Carcinosarcomas (CS) in gynecology are very infrequent and represent only 2â5% of uterine cancers. Despite surgical cytoreduction and subsequent chemotherapy being the primary treatment for uterine CS, the overall five-year survival rate is 30 ± 9% and recurrence is extremely common (50â80%). Due to the poor prognosis of CS, new strategies have been developed in the last few decades, targeting known dysfunctional molecular pathways for immunotherapy. In this paper, we aimed to gather the available evidence on the latest therapies for the treatment of CS. We performed a systematic review using the terms âuterine carcinosarcomaâ, âuterine Malignant Mixed Müllerian Tumorsâ, âtarget therapiesâ, âangiogenesis therapyâ, âcancer stem cell therapyâ, âprognostic biomarkerâ, and ânovel antibody-drugâ. Based on our results, the differential expression and accessibility of epithelial cell adhesion molecule-1 on metastatic/chemotherapy-resistant CS cells in comparison to normal tissues and Human Epidermal Growth Factor Receptor 2 (HER2) open up new possibilities in the field of target therapy. Nevertheless, future investigations are needed to clarify the impact of these new therapies on survival rate and medium-/long-term outcomes.
Target therapies for uterine carcinosarcomas: Current evidence and future perspectives
Vitale, Salvatore Giovanni;La Rosa, Valentina Lucia
;Valenti, Gaetano;Sapia, Fabrizio;Sarpietro, Giuseppe;Tropea, Alessandro;
2017-01-01
Abstract
Carcinosarcomas (CS) in gynecology are very infrequent and represent only 2â5% of uterine cancers. Despite surgical cytoreduction and subsequent chemotherapy being the primary treatment for uterine CS, the overall five-year survival rate is 30 ± 9% and recurrence is extremely common (50â80%). Due to the poor prognosis of CS, new strategies have been developed in the last few decades, targeting known dysfunctional molecular pathways for immunotherapy. In this paper, we aimed to gather the available evidence on the latest therapies for the treatment of CS. We performed a systematic review using the terms âuterine carcinosarcomaâ, âuterine Malignant Mixed Müllerian Tumorsâ, âtarget therapiesâ, âangiogenesis therapyâ, âcancer stem cell therapyâ, âprognostic biomarkerâ, and ânovel antibody-drugâ. Based on our results, the differential expression and accessibility of epithelial cell adhesion molecule-1 on metastatic/chemotherapy-resistant CS cells in comparison to normal tissues and Human Epidermal Growth Factor Receptor 2 (HER2) open up new possibilities in the field of target therapy. Nevertheless, future investigations are needed to clarify the impact of these new therapies on survival rate and medium-/long-term outcomes.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.