- Open Access
What does absence of lymph node in resected specimen mean after neoadjuvant chemoradiation for rectal cancer
© Lee et al.; licensee BioMed Central Ltd. 2013
- Received: 21 August 2012
- Accepted: 12 August 2013
- Published: 19 August 2013
The effect of insufficient node sampling in patients with rectal cancer managed by neoadjuvant chemoradiation followed by surgery has not been clearly determined. We evalulated the impact of insufficient sampling or even abscence of lymph nodes in the specimen on survival in patients at high-risk (T3, T4 or node positive) for rectal cancer.
We conducted a single institution, retrospective analysis of all patients who underwent surgical rectal resection following neoadjuvant chemoradiation for treatment of mid to lower rectal cancer between 1997 and 2009. ypNX was defined as the absence of lymph nodes retrieved in the resected specimen.
A total of 132 patients underwent resection for treatment of rectal cancer following neoadjuvant chemoradiation. Ninety four patients (71.2%) were considered as having node-negative disease, including ypNx and ypN0. In 38 patients (28.8%), the primary tumor was associated with regional lymph node metastases (ypNpos). The mean number of retrieved nodes per specimen was 14.2, respectively. The five-year overall survival from initial operation for the ypNx group was 100%, respectively. The estimated five-year overall survival for ypN0 and ypNpos was 84.0% and 60.3%, respectively (P =0.001). No significant differences in overall survival were observed between the ypNx and ypN0 group (P =0.302).
Absence of recovered LN in resected specimens after neoadjuvant chemoradiation was observed in 7.6% of specimens. Absence of LN should not be regarded as a risk factor for poor survival or as a sign of less radical surgery.
- Rectal neoplasm
- Neoadjuvant chemoradiation
It is estimated that approximately 50 ~ 60% of rectal cancers are considered to be locally advanced tumors with clinical stage T3 or T4 or node positive disease, characterized by poor prognosis due to increased incidence of systemic and local recurrence and decreased long-term survival . The preferred strategy for management of locally advanced mid to distal rectal cancer is multimodality treatment that includes radical surgery, chemotherapy, and radiation therapy. Radical surgery should be performed according to established surgical principles, which include en bloc resection of the tumor-bearing rectum and the adjacent lymphovascular pedicle, commonly referred to as total mesorectal excision .
The lymph node (LN) status remains one of the independant prognostic factors in rectal cancer. Patients without LN metastses have significantly better survival, compared to node positive patients, in the abscence of distant metastasis. However, a mininum number of LNs retrieved from the resected specimen is prerequisite to ensuring both adequate nodal sampling and surgical radicality . Several studies have demonstrated a significant survival benefit of patients with node negative disease with an increased number of recovered nodes [4–6]. Chemoradiation exerts effects not only on tumor down staging and rate of metastatic LN but also on the overall number of retrieved nodes [7, 8]. The number of LNs assessed pathologically is a combination of the aggressiveness of the surgeon in resecting widely around the primary tumor and of the didicated pathologist in searching the specimen for additional nodes. Inadequate retrieval of LNs is considered unacceptable for patients who have not undergone pretreatment and went straight to surgery. However, the effect of this finding in patients with rectal cancer managed by neoadjuvant chemoradiation followed by surgery has not yet been determined.
In an attempt to determine the impact of insufficient sampling (i.e. ypN ≤ 12) or even abscence of lymph nodes in the specimen (i.e. ypNx) on survival in these patients, we evaluated a cohort of patients who enrolled in our neoadjuvant chemoradiation protocol for patients with high-risk (T3, T4 or node positive) rectal cancer.
Between September 1997 and September 2009, 720 patients with rectal cancer underwent treatment at Gachon Medical Center. The inclusion criteria for the study were as follows: 1) lesion located no more than 10 cm from the anal verge; 2) clinical TNM stage II and III (T2-T4, or N positive and M0) on abdominopelvic computated tomography; 3) patients with histologically proven rectal carcinoma; 4) age ≥18 years; 5) patients who underwent preoperative chemoradiation; 6) mid (anal verge 6 cm to 10 cm) and lower (anal verge 1 cm to 5 cm) rectal cancer patients. Of the 720 patients screened for rectal resection, 132 patients fulfilled the inclusion criteria and were included in this retrospective analysis.
Initial staging included complete physical examination, digital rectal examination, colonoscopy, serum CEA (carcino-embryonic antigen) abdominal and pelvic spiral CT scans, and endorectal ultrasonography or rectal magnetic resonance imaging in selected patient chest X-ray.
All patients received two initial cycles of chemotherapy followed by pelvic radiation therapy plus chemotherapy. The concurrent chemotherapy was performed at the first and fifth week of radiation with bolus intravenous 5-fluorouracil 400 mg/m2 and leucovorin 20 mg/m2 for five days per week. All patients received external beam radiation therapy (median dose, 50.40 Gy; range 48.4 to 55.8 Gy), according the previously published techniques [9, 10]. Using 6 to 10 Mv photons, a 3- or 4-field technique was used.
Surgery was attempted at 6–8 weeks after completion of neoadjuvant chemoradiotherapy. All patients underwent low anterior resection or abdominoperineal resection and total mesorectal excision (TME) according to the surgical technique described by Heald et al.  as well as high ligation inferior mesenteric artery and en bloc resection of any suspected adjacent organ invasion. Four cycles of postoperative adjuvant chemotherapy with 5-fluorouracil 500 mg/m2 for five days was added.
Two pathologists performed meticulous dissection and retrieval of mesorectal lymph nodes. A rigorous search of the mesorectum was performed in order to identify as many lymph nodes as possible. Each lymph node was analyzed in its entirety in separate blocks. When fewer than 12 lymph nodes were found, an additional 24-hour surfixation in Bouin’s fluid was performed in order to facilitate recovery of residual lymph nodes. No clearing technique was performed. Patients were staged according to the American Joint Committee on Cancer recommendations . ypNX was defined as the absence of lymph nodes recovered in the resected specimen.
Surveillance for recurrence following surgery was outlined as follows: physical examination, serum CEA, chest X-ray, and spiral abdominal CT scan were performed every six months for three years, and annually thereafter.
The primary endpoint of the study was overall survival. Overall survival (OS) was estimated using the Kaplan-Meier method. OS was measured from the date of diagnosis to the date of death or the last follow-up visit. Survival rates were compared for statistical differences using log-rank analysis. Chi squared and ANOVA were used for categorical and numeral variables between groups. Multivariate analysis was performed using stepwise Cox proportional hazards regression modeling. P values less than .05 were considered statistically significant and all P values correspond to two-sided significance tests.
Patient characteristics (n = 132)
Number of patients
Primary tumor location
Pretreatment CEA, ng/mL*
Poorly or mucinous
Body mass index
The median interval time between completion of preoperative chemoradiation and surgery was 6.2 weeks (range, 4.4-8.6 weeks). Among the 132 patients, 52 (39.4%) underwent low anterior resections with or without protective ileostomy; 39 (29.5%) underwent ultralow low anterior resections with or without protective ileostomy; 22 (16.7%) underwent Hartmann’s procedure and 19 patients (14.3%) underwent abdominoperineal resections. A summary of patient characteristics is shown in Table 1. In this study, 92 patients (69.7%) underwent a sphincter saving operation without permanent colostomy.
TNM downstaging in a series of 132 rectal cancer patients treated with preoperative chemoradiotherapy
Lymph node status
Correlation of ypT stage and ypN stage (n = 132)
Clinicopathological characteristics of patients according to ypN status (n = 132)
P-value, ypNx vs ypN0
Number of patients
Mean age(yr) ± STD
66.9 ± 9.13
59.5 ± 8.80
58.5 ± 11.4
Primary tumor location
5.59 ± 5.98
4.02 ± 5.67
7.36 ± 17.73
Body mass index
22.18 ± 1.57
23.39 ± 3.14
22.86 ± 2.61
13.45 ± 7.59
17.9 ± 6.87
Risk factor analyses
Univariate predictors of adverse outcome (n = 132)
Primary tumor location
Pathologic N stage
Body mass index
Disease recurrence and survival
Recurrence according to ypN status (n = 132)
Cancer related mortality
Neoadjuvant chemotherapy and radiation therapy for treatment of locally advanced rectal cancer is a widely accepted treatment before surgical operation. Although it was initially used to improve rates of sphincter preservation and to optimize patient tolerance, the ideal number of nodes for rectal cancer surgery has been an issue of controversy. Many studies have demonstrated that the number of lymph nodes involved with a tumor has a strong impact on outcome for patients treated for rectal cancer . Indeed, the TNM staging system is based on whether one to three nodes are involved or four or more . An apparent increase in the number of retrieved nodes in patients with N1 or N2 disease, when compared to N0 disease, has been reported [3, 6]. Although there is no clear agreement on the absolute number of total retrieved nodes, [3, 13–15] the American Joint Committee on Cancer (AJCC) has recommended at least 12 lymph nodes as the standard for adequate staging of colon and rectal disease [12, 16]. The AJCC staging does not include an exception criteria for pretreated rectal cancer, which in fact may have several factors that interfere with lymph node retrieval after rectal cancer surgery. In addition, the impact of absence of lymph nodes in the resected specimen after radical surgery for treatment of mid to distal rectal cancer after neoadjuvant chemoradiation has not been clearly defined in terms of overall survival.
In this study, the mean number of lymph nodes recovered after neoadjuvant chemoradiation followed by radical surgery was 14.2 LN per specimen, whereas the rate of ypNx was 7.6%. Findings of this series showed a statistically significant higher number of nodes in node positive patients, compared with node negative patients. For example, Wong et al.  reported that a mean of 14 nodes was found in node negative patients, as compared with 20 nodes in node positive patients. Unlike the study reported by Gorog et al.  and Kuo et al. , in this study, body surface area did not affect the number of LN retrieved. The major weakness of this study is that the results are based on 11 patients with no recurrent disease after ypNx. The retrospective nature and small sample size might actually have affected statistical analysis.
In a population-based study, including 5000 patients with rectal cancer from the SEER (Surveillance, Epidemiology, and End Results) database, results of multivariate analysis showed that patients who underwent preoperative radiation had significantly fewer recovered nodes, as compared with patients treated by adjuvant therapy . The main reason for more retrieved nodes in this study may have resulted from complete total mesorectal excision with high ligation of inferior mesenteric vessels; however, a more likely explanation is the pathologist’s determination to retrieve as many nodes as possible.
The clinical impact of decreased retrieval of LN after neoadjuvant chemoradiation has not yet been clearly defined. It is generally believed that examining a greater number of nodes increases the likelihood of proper staging and thus might benefit from adjuvant therapy. Is survival in the ypNx population worse than that in the ypN0 population? In our series, the answer is no. The ypNx group exhibited a tendency toward better overall survival than the ypN0 group. The ypNx group may reflect an increased sensitivity to chemoradiation, which ultimately results in downstaging, as suggested by Habr-Gama et al. . In fact, some of patients with ypNx could have been node positive patients before neoadjuvant chemoradiation. The results of the current series should be interpreted with caution. Due to the retrospective nature of this study, the analysis of disease free survival, local recurrence free survival and overall survival lack significant variables having a major impact on the outcome. Based on our results, the authors of this study suggest that the current recommendation of minimum requirement for LN retrieved (i.e. more than 12 nodes) for proper staging in these subsets of patients may be inappropriate and that conduct of more larger studies comparing the therapeutic outcome of ypNx and ypN0 is definitely warranted.
A wide range of tumor responses after preoperative chemoradiation therapy have been reported [2, 6, 9, 21, 22]. The reason for this wide variability in tumor responses is unclear. The results of studies reporting predictive clinicopathologic factors of tumor response are controversial and patients in the ypNx group may be associated with increased sensitivity toward chemoradiation therapy, and, thus, toward better survival. Some molecular biomarkers and various enzymes that may predict tumor response to chemotherapy have been suggested [19, 23–25]. Neoadjuvant chemoradiation therapy has played a critical role in improving resectability and downstaging tumors. A variety of neoadjuvant chemoradiation regimens and radiosentisizers should be investigated for improvement of tumor response after chemoradiation and further prediction of tumor response.
In conclusion, absence of recovered LN in a resected specimen after neoadjuvant chemoradiation is rare and was observed in 7.6% in this series. Patients with ypNx after neoadjuvant chemoradiation and radical surgery may not be considered as patients at high risk for development of recurrence.
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