RecruitingPhase 2NCT06456359

Pasireotide as Maintenance Treatment in Synovial Sarcoma and Desmoplastic Small Round Cell Tumor

Pasireotide as Maintenance Treatment With Monthly Deep Intramuscular Injection in SSTR2/3/5-Expressing Synovial Sarcoma and Desmoplastic Small Round Cell Tumor


Sponsor

University Hospital Heidelberg

Enrollment

28 participants

Start Date

Dec 19, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

PAMSARC is a non-commercial interventional Phase 2 clinical trial of academic research institutions, with its primary goal being to improve medical treatment of fusion driven Desmoplastic small round cell tumor (DSRCT) and Synovial sarcoma (SySa) in young adults and adolsecents with male predominance. Current management of DSRCT and SySa includes chemotherapy, radiation and aggressive cytoreductive surgery. Despite advances in multimodal therapy, outcomes remain poor with frequent disease recurrence and very limited options for patients with advanced disease. Selected somatostatin receptor (SSTR) family members, i.e., SSTR2, SSTR3 and SSTR5, are frequently overexpressed in DSRCT and SySa, providing the rationale for treatment with somatostatin analogues (SSA). Pasireotide is a SSA with high affinity for SSTR1, -2, -3, and -5 and is approved for the treatment of Cushing's disease and acromegaly and has also shown activity in other cancers. In patients with advanced stage DSRCT and SySa, conventional chemotherapeutic approaches frequently lead to disease response, however, the duration of progression-free time after chemotherapy is short. The targeted approach with pasireotide after initial intensive multimodal treatment may have the potential to significantly improve outcome.


Eligibility

Min Age: 13 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a hormone-blocking drug called pasireotide as a maintenance therapy for two rare cancers — synovial sarcoma (a soft tissue cancer) and desmoplastic small round cell tumor (DSRCT). Maintenance therapy means treatment given to keep the cancer from coming back after the initial treatment has worked. **You may be eligible if...** - You have a confirmed diagnosis of DSRCT (at any stage) or synovial sarcoma (with metastatic or relapsed disease) - Your tumor shows high expression of specific receptors (SSTR2/3/5) determined by genetic testing - Your disease is stable or responding after completing standard treatment - You were profiled through a specific genomic research program (DKFZ/NCT/DKTK MASTER or INFORM) **You may NOT be eligible if...** - Your tumor does not show the required receptor expression - Your cancer is progressing on current treatment - You have not completed standard initial treatment Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGSignifor

Signifor 40 mg: each vial contains 40 mg pasireotide (as pasireotide pamoate). Signifor 60 mg: each vial contains 60 mg pasireotide (as pasireotide pamoate).


Locations(4)

National Center for Tumour Diseases, University Hospital Heidelberg

Heidelberg, Baden-Wurttemberg, Germany

Klinikum Stuttgart- Olga Hospital Zentrum für Kinder-, Jugend und Frauenmedizin

Stuttgart, Baden-Wurttemberg, Germany

Klinikum Stuttgart Studienzentrale Stuttgart Cancer Center, Tumorzentrum Eva-Mayr-Stihl

Stuttgart, Baden-Wurttemberg, Germany

Universitätsklinikum Essen Pädiatrische Hämatologie und Onkologie

Essen, North Rhine-Westphalia, Germany

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06456359


Related Trials