The Value of 68Ga-grazytracer PET in Monitoring Responses to Immunotherapy of Advanced Soft Tissue Sarcomas

December 9, 2024 updated by: Hu Jiajia, Ruijin Hospital
This study aims to investigate the value of 68Ga-grazytracer in predicting the efficacy of immunotherapy for advanced soft tissue sarcomas.

Study Overview

Status

Recruiting

Detailed Description

The investigators will number all participants, create a medical record file, and record their basic information (gender, age) as well as contact information and medical history information. All participants will undergo a 68Ga-grazytracer PET/CT after 3 cycles of immunotherapy to evaluate response. The imaging response measurements will be compared with the histopathological or clinical assessment results as gold standard.

Study Type

Observational

Enrollment (Estimated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Shanghai
      • Shanghai, Shanghai, China, 200001
        • Recruiting
        • Ruijin Hospital affiliated to Shanghai Jiao Tong University of Medicine
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Inpatients and outpatients at Ruijin Hospital who meet the inclusion criteria.

Description

Inclusion Criteria:

  1. Pathological and clinical diagnosis of advanced soft tissue sarcomas, pathological types include: fibrosarcoma, liposarcoma, undifferentiated pleomorphic sarcoma, epithelioid sarcoma, rhabdomyosarcoma, synovial sarcoma, alveolar soft-part sarcoma, leiomyosarcoma, clear cell sarcoma, malignant schwannoma, angiosarcoma.
  2. Consider immunotherapy or combined immunotherapy based on clinical judgement.
  3. Signed and dated informed consent form.
  4. Commitment to comply with research procedures and co-operation in the implementation of the full research process.
  5. Aged 6-80 years old.

Exclusion Criteria:

  1. Patients with serious illnesses that researchers consider unsuitable for participation in this clinical study. Such as severe heart and lung failure, severe bone marrow suppression, severe liver and kidney dysfunction, etc.
  2. Intestinal perforation, complete intestinal obstruction
  3. Pregnant women and women who may be pregnant, women who are breastfeeding.
  4. Non-compliant person

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Diagnosis of advanced soft tissue sarcomas
Patients diagnosis of advanced soft tissue sarcomas require immunotherapy or combination immunotherapy after evaluation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Standardized uptake value(SUV)
Time Frame: up to about 10 weeks
SUV of 68Ga-grazytracer uptake on PET/CT images for tumor lesions
up to about 10 weeks
Target-to-background ratio(TBR)
Time Frame: up to about 10 weeks
68Ga-grazytracer uptake ratio of tumor lesions to mediastinum and liver blood pool on PET/CT images.
up to about 10 weeks
Evaluation the responses to immunotherapy of advanced soft tissue sarcomas
Time Frame: up to about 10 weeks
The value of 68Ga-grazytracer PET in monitoring responses to immunotherapy of advanced soft tissue sarcomas
up to about 10 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Progress free survival
Time Frame: 1 years
Progress free survival
1 years
Overall survival
Time Frame: 1 years
Overall survival
1 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 15, 2024

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

July 31, 2027

Study Registration Dates

First Submitted

October 14, 2024

First Submitted That Met QC Criteria

October 14, 2024

First Posted (Actual)

October 16, 2024

Study Record Updates

Last Update Posted (Estimated)

December 13, 2024

Last Update Submitted That Met QC Criteria

December 9, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Advanced Soft Tissue Sarcomas

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