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Distribution of lymph node metastases in esophageal carcinoma [TIGER study]: study protocol of a multinational observational study
BMC Cancer volume 19, Article number: 662 (2019)
An important parameter for survival in patients with esophageal carcinoma is lymph node status. The distribution of lymph node metastases depends on tumor characteristics such as tumor location, histology, invasion depth, and on neoadjuvant treatment. The exact distribution is unknown. Neoadjuvant treatment and surgical strategy depends on the distribution pattern of nodal metastases but consensus on the extent of lymphadenectomy has not been reached. The aim of this study is to determine the distribution of lymph node metastases in patients with resectable esophageal or gastro-esophageal junction carcinoma in whom a transthoracic esophagectomy with a 2- or 3-field lymphadenectomy is performed. This can be the foundation for a uniform worldwide staging system and establishment of the optimal surgical strategy for esophageal cancer patients.
The TIGER study is an international observational cohort study with 50 participating centers. Patients with a resectable esophageal or gastro-esophageal junction carcinoma in whom a transthoracic esophagectomy with a 2- or 3-field lymphadenectomy is performed in participating centers will be included. All lymph node stations will be excised and separately individually analyzed by pathological examination. The aim is to include 5000 patients. The primary endpoint is the distribution of lymph node metastases in esophageal and esophago-gastric junction carcinoma specimens following transthoracic esophagectomy with at least 2-field lymphadenectomy in relation to tumor histology, tumor location, invasion depth, number of lymph nodes and lymph node metastases, pre-operative diagnostics, neo-adjuvant therapy and (disease free) survival.
The TIGER study will provide a roadmap of the location of lymph node metastases in relation to tumor histology, tumor location, invasion depth, number of lymph nodes and lymph node metastases, pre-operative diagnostics, neo-adjuvant therapy and survival. Patient-tailored treatment can be developed based on these results, such as the optimal radiation field and extent of lymphadenectomy based on the primary tumor characteristics.
NCT03222895, date of registration: July 19th, 2017.
Survival rates following an esophageal resection for esophageal carcinoma vary from a median of 25 to 74 months [1, 2]. An important parameter for survival is lymph node status [3,4,5,6,7,8,9,10,11,12]. The distribution of lymph node metastases depends on tumor characteristics such as tumor location, histology, invasion depth, and on neoadjuvant treatment [13,14,15,16,17,18,19,20]. However, the precise distribution pattern is unknown.
In the Netherlands, among other countries, curative treatment for patients with esophageal carcinoma consists of neoadjuvant chemoradiation followed by surgery [21, 22]. The radiation field during neoadjuvant treatment and the lymphadenectomy during surgery depend on the location of lymph node metastases but no consensus has been reached on the extent of the lymphadenectomy . If a distribution pattern of lymph node metastases of esophageal carcinoma can be identified, the optimal neoadjuvant and surgical treatment can be determined.
The administration of neoadjuvant therapy itself can also influence the distribution of lymph node metastases . Neoadjuvant chemoradiation may be able to sterilize metastatic lymph nodes. Lymph nodes inside the radiation field are affected by both radiotherapy and concurrent chemotherapy, whereas lymph nodes outside the radiation field are affected by chemotherapy only. Nevertheless, recent studies show that also after neoadjuvant therapy, the extend of lymphadenectomy is directly related to survival . Therefore, not only the metastatic behavior of untreated esophageal carcinoma is an important factor, also the pattern after neoadjuvant therapy can provide valuable information for the optimal extend of lymphadenectomy after chemo (radio)therapy.
Especially for adenocarcinoma the distribution of lymph node metastases has not yet been described in large series that report on a complete 2- or 3-field lymphadenectomy [13, 14]. Also, different classification systems for lymph node stations are used in current literature, leading to incomparable studies. Besides the limited and heterogeneous evidence, also the significant morbidity involved in esophageal surgery makes the treatment choices demanding considering that the removal of more lymph nodes may lead to a more invasive procedure, possibly increasing the risk for postoperative morbidity.
A large observational study could identify lymph node stations that should be resected in relation to tumor characteristics and may clarify if the same surgical strategy is justified in patients with and without neoadjuvant therapy. Furthermore, the prognostic value of different lymph node stations can be established. We thus propose a multicenter prospective study to determine the distribution of lymph node metastases in patients with resectable esophageal or gastro-esophageal junction carcinoma in whom a transthoracic esophagectomy with a 2- or 3-field lymphadenectomy is performed. This can be the foundation for a uniform worldwide staging system and establishment of the optimal surgical strategy for esophageal cancer patients.
The aim of the TIGER study is to evaluate the distribution of lymph node metastases in esophageal carcinoma specimens following transthoracic esophagectomy with a 2- or 3- field lymphadenectomy.
Study design and setting
TIGER is an international observational cohort study. The duration of the study will approximately be 7 years (2 years inclusion, 5 years follow-up). There are currently 50 participating centers distributed over 18 countries. Centers are located in The Netherlands (10), Sweden (1), Finland (1), Belgium (2), Germany (3), Swiss (1), France (1), Italy (5), Spain (2), United Kingdom (7), Ireland (2), Japan (4), Hong Kong (1), China (1), India (2), United States (5), Canada (1) and Brazil (1). Data from each participating hospital will be collected at the TIGER website (www.tigerstudy.net). Data collection forms can be assessed after login on the website. Each hospital has access to their own dataset.
All patients with a resectable (cT1-4a, N0–3, M0) esophageal or gastro-esophageal junction carcinoma.
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
Primary squamous cell or adenocarcinoma of the esophagus or esophago-gastric junction
Surgically resectable tumor (cT1-4a, N0–3, M0)
Adequate physical condition to undergo transthoracic surgery (ASA 1–3)
Transthoracic esophagectomy, either open or minimal invasive
A potential subject who meets any of the following criteria will be excluded from participation in this study:
Previous thoracic or abdominal (upper GI) surgery disturbing lymph drainage of the esophagus and stomach
Patients with in situ carcinoma or high-grade dysplasia
The aim is to include 5000 patients. This number suffices for descriptive purposes and clustering of metastases diffusion profiles into meaningful subgroups within predefined strata (patients with adenocarcinoma or squamous cell carcinoma, with and without neoadjuvant therapy, different tumor heights and invasion depths, and following a 2- or 3-field lymphadenectomy). In 2012, the incidence of esophageal cancer was 456.000 new cases worldwide . Only a small percentage of patients with esophageal cancer present with curable disease at time of diagnosis. The aim is to include all 5000 patients with resectable disease in the 50 participating centers in a 2-year time period.
The distribution of lymph node metastases in esophageal and esophago-gastric junction carcinoma specimens following transthoracic esophagectomy with at least 2-field lymphadenectomy in relation to tumor histology, tumor location, invasion depth and neoadjuvant therapy.
Accuracy of preoperative diagnostics (EUS and PET-CT) and added value of EBUS to existing staging with EUS/PET-CT
Prognostic value of different lymph node stations
Postoperative morbidity (anastomotic leakage, chyle leakage, pneumonia, recurrent nerve injury and arrhythmia)
30-days/in-hospital and 90-days mortality
3- and 5-year overall and disease-free survival
Distribution pattern of recurrence or metastases
In-field- or out-field nodal recurrence in case of neo-adjuvant chemoradiation
Number of harvested lymph nodes in patients who are treated with and without neo-adjuvant chemo (radio)therapy
Analysis of the phenomenon skip nodal metastases
Ratio of nodal metastases inside and outside the radiation field
Treatment of subjects
Preoperative staging will be performed according to national guidelines. This therefore, may differ per country. Usually, patients are staged with an endoscopy with biopsies, an endoscopic ultrasound, a PET-CT-scan of neck, thorax and abdomen and an ultrasound of the neck. An EBUS-TBNA will be performed if indicated. All patients are discussed in a multidisciplinary team (MDT).
A suspected lymph node is defined as a node larger than > 9 mm short axis or a node 5–9 mm short axis that is round, inhomogeneous and has an irregular border (2 out of 3). In case of PET-CT-scan, pathological nodes are those with FDG uptake, a short axis > 10 mm or those with a short axis between 5 and 9 mm that present with sharp borders.
In case of potentially curative disease (cT1-4a, N0–3, M0) patients may be treated with neoadjuvant therapy, this however, may differ per country and usually consists of chemotherapy or chemoradiotherapy.
One coronal, 1 sagittal and 3 axial CT-images of the radiation field is documented in the medical file, to assess lymph nodes stations incorporated in the radiation field. An anatomical description of the radiation field will be given according to highest and lowest radiated lymph node station. An in-field lymph node is defined as a lymph node within the clinical target volume. Clinical target volume fields as defined gross tumor volume plus a margin for sub-clinical disease spread.
After completion of neoadjuvant therapy patients will generally be restaged with a (PET-)CT scan to exclude distant metastases before patients are scheduled for surgery. In addition, the locoregional lymph nodes will be evaluated. The (PET-)CT will usually be performed 2–4 weeks after completion of neoadjuvant therapy.
If no metastases are detected, patients will be operated 5–12 weeks after completion of neoadjuvant therapy. This may differ per country and may depend on the type of neoadjuvant therapy. If no neoadjuvant therapy is administered patients are directly scheduled for surgery.
An esophageal resection with a 2- or 3-field lymphadenectomy can be performed via a thoracolaparoscopy, a thoracolaparotomy or a hybrid procedure and a cervical incision as indicated. A gastric tube or colonic interposition can be used for reconstruction. Lymph node stations may be dissected ex vivo (after enbloc resection with the specimen), in vivo, or partially ex and in vivo, and will be separately sent for pathological examination. Lymph node stations in close proximity to the tumor are preferably marked with sutures or beads to prevent damage to the specimen and circumferential resection margin.
Lymph node classification systems
Different classification systems are used in different countries to classify lymph node stations around the esophagus: the AJCC 8th edition esophageal cancer staging and the JES 11th edition esophageal cancer staging. In Fig. 1 and Table 1 these classifications have been combined for the purpose of this study.
In case of a 3-field lymphadenectomy stations 1–19 will be resected and in case of a 2-field lymphadenectomy stations 6–19 will be resected as usual. If not all lymph node stations are resected, patients can still be included in the study, however this has to be documented accurately. A video appendix and definitions of the individual lymph node stations are displayed and available for review on the TIGER study website.
The esophageal resection and lymphadenectomy specimens will be processed and analyzed according to national and international guidelines by the department of pathology. In addition to the separately sent lymph node stations, the esophageal surgical resection specimen will be carefully analyzed for retained lymph nodes and structures macroscopically suspicious for lymph nodes will be embedded. All lymph nodes under 5 mm will be totally embedded for microscopic evaluation, larger lymph nodes will be totally embedded in slices of 3–4 mm thick. Microscopically, a circumscript area of lymphoid cells containing a follicular architecture and/or a subcapsular sinus is identified as a lymph node. In the final report the exact localization and number of lymph nodes found will be reported.
Initial microscopic evaluation will be performed by standard H&E staining. In case of suspicion of micro-metastasis (0.2–2.0 mm) or isolated tumor cells in the lymph node, or in case of suspicion of residual tumor cells in patients with extensive response to neoadjuvant therapy, additional keratin stains will be performed. A metastatic lymph node is defined as a lymph node with tumor cells. Lymph nodes containing micro-metastasis or isolated tumor cells are also considered as metastatic lymph nodes but will be also recorded separately. Lymph nodes with regression after chemoradiation with isolated tumor cells will be considered as metastatic lymph nodes, however, these also will be recorded separately, so that the prognostic value of these isolated tumor cells can be determined. The same applies to fibrotic lymph nodes without vital tumor cells. These are so called preneoadjuvant therapy N+ nodes. In case of an adenocarcinoma of the esophagus, Her2-status will be analyzed (immunohistochemistry and SISH).
Patients will be followed up until 5 years after the operation. Follow-up will usually be scheduled (but differences between countries exist) every 3 months the first year, every 6 months the second until the fourth year and once yearly until the fifth year. Investigations are performed according to national guidelines.
Primary study parameter(s)
Numbers and percentages of resected lymph nodes and lymph node metastases will be given per lymph node station (Fig. 1). Tumor location and invasion depth will be categorized. Patients with adenocarcinoma and squamous cell carcinoma and patients with and without neoadjuvant therapy will be analyzed separately.
Secondary study parameter(s)
The sensitivity, specificity, and positive and negative predictive values of EUS and PET-CT will be reported. Perioperative morbidity and mortality will be summarized descriptively. For each patient group (squamous cell versus adenocarcinoma, with and without neoadjuvant therapy), explorative cluster analyses will be performed to identify subgroups of patients with different patterns of lymph nodes metastases. Potentially relevant characteristics at the time of surgery like age, gender, tumor location, tumor invasion depth, tumor differentiation, vaso-invasive growth will be included in the analysis. No restrictions will be applied to the number of clusters in each analysis, but the ratio of the largest cluster size to the smallest cluster size should preferably not exceed the value of 3 and/or the smallest cluster size should be minimally 30 patients. Characteristics introducing patient outliers will be excluded and one should further be able to attribute meaning to the resulting cluster profiles. Clusters that show the phenomenon of skip metastases will be noted. The resulting clusters will be evaluated for the diffusion pattern of future metastases during follow-up (descriptive analysis), the number of future metastases during follow-up (Poisson regression or generalized estimation equation, whichever appropriate), for 3- and 5-year overall and disease-free survival (Kaplan-Meier survival analysis). Multivariate analysis will be performed using the Cox hazard regression method. The univariate analysis, including all baseline parameters, will serve as the basis for the multivariate Cox hazard regression model. Variables showing association (p < 0.10) with survival in univariate analysis will be included in the multivariate analysis. Age and sex will be included in all multivariate analyses. Results are presented as hazard ratio with exact 95% confidence interval (95% CI). After 5-years of follow-up the efficacy index will be determined (incidence of metastases to an area (%) × 5-year overall survival rate (%)). A log-rank test, Mann-Whitney U test, or χ2-test will be used as indicated to compare groups. A value of p < 0.05 will be considered statistically significant.
The TIGER study is an international observational cohort study, with participation of worldwide renowned esophageal cancer centers, that will investigate the distribution of lymph node metastases is esophageal cancer. This global study group will be a unique international collaboration that will determine the pattern of lymph node metastases in both squamous cell and adenocarcinoma, since, especially in adenocarcinoma, this has not been investigated in multicenter prospective series before [11, 12]. The results of the TIGER study will provide a roadmap of the location of lymph node metastases in relation to tumor histology, tumor location, tumor invasion depth, number of lymph nodes and lymph node metastases, pre-operative diagnostics, neoadjuvant therapy and survival. In addition, it will be investigated whether neoadjuvant chemoradiotherapy and chemotherapy influence the presence and location of lymph node metastases, as some recent reports suggest that lymph nodes can become sterile after neoadjuvant treatment and only fibrosis is found in these lymph nodes . The prognostic value of positive lymph nodes, micrometastases, isolated tumor cells and fibrosis will be investigated. Patient-tailored treatment can be developed on the basis of the TIGER study results, such as the optimal radiation field and the extent of the lymphadenectomy and, additionally, it may aid in the development of a global uniform classification system.
Protocol version 6, date: 08-02-2019
Start recruitment: 03-03-2019
Approximate date recruitment completion: 03-03-2021
Availability of data and materials
The datasets generated and/or analyzed during the current study will be available from the corresponding author on reasonable request.
American Joint Committee on Cancer
Endobronchial ultrasound-transbronchial needle aspiration
Hematoxylin and eosin stain
- IRB :
Investigational Research Board
Japan Esophageal Society
Positron emission tomography-computed tomography
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Madhan Kupusammy is acknowledged for designing and developing the secure TIGER study website and online database. Affiliation: Virginia Mason Medical Center, Seattle, USA. Dana Hamers is acknowledged for designing the image of the TIGER classification of lymph node stations.
Professor Dr. Christophe Mariette, Head of the Department of Digestive and Oncologic Surgery, CHRU de Lille, France passed away in July 2017. Mariette was an internationally recognized surgeon and researcher and an important member of the TIGER study group. He will be greatly missed and the members of the TIGER study group respectfully dedicate this paper to his memory.
Funding has been obtained from the MLDS, the Egbers Stichting, Olympus, the SLMK fund and crowdfunding. The funding bodies did not have any role in the design of the study and will not have any role in collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
The Medical Ethics Review Committee of the Academic Medical Center has confirmed that the Medical Research Involving Human Subjects Act (WMO) does not apply to the TIGER study because of the observational nature of the study. An official approval by the IRB is therefore not required. An IRB waiver is obtained. Reference number: W17_069. Written informed consent for prospective data collection will be obtained from all patients prior to treatment.
Consent for publication
SL Is a member of the editiorial board (Associate Editor) of this journal. The other authors declare that they have no competing interests. The funding bodies did not have any role in the design of the study and will not have any role in collection, analysis, and interpretation of data and in writing the manuscript.
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