Results 301 to 310 of about 406,491 (336)
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The Lancet, 2020
BACKGROUND Pembrolizumab monotherapy showed durable antitumour activity and manageable safety in patients with metastatic triple-negative breast cancer.
J. Cortés +19 more
semanticscholar +1 more source
BACKGROUND Pembrolizumab monotherapy showed durable antitumour activity and manageable safety in patients with metastatic triple-negative breast cancer.
J. Cortés +19 more
semanticscholar +1 more source
Immunotherapy in Triple-Negative Breast Cancer
The Cancer Journal, 2021Abstract Triple-negative breast cancer (TNBC) is an aggressive subtype of mammary carcinoma. A subset of TNBC is immune activated, suggesting that immunotherapy may be a viable treatment strategy. Phase III clinical trials have shown that atezolizumab or pembrolizumab is well-tolerated in combination with chemotherapy, with progression-free ...
openaire +2 more sources
Sacituzumab Govitecan-hziy in Refractory Metastatic Triple-Negative Breast Cancer
BACKGROUND Standard chemotherapy is associated with low response rates and short progression‐free survival among patients with pretreated metastatic triple‐negative breast cancer.
Aditya Bardia +2 more
exaly +2 more sources
Chemoresistance Evolution in Triple-Negative Breast Cancer Delineated by Single-Cell Sequencing
SUMMARY Triple-negative breast cancer (TNBC) is an aggressive subtype that frequently develops resistance to chemotherapy. An unresolved question is whether resistance is caused by the selection of rare pre-existing clones or alternatively through the ...
Charissa Kim, Ruli Gao, Emi Sei
exaly +2 more sources
An overview of triple-negative breast cancer
Archives of Gynecology and Obstetrics, 2015Triple-negative breast cancer (TNBC) is a heterogeneous group of tumors comprising various breast cancers simply defined by the absence of estrogen receptor, progesterone receptor and overexpression of human epidermal growth factor receptor 2 gene.
Pankaj Kumar, Rupali Aggarwal
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Metastatic Triple-negative Breast Cancer
Clinical Oncology, 2011The triple-negative class (oestrogen receptor-negative, progesterone receptor-negative and human epidermal growth factor receptor 2 [HER2]-negative) comprises about 15% of breast cancer. It is associated with a poor prognosis compared with tumours that are positive for hormone receptors or HER2.
E A, Rakha, S, Chan
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Pathology of triple negative breast cancer
Seminars in Cancer Biology, 2021Triple negative breast cancer (TNBC) is a subtype of breast tumor lacking hormone receptors expression and HER2 gene amplification and represents 24 % of newly diagnosed breast neoplasms. In this review, pathological aspects of triple-negative breast cancer are illustrated, with particular attention to the seminal studies that defined this subtype of ...
Filippo, Borri, Annarita, Granaglia
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Epidemiology of triple negative breast cancers [PDF]
Triple negative (TN) breast cancers fail to express the three most common breast cancer receptors; i.e., estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor-2 (HER2). Accumulating data demonstrate that epidemiological risk factor profiles also vary between TN (ER-PR-HER2-) and other breast cancers, especially ...
Gretchen L, Gierach +2 more
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Overall Survival with Pembrolizumab in Early-Stage Triple-Negative Breast Cancer.
New England Journal of MedicineBACKGROUND In patients with early-stage triple-negative breast cancer, the phase 3 KEYNOTE-522 trial showed significant improvements in pathological complete response and event-free survival with the addition of pembrolizumab to platinum-containing ...
P. Schmid +22 more
semanticscholar +1 more source
Pharmacotherapy of triple-negative breast cancer
Expert Opinion on Pharmacotherapy, 2009The term 'triple-negative breast cancer' defines tumors that do not express estrogen receptors, progesterone receptors or Her2 on immunohistochemical analysis. This subgroup accounts for 15% of all types of breast cancer. Histologically, triple-negative breast cancers are poorly differentiated and are characterized by an aggressive clinical history.
Cagatay, Arslan +2 more
openaire +2 more sources

