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Trastuzumab beyond progression in HER2-positive advanced breast cancer: The Royal Marsden experience

Authors :
Waddell, T.
Kotsori, A.
Constantinidou, Anastasia
Yousaf, N.
Ashley, Sue
Parton, M.
Allen, M.
Starling, N.
Papadopoulos, P.
O'Brien, M.
Smith, I. E.
Johnston, S. L.
Constantinidou, Anastasia [0000-0001-5316-7574]
Source :
British Journal of Cancer, British journal of cancer
Publication Year :
2011
Publisher :
Nature Publishing Group, 2011.

Abstract

BACKGROUND: Recent UK clinical guidance advises against continuing trastuzumab (T) beyond disease progression (PD) in the absence of brain metastases in patients with HER-2 positive (+ ve) advanced breast cancer. We have retrospectively evaluated the outcome of patients with HER-2 + ve locally advanced (LA) or metastatic breast cancer (MBC) who continued T beyond PD, treated in our unit. METHODS: All HER-2+ ve patients on our prospectively maintained database with LA or MBC who received T beyond PD after adjuvant or one line of T for advanced disease were assessed for response and outcome. From the timepoint of T continuation beyond PD, we calculated the overall disease control rate, time to progression (TTP), and overall survival (OS). RESULTS: One hundred and fourteen patients with HER-2 + ve LA or MBC treated with T beyond PD were identified. The main site of disease was visceral in 84 (74%) patients. Seventy-six (66%) had one line of chemotherapy before continuation of T beyond PD and 21 (19%) had two or more. Post-progression, 66 (58%) received T combined with chemotherapy. Of the 93 (82%) patients with documented clinical or radiological response evaluation, 67 (59%) were considered as having stable disease or better. The median TTP was 24 weeks (95% CI: 21-28) and the median OS was 19 months (95% CI: 12-24). CONCLUSION: Our results from an unselected group of patients provide additional evidence that continuation of T beyond PD is of clinical benefit. © 2011 Cancer Research UK. 104 11 1675 1679

Details

Language :
English
ISSN :
15321827 and 00070920
Volume :
104
Issue :
11
Database :
OpenAIRE
Journal :
British Journal of Cancer
Accession number :
edsair.doi.dedup.....46f4ce17477c9f4dfdc3d01c7678d206