Changes in chemotherapy usage and outcome of early breast cancer patients in the last decade
- PMID: 27744486
- PMCID: PMC5090013
- DOI: 10.1007/s10549-016-4016-4
Changes in chemotherapy usage and outcome of early breast cancer patients in the last decade
Abstract
Background: During the last decade, neoadjuvant chemotherapy (NACT) of early breast cancer (EBC) evolved from a therapy intended to enable operability to a standard treatment option aiming for increasing cure rates equivalent to adjuvant chemotherapy (ACT). In parallel, improvements in the quality control of breast cancer care have been established in specialized breast care units.
Patients and methods: This study analyzed chemotherapy usage in patients with EBC treated at the Heidelberg University Breast Unit between January 2003 and December 2014.
Results: Overall, 5703 patients were included in the analysis of whom 2222 (39 %) received chemotherapy, 817 (37 %) as NACT, and 1405 (63 %) as ACT. The chemotherapy usage declined from 48 % in 2003 to 34 % in 2014 of the cohort. Further, the proportion of NACT raised from 42 to 65 % irrespective of tumor subtype. In addition, frequency of pathologic complete response (pCR) defined as no tumor residues in breast and axilla (ypT0 ypN0) at surgery following NACT increased from 12 % in 2003 to 35 % in 2014. The greatest effect was observed in HER2+ breast cancer with an increase in patients achieving pCR from 24 to 68 %.
Conclusions: The results mirror the refined indication for chemotherapy in EBC and its preferred usage as NACT in Germany. The increase in pCR rate over time suggests improvement in outcome accomplished by a multidisciplinary decision-making process and stringent measures for quality control.
Keywords: Adjuvant chemotherapy; Certified breast cancer unit; Early breast cancer; Neoadjuvant chemotherapy; Pathologic complete response.
Conflict of interest statement
There are no conflicts of interests (e.g., employment, consultancies, stock ownership, honoraria, paid expert testimony, patent applications/registrations, or grants, or other funding with regard to this study) for any of the authors. Ethics approval and consent to participate The study was approved by the ethics committee of the University of Heidelberg and in accordance with the Declaration of Helsinki. Because the study was deemed as without risk, including only anonymized analysis of routinely collected data, the ethics committee of the University of Heidelberg did not request approval for consent.
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References
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- AGO Breast Committee, Diagnosis and Treatment of Patients with Primary and Metastatic Breast Cancer, Guidelines of the AGO Breast Committee, Version 2016.1. http://www.ago-online.de/de/infothek-fuer-aerzte/leitlinienempfehlungen/.... Accessed 27 May 2016
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