Literature DB >> 18303485

Clinical course of breast cancer patients with metastases limited to the liver treated with chemotherapy.

Ozlem Er1, Debra K Frye, Shu-Wan C Kau, Kristine Broglio, Vicente Valero, Gabriel N Hortobagyi, Banu Arun.   

Abstract

PURPOSE: The purpose of this retrospective analysis was to describe the clinical course of patients with breast cancer with liver metastases alone who were treated on doxorubicin/cyclophosphamide or taxane-containing chemotherapy protocols at the M. D. Anderson Cancer Center. PATIENTS AND METHODS: A total of 2,193 patients with metastatic breast cancer were treated on prospective clinical protocols at the University of Texas M. D. Anderson Cancer between 1973 and 2003. Among those, 132 were identified as having the liver as the first site of metastatic disease. The following information was obtained from the medical records: gender, age, race, performance status, menopausal status, hormonal receptor status, laboratory data, primary treatment, prior systemic treatment, disease-free interval, extent of metastatic disease, response to chemotherapy, site of progression, time to tumor progression, overall survival, and cause of death.
RESULTS: Of the patients 62% received anthracycline-based regimens and 38% received anthracycline- and taxane-based regimens on various clinical protocols as the initial therapy for metastatic disease. The median follow-up of the patients was 52 months. The overall objective response rate was 66.4%; 16.4% of the patients achieved complete responses. The median time to progression was 14 months. Progression-free survival rates were 56% and 30% at 12 and 24 months, respectively. The median overall survival was 25 months. Sixteen patients (12.1%) survived longer than 60 months. There was a statistically inverse relation between a high lactate dehydrogenase level and achieving a complete response (P < 0.05). Age > or =50 years, extent of liver metastases, performance status, and lactate dehydrogenase and albumin levels are significantly related to progression-free survival (P < 0.05). Year of liver metastases diagnosis, extent of liver metastases, performance status, and albumin level are significantly related to overall survival (P < 0.05).
CONCLUSIONS: This retrospective analysis demonstrated that patients with liver metastases only had high objective response rates and encouraging results for median survival obtained with currently available cytotoxic agents.

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Year:  2008        PMID: 18303485     DOI: 10.1097/PPO.0b013e3181629a7b

Source DB:  PubMed          Journal:  Cancer J        ISSN: 1528-9117            Impact factor:   3.360


  11 in total

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3.  Clinical outcome of percutaneous RF-ablation of non-operable patients with liver metastasis from breast cancer.

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4.  Clinicopathological characteristics and prognostic risk factors of breast cancer patients with bone metastasis.

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5.  Breast cancer liver metastases: US-guided percutaneous radiofrequency ablation--intermediate and long-term survival rates.

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6.  Obesity is an independent predictor of poor survival in metastatic breast cancer: retrospective analysis of a patient cohort whose treatment included high-dose chemotherapy and autologous stem cell support.

Authors:  A von Drygalski; T B Tran; K Messer; M Pu; S Corringham; C Nelson; E D Ball
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7.  Locally ablative treatment of breast cancer liver metastases: identification of factors influencing survival (the Mammary Cancer Microtherapy and Interventional Approaches (MAMMA MIA) study).

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8.  Incidence and prognostic factors of patients with synchronous liver metastases upon initial diagnosis of breast cancer: a population-based study.

Authors:  Hai-Yun Zhao; Yue Gong; Fu-Gui Ye; Hong Ling; Xin Hu
Journal:  Cancer Manag Res       Date:  2018-11-20       Impact factor: 3.989

9.  Serological diagnosis of liver metastasis in patients with breast cancer.

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Journal:  Cancer Biol Med       Date:  2012-03       Impact factor: 4.248

10.  Complete response in a patient with liver metastases from breast cancer employing hepatic arterial infusion 5-fluorouracil based chemotherapy plus systemic nab-paclitaxel.

Authors:  Girolamo Ranieri; Ilaria Marech; Mariangela Porcelli; Francesco Giotta; Gennaro Palmiotti; Giuseppe Laricchia; Vito Fazio; Cosmo Damiano Gadaleta
Journal:  Oncotarget       Date:  2017-12-31
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