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   <subfield code="a">Prognostic implications of receptor discordance between primary and recurrent breast cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Akiko Matsumoto, Hiromitsu Jinno, Takeshi Murata, Tomoko Seki, Maiko Takahashi, Tetsu Hayashida, Kaori Kameyama, Yuko Kitagawa]</subfield>
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   <subfield code="a">Background: Discordance rates of hormone receptor (HR) and human epidermal growth factor-2 (HER2) status between primary and recurrent breast cancer were reported to be in the wide range of 10-40%, although its prognostic relevance remains to be elucidated. Methods: Fifty-five breast cancer patients had biopsies or resections of recurrent lesions. Pathological assessments of the HR and HER2 status of primary and recurrent lesions were performed in a single laboratory at Keio University Hospital. Tumors were classified as luminal (HR+ and HER2−), luminal/HER2 (HR+ and HER2+), HER2 (HR− and HER2+), or triple negative (HR− and HER2−). Results: Discordance rates in estrogen receptor (ER), progesterone receptor (PgR) and HER2 status between primary tumors and recurrent lesions were 16.4, 30.9 and 10.2%, respectively. Overall, 14 patients (25.5%) changed subtypes at recurrent lesions. Patients with a gain in ER and PgR status had a significantly longer disease-free interval compared with the corresponding concordant-negative patients (ER: 99.0 vs. 18.5months, p=0.037, PgR: 141.0 vs. 24.4months, p=0.011). Patients with a loss of HER2 status experienced a trend toward shorter time to progression, compared with patients who maintained HER2 positivity (4.0 vs. 18.4months, p=0.051). Conclusions: Discordance in receptor status between primary and recurrent breast cancers were seen in 10-30%. A gain in HR status was significantly associated with better prognosis.</subfield>
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   <subfield code="a">Japan Society of Clinical Oncology, 2014</subfield>
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   <subfield code="a">Breast cancer</subfield>
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   <subfield code="a">Receptor</subfield>
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   <subfield code="a">Discordance</subfield>
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   <subfield code="a">Prognosis</subfield>
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   <subfield code="a">Matsumoto</subfield>
   <subfield code="D">Akiko</subfield>
   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="a">Jinno</subfield>
   <subfield code="D">Hiromitsu</subfield>
   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="a">Murata</subfield>
   <subfield code="D">Takeshi</subfield>
   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="a">Seki</subfield>
   <subfield code="D">Tomoko</subfield>
   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="a">Takahashi</subfield>
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   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="a">Hayashida</subfield>
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   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="a">Kameyama</subfield>
   <subfield code="D">Kaori</subfield>
   <subfield code="u">Division of Pathological Diagnosis, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
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   <subfield code="u">Department of Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, 160-8582, Tokyo, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="t">International Journal of Clinical Oncology</subfield>
   <subfield code="d">Springer Japan</subfield>
   <subfield code="g">20/4(2015-08-01), 701-708</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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