Prolonged Disease Control after Myeloablative Chemotherapy, Autologous Transplantation and Immunotherapy in High-risk Early Breast Cancer
Background: Failure to eradicate all cancer stem cells, lymphocytopenia, and high levels of vascular endothelial growth factor (VEGF) may explain the limited efficacy of high dose-chemotherapy (HDCT) with peripheral progenitor cell transplantation (PBPCT) in high-risk early breast cancer with more t...
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Published in: | Anticancer research Vol. 30; no. 1; pp. 209 - 216 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
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International Institute of Anticancer Research
01-01-2010
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Subjects: | |
Online Access: | Get full text |
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Summary: | Background: Failure to eradicate all cancer stem cells, lymphocytopenia, and high levels of vascular endothelial growth factor
(VEGF) may explain the limited efficacy of high dose-chemotherapy (HDCT) with peripheral progenitor cell transplantation (PBPCT)
in high-risk early breast cancer with more than 10 axillary nodes (HRBC). Patients and Methods: With the aim of increasing
patient's lymphocyte count and reducing VEGF, wich could translate into an improved immune function and a better clinical
outcome, patients with HRBC, received HDCT, PBPCT and immunotherapy with interleukin-2 (IL-2) and 13-cis retinoic acid (RA).
Results: A total of 30 HRBC patients were entered into the study. Grade 4 hematological toxicity was universal, while major
adverse effects of IL-2 were fever, rash and autoimmune reactions. After a median follow-up of 61 months, immune function
improved with a statistically significant increase of lymphocyte count and a decrease in VEGF levels. This translated into
an unexpected 5-year relapse-free and overall survival rates of 76% and 85%, respectively. Conclusion: These data show that
IL-2 and RA administration after HDCT and PBPCT is feasible and, as well as giving a statistically significant improvement
in lymphocyte count and a decrease of VEGF, also seems to improve the expected clinical outcome. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0250-7005 1791-7530 |