About this trial
The main purpose of this study is to explore the feasibility of selecting treatment plans based on genomic variations guided by MTB in patients with advanced refractory solid tumors.
Eligibility criteria
Qualifiers
Recurrent or metastatic malignant solid tumors diagnosed by histology or cytology;
ECOG score 0-4 (3-4 points only for patients with tumor burden);
Those who fail or cannot tolerate standard treatment, or those who refuse standard treatment;
At least one measurable lesion that meets the RECIST 1.1 standard;
Disqualifiers
Patients who have actively undergone or are currently participating in clinical trials for treatment;
Serious or uncontrolled medical diseases (i.e. uncontrolled diabetes, chronic kidney disease, chronic lung disease or uncontrolled active infection, mental diseases/social conditions that limit the compliance with the research requirements) that the researchers think will confuse the research treatment response analysis;
Pregnant or lactating patients, or any patients with fertility, have not taken appropriate pregnancy prevention measures.
Trial design
Treatments tested in this trial
- Olaparib tablet
- Temozolomide capsule
- Anlotinib
- Trametinib tablet
- Dabrafenib
- Vebreltinib Enteric Capsules
- Alpelisib Pill
- Sacituzumab Govitecan-Hziy 180 MG
- Lenvatinib Capsules
- Pazopanib Pill
- Palbociclib Pill
- Chidamide
- PD-1/PD-L1/PD-1&CTLA4 inhibitor
- Target Gene
Treatment groups
9
Treatment groupsSee each treatment group below.