a Prospective Registration Study for Patients With Advanced Refractory Solid Tumors

NCT ID: NCT05177666

Last Updated: 2022-01-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-12-30

Study Completion Date

2024-03-30

Brief Summary

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This is a prospective registration study for patients with advanced refractory solid tumors. Patients who meet the eligibility criteria will be included to participate in the study, and baseline information to be collected after signed informed consent. Patients will choose for themselves whether to carry out targeted therapy or other appropriate treatment methods. And we plan to follow up for at least 12 months or until disease progression or death.

Detailed Description

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1. Screen and enroll 120 patients with refractory solid tumors, and sign informed consents;
2. Extract the clinical data, including gender, age, disease diagnosis, past treatment history and genetic test results, etc.;
3. Take biopsy samples and perform NGS testing on patients. After discussion by the Molecular Steering Committee (MTB), the recommendations for treatment guidance will be given based on treatment guidelines and clinical experience;
4. The patient and the clinician jointly select the treatment plan and follow-up until the patient's disease progresses. The follow-up time will be 1 year;
5. During the follow-up period, clinical treatment and routine examination information of patients will be collected;
6. If the patient fails to receive molecular targeted therapy or they cannot tolerate the adverse reaction of the drug after adequate treatment, the clinician will evaluate whether a second NGS resistance test is needed or the participant may withdraw from the study.

Conditions

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Feasibility Effectiveness Safety Targeted Molecular Therapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Targeted therapy

Based on next-generation sequencing (NGS) detection, after discussion by the Molecular Steering Committee (MTB), intervention guidance suggestions are given based on domestic and foreign guidelines and clinical experience, and finally the patient and clinician jointly choose the treatment plan.

Intervention Type DRUG

Other Intervention Names

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Entratinib Cabotinib Aletinib Enmetrastuzumab Trastuzumab Pertuzumab Vemurafenib Atilizumab Bevacizumab Erlotizumab

Eligibility Criteria

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Inclusion Criteria

* Recurrent or metastatic malignant solid tumor confirmed by histology or cytology
* Disease progression or intolerance after receiving standard treatment
* With evaluable lesions (RECIST 1.1 standard)
* Tumor tissue pieces with sufficient formalin-fixed paraffin-embedded (FFPE) can be used for genetic testing
* ECOG PS score 0-4 (3-4 points only for patients with tumor burden)
* Sign the informed consent form

Exclusion Criteria

* The subject is participating in any other clinical research;
* Researchers believe that serious or uncontrolled medical diseases (ie uncontrolled diabetes, chronic kidney disease, chronic lung disease, or uncontrolled active infections, mental illnesses/social conditions that restrict compliance with research requirements) that will confuse the analysis of research treatment response ;
* Patients during pregnancy or lactation
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tianjin Happy Life Technology Co., Ltd.

INDUSTRY

Sponsor Role collaborator

The University of Hong Kong-Shenzhen Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Yongmei Li, MD

Role: PRINCIPAL_INVESTIGATOR

The University of Hong Kong-Shenzhen Hospital

Weitang Wu

Role: PRINCIPAL_INVESTIGATOR

The University of Hong Kong-Shenzhen Hospital

Central Contacts

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Zhiyuan Xu, MD

Role: CONTACT

+86-18307555170

References

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Reference Type RESULT
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Other Identifiers

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V1

Identifier Type: -

Identifier Source: org_study_id

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