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NCT Number: NCT07593573

the Exploration of MTAP Deletion in Osteosarcoma by Immunohistochemistry

MTAP deletion frequently occurs in osteosarcoma, and PRMT5 has been identified as a synthetic lethal target for cancers with homozygous deletion of the MTAP gene, making it a promising target for anti-tumor drug development.This study aims to evaluate the overall status of MTAP deficiency in the tissues of osteosarcoma patients and its correlation with clinical features such as metastasis and immune subtypes by examining the MTAP protein expression levels in previous histological samples of the patients and combining this with their clinicopathological data.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

12 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Peking University People's Hospital

Beijing, Beijing Municipality, 100044, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • advanced recurrent and refractory osteosarcoma confirmed by histopathology;
  • initial treatment in the Orthopedic/Oncology Departments of Peking University People's Hospital or Peking University Shougang Hospital;
  • progression less than 6 months after first-line chemotherapy with a combination of high-dose methotrexate, doxorubicin, cisplatin and ifosfamide (first-line chemotherapy);
  • measurable lesions according to the Response Evaluation Criteria for Solid Tumors (RECIST 1.1) ;
  • Eastern Cooperative Oncology Group performance status ≤ 1 ;
  • acceptable haematologic, hepatic, and renal function.

Exclusion criteria

  • those who had been previously treated with antiangiogenic TKIs and single IE chemotherapy;
  • those who had severe or uncontrolled medical disorders that could jeopardize the outcomes of the study. These confounding conditions included, cardiac clinical symptoms or disease with left ventricular ejection fraction<50%, and hypertension that could not be well controlled with antihypertensive drugs.;
  • all patients were assessed by the sarcoma board including a thoracic surgeon with at least 10 years surgical experience. Patients with lung metastases only were carefully assessed for eligibility for metastasectomy, of whom those who were suitable for surgery were excluded from this study;
  • weight loss of 20% or more before illness;
  • brain or leptomeningeal metastasis;
  • surgical procedure or radiotherapy within 4 weeks of enrollment;
  • activegastroduodenal ulcer, previous condition associated with risk of bleeding or requiring anticoagulation;
  • proteinuria or hematuria, denutrition with albuminemia <25 g/L;
  • women who were pregnant or breast feeding, other malignancy;
  • positive HBV/HCV/HIV serology, and known allergy to the experimental agents.

Treatment and study plan

Primary outcomes

  1. Progression free survival

    Time frame: 2 years

    from the start of target treatment until disease progression or death, whichever came first.

Sponsors and collaborators

Lead sponsor

Peking University People's Hospital

Other

Collaborators

  • Sailan(Hangzhou)Biopharmaceutical Technology Co.,Ltd.

Registry information

Official study title

A Clinical Study on the Exploration of MTAP Deletion in Osteosarcoma Specimens by Immunohistochemistry

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 18, 2026
Registry last updated
May 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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