Metastatic breast cancer;
HER2 positive;
Survival;
Brain metastasis;
D O I:
暂无
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摘要:
Prior to availability of anti-HER2 therapies, HER2-positive metastatic breast cancer (MBC) was associated with a poor prognosis. Prospective randomized trials have demonstrated survival benefit from anti-HER2 treatments. Anecdotal observations have suggested that a small but meaningful fraction of patients with HER2-positive MBC may be “exceptional responders” with long survival. We hypothesized that demographic and/or clinicopathologic characteristics can be identified to distinguish short-term from long-term survivors. A retrospective, single-institution review of 168 patients with HER2-positive MBC who received treatment with anti-HER2 therapy in the metastatic setting was performed. Cox proportional hazards analysis was used to assess factors associated with long-term survival. Median overall survival from the time of breast cancer recurrence was 3.9 years (95 % CI 3.4–5.2). From the time of diagnosis of MBC, 56 (33 %) survived for 5 or more years and 12 (7 %) survived more than 10 years. Of the 66 patients diagnosed with central nervous system metastases, 9 (14 %) survived more than 5 years following that diagnosis. Younger age at diagnosis, lower stage, hormone receptor positive status, and only having one organ involved at diagnosis were associated with longer survival. Four patients discontinued anti-HER2 therapy and are without evidence of progression of disease after a median 7.4 years (0.2–12.0) since stopping therapy. In a cohort of patients with HER2-positive MBC treated primarily with trastuzumab and lapatinib, 7 % of patients were “exceptional responders.” Combining these clinical factors with molecular determinants of prolonged survival may provide insights for individualizing treatment selection.
机构:
Univ Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USAUniv Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USA
Avelino, Alzira R. M.
Pulipati, Soumya
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Univ Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USAUniv Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USA
Pulipati, Soumya
Jamouss, Kevin
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机构:
Univ Massachusetts, Chan Med Sch Baystate, Dept Internal Med, Springfield, MA USAUniv Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USA
Jamouss, Kevin
Bhardwaj, Prarthna V.
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机构:
Univ Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USAUniv Massachusetts, Div Hematol Oncol, Chan Med Sch Baystate, Springfield, MA 01107 USA
机构:
Erzincan Univ, Fac Med, Dept Internal Med, Med Oncol, Erzincan, Turkey
A Yurtaslan Ankara Oncol Traning & Res Hosp, Dept Med Oncol, Ankara, TurkeyErzincan Univ, Fac Med, Dept Internal Med, Med Oncol, Erzincan, Turkey
机构:
European Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Univ Milan, Dept Oncol & Hematol, Milan, ItalyEuropean Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Tarantino, Paolo
Morganti, Stefania
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机构:
European Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Univ Milan, Dept Oncol & Hematol, Milan, ItalyEuropean Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Morganti, Stefania
Uliano, Jacopo
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机构:
European Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Univ Milan, Dept Oncol & Hematol, Milan, ItalyEuropean Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Uliano, Jacopo
Giugliano, Federica
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机构:
European Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Univ Milan, Dept Oncol & Hematol, Milan, ItalyEuropean Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Giugliano, Federica
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Crimini, Edoardo
Curigliano, Giuseppe
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机构:
European Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy
Univ Milan, Dept Oncol & Hematol, Milan, ItalyEuropean Inst Oncol IRCCS, Div New Drugs & Early Drug Dev, I-20141 Milan, Italy