A 2 Stage Trial of Lenalidomide (REV) in Asymptomatic Ovarian Cancer Patients With Increasing CA 125 in Late Relapse

Inclusion Criteria:

Stage A: Patient:

* aged \> 18 years.
* with a histological proven diagnosis of epithelial cancer of the ovary, the fallopian tube or extra-ovarian papillary serous tumors.
* with asymptomatic disease in progression detected by increase of CA 125 levels according to GCIG criteria during systematic follow-up, with or without measurable lesions.
* with disease in progression \> 6 months after a first or second line including a platinum derivative. Patients should have received previously a taxane derivative.
* Adequate bone marrow, renal and hepatic function defined as: . WBC \> 3.0 x 109/L or Neutrophils (ANC) \> 1,5 x 109/L; Platelets \> 100 x 109/L; Hemoglobin \> 6 mmol/L (10,0 mg/dL); Bilirubin \< 2 x upper normal limit of normal range; Estimated glomerular filtration rate \> 50 ml/mn according to Cockroft-Gault formula.
* with ECOG performance status = 0 or 1.
* with a life expectancy of at least 16 weeks
* who have given their signed and written informed consent to participate in the trial after fully understanding the implication and constraints of the protocol.

Stage B: Patients

* aged \> 18 years.
* with a histological proven diagnosis of epithelial cancer of the ovary, the fallopian tube or extra-ovarian papillary serous tumors.
* with disease in progression \> 6 months after a first or second line including a platinum derivative. patients should have received previously a taxane derivative.
* Measurable disease by RECIST or evaluable disease by GCIG (CA-125).
* Patients included in stage A with disease in progression under lenalidomide could be eligible in phase B if they did not experience unacceptable toxicity under lenalidomide in stage A. Patients should stop lenalidomide for 7 days before entry in stage B (7 days wash out).
* Adequate bone marrow, renal and hepatic function defined as: . WBC \> 3.0 x 109/L or Neutrophils (ANC) \> 1,5 x 109/L; Platelets \> 100 x 109/L; Hemoglobin \> 6 mmol/L (10,0 mg/dL); Bilirubin \< 2 x upper normal limit of normal range; Estimated glomerular filtration rate \> 50 ml/mn according to Cockroft-Gault formula.
* with LVEF under normal range
* with ECOG performance status = 0 or 1.
* with a life expectancy of at least 16 weeks.
* who have given their signed and written informed consent to participate in the trial after fully understanding the implication and constraints of the protocol.

Exclusion Criteria:

* Ovarian tumors of low malignant potential (borderline tumors).
* Non-epithelial ovarian or mixed epithelial/non epithelial tumors (e.g. mixed Mullerian tumors).
* Patients with a prior diagnosis of any malignancy not cured by surgery alone less than 5 years before study entry (except in situ carcinoma of the cervix or adequately treated basal cell carcinoma of the skin).
* Patients who have received previous radiotherapy.
* Presence of symptomatic brain metastases.
* Patients with a history of seizure disorder or central nervous system disorders; pre-existing motor or sensory neurologic pathology or symptoms \> NCI-CTC grade 1.
* History of congestive heart failure (NYHA Classification \> 2, even if medically controlled. History of clinical and electrocardiographically documented myocardial infarction within the last 6 months. History of atrial or ventricular arrhythmias (≥ LOWN II).
* Thrombosis or anti-thrombosis treatment within 6 months.
* History of visceral bleeding, gastrointestinal ulcer in 6 months.
* Obstructive or sub-occlusive disease.
* Patients with severe active infection.
* Concurrent severe medical problems unrelated to malignancy which would significantly limit full compliance with the study or expose the patient to extreme risk or decreased life expectancy.
* Fertile women not using adequate contraceptive methods, or who are pregnant or breast feeding.
* Histories of allergy or sentimentality known about the similar chemical compounds in the carboplatine, either in the doxorubicine liposomale pégylée, or in one of the constituents of the lenalidomide.
* Patient having developed a knotty erythema characterized by a rash with desquamation during grip(taking) of thalidomide or a medicine similaire.
* Previous administration of lenalidomide.
* Seropositivity known about the virus of the human immunodeficiency (HIV), or pathology bound to the syndrome of acquired immunodeficiency (AIDS) or hepatitis activates type A, B or C.
* Administration of other simultaneous chemotherapeutic drugs, or hormonal therapy, or simultaneous radiotherapy during the study treatment period (hormone replacement therapy is allowed as are steroid antiemetics).
* Dementia or significantly altered mental status that would prohibit the understanding and giving of informed consent.