To analyze data obtained in a representative number of patients with primary rectal cancer with respect to lymph node diagnostics and related tumor stages.
Methods
In pT2-, pT3-, and pT4 rectal cancer lesions, the impact of investigated lymph nodes on the frequency of pN+ status, the cumulative risk of metachronous distant metastases, and overall survival was studied by means of a prospective multicenter observational study over a defined period of time.
Results
From 2000 to 2011, the proportion of surgical specimens with ≥ 12 investigated lymph nodes increased significantly, from 73.6% to 93.2% (p < 0.001; the number of investigated lymph nodes from 16.2 to 20.8; p < 0.001). Despite this, the percentage of pN+ rectal cancer lesions varied only non-significantly (39.9% to 45.9%; p = 0.130; median, 44.1%). For pT2-, pT3-, and pT4 rectal cancer lesions, there was an increasing proportion of pN+ findings correlating significantly with the number of investigated lymph nodes up to n = 12 investigated lymph nodes. Only in pT3 rectal cancer was there a significant increase in pN+ findings in case of > 12 lymph nodes (p = 0.001), but not in pT2 (p = 0.655) and pT4 cancer lesions (p = 0.256). For pT3pN0cM0 rectal cancer, the risk of metachronous distant metastases and overall survival did not depend on the number of investigated lymph nodes.
Conclusion
In rectal cancer, at least n = 12 lymph nodes are to be minimally investigated. The investigation of fewer lymph nodes is associated with a higher risk of false-negative pN0 findings. In particular, in pT3 rectal cancer, the investigation of more than 12 lymph nodes lowers the risk of false-negative pN0 findings. An upstaging effect by the investigation of a possibly maximal number of lymph nodes could not be detected.
Hinweise
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Introduction
For years, retrieval staging has been a paradigm in colorectal cancer surgery. However, recently published analyses have demonstrated that a maximum number of regional lymph nodes is required for accurate tumor but the proportion of node-positive colorectal cancers has not increased over the years, despite steadily increasing numbers of lymph nodes examined in colorectal cancer specimens [1‐4]. These analyses generated some doubt regarding the hypothesis that “upstaging” of colorectal cancers occurs as the number of examined lymph nodes increases, and suggest that examination of more than 12 lymph nodes (or as many lymph nodes as possible) might not be beneficial with respect to staging accuracy.
Interestingly, Parsons et al. and Erning et al. found that a higher number of removed lymph nodes is indeed associated with improved long-term survival, even though the proportion of lymph node-positive cancers identified is not increased. This seems to be true for both node-negative and node-positive disease. Other authors have reported similar observations [5, 6].
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Based on a multicenter database of surgically treated rectal cancer patients, the analysis presented here aimed at examining the role of lymph node harvest as a component of adequate histopathological tumor staging as well as the association between the total number of lymph nodes examined and the number of tumor-positive lymph nodes. Moreover, longitudinal changes in lymph node diagnostics during the study period were evaluated.
Methods
Database
The analysis is based on data collected within the prospective multicenter observational study on rectal cancer surgery conducted by the Institute for Quality Assurance in Operative Medicine at Otto-von-Guericke University, Magdeburg, Germany (as previously reported [7‐16]). Within this database, patient-, tumor-, and treatment-related parameters obtained in patients with newly diagnosed rectal cancer (defined as cancer located within 16 cm of the anal verge) were recorded. Tumor staging was achieved using CT scan (98%), EUS (80%), and MRI (36%) according to the regional clinical care as established at the time of analysis. In all cases with tumor lesion at the middle and lower third of the rectum, TME was performed (patients with rectal cancer at the upper third underwent PME or TME).
Paraaortic lymphadenectomy (and D3 lymphadenectomy) was not defined as a standard part of oncological resection. However, if this extensive lymphadenectomy was performed, it is was not precisely documented.
According to the guideline-based recommendations, as standard, D2 lymphadenectomy was performed.
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Informed consent from all patients is required prior to data entry into the database. Surgical departments of all levels of care throughout Germany are encouraged to enter their data; however, participation in the study is voluntary (the precise number of actively practicing surgeons at the time of data documentation was not registered).
Study population
For the present analysis, all patients entered into the database from January 1, 2000, to December 31, 2011, were investigated if they fulfilled the following criteria:
i
Primary radical surgery for rectal cancer without neoadjuvant treatment;
ii
Availability of complete histopathological tumor classification.
Patients who had undergone chemoradiation as indicated were not included in the study. In addition, patients who had undergone non-radical rectal cancer surgery (e.g., local tumor excision) were also not registered.
Assessment of lymph node numbers and lymph node tumor positivity
Changes in the following parameters over the study period were determined:
Mean total number of lymph nodes examined per specimen;
Proportion of specimens containing at least12 lymph nodes;
Proportion of specimens with lymph node-positive cancers.
Moreover, the impact of tumor growth through the rectal wall (“pT stage”) on lymph node metastases was described. The association between the number of lymph nodes examined per specimen and the rate of detected lymph node-positive cancers was also examined separately for each of the pT stages 2, 3, and 4.
To account for possible bias inflicted by improvements in lymph node diagnostics implemented during the study period, additional analysis was undertaken using exclusively data from institutions having contributed to the registry throughout the entire period studied (2000–2011). For each institution, the average number of lymph nodes examined per specimen in the years 2000 and 2001 were compared to the corresponding numbers from years 2010 and 2011. Based on these comparisons, the institutions were subdivided into those in which the number of lymph nodes examined had
i
increased significantly from 2000/2001 to 2010/2011, and
ii
remained unchanged.
Within both groups, the rate of node-positive cancers was compared between the years 2000/2001 and 2010/2011.
Additionally, the association between lymph node metastasis and synchronous distant metastasis as well as metachronous distant metastasis diagnosed after potentially curative rectal resection was studied. For the latter, oncological long-term outcome data for patients recorded between 2005 and 2007 were collected and used to analyze the influence of UICC tumor stage, pN stage, and number of lymph nodes examined (in categories of less than 12 lymph nodes: LN class 1; 12 through 17 lymph nodes: LN class 2; 18–23 lymph nodes: LN class 3; or more than 23 lymph nodes: LN class 4) on the emergence of metachronous distant metastases.
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Statistics
SPSS version 22.0 (IBM® SPSS Statistics, Ehningen, Germany) was used for statistical data analysis. Comparison of continuous parameters was performed using student’s t-test (in case of two groups) or univariate analysis of variance (one-way ANOVA, in case of more than two groups). Results are presented as mean values and 95% confidence intervals (CI). Chi2-test was used to compare categorical parameters. A two-sided p-value of < 0.05 was considered significantly different.
Univariate analysis of oncological long-term outcomes was performed using the Kaplan-Meier method and results were compared between groups using the log-rank test. Again, a two-sided p-value of < 0.05 was considered significantly different.
Results
Within the 12-year study period (01/01/2000 through 12/31/2011), data from n = 23,773 patients undergoing primary radical resection for rectal cancer without neoadjuvant treatment for whom complete histopathological tumor classification was available were entered into the observational study database. As the proportion of patients who received neoadjuvant treatment and had to be excluded from the analysis increased, a steady decline of patients available for study entry over the 12-year period was observed. Moreover, a significant increase in mean age, proportion of patients in UICC tumor stage IV, and proportion of patients whose tumors were located > 12 cm from the anal verge was recorded.
In Table 1, patient characteristics over the study period from 2000–2011 are shown.
Table 1
Changes in patients characteristics over time
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
2010
2011
p-value
Patients (n)
2752
2835
2727
2523
2181
1942
1636
1480
1705
1471
1268
1253
–
Patients’ age, years; mean (95% CI)
66.7
(66.3–67.1)
67.0
(66.6–67.4)
66.8
(66.5–67.2)
67.7
(67.3–68.0)
68.1
(67.7–68.4)
68.5
(68.1–69.0)
69.3
(68.8–69.8)
69.8
(69.3–70.4)
69.1
(68.6–69.6)
68.9
(68.4–69.5)
69.8
(69.2–70.5)
69.9
(69.3–70.5)
< 0.001*
Gender (m:f)
1.37:1
1.41:1
1.48:1
1.37:1
1.39:1
1.36:1
1.32:1
1.40:1
1.39:1
1.35:1
1.38:1
1.35:1
0.955
UICC stage
< 0.001*
UICC I (%)
28.7
29.8
28.7
30.8
31.8
30.2
31.0
33.1
32.4
28.2
29.8
28.5
UICC II (%)
24.4
24.0
25.0
22.8
23.1
21.2
23.0
23.9
21.5
22.9
22.0
22.2
UICC III (%)
33.2
32.5
32.8
32.4
32.2
31.2
29.2
26.1
28.0
29.2
28.2
29.4
UICC IV (%)
13.8
13.7
13.5
14.0
12.9
17.5
16.8
17.0
18.1
19.6
20.0
19.9
Tumor location
< 0.001*
12–15.9 cm (%)
24.7
26.5
28.1
30.4
32.0
35.3
35.6
37.4
42.4
40.2
40.8
42.1
8–11.9 cm (%)
34.9
33.9
31.6
31.8
32.2
31.7
31.8
31.2
27.2
29.0
27.4
27.1
4–7.9 cm (%)
25.1
25.1
25.6
24.1
21.1
22.0
21.0
20.1
19.6
20.5
22.2
19.2
< 4 cm (%)
15.3
14.5
14.7
13.6
14.7
11.0
11.6
11.4
10.8
10.3
9.7
11.5
m male, f female
*statistically significant p-value
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The rate of rectal cancer specimens from which at least 12 lymph nodes were retrieved and examined increased from 73.6% to 93.2% (p < 0.001) during the study period. Correspondingly, the mean number of lymph nodes harvested from each specimen increased from 16.2 to 20.8 (p < 0.001; Table 2). In spite of these numerical improvements in lymph node diagnostics, only a minor non-significant variation in the rate of patients diagnosed with lymph node-positive cancer was observed (p = 0.130). The mean number of tumor-bearing lymph nodes per specimen did not change significantly during the study period regardless of whether all patients or only pN+ patients were analyzed (lymph nodes per specimen 2.2–2.6, p = 0.331, and 5.2–5.8, p = 0.479, respectively; Table 2).
Table 2
Changes in specimen characteristics over the years
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
2010
2011
p-value
≥12 LN examined (%)
73.6
76.7
80.4
80.5
81.2
82.2
83.9
86.1
83.1
85.7
91.8
93.2
< 0.001*
Examined LN; mean (95% CI)
16.2
(15.8–16.5)
16.4
(16.1–16.8)
16.9
(16.6–17.2)
17.1
(16.8–17.4)
17.4
(17.0–17.8)
17.9
(17.5–18.4)
17.3
(17.0–17.7)
17.8
(17.3–18.2)
17.5
(17.1–17.9)
18.9
(18.4–19.4)
19.9
(19.4–20.5)
20.8
(20.2–21.3)
< 0.001*
Positive LN; mean (95% CI)
2.5
(2.3–2.7)
2.3
(2.1–2.5)
2.4
(2.2–2.6)
2.4
(2.2–2.6)
2.3
(2.1–2.5)
2.3
(2.1–2.5)
2.4
(2.2–2.7)
2.2
(2.0–2.5)
2.5
(2.2–2.7)
2.6
(2.3–2.8)
2.6
(2.3–2.9)
2.6
(2.3–2.9)
0.331
pN+ (%)
45.1
44.7
44.0
44.2
42.9
45.0
43.8
39.9
43.8
45.1
44.5
45.9
0.130
pT category
< 0.001*
pT1 (%)
8.2
8.6
8.2
11.7
11.0
12.5
11.7
14.4
14.3
12.0
13.2
12.5
pT2 (%)
27.4
28.7
28.2
26.2
29.2
26.6
27.3
26.8
26.0
24.6
25.0
23.9
pT3 (%)
57.3
55.9
56.1
54.4
52.5
53.1
52.1
48.7
49.1
51.5
49.4
51.8
pT4 (%)
7.1
6.8
7.6
7.7
7.2
7.8
9.0
10.1
10.6
11.9
12.4
11.8
LN lymph node(s)
*statistically significant p-value
Considering the tumor infiltration depth, pT1 and pT4 cancers showed a slight increase (from 8.2% to 12.5% and from 7.1% to 11.8%, respectively) over the study period. Conversely, the rate of pT2 and pT3 cancers decreased (Table 2).
Fig. 1 shows the probability of lymph node metastasis (pN+) as well as distant metastasis diagnosed on preoperative imaging or intraoperatively as a function of tumor infiltration depth (pT category). Both lymph node metastasis and distant metastasis were significantly more likely to be diagnosed in patients with a more advanced pT stage (p < 0.001). The likelihood graphs for lymph node and distant metastases are parallel.
Fig. 1
Frequency of lymph node metastases and clinically apparent distant metastases depending on depth of tumor invasion (pT)
×
The probability of synchronous distant metastasis as a function of lymph node involvement (pN0 vs. pN1 vs. pN2) can be seen in Fig. 2a for pT categories 1 through 4. In each of these pT categories, more extensive lymph node involvement was significantly associated with an increase in the probability of distant metastasis diagnosed synchronously with the primary tumor. Moreover, the number of tumor-positive lymph nodes had a significant impact on the probability of distant metastases (p < 0.001, Fig. 2b), whereas in node-negative patients, no association between the number of lymph nodes examined and the probability of synchronous distant metastasis was found. The average risk for pN0 patients to be diagnosed with synchronous distant metastases was 4.5% (Fig. 2c).
Fig. 2
Frequency of synchronous distant metastasis depending on: a nodal positivity and pT category of rectal cancer; b number of positive lymph nodes; c number of examined negative lymph nodes
×
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Impact of lymph node involvement on metachronous distant metastasis
Follow-up data of 70% of the patients entered into the database between 2005 and 2007 (n = 2733 of 3930; best follow-up data quality during this time period) were available to analyze the association between initial lymph node involvement and the development of metachronous metastatic disease. Median follow-up was 55.0 (95% CI: 53.9–56.1) months. Fig. 3a shows the cumulative risk for metachronous metastasis after potentially curative rectal resection as a function of UICC tumor stage, whereas Fig. 3b shows its association with the initially diagnosed pN category. While patients with lymph node-negative cancer had a 6.7% cumulative risk of developing distant metastases at 4 years, this was 19.4% for patients with node-positive cancers (p < 0.001). The cumulative risk for patients with pN1 vs. pN2 nodal status was only marginally different (18.0% vs. 21.8%, respectively; p = 0.017).
Fig. 3
Cumulative risk for metachronous metastasis as a function of a UICC tumor stage, b pN stage. cum cumulative, fu follow-up
×
Impact of the total number of lymph nodes examined on detection of tumor-involved lymph nodes
The association between the total number of lymph nodes examined per specimen and the pN category assigned (pN0 vs. pN1 vs. pN2) is shown in Fig. 4a–c for pT categories 2, 3, and 4. A significant impact of the total number of lymph nodes on the detection of tumor-involved lymph nodes was found for each of these pT categories (pT2: p = 0.002, pT3: p < 0.001, pT4: p = 0.002). 11.6% of pT2 cancers were diagnosed as being lymph node positive (pN1 + pN2) if less than six lymph nodes were examined whereas this was 25.5% in patients who had more than 20 lymph nodes examined (Fig. 4a). Among patients with pT3 and pT4 cancers, the rates of lymph node positivity were 33.7% and 40.5% if less than six lymph nodes were examined as opposed to 61.1% and 76.9% if more than 20 lymph nodes were investigated. Thus, approximately twice as many patients in all three pT categories were diagnosed as having node-positive cancer if they had more than 20 as opposed to less than six lymph nodes examined. Within the groups of patients with pT2 and pT4 cancers, the detection rate of tumor-involved lymph nodes did not increase any further beyond 12 examined lymph nodes (19.1% vs. 25.5%, p = 0.655; and 76.6% vs. 77.0%, p = 0.256, respectively; Fig. 4a, c). In contrast, in patients with pT3 cancers, examination of more than 20 nodes did result in a significant increase in detection of positive lymph nodes as compared to examination of only 12 lymph nodes (49.2% vs. 66.1%, p = 0.001; Fig. 4b).
Fig. 4
Association between investigated lymph node count and pN category in rectal cancer with no neoadjuvant chemoradiation: a pT2 category (n = 6364; p < 0.001); b pT3 category (n = 12,568; p < 0.001); c pT4 category (n = 2027; p < 0.001)
×
Impact of the total number of lymph nodes examined on metachronous distant metastasis and overall survival
The number of lymph nodes examined in patients with node-negative cancers (pN0) was not significantly associated with the probability of developing metachronous distant metastasis in any of the pT categories pT2, pT3, and pT4. Fig. 5 shows the cumulative risk for distant metastasis in lymph node (LN) classes 1 through 4 (see Patients and methods) for patients initially diagnosed with pT3 pN0 cM0 cancers. The cumulative risk for the development of distant metastasis was 6.2%, 8.6%, 9.0%, and 15.2% in LN classes 1 through 4, respectively (log-rank test).
Fig. 5
Risk of metachronous distant metastases depending on lymph node count after curative radical resection of pT3 pN0 cM0 rectal cancer. cum cumulative, fu follow-up
Fig. 6
Untreated (p)T3 rectal cancer (no neoadjuvant radio[chemo]therapy) of one selected patient with tumor imaging, macroscopic specimen, and histological imaging (HE): a Preoperative MRI. b TME specimen (perspective from ventral: left; from dorsal: right). c T3a stage (according to invasion depth); satellite panel: histopathological image (HE). d Representative imaging for N‑stage (lymph nodes increased but not tumor infiltrated); satellite panel: histopathological image (HE)
×
×
Stage migration
The impact of the number of examined lymph nodes on the detection of tumor-positive lymph nodes was compared between participating institutions that did (group 1) and did not (group 2) report an increase in the total number of lymph nodes examined per specimen between the years 2000/2001 and 2010/2011. Only pT3 cancers were investigated for this analysis. Results are shown in Table 3. Hospitals of group 1 reported an increase in the mean number of examined lymph nodes from 16.7 to 26.9 (p < 0.001), whereas in hospitals of group 2, the lymph node harvest remained stable (17.6 vs. 18.0, p = 0.472). Despite the significant increase in the total lymph node number per specimen in group 1, the mean number of tumor-involved lymph nodes as well as the rate of node-positive (pN+) cancers remained unchanged (57.5% vs. 55.6%, p = 0.673). In hospitals of group 2, there was also no change in the mean number of tumor-involved lymph nodes (p = 0.129). A tendency towards a decrease in the rate of lymph node-positive cancers was observed in this group (60.9% vs. 53.4%); however, this was not statistically significant (p = 0.097).
Table 3
Prognosis-relevant parameters in lymph node diagnostics comparing surgical departments with increased (group 1) and similar numbers of investigated lymph nodes (group 2) in pT3 rectal cancer during study period
Time period
2000–2001
Time period
2010–2011
p-value
Group 1 (hospitals, n=20)
Patients (n)
465
247
–
No. of investigated LN; mean (95% CI)
16.7
(16.1–17.4)
26.9
(25.0–28.8)
< 0.001
No. of Tu-infiltrated LN; mean (95% CI)
2.9
(2.5–3.4)
3.3
(2.5–4.1)
0.443
Portion of pN-negative cancer lesions (%)
42.5
44.4
0.673
Portion of pN-positive cancer lesions (%)
57.5
55.6
Group 2 (hospitals, n=20)
Patients (n)
284
193
–
No. of investigated LN; mean (95% CI)
17.6
(16.8–18.4)
18.0
(17.1–19.0)
0.472
No. of Tu-infiltrated LN; mean (95% CI)
3.3
(2.8–3.9)
2.8
(2.2–3.4)
0.219
Portion of pN-negative cancer lesions (%)
39.1
46.6
0.097
Portion of pN-positive cancer lesions (%)
60.9
53.4
LN lymph node(s), No. number, Tu tumor
Discussion
Results from analyses encompassing long time periods may be influenced by a variety of factors that may not remain constant during the study period, which, thus, may bias their interpretation. For example, a lack of upstaging in spite of an increased lymph node harvest may also be due to an increase in patients being diagnosed at an earlier disease stage as a result of the growing use of screening colonoscopy in the population analyzed.
The principal results of the analysis of data from an observational study presented here include a significant increase in the number of lymph nodes examined per rectal cancer specimen (Fig. 6) during the study period, which leads to a rising proportion of specimens with a minimum of 12 lymph nodes retrieved. Within pT categories 2 through 4, examination of more lymph nodes leads to identification of more lymph node-positive cancers. Moreover, it has been confirmed that lymph node involvement in rectal cancer is an important indicator for established metastatic disease as well as a predictor for metachronous development of distant metastasis. However, the continuously rising number of lymph nodes examined per specimen during the study period was not associated with a similar increase in the rate of lymph node-positive cancers identified. Thus, it could not be demonstrated that more accurate tumor staging by examination of more lymph nodes leads to consecutive upstaging in rectal cancer. Correspondingly, the cumulative risk of distant metastases following potentially curative resection of pT3 pN0 cM0 rectal cancer was not dependent on the number of lymph nodes examined.
Similar results of a literature search were presented by Hogan et al. [3], demonstrating relatively little variation in the rate of lymph node-positive rectal cancers, which fluctuated at around 40% out of a total sample of 240,081 rectal cancers over the past two decades. These authors proposed the concept of a “nodal positivity constant.” Similarly, Parsons et al. [1] analyzed 86,394 colon cancer patients included in the SEER database between 1998 and 2008. Despite a significant increase in the number of lymph nodes examined, again, a relatively constant rate of node-positive cancers of approximately 40% was found. These results are comparable to the 44% rate of node-positive cancers found in the observational study database presented here and have been confirmed by other authors [2, 4], putting the concept of tumor upstaging through more meticulous lymph node examination into question. Interestingly, though, an association between the increase in the number of examined lymph nodes and improved survival, both for lymph node-negative and for lymph node-positive cancers, has been reported [1, 2, 6, 7]; however, this has not been confirmed by all authors [19]. In the current analysis, no association between the number of lymph nodes examined and the rate of metachronous distant metastatic disease was found.
Baxter et al. [20], in an analysis of the SEER data, identified a threshold of 13 examined lymph nodes for identification of lymph node involvement in pT3 colon cancer specimens, exceeding of which does not lead to detection of more lymph node-positive cancers. Correspondingly, the present analysis demonstrates that examination of more than 12 lymph nodes in pT2 and pT4 rectal cancer specimens not treated with neoadjuvant radiotherapy does not increase the detection rate of pN+ cancers. Only in pT3 specimens did we identify a further 11.9% increase in the detection of lymph node positivity if more than 12 lymph nodes were investigated. Very likely, these observations are the result of the process of lymphatic metastatic spread over time and the distribution of locoregional lymph nodes as well as their pattern of tumor involvement. In a study by Langman et al. [21], 83% of tumor-involved lymph nodes were located either adjacent to the tumor itself or in the mesorectum proximal to the tumor lesion, whereas only 3% of involved lymph nodes were found distally to the tumor mass towards the anal verge. Apart from the mesorectum, 16% of involved lymph nodes were located alongside the superior rectal artery or the inferior mesenteric artery. Only 0.3% were located elsewhere in the mesentery of the sigmoid colon. The proportion of lymph nodes located in the mesorectum among all identified lymph nodes in the specimen (mesorectum, vascular pedicle, and sigmoid colon mesentery) was only 40%. The median number of lymph nodes identified in the mesorectum was 16. This underscores that examination of 12 mesorectal lymph nodes yields a very high probability of accurate detection or exclusion of lymph node metastases in rectal cancer. In comparison, the chance of detecting tumor-involved lymph nodes outside the mesorectum when all mesorectal lymph nodes are free of tumor appears to be small. This is further highlighted by reports demonstrating that pN0 tumor status in colorectal cancer can be correctly identified in 99.2% or 98.2% by the examination of all lymph nodes within 3 cm or 5 cm proximally and distally to the tumor, respectively [22, 23], even though the rate of false-negative results was higher in rectal cancer compared to colon cancer. Langman et al. [21] also identified lymph node “skip” metastases along the vascular pedicle in 2% of all pN+ rectal cancer specimens: 9% of the specimens had tumor-involved lymph nodes at more than 5 cm from the tumor even if all lymph nodes located within 5 cm of the tumor were free of metastases. This translates into a theoretical 11% false-negative rate if lymph node examination is limited to the peritumoral tissue within 5 cm of the tumor, mostly in pT3 cancers. Among all specimens analyzed, the false-negative pN assessment rate would have been 3.3%.
Even though no upstaging effect was found, an increase in the number of lymph nodes examined was associated with improved survival in colon cancer patients in the analysis by Parsons et al. [1] and confirmed by other authors [18, 27]. Some authors [3] have suggested that these counterintuitive observations may be the result of heterogeneity in individual immune responses. A more pronounced immune response may facilitate detection of both non-involved and involved lymph nodes, which may result in more lymph nodes identified by the pathologist in specimens from these individuals. This may lead to bias, as an enhanced immune response may also be associated with better prognosis and improved long-term survival, as demonstrated by Pages et al. [25, 26, 28]. In our analysis, patients with more examined lymph nodes did not demonstrate better long-term survival nor a decreased risk of metachronous metastatic disease, which may be the result of the relatively low proportion of specimens with fewer than 12 lymph nodes found during the study period.
By separately analyzing data from hospitals that did and did not report an increase in the number of examined lymph nodes during the course of the study period, we attempted to determine whether the expected upstaging effect through improved lymph node diagnostics was altered by a tendency towards earlier detection of rectal cancers over the years. Although a more pronounced stage migration towards UICC stage II was found in hospitals in which the number of examined lymph nodes had remained unchanged during the study period (7.5% vs. 1.9%), this difference was not statistically significant. A similar comparative analysis of institutions (A, B, and C) demonstrating different developments in lymph node diagnostics over a defined time period was reported by Storli et al. [4]. In hospitals A and C, an increase in the number of lymph nodes examined per specimen was achieved through optimized surgery (A) or lymph node preparation (C), whereas in hospital B, the number of examined lymph nodes per specimen as well as the proportion of specimens with at least 12 lymph nodes examined remained unchanged. Still, a decrease in the number of tumor-involved lymph nodes as well as a non-significant trend from UICC stage III towards UICC stage II was found in hospital B. This was also observed in hospital A (optimized surgery) but not in hospital C (intensified lymph node diagnostics). Our results do not permit conclusion that the expected upstaging effect through more meticulous lymph node diagnostics has been offset by a tendency towards earlier detection of colorectal cancer.
However, as a possible limitation, it needs to be taken into consideration that pathology units use different methods to search for nodes, resulting in difficult comparison of the literature data. In addition, it must also be taken into account that radiotherapy lowers the number of nodes detected and this has good prognostic value. In addition, lymph node harvest is an indirect indicator of appropriate surgery and, thus, of better oncological outcome.
In conclusion, the presented analysis underscores the demand for a minimum number of 12 examined lymph nodes in rectal cancer specimens. Examination of fewer lymph nodes is associated with a higher rate of false-negative pN staging.
Our data do not demonstrate that maximizing the number of examined lymph nodes per specimen results in tumor upstaging. Despite an increase in investigated lymph nodes, there was no detectable shift of tumor stages.
Conclusion
There is a demand for a minimum of 12 examined LN in untreated (no neoadjuvant treatment) rectal cancer specimens.
Examination of fewer LN is associated with a higher rate of false-negative pN staging.
Further increasing the number of examined LN beyond 12 may decrease the false-negative rate, especially in pT3 cancers.
The data do not demonstrate that maximizing the number of examined LN per specimen results in tumor upstaging.
Despite an increase in investigated lymph nodes, there was no detectable shift of tumor stages.
Declarations
Conflict of interest
H. Ptok, F. Meyer, R.S. Croner, I. Gastinger, and B. Garlipp declare that they have no competing interests.
Ethical standards
Research involving human participants and/or animals. The study was performed according to the guidelines and ethical standards of the Declaration of Helsinki for Biomedical Research from 1964 by the World Medical Association and its further amendments, the policy of the local institutional ethics committees, as well as according to the requirements of Good Clinical Research and Good Clinical Practice. Data generation, documentation, and evaluation was performed according to prerequisites of data protection law of the German district Saxony-Anhalt and according to federal law. With regard to the study concept, it can be stated that a (potential) danger for study participants can be definitely excluded. There is no imponderable risk or side effect for the patient. Informed consent. Each patient signed an informed consent form prior to i) surgery, including appropriate explanation of the surgical intervention and potential complications, and ii) generation and documentation of data in the patient data registry.
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