NSCLC Relapse Therapy After Surgery and Peri-operative Chemotherapy

You may not be if

• Previous history of adjuvant or neoadjuvant chemotherapy (at least 2 full cycles of a platinum containing regimen)
• Initial stage pT1N0 to pT3N2 (TNM classification 1999), complete resection. T4 tumours (several nodules in the same lobe) and M1 tumours (several nodules in the same lung) N0-2 completely resected are allowed to inclusion. Histological complete response tumours (pT0N0) after neoadjuvant chemotherapy are allowed to inclusion.
• At least one unidimensionally measurable disease (RECIST criteria) (lesions must have clearly defined margins on X-ray, CT-scan, MRI or ultra-sound (US) examination and should measure at least 1 cm if assessed by CT, MRI or US and at least 2 cm if assessed by X-ray, target lesions should be selected outside a previously irradiated field ). PET scans and ultra sonography are not allowed
• ECOG Performance status 0 to 1).
• Patients with adequate biological functions:
• Written informed consent from patient.
• The effects of docetaxel, cisplatin and carboplatin on the developing human fetus at the recommended therapeutic dose are unknown. For this reason and because docetaxel, cisplatin and carboplatin as well as other therapeutic agents used in this trial are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
• Life expectancy \> 12 weeks
• Patient compliance and geographic proximity that allow adequate follow-up.
• Patient affiliated to a social insurance program
• Previous treatment with docetaxel.
• Hypersensitivity to docetaxel, cisplatin, carboplatin or polysorbate 80 (excipient).
• Previous history of cancer other than Non small cell lung cancer, in situ carcinoma of the uterine cervix and basal cell carcinoma of the skin.
• Patients previously treated by an investigational agent in the last 30 days.
• Patient treated with preoperative platin based chemotherapy, achieving a progression of disease after treatment evaluation.
• Patients non responders to preoperative chemotherapy and whose tumor specimen did not disclose any necrosis nor tumoral modification thus confirming the lack of chemosensitivity to platin based chemotherapy
• Patient treated with platin based adjuvant chemotherapy, relapsing within the first 6 months after surgery.
• Patients with a peripheral neuropathy grade CTC \>= 2
• Patients unable to fulfill protocol requirements
• Serious concomitant morbidity incompatible with the study (at the discretion of the investigator).
• Relapse within the month following lung cancer resection or adjuvant chemotherapy
• Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.
• Significant loss of weight (\> 10 %) in the 6 weeks preceding patient selection.
• Concomitant administration of another anti cancer treatment
• Pregnant women are excluded from this study. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother, breastfeeding should be discontinued.
• Patient under legal protection.