Uterine or Soft Tissue Leiomyosarcoma Clinical Trial
Randomised Phase III Multicentric Study Comparing Efficacy of Doxorubicin With Trabectedin Followed by Trabectedin in Non-progressive Patients Versus Doxorubicine Alone as First-line Therapy in Patients With Metastatic or Unresectable Leiomyosarcoma (Uterine or Soft Tissue)
The objective of LMS04 study is to better define the treatment strategy for patients with
metastatic leiomyosarcoma (uterine or soft tissue), as well as identifying the best first
line therapeutic option for these patients. LMS04 will test a new strategy for first line
therapy LMS sarcoma compare to the reference therapy (6 cycles of doxorubicin alone): the
interest of the association of trabectedin to doxorubicin in first line treatment followed
by trabectedin alone for non-progressive patients after 6 cycles of the association of
trabectedin and doxorubicin (the LMS02 design).
LMS04 will be the first phase III randomized study specifically dedicated to soft tissue leiomyosarcoma in first line metastatic disease.
It is planned to compare a new doxorubicin combination (including trabectedin) with very encouraging results followed by trabectedin maintenance therapy for non-progressive patients to doxorubicin alone. Prospective ancillary translational studies will attempt to define profiles of patients who could benefit from this new chemotherapy in an exploratory way.
The validation of a new first line option specific for LMS, identifying clinical factors that characterize aggressiveness and responsiveness to treatment aims to have an important in the spirit of personalized medicine in this rare and deadly disease.
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment