A Safety Study Utilizing Yondelis and Doxorubicin in Patients With a Type of Cancer Called Soft Tissue Sarcoma
NCT00102609
Neoplasms, Neoplasms by Histologic Type
View Trial DetailsNCT Number: NCT06749600
This observational study aims to gather comprehensive data on primary ovarian leiomyosarcoma (POLMS). This extremely rare malignancy accounts for less than 3% of primary ovarian malignancies and has an incidence of only 1% among ovarian cancers. This national, retrospective and prospective multicenter study will collect and analyze historical cases of POLMS with remote diagnoses accessed through clinical case reviews and newly identified cases. The study aims to expand a previously identified series of 113 cases described in the literature, uncovering patterns in diagnosis, treatment, and outcomes and ultimately establishing evidence-based guidelines for the optimal management of this rare and aggressive cancer.
Interested in participating?
Request Info18 year–99 year
Female
Observational
AOU Policlinico di Modena, Modena, Italy
This study adopts a national, multicenter, observational design, incorporating both retrospective and prospective methodologies to collect and analyze primary ovarian leiomyosarcoma (POLMS) cases. The retrospective component will include cases diagnosed since 1980, leveraging institutional archives and clinical case reviews.
Data collection will be standardized using an electronic Case Report Form (eCRF) implemented on REDCap. All data will be centralized for uniformity and undergo rigorous validation to ensure consistency across centers. Findings will be reported in aggregated form to preserve patient confidentiality.
The study will gather extensive data points, including:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 3 years observation period
Correlation between survival outcomes and treatments (type of surgery ,type of chemotherapy, hormone therapy, radiotherapy).
Time frame: through study completion, an average of 1 year
Number of mitotic figures and levels of Ki67 expression in immunohistochemical staining
Time frame: 3 years observation period
Correlation between survival outcomes and mitotic index
Time frame: 3 years observation period
Time from diagnosis to death from any cause, measured in months.
Time frame: 3 years observation period
Time from diagnosis to disease progression or death, whichever occurs first, measured in months.
Contact information is provided by the study sponsor or research team.
Azienda USL Reggio Emilia - IRCCS
Other Gov
Acronym: POLMS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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