| Literature DB >> 27641463 |
Frédéric Selle1, Joseph Gligorov2, Daniele G Soares1, Jean-Pierre Lotz3.
Abstract
The concept of high-doses chemotherapy was developed in the 1980s based on in vitro scientific observations. Exposure of tumor cells to increasing concentrations of alkylating agents resulted in increased cell death in a strong dose-response manner. Moreover, the acquired resistance of tumor cells could be overcome by dose intensification. In clinic, dose intensification of alkylating agents resulted in increased therapeutic responses, however associated with significant hematological toxicity. Following the development of autologous stem cells transplantation harvesting from peripheral blood, the high-doses of chemotherapy, initially associated with marked toxic effects, could be more easily tolerated. As a result, the approach was evaluated in different types of solid tumors, including breast, ovarian and germ cell tumors, small cell lung carcinoma, soft tissue sarcomas and Ewing sarcoma. To date, high-doses chemotherapy with hematopoietic stem cells support is only used as a salvage therapy to treat poor prognosis germ cell tumors patients with chemo-sensitive disease. Regarding breast and ovarian cancer, high-doses chemotherapy should be considered only in the context of clinical trials. However, intensive therapy as an approach to overcome resistance to standard treatments is still relevant. Numerous efforts are still ongoing to identify novel therapeutic combinations and active treatments to improve patients' responses.Entities:
Keywords: Autogreffe de cellules-souches; Autologous stem cell transplant; Breast cancer; Cancer de l’ovaire; Cancer du sein; Germ cell tumors; Hautes doses de chimiothérapie; High-dose chemotherapy; Ovarian cancer; Solid tumors; Tumeurs germinales; Tumeurs solides
Mesh:
Substances:
Year: 2016 PMID: 27641463 DOI: 10.1016/j.bulcan.2016.08.002
Source DB: PubMed Journal: Bull Cancer ISSN: 0007-4551 Impact factor: 1.276