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1.
Clin. transl. oncol. (Print) ; 18(6): 541-549, jun. 2016. tab, ilus
Article in English | IBECS | ID: ibc-152748

ABSTRACT

Aberrations in the PI3K signaling pathway are frequently observed in patients with breast cancer. Because of that, PI3K inhibitors are attractive options for the treatment of breast cancer because PI3K is the most proximal component of the pathway other than receptor tyrosine kinases. Buparlisib is a potent and highly specific oral pan-class I PI3K inhibitor, which is currently under investigation in patients with breast cancer. In this article, we describe the PI3K signaling pathway, the prognostic value of PI3K pathway mutations, as well as the mechanism of action of buparlisib. Lastly, we discuss preliminary results of preclinical and clinical studies showing the efficacy and safety profile of this agent in breast cancer patients (AU)


No disponible


Subject(s)
Humans , Female , Antineoplastic Combined Chemotherapy Protocols/analysis , Breast Neoplasms/diagnosis , Breast Neoplasms/drug therapy , Phosphatidylinositol 3-Kinases/analysis , Prognosis , Estrogen Receptor Modulators/analysis , Estrogen Receptor Modulators/therapeutic use , Neoplasm Metastasis/diagnosis , Neoplasm Metastasis/drug therapy
2.
Clin. transl. oncol. (Print) ; 17(12): 939-945, dic. 2015. tab
Article in English | IBECS | ID: ibc-147432

ABSTRACT

Breast cancer is a major public health problem. Despite remarkable advances in early diagnosis and treatment, one in three women may have metastases since diagnosis. Better understanding of prognostic and predictive factors allows us to select the most appropriate adjuvant therapy in each patient. In these guidelines, we summarize current evidence for the medical management of early-stage breast cáncer (AU)


No disponible


Subject(s)
Humans , Female , /standards , Breast Neoplasms/metabolism , Public Health , Mammography/methods , Mastectomy/methods , Mastectomy/nursing , Therapeutics/methods , Breast Neoplasms/drug therapy , Breast Neoplasms/radiotherapy , Public Health/legislation & jurisprudence , Public Health/methods , Mammography/instrumentation , Sentinel Lymph Node Biopsy/nursing , Mastectomy/classification , Therapeutics/standards
3.
Clin. transl. oncol. (Print) ; 15(3): 205-210, mar. 2013. tab
Article in English | IBECS | ID: ibc-127079

ABSTRACT

BACKGROUND: Use of breast magnetic resonance imaging (MRI) to detect breast cancer has generated significant debate. We analyze the role of breast MRI in the detection of additional disease and the need to perform additional biopsies in early breast carcinoma patients. In addition, we correlate the detection of new foci with tumor pathological features. METHODS: Early breast carcinoma patients that had undergone an MRI as well as a mammography as diagnostic procedures were included in the study. The following pathologic features were studied: carcinoma type, histological grade, estrogen receptors (ER), progesterone receptors (PR), HER2 and Ki67. Univariate analysis was conducted to ascertain significant correlation among detection of new foci and each of the tumor pathological features. RESULTS: Data from 98 patients have been analyzed: median age 49 years (range 35-79); carcinoma type: (a) infiltrative ductal carcinoma (n = 73, 74 %), (b) infiltrative lobular cancer (n = 12, 12 %), (c) ductal carcinoma in situ (n = 6, 6 %); amplified HER2 (n = 18, 18 %); grade III (n = 33, 33 %); Ki67 ≥ 25 % (n = 33, 33.67 %); positive ER and PR (n = 79, 80 %); triple negative tumors (n = 8, 8 %). MRI detected additional disease in 38 cases (39.58 %), and 20 led to an additional biopsy (20.4 %). Thirty-eight patients (39 %) underwent mastectomy. We found a statistically significant correlation between new foci in MRI and high Ki67 ≥ 25 % (p < 0.005). No other statistically significant correlation was established. CONCLUSION: MRI detected additional disease in 39 % cases, requiring an additional biopsy 20 %. Tumors with high proliferative index were significantly correlated with the detection of new foci in MRI (AU)


Subject(s)
Humans , Female , Adult , Aged , Breast Neoplasms/diagnosis , Carcinoma, Ductal, Breast/diagnosis , Carcinoma, Intraductal, Noninfiltrating/diagnosis , Carcinoma, Lobular/diagnosis , Magnetic Resonance Imaging , Breast Neoplasms/metabolism , Carcinoma, Ductal, Breast/metabolism , Carcinoma, Intraductal, Noninfiltrating/metabolism , Carcinoma, Lobular/metabolism , Early Detection of Cancer , Prognosis , /metabolism , Receptors, Progesterone , Retrospective Studies
4.
Clin. transl. oncol. (Print) ; 9(5): 317-322, mayo 2007. tab
Article in English | IBECS | ID: ibc-123312

ABSTRACT

INTRODUCTION: The purpose of this phase II study was to evaluate the efficacy and safety of neoadjuvant docetaxel/gemcitabine treatment in a biweekly regimen. MATERIALS AND METHODS: Patients with stage II/III breast cancer were treated with docetaxel (65 mg/m(2)) followed by gemcitabine (2500 mg/m(2)) every 2 weeks for 6 cycles. Patients with a clinical response or stable disease underwent mastectomy or breast-conserving surgery plus axillary dissection. After surgery, patients received 4 cycles of standard doxorubicin 60 mg/m(2) and cyclophosphamide 600 mg/m(2) every 21 days. RESULTS: Thirty-five patients were included in the trial. The overall response rate was 71.4% (95% CI: 53.7-85.4), with 8 complete and 17 partial responses. Breast conservation was possible in 59% of the patients. Toxicity was manageable. CONCLUSIONS: We consider biweekly docetaxel and gemcitabine could be an active and tolerable regimen option in the neoadjuvant setting sequentially with standard adjuvant doxorubicin-cyclophosphamide in patients with stage II or III breast cancer (AU)


Subject(s)
Humans , Female , Adult , Middle Aged , Aged , Clinical Trials, Phase II as Topic/methods , Clinical Trials, Phase II as Topic , Antineoplastic Agents/therapeutic use , Breast Neoplasms/drug therapy , Breast Neoplasms/pathology , Cyclophosphamide/therapeutic use , Doxorubicin/therapeutic use , Deoxycytidine/therapeutic use , Chronotherapy/methods , Taxoids/administration & dosage , Chemotherapy, Adjuvant/methods , Drug Administration Schedule , Neoadjuvant Therapy , Neoplasm Staging/methods , Neoplasm Staging
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