Background
Precise pathologic information is essential for clinical decision-making in patients with solid tumors, including those in the pancreaticoduodenal area (i.e., pancreatic, common bile duct, and ampullary cancers). Therefore, minimizing the risk of misclassification by harvesting an adequate number of lymph nodes is important not only for prognostic stratification but also for implementation of adjuvant therapy when indicated.
The accuracy of staging lymph node status is directly proportional to the number of lymph nodes retrieved and the optimum cutoff value minimizing the stage migration phenomenon reported previously for pancreatic cancer varies from 10 to 15 [
1,
2]. Moreover, many studies suggested that removing at least ten lymph nodes is significantly associated with improved survival regardless of the presence of nodal metastases [
1,
3,
4]. Others suggested that pathologic assessment of more than 12 lymph nodes may provide more accurate survival estimates for patients with node-negative disease [
5,
6]. Based on these observations, at least 12 lymph nodes are required for adequate staging for pancreatoduodenectomy specimens of pancreatic, distal bile duct, and ampullary cancer according to the most recent edition of the American Joint Committee on Cancer (AJCC) TNM classification [
7]. Contrary to these recommendations only about seven to eight nodes are dissected in many institutions worldwide [
2,
3,
8‐
10]. This carries the risk of understaging, as an inadequate assessment of regional lymph nodes may erroneously identify node-positive patients as node negative.
Several previous reports demonstrated marked improvements in lymph node counts by adopting adequate methods of specimen processing by dedicated pathologists [
11‐
14]. Surprisingly, there are hardly any studies that discuss other factors affecting retrieval of the optimal 12 lymph nodes according to the current recommendations of AJCC in patients undergoing pancreatoduodenectomy for cancers of the periampullary area. As understaging may have important therapeutic implications in routine clinical practice, the aim of this study was to investigate the impact of clinical and pathological factors on the likelihood of identifying the appropriate number of lymph nodes for cancers of the pancreatic head, ampulla of Vater, and common bile duct.
Discussion
Appropriate evaluation of lymph nodes in patients with solid tumors has obvious implications for more accurate staging. This study has demonstrated that the adequate lymph node yield with standard pathologic processing of pancreatoduodenectomy specimens in patients with suspected periampullary malignancy is influenced by only three factors, i.e., tumor diameter, metastases to lymph nodes and extent of lymphadenectomy. Moreover, evaluation of 12 or more nodes was associated with survival benefit in patients with pancreatic cancer.
The amount of lymphatic tissue and numbers of lymph nodes in the upper abdomen vary among individuals [
19]. However, the yield of lymph nodes in all surgical specimens, including pancreatoduodenectomy, is mostly influenced by three main groups of variables, i.e., those related to the patient and underlying pathology, to surgical intervention, and to pathologic assessment of the specimen. Although tissue processing and thoroughness of the pathologic examination are the key factors for identifying lymph nodes in surgical specimens, there is no general agreement regarding the appropriate pathological evaluation of pancreatoduodenectomy specimens, leading to ambiguities in defining R1 resections and marked variability in counts of lymph nodes identified in the peripancreatic tissue [
20,
21]. The average number of lymph nodes identified in such specimens with standard techniques of pathology sampling is five to seven [
20]. Rarely, the number reaches 15 to 29 in some studies examining anatomic distribution of peripancreatic lymph nodes or those applying meticulous processing of the specimen [
12,
22,
23]. The use of a standardized protocol for harvesting lymph nodes in our department and the fact that almost 70 % of the specimens were examined by a single pathologist minimize the risk that pathologist-related variability could bias results of the current study and give the opportunity to evaluate the influence of other factors on nodal yield.
There are very few studies reporting variables affecting the number of lymph nodes dissected in pancreatic surgery. Govindarajan et al. in a population of 2111 patients subject to pancreatoduodenectomy or total pancreatectomy for pancreatic head cancer from 1998 through 2003 and identified from the Surveillance, Epidemiology and End Results (SEER) registry found that younger age, female sex, tumor diameter >2 cm, and node-positive status increased the overall nodal count by 10 to 18 % [
3]. Another analysis of the same database, but covering the period from 1993 through 2003, demonstrated that the likelihood of removing ten or more lymph nodes among 5465 pancreatoduodenectomies for periampullary carcinomas was higher in females, tumor diameter ≥2 cm, pancreatic head cancers, and metastases to regional lymph nodes [
1]. However, the use of SEER data carries several disadvantages, including the unavailability of some variables potentially affecting lymph node counts such as BMI or the extent of lymphadenectomy. Another important issue that has not been addressed before is variability in lymph node counts among different surgeons and pathologists. In contrast with both previous studies, our database provides much more detailed information necessary to better characterize potential predictors of nodal yield.
The association between the lymph node yield and node positivity, as found in this study, is somewhat controversial. Besides the SEER studies, two previous reports suggested that in patients with pancreatic cancer subject to various pancreatic resections there was a significant difference in the total lymph node count in cases with or without nodal metastases of 19 vs 13 (
P = 0.02) [
5] and 15 vs 10 (
P < 0.001) [
24]. However, some other studies failed to confirm such a relationship [
6,
25‐
27]. These discrepancies may derive from two potential aspects. First, the presence of enlarged, metastatic nodes may force the operating surgeon to a more extended dissection, and second, metastatic lymph nodes are usually larger and thus easier to identify by the pathologist. The proportion of patients subject to radical lymphadenectomy in our study was not influenced by the presence of metastatic lymph nodes, but the overall median number of nodes was significantly higher in this group (18 vs 15,
P < 0.001). As a subsequent analysis in individual nodal stations revealed that the median count among subjects with metastatic nodes was higher only for pancreaticoduodenal stations (9 vs 7,
P = 0.040), we may assume that lymph node metastases did not affect the extent of surgery.
As reasonably expected, our study revealed that performing radical lymph node dissection, including para-aortic nodes, is the most significant factor and the only surgeon-dependent one to achieve the recommended nodal yield. Although none of the prospective randomized clinical trials on the extent of lymphadenectomy in periampullary malignancies analyzed variables that potentially affect nodal yield, median numbers of lymph nodes dissected in these studies during standard pancreatoduodenectomy was 13 to 17 and for extended 20 to 36 [
23,
25,
28,
29]. The idea of radical dissection is further supported by data accumulated over recent years suggesting that the incidence of lymph node metastasis to para-aortic nodal stations in periampullary malignancies is relatively high and an appropriate degree of lymphadenectomy is necessary to achieve an R0 resection [
30‐
35]. Although a recent meta-analysis of sixteen studies comprising 1909 patients comparing outcomes of standard and extended pancreatoduodenectomy showed similar perioperative morbidity and mortality rates, it also emphasized no improved survival after the latter procedure (hazard ratio 0.77,
P = 0.100) [
36]. Therefore, the only benefit of the latter procedure seems to be associated with more accurate staging of nodal disease even if some controversies still exist about station 16b1 considered as one of the major lymphatic drainage routes for pancreatic head cancer [
18].
Removal of the recommended number of lymph nodes was not associated with any clear survival benefit in the whole population of patients with periampullary malignancies. However, if the tumors were analyzed separately, pancreatic cancer demonstrated better survival among patients with ≥12 lymph nodes resected regardless the extent of lymphadenectomy. This is similar to some observations using cutoff values of 10 or 12 lymph nodes; however, the relationship between node counts and survival is not clear as previous studies on periampullary malignancies reported conflicting results [
1,
3‐
6,
37].
The limitations of the present study are related to its retrospective design and potential bias resulting from such analyzes. In particular, we were unable to account for the premises for performing a more extensive lymph node dissection, such as finding suspicious nodes intraoperatively or decisions made a priori, even though data analysis showed no such correlation. Nevertheless, the lack of major changes observed over time in the absolute number of lymph nodes harvested and the proportion of patients with ≥12 nodes support the assumption that the surgical technique remained unchanged over the study period.
Conclusions
In conclusion, this study demonstrated that only few factors were associated with the likelihood of removing at least 12 lymph nodes in surgical specimens of patients subject to pancreatoduodenectomy for suspected periampullary malignancy, i.e., tumor diameter, lymph node metastases, and radical lymphadenectomy. However, the latter and the only modifiable factor offered no clear survival benefit in previous randomized clinical trials and potentially may increase postoperative morbidity. Therefore, appropriate pathology training should be considered to increase nodal yield rather than more aggressive lymphatic dissection.
Acknowledgements
Not applicable.