TY - JOUR
T1 - Lymphovascular invasion and nodal metastasis in intramucosal adenocarcinoma of the esophagus and esophagogastric junction
AU - Li, Zhi Gang
AU - Zhu, Hui
AU - Shi, Hong
AU - Xie, Hao
AU - Goldblum, John R.
AU - Thota, Prashanthi N.
AU - Liu, Xiuli
N1 - Publisher Copyright:
© 2015 Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and Wiley Publishing Asia Pty Ltd.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - Objective: To evaluate the tumor parameters predictive of lymphovascular invasion (LVI) and nodal metastases in intramucosal adenocarcinoma (IMAC) of the esophagus and esophagogastric junction. Methods: In all, 171 cases of IMAC from esophagectomy database (1986-2009) were reviewed. LVI was evaluated on HE and by immunohistochemistry stain for D2-40 (in selected cases). Univariate analysis was performed to identify predictors for LVI (in this cohort) and nodal metastasis (for pooled data from literature review). Results: Altogether 150 IMAC were included in the study after histology review; 7 (4.7%) showed LVI and one (0.7%) had nodal metastasis. LVI-positive IMAC were thicker (tumor thickness 3.0±2.8mm vs 1.3±1.2mm, P=0.01), and more likely to invade the outer muscularis mucosae (M3) (P=0.004), be poorly differentiated (P<0.001), and to show a nodular or plaque-like lesion (P=0.04) compared with LVI-negative IMAC. Patients' age, gender, the frequency of tumor multifocality, ulceration and tumor size were not significantly different between these two groups. The pooled rates of LVI and nodal metastases in IMAC from five published studies and this cohort were 6.0% (range 2.9-16.7%) and 3.4% (range 0-10.0%), respectively. Pooled analysis of studies with histology review showed that LVI in IMAC was associated with a nodal metastases rate of 27.3%. Conclusion: For IMAC of the esophagus and esophagogastric junction, LVI is associated with tumor thickness, M3 invasion, poor differentiation and the presence of nodular or plaque-like lesion; by pooled analysis, it is associated with a risk of nodal metastasis of 27.3%.
AB - Objective: To evaluate the tumor parameters predictive of lymphovascular invasion (LVI) and nodal metastases in intramucosal adenocarcinoma (IMAC) of the esophagus and esophagogastric junction. Methods: In all, 171 cases of IMAC from esophagectomy database (1986-2009) were reviewed. LVI was evaluated on HE and by immunohistochemistry stain for D2-40 (in selected cases). Univariate analysis was performed to identify predictors for LVI (in this cohort) and nodal metastasis (for pooled data from literature review). Results: Altogether 150 IMAC were included in the study after histology review; 7 (4.7%) showed LVI and one (0.7%) had nodal metastasis. LVI-positive IMAC were thicker (tumor thickness 3.0±2.8mm vs 1.3±1.2mm, P=0.01), and more likely to invade the outer muscularis mucosae (M3) (P=0.004), be poorly differentiated (P<0.001), and to show a nodular or plaque-like lesion (P=0.04) compared with LVI-negative IMAC. Patients' age, gender, the frequency of tumor multifocality, ulceration and tumor size were not significantly different between these two groups. The pooled rates of LVI and nodal metastases in IMAC from five published studies and this cohort were 6.0% (range 2.9-16.7%) and 3.4% (range 0-10.0%), respectively. Pooled analysis of studies with histology review showed that LVI in IMAC was associated with a nodal metastases rate of 27.3%. Conclusion: For IMAC of the esophagus and esophagogastric junction, LVI is associated with tumor thickness, M3 invasion, poor differentiation and the presence of nodular or plaque-like lesion; by pooled analysis, it is associated with a risk of nodal metastasis of 27.3%.
KW - Esophageal neoplasms
KW - Esophagogastric junction
KW - Intramucosal adenocarcinoma
KW - Lymphatic metastasis
KW - Lymphovascular invasion
UR - http://www.scopus.com/inward/record.url?scp=84928536934&partnerID=8YFLogxK
U2 - 10.1111/1751-2980.12230
DO - 10.1111/1751-2980.12230
M3 - Article
C2 - 25620066
AN - SCOPUS:84928536934
SN - 1751-2972
VL - 16
SP - 197
EP - 204
JO - Journal of Digestive Diseases
JF - Journal of Digestive Diseases
IS - 4
ER -