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Esophageal NeoplasmsTIGERNCT03222895

Distribution of Lymph Node Metastases in Esophageal Carcinoma

An observational study of Esophageal Neoplasms and Lymph Node Metastases, run by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) at 19 sites in 14 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Background: Lymph node status is an important prognostic parameter in esophageal carcinoma and an independent predictor of survival. Distribution of metastatic lymph nodes may vary with tumor location, tumor histology, tumor invasion depth and neoadjuvant therapy. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Esophageal Neoplasms, Lymph Node Metastases
How many people
5,000 participants
Where
19 sitesin 14 countries
Study dates
1 Mar 2019to 1 Jun 2028
How long will I take part?
5 Years
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: All patients with esophageal cancer who will undergo a transthoracic esophagectomy with a 2- or 3 field lymphadenectomy for esophageal cancer in one of the participating centers during the inclusion period.

Who may be able to join

  • Primary squamous cell or adenocarcinoma of the esophagus or esophago-gastric junction
  • Surgically resectable (cT1-4a, N0-3, M0)
  • Adequate physical condition to undergo transthoracic surgery (ASA 1-3)
  • Transthoracic esophagectomy

Who cannot join

  • Previous thoracic or abdominal (upper GI) surgery disturbing lymph drainage of the esophagus and stomach
  • Patients with in situ carcinoma or high grade dysplasia

Trial locations and contacts

19 sites in 14 countries. Contact the study team or a site near you to ask about taking part.

Suzanne S Gisbertz, MD, PhD contact

+31205669111

s.s.gisbertz@amc.nl

Eliza RC Hagens, BSc contact

+31205669111

e.r.hagens@amc.uva.nl

19 sites in 14 countries

Italy3 sites, 3 recruiting
  • IRCCS Policlinico San Donato

    Milan, 20097

    L. Bonavina, MD, PhD

    Recruiting
  • Ospedale San Raffaele

    Milan

    Riccardo Rosati, MD

    Recruiting
  • University of Verona

    Verona, 37129

    G. de Manzoni, MD, PhD

    Recruiting

Other trials in Italy

Japan3 sites, 3 recruiting
  • Uonuma Institute and Niigata University

    Niigata, 9502292

    S. Kosugi, MD, PhD

    Recruiting
  • Keio University School of Medicine

    Tokyo, 1088345

    Y. Kitagawa, MD, PhD

    Recruiting
  • The Cancer Institute Hospital of JFCR

    Tokyo, 1358550

    M. Watanabe, MD, PhD

    Recruiting

Other trials in Japan

Netherlands2 sites, 2 recruiting
  • Ziekenhuisgroep Twente, Almelo & Hengelo

    Almelo

    E. Kouwenhoven, MD, PhD

    Recruiting
  • Amsterdam UMC

    Amsterdam

    Suzanne S Gisbertz, MD PhD

    Recruiting

Other trials in Netherlands

United States1 site, 1 recruiting
  • MD Anderson Cancer Center

    Houston, Texas, 77030

    W.L. Hofstetter, MD, PhD

    Recruiting

Other trials in United States

Brazil1 site, 1 recruiting
  • Instituto Nacional de Câncer

    Rio de Janeiro

    C.E. Pinto, MD, PhD

    Recruiting

Other trials in Brazil

Canada1 site, 1 recruiting
  • University of Toronto

    Toronto

    Gail Darling, MD PhD

    Recruiting

Other trials in Canada

China1 site, 1 recruiting
  • Fudan University Shanghai Cancer Center

    Shanghai, Yangpu, 200032

    H. Chen, MD, PhD

    Recruiting

Other trials in China

Finland1 site, 1 recruiting
  • Hospital District of Helsinki and Uusimaa

    Helsinki, 000260

    J. Räsänen, MD, PhD

    Recruiting

Other trials in Finland

Germany1 site, 1 recruiting
  • University Medical Center of the Johannes Gutenberg University

    Mainz, 55131

    P. Grimminger, MD, PhD

    Recruiting

Other trials in Germany

Greece1 site, 1 recruiting
  • University of Athens, School of Medicine

    Athens, 11527

    D. Theodorou, MD, PhD

    Recruiting

Other trials in Greece

Hong Kong1 site, 1 recruiting
  • University of Hong Kong

    Hong Kong, 102

    S.Y.K Law, MD, PhD

    Recruiting

Other trials in Hong Kong

India1 site, 1 recruiting
  • Tata Memorial Centre

    Mumbai

    C.S. Pramesh, MD, PhD

    Recruiting

Other trials in India

Spain1 site, 1 recruiting
  • Hospital Universitario del Mar

    Barcelona, 08003

    M. Pera, MD, PhD

    Recruiting

Other trials in Spain

Sweden1 site, 1 recruiting
  • Karolinska Institutet

    Stockholm, 17177

    M. Nilsson, MD, PhD

    Recruiting

Other trials in Sweden

About this study

Background: Lymph node status is an important prognostic parameter in esophageal carcinoma and an independent predictor of survival. Distribution of metastatic lymph nodes may vary with tumor location, tumor histology, tumor invasion depth and neoadjuvant therapy. Surgical strategy depends on the distribution pattern of nodal metastases but consensus on the extent of lymphadenectomy differs worldwide. Especially for adenocarcinoma the distribution of lymph node metastases has not yet been described in large series. Aim of the present study is to evaluate the distribution of lymph node metastases in esophageal carcinoma specimens following transthoracic esophagectomy with at least a 2-field lymphadenectomy.

Methods: The TIGER-study is a multinational observational cohort study. All 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 sent for pathological examination. Cluster analysis will be performed to identify patterns of metastases in relation to tumor location, tumor histology, tumor invasion depth and neoadjuvant therapy.

Conclusion: TIGER 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 on the basis of these results, such as the the optimal radiation field and extent of lymphadenectomy based on the primary tumor characteristics.

Read the detailed description

Primary Objective:

Aim of the TIGER study is to evaluate the distribution of lymph node metastases in esophageal carcinoma specimens following transthoracic esophagectomy with at least 2-field lymphadenectomy.

Secondary Objective(s):

  • Accuracy of preoperative diagnostics (especially EUS and PET-CT) and added value of EBUS (endobronchial ultrasonography) to existing staging with EUS (endoscopic ultrasonography)/PET-CT
  • Prognostic value of different lymph node stations
  • Three- and 5-year overall and disease free survival
  • Distribution pattern of recurrence or metastases
  • Number of harvested lymph nodes in patients who are treated with and without neo-adjuvant chemoradiotherapy
  • Frequency of skip nodal metastases
  • Ratio of nodal metastases inside and outside the radiation field o Lymph node metastases will be defined as inside or outside the radiation field nodes.

Study design:

TIGER is a multinational observational cohort study. The duration of the study will approximately be 7 years (2 years inclusion, 5 years follow-up). The participating centers are distributed over 18 countries.

Sample size calculation:

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. We aim to include all patients with resectable disease in participating centers in a 2 year time period. We aim to include 5000 patients. This number suffices for (i) descriptive purposes and (ii) 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).

Study procedures:

Patients will not undergo any additional procedures for the study. This is an observational study only. Patients will be treated according to national guidelines.

Follow-up:

Patients will be followed up for 5 years after the operation according to national guidelines. Follow-up will be scheduled every three months the first year, every six months the second until the fourth year and once yearly until the fifth year. Investigations are performed according to national guidelines. In the Netherlands, these are performed on indication of patients' complaints.

Statistical analysis:

Primary study parameter(s):

Numbers and percentages of resected lymph nodes and lymph node metastases will be given per lymph node station. 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. Also patients following a 2- or 3-field lymphadenectomy 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 mentioned in 5.4, explorative cluster analyses will be done to identify subgroups of patients with different patterns of lymph nodes metastases, tumor locations and invasion depths. Potentially relevant other characteristics at the time of surgery like age, gender, 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 (%) x 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. Statistical analysis will be performed with SPSS 21.0 software (SPSS, Inc., Chicago, IL, USA). No formal power analysis or sample size calculation will be performed, but the 5,000 inclusions will suffice for an exploratory study.

Other study parameters:

Baseline characteristics will be presented in a baseline table. Clinical and pathology data will be presented in separate tables.

Study population:

Central data management is organized via the secured TIGER database that can be found on TIGERstudy.net. Patient inclusion and data registration of these patients will be done by the participating local PI, surgeon or fellow for the center they are representing on the TIGER website. The local PI is responsible for the inclusion and data registration of all eligible patients in his or her center.

All patients with resectable esophageal carcinoma undergoing transthoracic esophageal resection are eligible for inclusion.

Patients will be treated according to national guidelines and may be neo-adjuvantly treated with chemotherapy or chemoradiation. An esophagectomy with a 2- or 3-stage lymphadenectomy will be performed followed by a gastric tube or colonic interposition for reconstruction. All lymph node stations will be excised and separately sent for pathological examination. Initial microscopic evaluation will be performed by standard H\&E staining. In case of suspicion of micro-metastasis 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. For the TIGER-study a new lymph node classification is designed, and lymph nodes will be recorded according to that classification system. Patients will be followed-up for 5 years after the operation.

Keywords
Esophageal Neoplasms, Lymph node metastases, Esophagectomy
Medical subject headings
Esophageal Neoplasms, Lymphatic Metastasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03222895
Study groupRoleWhat they receive
TIGER study cohortThis is the entire patient cohort. Alle patients with resectable esophageal cancer undergoing a transthoracic esophagectomy with at least a 2-field lymphadenectomy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Distribution of lymph node metastases

    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.

    Measured: 2 years

Secondary outcomes (7)
  1. Accuracy of preoperative diagnostics

    Accuracy of preoperative diagnostics (especially EUS and PET-CT) and added value of EBUS to existing staging with EUS/PET-CT

    Measured: 2 years

  2. Prognostic value of different lymph node stations

    Prognostic value of different lymph node stations

    Measured: 2 years

  3. Distribution pattern of recurrence or metastases

    Distribution pattern of recurrence or metastases, In-field- or out-field nodal recurrence in case of neo-adjuvant chemoradiation

    Measured: 2 years

  4. Number of harvested lymph nodes in patients who are treated with and without neo-adjuvant chemoradiotherapy

    Number of harvested lymph nodes in patients who are treated with and without neo-adjuvant chemoradiotherapy

    Measured: 2 years

  5. Skip nodal metastases

    Analysis of the phenomenon skip nodal metastases

    Measured: 2 years

  6. Ratio of nodal metastases inside and outside the radiation field

    Ratio of nodal metastases inside and outside the radiation field

    Measured: 2 years

  7. 3- and 5-year overall and disease free survival

    3- and 5-year overall and disease free survival in relation to the lymph node distribution pattern

    Measured: 7 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Jul 2017
  2. Study start1 Mar 2019
  3. Primary completion1 Jan 2025 (estimated)
  4. Study completion1 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
5,000 participants (estimated)
Target duration
5 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT03222895
Sponsor's protocol ID
W17_069
Acronym
TIGER
Status last verified
Feb 2024
First submitted
17 Jul 2017
Last updated
13 Feb 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Hagens ERC, van Berge Henegouwen MI, van Sandick JW, Cuesta MA, van der Peet DL, Heisterkamp J, Nieuwenhuijzen GAP, Rosman C, Scheepers JJG, Sosef MN, van Hillegersberg R, Lagarde SM, Nilsson M, Rasanen J, Nafteux P, Pattyn P, Holscher AH, Schroder W, Schneider PM, Mariette C, Castoro C, Bonavina L, Rosati R, de Manzoni G, Mattioli S, Garcia JR, Pera M, Griffin M, Wilkerson P, Chaudry MA, Sgromo B, Tucker O, Cheong E, Moorthy K, Walsh TN, Reynolds J, Tachimori Y, Inoue H, Matsubara H, Kosugi SI, Chen H, Law SYK, Pramesh CS, Puntambekar SP, Murthy S, Linden P, Hofstetter WL, Kuppusamy MK, Shen KR, Darling GE, Sabino FD, Grimminger PP, Meijer SL, Bergman JJGHM, Hulshof MCCM, van Laarhoven HWM, Mearadji B, Bennink RJ, Annema JT, Dijkgraaf MGW, Gisbertz SS. Distribution of lymph node metastases in esophageal carcinoma [TIGER study]: study protocol of a multinational observational study. BMC Cancer. 2019 Jul 4;19(1):662. doi: 10.1186/s12885-019-5761-7.

    PubMed 31272485

Questions about this trial

What is this clinical trial studying?

An observational study of Esophageal Neoplasms and Lymph Node Metastases, run by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) at 19 sites in 14 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 19 sites in Italy, Japan, Netherlands, United States, Brazil and 9 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Suzanne S Gisbertz, MD, PhD (+31205669111, s.s.gisbertz@amc.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Distribution of lymph node metastases (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03222895, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Feb 2024.

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