.014 | ||||||
| Yes | 62 | 47.5 | 29.3 | 46.80 | 1 (Reference) | ||
| No | 44 | 31.2 | 18.9 | 30.21 | 1.753 (1.107–2.776) | 0.017 | |
| Perineural invasion | 0.029 | ||||||
| No | 10 | 60.0 | 50.0 | 61.97 | 1 (Reference) | ||
| Yes | 93 | 31.1 | 14.8 | 26.77 | 1.448 (0.601–3.489) | 0.409 | |
| Lymphovascular invasion | 0.107 | ||||||
| No | 44 | 44.7 | 21.1 | 39.60 | |||
| Yes | 51 | 25.7 | 18.0 | 25.75 | |||
YSR, year survival rate; MST, mean survival time; HR, hazard ratio; CI, confidence interval; DPS, distal pancreatosplenectomy; RAMPS, radical antegrade modular pancreatosplenectomy; ASA, American Society of Anesthesiologists; CEA, carcinoembryonic antigen; CA19-9, cancer antigen 19-9.
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MDPI and ACS Style
Kwon, J.; Lee, H.; Kim, H.; Kim, S.H.; Yang, J.D.; Lee, W.; Lee, J.S.; Shin, S.H.; Kim, H.J. Comparison of Survival Outcomes between Radical Antegrade Modular Pancreatosplenectomy and Conventional Distal Pancreatosplenectomy for Pancreatic Body and Tail Cancer: Korean Multicenter Propensity Score Match Analysis. Cancers 2024, 16, 1546. https://doi.org/10.3390/cancers16081546
AMA Style
Kwon J, Lee H, Kim H, Kim SH, Yang JD, Lee W, Lee JS, Shin SH, Kim HJ. Comparison of Survival Outcomes between Radical Antegrade Modular Pancreatosplenectomy and Conventional Distal Pancreatosplenectomy for Pancreatic Body and Tail Cancer: Korean Multicenter Propensity Score Match Analysis. Cancers. 2024; 16(8):1546. https://doi.org/10.3390/cancers16081546
Chicago/Turabian StyleKwon, Jaewoo, Huisong Lee, Hongbeom Kim, Sung Hyun Kim, Jae Do Yang, Woohyung Lee, Jun Suh Lee, Sang Hyun Shin, and Hee Joon Kim. 2024. "Comparison of Survival Outcomes between Radical Antegrade Modular Pancreatosplenectomy and Conventional Distal Pancreatosplenectomy for Pancreatic Body and Tail Cancer: Korean Multicenter Propensity Score Match Analysis" Cancers 16, no. 8: 1546. https://doi.org/10.3390/cancers16081546
APA StyleKwon, J., Lee, H., Kim, H., Kim, S. H., Yang, J. D., Lee, W., Lee, J. S., Shin, S. H., & Kim, H. J. (2024). Comparison of Survival Outcomes between Radical Antegrade Modular Pancreatosplenectomy and Conventional Distal Pancreatosplenectomy for Pancreatic Body and Tail Cancer: Korean Multicenter Propensity Score Match Analysis. Cancers, 16(8), 1546. https://doi.org/10.3390/cancers16081546
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