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DOI 10.1016/j.clbc.2015.10.005

Медицинская библиотека · Clinical breast cancer · 2015

A Phase II Randomized Study of Lapatinib Combined With Capecitabine, Vinorelbine, or Gemcitabine in Patients With HER2-Positive Metastatic Breast Cancer With Progression After a Taxane (Latin American Cooperative Oncology Group 0801 Study).

Gómez Henry L, Neciosup Silvia, Tosello Célia, Mano Max, Bines José, Ismael Gustavo, Santi Patrícia X, Pinczowski Hélio, Nerón Yeni, Fanelli Marcello, Fein Luis, Sampaio Carlos, Lerzo Guillermo, Capó Adolfo, Zarba Juan J, Blajman César, Varela Mirta S, Martínez-Mesa Jeovany, Werutsky Gustavo, Barrios Carlos H

Клиническое исследование II фазыСтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Novel targeted agents and combinations have become available in multiple lines of treatment for human epidermal growth factor receptor 2-positive (HER2(+)) metastatic breast cancer (MBC). In this context, alternatives to the lapatinib (L) and capecitabine (C) regimen, evaluating L combined with other cytotoxic drugs, are warranted.

PATIENTS AND

METHODS

In the present phase II, multicenter study, patients with HER2(+) MBC with progression after taxane were randomized between L, 1250 mg, combined with C, 2000 mg/m(2) on days 1 to 14 (LC), vinorelbine (V), 25 mg/m(2) on days 1 and 8 (LV), or gemcitabine (G), 1000 mg/m(2) on days 1 and 8 (LG), every 21 days. The primary endpoint was the overall response rate.

RESULTS

A total of 142 patients were included from 2009 to 2012. No differences were found in the patient baseline characteristics. The median age was 51 years, 69% were postmenopausal, 32% had liver metastasis, 57% were hormone receptor negative, and 48% had been previously treated with trastuzumab. The overall response rate was 49% (95% confidence interval [CI], 34.8%-63.4%), 56% (95% CI, 40%-70.4%), and 41% (95% CI, 27%-56.8%) in the LC, LV, and LG groups, respectively. The median progression-free survival was 9 months in the LC arm and 7 months in the other 2 arms (P = .28). The most common grade 3 and 4 adverse events were hand-foot syndrome (18%), diarrhea (6%), and increased alanine aminotransferase/aspartate aminotransferase (4%) in the LC arm; neutropenia (36%), diarrhea (9%), and febrile neutropenia (6%) in the LV arm; and neutropenia (47%), alanine aminotransferase/aspartate aminotransferase (13%), and rash (4%) in the LG arm.

CONCLUSION

LV and LG seem to be active combinations in patients with HER2(+) MBC after taxane failure. The overall toxicity was manageable in all regimens.

Для цитирования: Gómez Henry L, Neciosup Silvia, Tosello Célia, Mano Max, Bines José, Ismael Gustavo, Santi Patrícia X, Pinczowski Hélio, Nerón Yeni, Fanelli Marcello, Fein Luis, Sampaio Carlos, Lerzo Guillermo, Capó Adolfo, Zarba Juan J, Blajman César, Varela Mirta S, Martínez-Mesa Jeovany, Werutsky Gustavo, Barrios Carlos H. A Phase II Randomized Study of Lapatinib Combined With Capecitabine, Vinorelbine, or Gemcitabine in Patients With HER2-Positive Metastatic Breast Cancer With Progression After a Taxane (Latin American Cooperative Oncology Group 0801 Study).. Clinical breast cancer. 2015. DOI: 10.1016/j.clbc.2015.10.005.

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