Registry collecting health information about Desmoplastic Small Round Cell Tumor
Official title: Registry for Patients With Desmoplastic Small Round Cell Tumor
Run by Memorial Sloan Kettering Cancer Center · NCT04690374 · Data updated 2026-11-12
This study is collecting health information from people with Desmoplastic Small Round Cell Tumor to help researchers learn more about the condition and improve future treatments.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 250 (estimated) |
| Sponsor | Memorial Sloan Kettering Cancer Center Academic / other |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | December 22, 2020 |
| Main results expected | December 2027 |
| Study ends | December 2027 |
| Registry record updated | January 12, 2026 |
| Trial ID | NCT04690374 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals diagnosed with Desmoplastic Small Round Cell Tumor who are willing to share their clinical data.
✕Probably not a fit
Patients who are unwilling to provide consent or share their clinical data may not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry collects health information from individuals diagnosed with Desmoplastic Small Round Cell Tumor (DSRCT). The aim is to create a comprehensive database that enhances understanding of DSRCT and supports current and future research efforts. Participants of any age are encouraged to contribute their historical and longitudinal clinical data to aid in this initiative.
Why it matters
Potential benefit: If successful, this registry could lead to improved understanding and treatment options for patients with DSRCT.
How similar studies have gone: While this registry approach is common, the specific focus on DSRCT may provide novel insights that have not been extensively explored in previous studies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants must have a diagnosis of desmoplastic small round cell tumor * Participants may be of any age as long as the appropriate consent and assent may be obtained * Willing to provide historical and longitudinal clinical data Exclusion Criteria: * Participant unwilling to provide consent or share historical and longitudinal clinical data
Where it's running
-
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York, United States Recruiting
Study contacts
- Principal investigator: Emily Slotkin, MD — Memorial Sloan Kettering Cancer Center
- Study coordinator: Emily Slotkin, MD
- Email: slotkine@mskcc.org
- Phone: 1-833-675-5437
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Lurbinectedin plus irinotecan for advanced desmoplastic small round cell tumor
This study will try lurbinectedin combined with irinotecan in people 15 and older whose desmoplastic small round cell tumor has come back or spread after anthracycline chemotherapy.
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This study will try removing alpha/beta T cells and B cells from donor stem cell grafts and giving zoledronic acid to see if it helps children and young adults (6 months to 25 years) with relapsed or high‑risk solid tumors tolerate allogeneic transplant and reduce relapse.
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Using pasireotide to treat advanced synovial sarcoma and desmoplastic small round cell tumor
This study is testing if the drug pasireotide can help young people with advanced synovial sarcoma and desmoplastic small round cell tumors stay healthy longer after their initial treatments.
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MASCT-I plus doxorubicin and ifosfamide as first-line treatment for advanced soft tissue sarcoma
This trial will test whether adding MASCT-I to standard chemotherapy (doxorubicin and ifosfamide) helps adults with advanced soft tissue sarcoma respond better or live longer.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.