Patient-derived tumor-like cell clusters for drug testing in cancer therapy

Abstract
Several patient-derived tumor models emerged recently as robust preclinical drug-testing platforms. However, their potential to guide clinical therapy remained unclear. Here, we report a model called patient-derived tumor-like cell clusters (PTCs). PTCs result from the self-assembly and proliferation of primary epithelial, fibroblast, and immune cells, which structurally and functionally recapitulate original tumors. PTCs enabled us to accomplish personalized drug testing within 2 weeks after obtaining the tumor samples. The defined culture conditions and drug concentrations in the PTC model facilitate its clinical application in precision oncology. PTC tests of 59 patients with gastric, colorectal, or breast cancers revealed an overall accuracy of 93% in predicting their clinical outcomes. We implemented PTC to guide chemotherapy selection for a patient with mucinous rectal adenocarcinoma who experienced recurrence with metastases after conventional therapy. After three cycles of a nonconventional therapy identified by the PTC, the patient showed a positive response. These findings need to be validated in larger clinical trials, but they suggest that the PTC model could be prospectively implemented in clinical decision-making for therapy selection.
Funding Information
  • National Natural Science Foundation of China (71532001)
  • National Natural Science Foundation of China (11971039)
  • National Natural Science Foundation of China (81827809)
  • National Natural Science Foundation of China (81421004)
  • National Natural Science Foundation of China (31870805)
  • National Natural Science Foundation of China (81773214)
  • National Key Basic Research Project of China (2016YFC0207705)
  • National Key Basic Research Project of China (2018YFA0108101)
  • Peking University Clinical Scientist Program (BMU2019LCKXJ011)
  • ‘San Ming’ Project of Shenzhen City (SZSM201612051)
  • Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support (ZYLX201701)