Uterine sarcomas constitute a rare group of neoplasms characterized by an aggressive clinical course and poor prognosis. It is this rarity that has resulted in clinical-trial reports and literature reviews including a broad range of histological subtypes of sarcoma. This has a detrimental effect on interpretation and application of the results; the pathological subtype demands a tailored approach. Surgical resection remains the mainstay of treatment for non metastatic uterine sarcomas. Although adjuvant radiation therapy has reportedly been of little survival value, it appears to improve local control and may delay recurrence. The role of adjuvant chemotherapy has yet to be established; however, bearing in mind the limitations and assumptions in the pooling of data the therapeutic options should be based on the pathological subtype. Considering the poor overall survival in uterine sarcomas, the need for new therapeutic agents is critical. New drugs with possible activity in uterine sarcomas include trabectedin, temozolomide, liposomal doxorubicin and gemcitabine.
Isabelle Ray‐Coquard, Paolo G. Casali, Sabrina Croce, Fiona M. Fennessy, D. Fischerová, Robin L. Jones, Roberta Sanfilippo, Ignacio Zapardiel, Frédéric Amant, Jean Yves Blay, Javier Martín‐Broto, Antonio Casado, Sarah Chiang, Angelo Paolo Dei Tos, Rick L. M. Haas, Martee L. Hensley, Peter Hohenberger, Jae‐Weon Kim, Se Ik Kim, Mehmet Mutlu Meydanlı, Patricia Pautier, Albiruni R. Abdul Razak, Jalid Sehouli, Winan J. van Houdt,
Discussion(0)
No comments yet. Be the first to comment.