Table.2:
Identifier | Cancer type | Exosome source | Treatment strategy |
---|---|---|---|
NCT01159288 | NSCLC | Tumor antigen-loaded DC-derived exosomes | Metronomic cyclophosphamide (mCTX) treatment followed by vaccinations with exosomes. Findings: mCTX inhibits immunosuppressive Treg fucntions and exosomes activate innate and adaptive immunity. |
NCT03985696 | Non-Hodgkin B-cell lymphoma | Exosomes purified from patients and cancer cells | CD20 and PDL1 expression in exosomes are analyzed to study their prognostic significance on patient outcome and rituximab response. |
NCT02869685 | NSCLC | Plasma | PDL1 levels in plasma exosomes are analyzed after 24h and 48h of radiotherapy. If PDL1 is upregulated, radiotherapy can be combined with immunotherapy to increase treatment efficacy. |
NCT02977468 | Triple negative breast cancer | Serum | Testing if pembrolizumab treatment alters the expression of immune tolerance markers like PDL1 in the primary tumor, circulating lymphocytes, and serum exosomes. |
NCT04427475 | NSCLC | Plasma | Exosomal PDL1 and mRNAs are analyzed in stage IV EGFR/ALK wild-type NSCLC patients before and after treatment with anti-PD1 (pabolizumab or nafulizumab) |
NCT02507583 | Malignant glioma | Tumor cells | Patients’ tumor cells are taken, treating them with investigational drug insulin-like growth factor receptor-1 Antisense Oligodeoxynucleotide (IGF-1R/AS ODN) and reimplanting into patients. As the tumor cells die inside the patient, they release tumor antigen containing exosomes, which can activate immune cells. |
NCT03854032 | Stage II-IV head and neck squamous cell cancer | Peripheral blood | Patients are treated with Nivolumab and BMS986205, an indoleamine 2, 3-dioxygenase 1 inhibitor (IDO1i). Exosomes abundance and composition before and after therapy are analyzed. |
NCT02535247 | NK and T cell non-Hodgkin lymphoma | Peripheral blood | Patients are treated with pembrolizumab alone or combined with copanlisib. Exosomes are profiled for PDL1 expression. |