2006
DOI: 10.1016/s1470-2045(06)70948-2
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Effectiveness of switching from adjuvant tamoxifen to anastrozole in postmenopausal women with hormone-sensitive early-stage breast cancer: a meta-analysis

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Cited by 229 publications
(122 citation statements)
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“…Where under-reporting is considered a potential source of bias, CLBC is probably more likely to be under-reported in trial datasets than IBTR, so this is unlikely to account for the excess of CLBC compared to ipsilateral NP. Although adjuvant systemic therapies, including endocrine and cytotoxic therapies, reduce the incidence of new primary tumors (14,31), there is no a priori reason to think that this effect will be greater on the ipsilateral than on the contralateral breast. Finally, although the risk of CLBC is increased after radiotherapy, there is no reason to believe that this risk is proportionately greater than the risk of radiation-induced cancers in the ipsilateral breast.…”
Section: Discussionmentioning
confidence: 99%
“…Where under-reporting is considered a potential source of bias, CLBC is probably more likely to be under-reported in trial datasets than IBTR, so this is unlikely to account for the excess of CLBC compared to ipsilateral NP. Although adjuvant systemic therapies, including endocrine and cytotoxic therapies, reduce the incidence of new primary tumors (14,31), there is no a priori reason to think that this effect will be greater on the ipsilateral than on the contralateral breast. Finally, although the risk of CLBC is increased after radiotherapy, there is no reason to believe that this risk is proportionately greater than the risk of radiation-induced cancers in the ipsilateral breast.…”
Section: Discussionmentioning
confidence: 99%
“…Tamoxifen, a selective estrogen receptor modulator, was the standard of care for such patients for nearly 20 years; it can significantly reduce recurrence and breast cancer-related death in patients prescribed about 5 years of adjuvant treatment [1]. However, the third-generation aromatase inhibitors (AIs) anastrozole, letrozole, and exemestane have proven more effective than tamoxifen at improving disease-free survival (DFS), whether given as upfront (initial) adjuvant therapy, as sequential or switch therapy following approximately 2-3 years of prior tamoxifen, or as extended adjuvant therapy following 5 years of tamoxifen treatment [2][3][4][5][6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…One of the primary unresolved considerations is whether these drugs should be used instead of tamoxifen as initial adjuvant treatment for postmenopausal women with successfully resected EBC, or whether 2-3 years of tamoxifen should precede the implementation of AI therapy. The latter strategy, using either exemestane [Intergroup Exemestane Study (IES)] or anastrozole (Arimidex Nolvadex [ARNO] 95 study and others) as endocrine therapy following 2-3 years of tamoxifen, potentially offers treatment cost savings relative to upfront AIs and significant improvements in DFS, event-free survival (EFS), and overall survival (OS) relative to tamoxifen alone [5][6][7]11]. A significant caveat of the switching approach is that it effectively ''misses'' a sizable number of women who may relapse during the initial treatment period with tamoxifen; these patients have been excluded from AI switching trials such as the IES and ARNO 95 [5,11].…”
Section: Introductionmentioning
confidence: 99%
“…Although aromatase inhibitors do prolong disease-free survival compared to tamoxifen [3], tamoxifen still has a major role in breast cancer treatment [4]. In addition, a survival benefit has been shown for sequential tamoxifen and an aromatase inhibitor [5,6]. A molecular test helping clinicians to make a choice between starting with either tamoxifen, an aromatase inhibitor or rather with chemotherapy would have enormous potential for tailoring treatment.…”
Section: Introductionmentioning
confidence: 99%