MEMORI: Evaluation for the Individualization of Therapy in Adenocarcinomas of the Gastroesophageal Junction
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Non-Responder Oxaliplatin Epirubicin Capecitabine 5-FU Carboplatin Paclitaxel Radiation Biopsy |
Drug: Oxaliplatin
130 mg/m2
Other Names:
Drug: Epirubicin
50 mg/m2
Other Names:
Drug: Capecitabine
625 mg/m2
Other Names:
Drug: 5-FU
200 mg/m2
Other Names:
Drug: Carboplatin
2 mg/ml min
Other Names:
Drug: Paclitaxel
50 mg/m2
Other Names:
Radiation: radiation
total dosage 41,4 Gy
Other Names:
Procedure: Biopsy
translational analysis
Other Names:
|
| Active Comparator: Responder Oxaliplatin Epirubicin Capecitabine 5-FU Biopsy |
Drug: Oxaliplatin
130 mg/m2
Other Names:
Drug: Epirubicin
50 mg/m2
Other Names:
Drug: Capecitabine
625 mg/m2
Other Names:
Drug: 5-FU
200 mg/m2
Other Names:
Procedure: Biopsy
translational analysis
Other Names:
|
Outcome Measures
Primary Outcome Measures
- R0 resection rate [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 Outcome Measures
- Regression [1 day of surgery (in between day 28 to day 43 after radio-chemotherapy)]
Histological regression defined by Becker Criteria
- Overall survival [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)
- Disease-free survival [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"
- Quality of life [from day 0 to follow up visit 6 (24 months after surgery)]
Quality of life, analyzed via EORTC QLQ-C30 and EORTC QLQ-OG25 questionnaires
- Metabilic response rate [from day 0 to one time point of time period day 14 to 28 after chemotherapy]
Metabolic response rate under neoadjuvant chemotherapy
- Translational analysis [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
- Adverse Events [from day 0 to follow up visit 6 (24 months after surgery)]
Occurence of AEs
Eligibility Criteria
Criteria
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
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | 2nd department of the Medical Clinic of the Technical University Munich | Munich | Bavaria | Germany | 81675 |
Sponsors and Collaborators
- Technische Universität München
Investigators
- Principal Investigator: Jens Siveke, Prof. Dr., II. Medizinische Klinik, Klinikum rechts der Isar (MRI) der TUM,Ismaninger Str. 22
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MEM-0000-SIV-0028-I