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dc.contributor.authorWaddell, T.en
dc.contributor.authorKotsori, A.en
dc.contributor.authorConstantinidou, Anastasiaen
dc.contributor.authorYousaf, N.en
dc.contributor.authorAshley, Sueen
dc.contributor.authorParton, M.en
dc.contributor.authorAllen, M.en
dc.contributor.authorStarling, N.en
dc.contributor.authorPapadopoulos, P.en
dc.contributor.authorO'Brien, M.en
dc.contributor.authorSmith, I. E.en
dc.contributor.authorJohnston, S. L.en
dc.creatorWaddell, T.en
dc.creatorKotsori, A.en
dc.creatorConstantinidou, Anastasiaen
dc.creatorYousaf, N.en
dc.creatorAshley, Sueen
dc.creatorParton, M.en
dc.creatorAllen, M.en
dc.creatorStarling, N.en
dc.creatorPapadopoulos, P.en
dc.creatorO'Brien, M.en
dc.creatorSmith, I. E.en
dc.creatorJohnston, S. L.en
dc.date.accessioned2018-06-22T09:53:26Z
dc.date.available2018-06-22T09:53:26Z
dc.date.issued2011
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41839
dc.description.abstractBACKGROUND: 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.en
dc.language.isoengen
dc.sourceBritish journal of canceren
dc.subjectMetastatic breast canceren
dc.subjectTrastuzumaben
dc.subjectHer2 positiveen
dc.titleTrastuzumab beyond progression in HER2-positive advanced breast cancer: The Royal Marsden experienceen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1038/bjc.2011.138
dc.description.volume104
dc.description.issue11
dc.description.startingpage1675
dc.description.endingpage1679
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidConstantinidou, Anastasia [0000-0001-5316-7574]
dc.gnosis.orcid0000-0001-5316-7574


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