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Completed

NCT Number: NCT02287129

Evaluation for the Individualization of Therapy in Adenocarcinomas of the Gastroesophageal Junction

Metabolic and Molecular Response evaluation for the individualization of therapy in adenocarcinomas of the gastroesophageal junction by evaluation of the R0 resection rate for patients with metabolically (ie, according to PET criteria) chemotherapy-resistant locally advanced AEG, who receive an intensified neoadjuvant chemoradiotherapy (INRCT). Additonal efforts will be done by investigation of molecular and metabolic biomarkers in relation to their predictive and prognostic value by correlating them with histopathologic responses and clinical outcome in an exploratory approach.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

2nd department of the Medical Clinic of the Technical University Munich

Munich, Bavaria, 81675, Germany

About this study

Adenocarcinomas of the esophagus and the esophagogastric junction (AEG) are clinically-topographically divided into subtypes I-III according to the Siewert classification and show an increased incidence. Neoadjuvant and/or perioperative chemotherapy or preoperative radiochemotherapy is well established in the management of AEG. However, a significant number of patients do not respond to preoperative chemotherapy, suffering from toxicity and facing a worse outcome due to lower R0 resection rates. Previous results from the MUNICON-1 and MUNICON-2 trials have shown that PET-based therapy individualization can be successfully integrated in neoadjuvant treatment algorithms.

Tumor-free resection edges (R0) constitute the greatest prognostic advantage in terms of overall survival. However, the R0 resection rates for patients who, according to early metabolic response evaluation, have not responded to the chemotherapy, have not been satisfactory, even after conversion to an - albeit moderate - radiochemotherapy in the MUNICON-2 trial. Thus, this patient population (so-called non responders) so far lack a beneficial neoadjuvant therapy modality.

Based on these results, the primary goal of MEMORI study is to evaluate the R0 resection rate for patients with metabolically (ie, according to PET criteria) chemotherapy-resistant locally advanced AEG, who receive an intensified neoadjuvant chemoradiotherapy (INRCT). Secondary it is planned to investigate molecular and metabolic biomarkers in relation to their predictive and prognostic value by correlating them with histopathologic responses and clinical outcome in an exploratory approach.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed AEG I-III
  • Potentially R0 - resectable AEG and primary tumor category UT2 -4
  • Functional operability : Exclusion of OP - limiting comorbidities
  • Intense FDG tracer uptake of the tumor during Baseline PET/CT examination and thus suitability for monitoring and early response prediction by FDG - PET ( [ 18F ] - FDG uptake in the tumor at baseline > 1.35 x liver SUV + 2 x standard deviation of the liver SUV)
  • Performance status (ECOG ) 0 or 1
  • Age : ≥ 18
  • creatinine clearance > 60ml/min measured in a 24 h urine or calculated with the Cockgroft -Gault formula
  • bilirubin ≤ 1.5 times upper limit of normal , serum transaminases (GOT

/ GPT ) ≤ 3 times ULN

  • leukocytes ≥ 3.5 g / l, platelet ≥ 100 g / l
  • Negative pregnancy test (determination of beta- HCG in urine or serum) in women of childbearing potential
  • A signed consent form after implementation of medical education

Exclusion criteria

  • Existing distant metastases (M1b)
  • Tumor infiltration into the tracheobronchial system
  • Previous radiotherapy targeted at the thorax
  • Lack of ability of the patient to adhere to the protocol rules
  • Manifest heart failure despite optimal medication> NYHA I
  • existing angina pectoris at rest or undergoing stress without clarification via interventional cardiology and / or myocardial infarction within the last 6 months
  • Existing pregnancy or lactation
  • childbearing or fertility without using recognized safe methods of contraception
  • Coexisting other malignant diseases with the exception of a non-melanomatuous, localized skin tumor or carcinoma in situ of the cervix
  • absence of a signed consent form

Treatment and study plan

Oxaliplatin

Drug

130 mg/m2

Other names: Oxaliplan

Epirubicin

Drug

50 mg/m2

Other names: Epi Teva

Capecitabine

Drug

625 mg/m2

Other names: Xeloda

5-FU

Drug

200 mg/m2

Other names: 5-FU medac

carboplatin

Drug

2 mg/ml min

Other names: Carboplatin SUN

paclitaxel

Drug

50 mg/m2

Other names: Taxomedac

Radiation

Radiation

total dosage 41,4 Gy

Other names: intensitive neoadjuvant radiochemotherapy (INRCT)

Biopsy

Procedure

translational analysis

Other names: esophagogastroduodenoscopy

Primary outcomes

  1. R0 resection rate

    Time frame: 1 day of surgery (in between day 28 to day 43 after radio-chemotherapy)

    R0 resection rate of patients suffering from metabolically (following PET criteria) chemotherapy-resistant, locally advanced AEG, who receive a more intensive neoadjuvant radio-chemotherapy (INRCT)

Secondary outcomes

  1. Regression

    Time frame: 1 day of surgery (in between day 28 to day 43 after radio-chemotherapy)

    Histological regression defined by Becker Criteria

  2. Overall survival

    Time frame: from day 0 to follow up visit 6 (24 months after surgery)

    Overall survival defined as period from start of study to death (if necessary censored by end of follow-up period)

  3. Disease-free survival

    Time frame: from day 0 to follow up visit 6 (24 months after surgery)

    Disease-free survival, defined as period from start of study to earlier occurring event: death or relapse until end of follow-up; Relapse will be separated into events of "local failure", "distant failure" and "local and distant failure"

  4. QLQ-C30

    Time frame: from day 0 to follow up visit 6 (24 months after surgery)

    Quality of life, analyzed via EORTC QLQ-C30 questionnaires

  5. Metabilic response rate

    Time frame: from day 0 to one time point of time period day 14 to 28 after chemotherapy

    Metabolic response rate under neoadjuvant chemotherapy

  6. Translational analysis

    Time frame: 1 day of surgery (in between day 28 to day 43 after radio-chemotherapy)

    Translational analysis for identification of tumor determinants relevant for prognosis and therapy

  7. Adverse Events

    Time frame: from day 0 to follow up visit 6 (24 months after surgery)

    Occurence of AEs

  8. QLQ-OG25

    Time frame: from day 0 to follow up visit 6 (24 months after surgery)

    Quality of life, analyzed via EORTC QLQ-OG25 questionnaires

Sponsors and collaborators

Lead sponsor

Technical University of Munich

Other

Registry information

Official study title

Metabolic and Molecular Response Evaluation for the Individualization of Therapy in Adenocarcinomas of the Gastroesophageal Junction

Acronym: MEMORI

Important dates

Study start
2014
Primary completion
2020
Study completion
2020
First posted
Nov 10, 2014
Registry last updated
Nov 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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