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Total Neoadjuvant Therapy for Lymph Node-positive Adenocarcinoma of the OESophagus and Oesophagogastric Junction: a Phase II Study

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Both neoadjuvant chemoradiotherapy (CROSS) and neoadjuvant chemotherapy (FLOT) have demonstrated overall survival benefit over surgery alone in esophageal and esophagogastric junction (EGJ) cancer. Despite these survival gains, the prognosis remains poor, especially in patients with nodal-positive adenocarcinoma (cN+ AC) (5-year survival 36%, compared to 55% for cN0). This highlights the need for more effective treatment options, and justifies treatment intensification in these patients. The aim of this study is to determine the efficacy and feasibility of TNT FLOT-CROSS and TNT CROSS-FLOT in patients with resectable, cN+ AC of the esophagus or EGJ.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ • Patients with cT2-4aN+M0 resectable adenocarcinoma of the oesophagus or EGJ (Siewert type I-II) according to the 8th edition of the Union for International Cancer Control (UICC) TNM classification for Esophageal Cancer who are planned to undergo nCRT or FLOT (43). In case of stage cT4a, curative resectability has to be explicitly verified by the multidisciplinary tumor board.

⁃ Clinical N+ status should be determined by EUS or 18F-FDG PET/CT. Clinical M0 status must be determined by 18F-FDG PET/CT.

• Maximum of 4 cm ingrowth in the cardia, measured by upper endoscopy.

• In case of tumor and/or lymph node involvement below the diaphragm, the most proximal involved lymph node station cannot be higher than N7 (Appendix C).

• In case of no tumor or lymph node involvement below the diaphragm, the most proximal involved lymph node station cannot be higher than N4 (Appendix C).

• Age ≥ 18 years. For patients aged 70 years or older, a geriatric screening tool (G8) should be used to assess functioning across the domains. If a patient has a score of 14 or lower on the G8, a comprehensive geriatric assessment (CGA) should be done prior to inclusion (Appendix D).

• No prior abdominal, thoracic or cervical radiotherapy overlapping with the CROSS irradiation fields.

• No prior cytotoxic chemotherapy for oesophageal cancer.

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1 (44).

• Weight loss \<10%.

• Adequate cardiac and respiratory function (cardiac or pulmonary function tests such only necessary in symptomatic patients).

• Adequate bone marrow function (White Blood Cells \>3x109/L; Haemoglobin \>5.5 mmol/L; platelets \>100x109/L). In the event of transfusions, the last red blood cell transfusion should be more than 2 weeks before inclusion.

• Adequate renal function (Glomerular Filtration Rate \>50 ml/min) or serum creatinine ≤1.5 x upper limit of normal (ULN) and adequate liver function (total bilirubin \<1.5x Upper Level of Normal (ULN); Aspartate transaminase (AST) \<2.5x ULN and Alanine transaminase (ALT) \<3x ULN.

• A negative serum pregnancy test in women of child-bearing potential during screening period.

• Use of adequate contraception during the study up to 3 months after the end of the study.

• Written informed consent and ability to understand the nature of the study and the study-related procedures and to comply with them.

Locations
Other Locations
Netherlands
Ziekenhuisgroep Twente
NOT_YET_RECRUITING
Almelo
Amsterdam UMC
NOT_YET_RECRUITING
Amsterdam
Antoni van Leeuwenhoek/Nederlands Kanker Instituut
NOT_YET_RECRUITING
Amsterdam
Gelre ziekenhuis
NOT_YET_RECRUITING
Apeldoorn
Catharina Ziekenhuis
NOT_YET_RECRUITING
Eindhoven
Frisius medisch centrum
NOT_YET_RECRUITING
Leeuwarden
Leids Universitair Medisch Centrum
NOT_YET_RECRUITING
Leiden
Radboud Universitair Medisch Centrum
NOT_YET_RECRUITING
Nijmegen
Erasmus Medical Centre
RECRUITING
Rotterdam
Elisabeth Tweesteden Ziekenhuis
NOT_YET_RECRUITING
Tilburg
Contact Information
Primary
Bianca Mostert, MD, PhD
b.mostert@erasmusmc.nl
+31107041906
Backup
Esmee A de Bruijn, MD
e.debruijn@erasmusmc.nl
0031107034523
Time Frame
Start Date: 2025-09-12
Estimated Completion Date: 2029-12-01
Participants
Target number of participants: 216
Treatments
Experimental: TNT FLOT-CROSS
Patients allocated to the TNT FLOT-CROSS arm will be treated with 4 cycles of FLOT chemotherapy followed by a response evaluation consisting of a CT-scan and upper endoscopy with bite-on-bite biopsies of the primary tumor site and of any other suspected lesions in the esophagus. Patients with distant metastases will go off-study. All other patients will proceed to CROSS chemoradiotherapy.
Experimental: TNT CROSS-FLOT
Patients allocated to the TNT CROSS-FLOT arm will be treated with CROSS chemoradiotherapy followed by a response evaluation consisting of a CT-scan and upper endoscopy with bite-on-bite biopsies of the primary tumor site and of any other suspected lesions in the esophagus. Patients with distant metastases will go off-study. All other patients will proceed to FLOT chemotherapy.
Related Therapeutic Areas
Sponsors
Leads: Erasmus Medical Center

This content was sourced from clinicaltrials.gov

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