
Pancreatic ductal adenocarcinoma is a malignant tumor that has one of the most dismal prognoses. In 2003, Strasberg et al. [1] introduced the concept of “radical antegrade modular pancreatosplenectomy (RAMPS),” which involves neck-level resection; complete N1 and N2 dissection, including gastroduodenal, infrapancreatic, splenic, gastrosplenic, celiac, and superior mesenteric artery (SMA) nodes; and
Despite its well-established feasibility and safety [2–4], minimally invasive RAMPS (MI-RAMPS) is more complex and technically challenging than open RAMPS. Notwithstanding the complexity and wide extent of dissection in the original RAMPS, the survival benefit remains inconclusive [5,6]. Therefore, several modified RAMPS procedures have been suggested. In this literature review, we examined the advantages and disadvantages of RAMPS and the indications for the original and modified RAMPS.
The total retrieved LN count and R0 resection rate are significantly higher in RAMPS than in conventional DP [5–11]. However, a higher LN yield and a higher R0 resection rate do not indicate better survival. Several meta-analyses have shown better 1-year survival with RAMPS [8,10], whereas other meta-analyses reported no differences in survival outcomes between RAMPS and conventional DP [5,6,9,11]. Therefore, despite the high number of LN harvested and the R0 resection rate, the survival benefit, which is the ultimate goal, is inconclusive.
Extensive resection of the pancreas can result in pancreatic exocrine and endocrine insufficiencies. The prevalence of new-onset diabetes mellitus (DM) is higher after DP than after pancreaticoduodenectomy (PD). In a study by Thomas et al. [12], the prevalence of new-onset DM was 38.59% and 28.69% after DP and PD, respectively. Shirakawa et al. [13] evaluated the risk factors for new-onset DM in patients who underwent DP. The resection of a pancreatic volume >44% was a significant independent risk factor. Using the three-dimensional (3D) slicer, an open-source 3D reconstruction program, the volume of the pancreatic head, body, and tail was measured on images obtained from computed tomography scans of 50 patients who underwent DP. The head and body were divided along the portal vein, and the body and tail were divided along the aortic left border, and the mean volumes were 47.10%, 14.16%, and 38.74% in the head, body, and tail, respectively (Fig. 1A). The sum of the volume of the body and tail was more than 44% (Fig. 1B), which was higher than the cutoff point for the resected volume as a significant risk factor for post-DP new-onset DM in 42 of the 50 patients (84.0%). There are few studies on the incidence of DM according to pancreatic resection volume in DP. However, the lower incidence of new-onset DM following central pancreatectomy compared with DP was well-elucidated in many studies [14–17]. Therefore, a large amount of pancreatic resection may be a risk factor for the development of DM after pancreatectomy, and the majority of patients who undergo RAMPS may be at risk of post-pancreatectomy DM. Similarly, the occurrence of pancreatic exocrine insufficiency after DP is higher than after central pancreatectomy [14–16]. Excessive pancreatectomy may also be a risk factor for postoperative pancreatic exocrine insufficiency. However, more investigations are needed for more clear evidence.
Extensive LN dissection is a time-consuming and complex procedure. Extended lymphadenectomy during PD does not ensure better survival in cancer of the head of the pancreas [18]. Furthermore, extensive LN dissection confers a potential risk of complications, such as vascular complications and chyle leak. Therefore, the extent of LN dissection should be selected according to the necessity. Imamura et al. [19] calculated the efficacy index of LN dissection based on the frequency of metastasis and 5-year survival. The efficacy index of celiac and common hepatic artery (CHA) node dissection was zero in pancreatic tail cancer. Moreover, the efficacy index of splenic hilar node dissection was zero in pancreatic body cancer. Ishida et al. [20] analyzed the frequency of LN metastasis according to the portal vein-to-tumor distance. The CHA, celiac, and SMA node metastases were observed only in cases wherein the tumor was located within 20 mm of the portal vein. Similarly, Tanaka et al. [21] reported that, when the tumor was confined to the tail of the pancreas, metastases to the CHA, celiac, and SMA nodes were nearly absent. Based on these results, it can be inferred that lymphadenectomy around the CHA, celiac axis, and SMA is not mandatory in cases where the tumor is confined to the pancreatic tail. Furthermore, splenic hilar node dissection and deep posterior dissection are not required in pancreatic body cancer.
The modified RAMPS is not a specific technique, but rather an optimization of the extent of LN dissection, pancreatic resection level, and posterior dissection plane from that of the RAMPS in accordance with the tumor location, without compromise of the oncologic principle. Therefore, the original RAMPS could be the optimal procedure for cancer extending from the body to the tail of the pancreas. However, if the tumor is only confined to the pancreatic tail, the pancreas might be divided at the left border of the aorta, and the LN dissection around the CHA, celiac axis, and SMA may be omitted [21]. If the tumor is confined to the right side of the left border of the aorta, deep posterior dissection and splenectomy could be omitted.
Modified RAMPS comprises a small modification of the original RAMPS and therefore, the modified MI-RAMPS is not a difficult procedure to master for surgeons who are familiar with the original MI-RAMPS, which provides the basic technique for the successfully modified MI-RAMPS. Our center usually makes use of four ports for laparoscopic original RAMPS as depicted in Fig. 2A. When the resection level is planned at the left aortic border, the locations of the ports are slightly shifted to left side (Fig. 2B).
The LN 8a can be easily found and dissected via the lesser omentum. The junction of the CHA and gastroduodenal artery (GDA) is usually located below LN 8a (Fig. 3A). The anterior surface of the portal vein is identified within a triangle, which is composed of the CHA, GDA, and the upper border of the pancreatic neck (Fig. 3B). After identifying the anterior surface of the superior mesenteric vein (SMV) at the inferior border of the pancreatic neck, the pancreatic neck is encircled and divided (Fig. 3C). The early division of the pancreatic neck facilitates LN dissection around the pancreatic neck, which is followed by the identification of the splenoportal junction and ligation and division of the splenic vein. The SMA lies below the root of the SMV. The gastroduodenal node and infrapancreatic node are located within a triangle composed of the portal vein, CHA, and SMA (Fig. 3D). In the lateral view, the gastroduodenal and infrapancreatic node dissection is not performed at a level that is deeper than the SMA (Fig. 3E). The dissection proceeds from the pancreatic neck-to-tail direction. When the root of the splenic artery is identified, it is ligated and divided. By dividing the splenic artery, celiac node dissection is facilitated (Fig. 3F).
After identifying the celiac axis and SMA, dissection proceeds along the left side of the celiac axis and SMA. Then, the dissection plane reaches the left side of the aorta because the celiac axis and SMA usually originate from the left side rather than from the center of the aorta (Fig. 4A). The inferior mesenteric vein (IMV) is a helpful landmark to distinguish the mesocolon from Gerota fascia. After the division of the IMV, the mesocolon is pulled down to explore the anterior surface of the left renal vein below the junction of the SMA and mesocolon (Fig. 4B). The Gerota fascia is dissected along the inferior border of the left renal vein toward the left kidney (Fig. 4C). The left adrenal gland is located at the anterior aspect, rather than along the superior portion of the left kidney. The anterior surface of the left adrenal gland and left adrenal vein are usually found at the same level as the anterior surface of the aorta (Fig. 4D). After completion of the RAMPS, the CHA, celiac axis, SMA, renal vein, and left kidney are exposed (Fig. 5).
The left aortic border is difficult to identify in the view of a minimally invasive surgery. In addition, the aorta is often torturous. Therefore, the SMA is a more helpful landmark than the left aortic border in minimally invasive settings. Sometimes, the location of the coronary vein, splenic artery, and IMV constitute other helpful landmarks to identify the level of pancreatic resection at the left aortic border.
Routine extensive LN dissection and removal of a large amount of the pancreatic parenchyma in RAMPS does not improve survival outcomes in left-sided pancreatic cancer. The key principles of the RAMPS are “adequate LN dissection and margin-negative resection.” Furthermore, the ultimate goal is to improve survival. The modified RAMPS can be defined as an optimized and reduced form of the RAMPS according to the tumor location without compromising oncologic principles. By optimal modification, unnecessary loss of the pancreatic parenchyma and unnecessary risk of complications may be avoided without disadvantage to the survival outcome. The surgeon should be familiar with the original MI-RAMPS for successfully performing the modified MI-RAMPS. To elucidate the efficacy of the modified RAMPS, a large-scale, well-designed study is needed.
The author has no conflicts of interest to declare.
None.
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