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   <subfield code="a">Efficacy and safety of neoadjuvant chemotherapy with concurrent liposomal-encapsulated doxorubicin, paclitaxel and trastuzumab for human epidermal growth factor receptor 2-positive breast cancer in clinical practice</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Joaquín Gavilá, Ángel Guerrero, Miguel Climent, Aranzazu Fernández, Francisco Gozalbo, María Carrascosa, Josefina Camps, Vicente Guillem, Amparo Ruiz]</subfield>
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   <subfield code="a">Background: Based on previous results obtained with non-pegylated liposomal-encapsulated doxorubicin (TLC-D99) together with paclitaxel and trastuzumab in patients with human epidermal growth factor receptor 2 (HER2)-positive locally advanced or metastatic breast cancer (BC), a similar regimen was evaluated in the neoadjuvant setting in a prospectively selected series of consecutive patients with clinical stage II-III BC. Primary and secondary objectives included the rate of pathologic complete response (pCR), safety, and predictive factors of pCR. Methods: Patients received six cycles of TLC-D99 (50mg/m2 every 3weeks), paclitaxel (80mg/m2 weekly) and trastuzumab (4mg/kg initial dose and 2mg/kg weekly). All patients underwent surgery after treatment. pCR was defined as the absence of invasive cancer cells in the breast and the axilla. Results: Sixty-two patients with a median age of 46.6 years were analyzed. Stage IIIA was diagnosed in 43.5% of patients and 14.5% had inflammatory BC. Conservative surgery was performed in 46.8% of the patients and pCR was achieved in 63% (95% CI 50.5-75.5). Patients with estrogen receptor (ER)-negative tumors presented a significantly higher pCR rate than patients with ER-positive tumors (74.4 vs 43.5%; P=0.028). Forty-five patients (72.6%) completed study treatment and 80.6% received at least five treatment cycles. No patients developed congestive heart failure and 14.5% of patients showed a≥10% decrease in the left ventricular ejection fraction. Conclusion: The triple combination therapy assessed is effective and safe, offering a high pCR rate in patients with HER2-positive BC.</subfield>
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   <subfield code="a">Japan Society of Clinical Oncology, 2014</subfield>
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   <subfield code="a">Antibodies</subfield>
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   <subfield code="a">Breast neoplasm</subfield>
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   <subfield code="a">Drug therapy</subfield>
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   <subfield code="a">Prospective study</subfield>
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   <subfield code="a">Gavilá</subfield>
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   <subfield code="u">Medical Oncology Service, Fundación Instituto Valenciano de Oncología, C/Gregorio Gea, 31, 46009, Valencia, Spain</subfield>
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   <subfield code="a">Guerrero</subfield>
   <subfield code="D">Ángel</subfield>
   <subfield code="u">Medical Oncology Service, Fundación Instituto Valenciano de Oncología, C/Gregorio Gea, 31, 46009, Valencia, Spain</subfield>
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   <subfield code="a">Climent</subfield>
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   <subfield code="u">Medical Oncology Service, Fundación Instituto Valenciano de Oncología, C/Gregorio Gea, 31, 46009, Valencia, Spain</subfield>
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   <subfield code="u">Pathological Anatomy Service, Fundación Instituto Valenciano de Oncología, C/Gregorio Gea, 31, 46009, Valencia, Spain</subfield>
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   <subfield code="u">Medical Oncology Service, Fundación Instituto Valenciano de Oncología, C/Gregorio Gea, 31, 46009, Valencia, Spain</subfield>
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   <subfield code="u">Medical Oncology Service, Fundación Instituto Valenciano de Oncología, C/Gregorio Gea, 31, 46009, Valencia, Spain</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">International Journal of Clinical Oncology</subfield>
   <subfield code="d">Springer Japan</subfield>
   <subfield code="g">20/3(2015-06-01), 480-489</subfield>
   <subfield code="x">1341-9625</subfield>
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   <subfield code="c">XK010000</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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