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Oncological Disease » Articles » Ovarian Cancer in Relapse: Medical Management Approaches
Thursday, 04 December, 2008



Ovarian Cancer in Relapse: Medical Management Approaches

Eric Pujade-Lauraine Département d’Hématologie et d’Oncologie Médicale, Hôpital Hôtel-Dieu, Paris, France and Centre Léon Bérard, Lyon, France , Jean-Paul Guastalla

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Conclusions

Significant progress has recently been made in defining the optimal therapeutic strategy for recurrent ovarian cancer. The combination of paclitaxel with carboplatin is currently considered as the standard chemotherapy for the treatment of relapsing patients with a therapy-free interval over six months. Regimens substituting new drugs such as gemcitabine or pegylated liposomal doxorubicin to paclitaxel in association with carboplatin may offer platinum-based combinations with better toxicity profile and quality–of–life. In addition, the availability of several new drugs with activity in ovarian cancer has allowed a better control of recurrences with survival prolongation.

Nevertheless, even these strategies may prove insufficiently effective, and continued study of novel therapies designed to target specific molecular mechanisms of tumour growth may ultimately be the only hope. We hope the next decade will yield significant progress in the treatment of this deadly disease.
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Author(s) Biography
Eric Pujade-Lauraine is the Head of the French GINECO Group devoted to clinical research in gynaecologic cancer. He is also the Head of the Medical Oncology Unit in the Department of Haematology- Medical Oncology at Hôpital Hôtel- Dieu in Paris, France. While receiving his medical degree from the University of Paris VI, he was an intern at Assistance Publique des Hôpitaux de Paris. He later earned his PhD from the University of Paris VI, where he is now a Professor of Medical Oncology. As well as serving on several advisory boards, Dr Pujade-Lauraine is also a member of the American Society of Clinical Oncology, the European Society for Medical Oncology, and the Gynecologic Cancer Intergroup.

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