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A registry study of pleuropulmonary blastoma and Dicer 1 related conditions

A registry study of pleuropulmonary blastoma and Dicer 1 related conditions

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024756
Enrollment
Unknown
Registered
2019-07-26
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pleuropulmonary blastoma

Interventions

Case series:Nil

Sponsors

National Center for Children's Health; Capital Medical University, Beijing Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: This study plans to recruit patients from various children's cancer centers in China. Those who meet one of the following conditions will be registered. Eligible diagnoses include SUSPECTED OR CONFIRMED: 1) Pleuropulmonary blastoma (PPB); 2) varian Sertoli-Leydig cell tumor or gynandroblastoma; 3) Gynandroblastoma; 4) Renal sarcoma; 5) Pulmonary sarcoma; 6) Embryonal rhabdomyosarcoma of the female genitourinary tract (ovary, fallopian tube, uterus); 7) Any other cancer documented by genetic testing to be DICER1-related; Prior therapy: There are no prior therapy restrictions; Be able to provide informed consent.

Exclusion criteria

Exclusion criteria: Patients who may not be able to comply with the protocol, who are unable to cooperate or patients who are believed that other conditions are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Overall survival;Disease free survival;

Secondary

MeasureTime frame
best overall response to chemotherapy;

Countries

China

Contacts

Public ContactXiaoli Ma, Qi Zeng

National Center for Children's Health; Capital Medical University, Beijing Children's Hospital

mxl1123@vip.sina.com+86 010-59617612

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026