Study Hypothesis: PANCHO is a prospective randomized, predictive marker study, evaluating the interaction between the potential predictive marker 'p53 genotype' and response to induction chemotherapy in patients with esophageal cancer considered resectable. 170 patients with measurable disease will be enrolled in this study. After testing the marker genotype (two genotypes: p53 normal or p53 mutant) patients will be stratified according to histological subtype only (adeno- or squamous cell carcinoma) and will be randomly assigned to receive 3 cycles of either 5-fluorouracil (5FU)/cisplatin or docetaxel monotherapy as neoadjuvant therapy. All patients will be rendered to subsequent surgery in order to assess both clinical and pathohistological response.
PANCHO will test the hypothesis that p53 genotype is predictive for response to chemotherapy. The study uses the marker by treatment interaction design. In this design, we assume that the status of the marker splits the whole population into two distinct groups (p53 normal versus p53 mutant). Patients in each marker group are randomly assigned to two different treatments, and planned statistical analysis is to test whether one treatment is superior to the other within each marker group separately. The marker information but not the treatment is blinded to the patient and the investigators.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
170
5 FU 1000mg/m2; days 1-5; 3 cycles: q21 Cisplatin 80mg/m2; day 1; 3 cycles: q21
Docetaxel 75mg/m2, day 1; 3 cycles; q21
Landesklinikum St. Pölten
Sankt Pölten, Lower Austria, Austria
Landesklinikum Wiener Neustadt
Wiener Neustadt, Lower Austria, Austria
Rudolfstiftung
Vienna, State of Vienna, Austria
SMZ OST
Vienna, State of Vienna, Austria
Wilhelminenspital
Vienna, State of Vienna, Austria
Medical University Innsbruck
Innsbruck, Tyrol, Austria
Landesklinikum Feldkirch
Feldkirch, Vorarlberg, Austria
Landeskrankenhaus Leoben
Leoben, Austria
Krankenhaus der Elisabethinen
Linz, Austria
Krankenhaus der Barmherzigen Brüder
Stankt Veit, Austria
...and 3 more locations
Tumor response (clinical and pathological) to neoadjuvant treatment in relation to p53 genotype
Time frame: 12 weeks
Complete pathological response and relation to p53 genotype
Time frame: 12 weeks
Complete tumor resection rate
Time frame: 12 weeks
Perioperative morbidity and mortality
Time frame: 16 weeks
Disease free and overall survival and relation to p53 genotype
Time frame: 2 years
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