Squamous Cell Carcinoma
Conditions
Keywords
ESCC NAL-IRI
Brief summary
The aim of our study is to evaluate the efficacy and safety of NALIRI plus 5FU versus paclitaxel as a second-line therapy in patients with locally advanced or metastatic ESCC who had failed to cisplatin- or oxaliplatin-based first-line chemotherapy. The hypotheses are as follows: H0: the percentage of patients alive at 9 months of 40% is not useful. H1: the percentage of patients alive at 9 months of 60% is expected.
Detailed description
Principal objective: • To evaluate the survival of patients at 9 months Secondary objectives: * Progression-free survival (PFS) (clinical and/or radiological) * Overall survival (OS) * Best response rate during treatment according to RECIST 1.1 criteria (according to the investigator and the centralised review committee) * Toxicity (NCI CTC 4.0) * Quality of life (QLQ-C30 and OES18 questionnaires of the EORTC) Arm A (experimental arm): Nal IRI plus LV5-FU (D1=D28) Nal-IRI: 70 mg/m² intravenous over 90 minutes Followed by intravenous folinic acid 400 mg/m² over 30 minutes or L-folinic acid: 200 mg/m² over 30 minutes And then 5-FU 2,400 mg/m² over 46 hours on D1 to D14 Arm B (control arm): PACLITAXEL (D1=D28) Paclitaxel: 80 mg/m² at D1, D8 and D15 Patients will be randomized in a 1:1 ratio using the minimisation technique. Randomisation will be stratified based on the following factors: * Centre * WHO performance status: 0/1 versus 2 An analysis of circulating tumour DNA (using genetic mutations, in particular, TP53, and DNA methylation analyses) will be performed before the 1st cycle of treatment and at D28, in order to look for factors predictive of response to treatment (decrease in unbound DNA).
Interventions
DRUGOnivyde
onivyde will be administered first, followed by folinic acid or L-folinic acid and then 5-FU at D1 and D14.
DRUGPaclitaxel
Paclitaxel : 80 mg/m2 IV during 60 minutes at D1, D8 and D15
Sponsors
Shire
Servier
Federation Francophone de Cancerologie Digestive
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
All initial characteristics will be described in the overall population and by treatment arm. Evaluation criteria related to efficacy and safety will be described by treatment arm. Initial characteristics of best response and toxicities will be evaluated using usual statistics: for quantitative variables: mean, standard deviation, median, interquartile interval and range and for qualitative variables: frequencies and percentages. For the primary evaluation end point, a one-sided 95% confidence interval (CI) will be calculated in the experimental arm.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically proven metastatic oesophageal squamous cell carcinoma * Patient in failure with 1st-line treatment with oxaliplatin or cisplatin. Patients presenting with resectable disease treated with surgery or neoadjuvant or adjuvant chemotherapy with oxaliplatin or cisplatin (with or without radiotherapy) can be included if a recurrence has occurred less than 6 months after the end of treatment * Age ≥ 18 years * Unresectable disease, measurable or not, according to RECIST 1.1 criteria * WHO performance status ≤ 2 * Neutrophils ≥ 1500/mm3 (without use of haematopoietic growth factors), platelets ≥ 100 000/mm3, haemoglobin ≥ 9 g/dl (blood transfusions are authorised for patients with a haemoglobin less than 9 g/dl) * Total bilirubin ≤ 2 x ULN (biliary drainage is authorised in case of a biliary obstruction); albumin ≥ 25 g/L; AST ≤ 2.5 x ULN, and ALT ≤ 2.5 x ULN (≤ 5 x ULN in case of hepatic metastases) * Creatinine clearance ≥ 50 ml/min according to MDRD formula * A normal ECG or ECG with no clinically significant findings * Patient able to understand and to sign the informed consent form (or who has a legal guardian able to do so for him/him) * Women of childbearing potential must have a negative pregnancy blood or urine test within 7 days prior to inclusion * Women of childbearing potential, as well as men (who have sexual relations with women of childbearing potential) must agree to use an effective method of contraception throughout this study and during the 6 months following administration of the last dose of the study medicinal product * Patient who is a beneficiary of the Social security system * Patient for whom regular follow-up is possible.
Exclusion criteria
* Known brain or bone metastases * Clinically significant gastrointestinal disorders, including hepatic, haemorrhagic, inflammatory, obstructive disorders or diarrhoea \> grade 1 * History of chronic inflammatory bowel disease * Gilbert's syndrome * Interstitial lung disease * Treatment with St John's Wort * Medical history of Whipple procedure * Body mass index \< 18.5 kg/m2 * Combination with sorivudine and others analogues as brivudine (irreversibly inhibits the enzyme dihydropyrimidine dehydrogenase) * History of progressive cancer or in remission of less than 3 years duration (patients who present with a cancer in situ or basal cell or squamous cell skin cancer during the last 3 years are eligible). * Severe arterial thromboembolic events (myocardial infarction, unstable angina, stroke) less than 3 months before inclusion * NYHA class III or IV congestive heart failure, ventricular arrhythmia or uncontrolled blood pressure * Significant neuropathy ≥ grade 2 according to NCI CTCAE criteria (National Cancer Institute Common Terminology Criteria for Adverse Events) v.4.0. * Known hypersensitivity or allergy to a component of the medicinal products used in the study. * Known DPD deficiency
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| survival at 9 months | 9 months | The principal objective is to evaluate survival at 9 months in patients presenting with metastatic oesophageal squamous cell carcinoma (OSC) treated with Nal-IRI/LV5-FU or with paclitaxel. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival | 5 years | Clinical Progression-free survival and/or radiological Progression free survival will be evaluated |
| Overall survival (OS) | 1 year | evaluate the overall survival |
| Best response rate during treatment | 6 months | Best response rate during treatment according to RECIST 1.1 criteria (according to the investigator and with centralised review) |
| Toxicity (NCI-CTC v4) | 6 months | all observed toxicities, graded according to NCI-CTC v4 and the SAE |
| Quality of life (questionnaires) | 6 months | Quality of life (QLQ-C30 questionnaires of EORTC) and OES18 questionnaires of EORTC |
Countries
France
Outcome results
None listed