Myocet ® - Carboplatine in Ovarian Cancer in Relapse, Sensitive to the Platinum (MYCA)

ARCAGY/ GINECO GROUP

Status and phase

Completed

Phase 2

Phase 1

Conditions

Ovarian Cancer

Treatments

Drug: carboplatin and liposomal doxorubicin

Study type

Interventional

Funder types

Other

Identifiers

NCT01705158

MYCA (GINECO-OV220)

2012-001999-10 (EudraCT Number)

Details and patient eligibility

About

The purpose of this study is to determine the efficacy and the safety of the association of carboplatine and liposomal doxorubicin in patient with ovarian cancer in relapse, sensitive to platin.

Full description

In front of a shortage of Caelyx, the implementation of an alternative treatment must be considered to treat patients with ovarian cancer in relapse, sensitive to platin: associate the carboplatin with another drug of the family of the doxorubicin: liposomal doxorubicin (Myocet®).

Enrollment

87 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

First or second relapse of a carcinoma of the ovary, the fallopian tubes or the peritoneal tissue histological proved.
Interval without progress > 6 months after the last administration of a salt of platinum(deck).
Measurable Disease (according to the criteria RECIST 1.1) or an assessable disease according to CA-125 (according to the criteria of the GCIG).
Satisfactory biological Balance sheet(Assessment), according to the following criteria:
- Neutrophiles > 1,5x 109/L, Plaques > 100 x 109/L, Haemoglobin > 9,0 g/dL.
- Bilirubine < 1.5 x LSN (Normal Superior Limit), transaminases and alkaline phosphatase < 2. 5 x LSN.
- Creatinin clearance > 50 mL/min calculated according to the formula of Cockroft-Gault or MDRD.
Performance status < 2.
Life expectancy of at least 12 weeks.
Age > 18 years.
Capacity to follow the protocol.
Consent signed before any procedure of inclusion.
Membership in a national insurance scheme.

Exclusion criteria

Tumor of mild histology or borderline, or malignant not epithelial tumor of the ovary, the fallopian tubes or the peritoneal tissue(eg. tumor of germ cells, tumor of the sexual cords and the stroma).
History of abdominal or pelvic radiotherapy.
Patient having received more than 2 lines of chemotherapy.
Patient in 3rd relapse or more.
History of another malignant tumor during the last 5 years, with the exception of a carcinoma in situ by the neck of the womb or by a squamous-cell carcinoma of the skin treated in a adequate way or any solid tumor considered in forgiveness completes without relapse for at least 5 years.
Patients having a stubborn illness in the platinum, (eg. progress during the last chemotherapy or in 6 months following the last administration of platinum).
Occlusive or sub-occlusive disease or presence of symptomatic intellectual metastases.
Heart disorder dissuading the use of an anthracycline.
Left venticular ejection fraction (LVEF) defined by MUGA/ECHO < 50%.
Wait presenting a severe infection.
Woman old enough to procreate not using adequate contraceptive method.
Concomitant disease not allowing a surgery and/or a chemotherapy.
Pathology severe or concomitant not compatible with the taking of the study treatment or the participation of the patient in the study.