TY - JOUR
T1 - The evolving role of endocrine therapy for breast cancer
AU - Jinno, Hiromitsu
AU - Ikeda, Tadashi
AU - Takayama, Shin
AU - Kitajima, Masaki
N1 - Funding Information:
This project is supported by the 3 M non-tenured faculty program and the National Science Foundation #1362256. We would like to thank Dr Zhiqiang Fang for folding resistance measurement, Dr Yuhuang Wang and Mr Brendan Meany for UV-Vis spectrum measurements, and Dr Jeremy Munday and Mr Joe Murphy for angular light scattering measurements. The Maryland Nanocenter and its NispLab are also greatly acknowledged. Dr Jianhua Zou and Dr Junbiao Peng would like to thank 973 chief project (No. 2015CB655000), the National Natural Science Foundation of China (No. 61574061 and 61574062), Science and Technology Project of Guangdong Province (No. 2014B090915004, 2014B090916002 and 2015B090914003). Dr Tao acknowledges the funding of the State Key Laboratory of Pulp and Paper Engineering, South China University of Technology (Grant No. 201233 and 2014C17), and the funding of the Guangdong Province Industrial Science and technology projects (Grant No. 2013B010406003).
PY - 2006/3
Y1 - 2006/3
N2 - The indirect comparison of LHRH agonist with tamoxifen showed similar efficacy in the adjuvant treatment of premenopausal endocrine-responsive breast cancer patients. Furthermore, LHRH agonist is as effective as cyclophosphamide, methotrexate and 5-fluorouracil chemotherapy. Data concerning combination of LHRH agonist with third-generation aromatase inhibitors are still lacking. Moreover, duration of therapy with LHRH agonist is still a matter of debate. In randomized clinical trials, each of the third-generation aromatase inhibitors (AIs) has demonstrated efficacy in the adjuvant treatment of postmenopausal women with receptor' -positive tumors. Anastrozole has been shown to improve disease-free survival when compared with tamoxifen, letrozole has been shown to further reduce the rate of breast cancer events when given as extended adjuvant therapy in women completing between 4.5 and 6 years of tamoxifen, and exemestane has been shown to improve disease-free survival when substituted for tamoxifen after an initial 2-3 years of adjuvant therapy. Although long-term follow-up for safety and overall survival continues in each of these trials, currently available data suggest that an AI should now be included as part of adjuvant endocrine therapy for the great majority of receptor-positive postmenopausal patients.
AB - The indirect comparison of LHRH agonist with tamoxifen showed similar efficacy in the adjuvant treatment of premenopausal endocrine-responsive breast cancer patients. Furthermore, LHRH agonist is as effective as cyclophosphamide, methotrexate and 5-fluorouracil chemotherapy. Data concerning combination of LHRH agonist with third-generation aromatase inhibitors are still lacking. Moreover, duration of therapy with LHRH agonist is still a matter of debate. In randomized clinical trials, each of the third-generation aromatase inhibitors (AIs) has demonstrated efficacy in the adjuvant treatment of postmenopausal women with receptor' -positive tumors. Anastrozole has been shown to improve disease-free survival when compared with tamoxifen, letrozole has been shown to further reduce the rate of breast cancer events when given as extended adjuvant therapy in women completing between 4.5 and 6 years of tamoxifen, and exemestane has been shown to improve disease-free survival when substituted for tamoxifen after an initial 2-3 years of adjuvant therapy. Although long-term follow-up for safety and overall survival continues in each of these trials, currently available data suggest that an AI should now be included as part of adjuvant endocrine therapy for the great majority of receptor-positive postmenopausal patients.
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M3 - Review article
C2 - 16529048
AN - SCOPUS:33744747624
SN - 0047-1852
VL - 64
SP - 547
EP - 554
JO - Nihon rinsho. Japanese journal of clinical medicine
JF - Nihon rinsho. Japanese journal of clinical medicine
IS - 3
ER -