Abstract

Simple SummaryMost breast cancer patients receive chemotherapy as part of their treatment. Unfortunately, treatment outcomes cannot be predicted with the current methods. Therefore, in the preset study, we explore the feasibility of a functional sensitivity test for the chemotherapeutic agents cisplatin and docetaxel on breast cancer tissue slices in culture. We show that these two agents need to be analyzed differently; cisplatin treatment resulted in cell death and a reduction in proliferation, whereas docetaxel could be assessed by determining the relative numbers of cells in mitosis. We also took the next step towards clinic application by adapting this test for biopsies from metastatic breast tumors. This test is now ready for a direct evaluation of its predictive value in clinical trials.Background chemotherapy is part of most breast cancer (BC) treatment schedules. However, a substantial fraction of BC tumors does not respond to the treatment. Unfortunately, no standard biomarkers exist for response prediction. Therefore, we aim to develop ex vivo sensitivity assays for two types of commonly used cytostatics (i.e., platinum derivates and taxanes) on organotypic BC tissue slices. Methods: Ex vivo cisplatin sensitivity assays were established using organotypic tissue slices derived from the surgical resection material of 13 primary BCs and 20 fresh histological biopsies obtained from various metastatic sites. Furthermore, tissue slices of 10 primary BCs were used to establish a docetaxel ex vivo sensitivity assay. Results: Cisplatin sensitivity was assessed by tissue morphology, proliferation and apoptosis, while the relative increase in the mitotic index was discriminative for docetaxel sensitivity. Based on these read-outs, a scoring system was proposed to discriminate sensitive from resistant tumors for each cytostatic. We successful completed the cisplatin sensitivity assay on 12/16 (75%) biopsies as well. Conclusions: We developed an ex vivo cisplatin and docetaxel assay on BC slices. We also adapted the assay for biopsy-sized specimens as the next step towards the correlation of ex vivo test results and in vivo responses.

Highlights

  • Chemotherapy remains the cornerstone of breast cancer (BC) treatment, despite increasing possibilities for targeted therapies

  • We previously measured the anthracycline sensitivity of primary BC samples based on tissue morphology, proliferation and apoptosis after the treatment of freshly cut slices ex vivo [2]

  • We first established the optimal conditions for the ex vivo sensitivity assay in organotypic tissue slices from patient-derived xenograft (PDX) tumors with known in vivo cisplatin sensitivity

Read more

Summary

Introduction

Chemotherapy remains the cornerstone of breast cancer (BC) treatment, despite increasing possibilities for targeted therapies. The demand for predictive biomarkers is high. Such biomarkers for classic chemotherapies do not yet exist despite extensive research [1], probably because of the multifactorial nature of their mechanisms of action. As DNA sequence or gene expression analysis has not yet yielded validated biomarkers, the direct determination of tumor sensitivity using functional assays appears to be an attractive alternative. For this purpose, viable tumor material is cultured and treated ex vivo. Our method maintained the breast tumor cells in their natural micro-environment and enabled ex vivo screening for chemotherapeutic drug sensitivities

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call