Tamoxifen or femara

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  1. SergeyKRK Moderator

    Tamoxifen or femara


    The antiestrogen tamoxifen has potent activity against estrogen receptor–positive breast cancer, but two nonsteroidal aromatase inhibitors, letrozole and anastrozole, show considerable advantages over tamoxifen with respect to patient survival and tolerability. To determine the optimal way to use letrozole and tamoxifen, we studied their effects on a breast tumor xenograft model, MCF-7Ca, that is responsive to both antiestrogens and aromatase inhibitors. Female ovariectomized BALB/c athymic nude mice carrying xenograft tumors were treated daily subcutaneously with one of the following first-line therapies for varying durations: no drug (control), tamoxifen (100 μg/day) alone, letrozole (10 μg/day) alone, both drugs at the same time, or alternating 4-week courses of each drug (beginning with a course of tamoxifen or beginning with a course of letrozole). Tumor volumes and weights were estimated using linear mixed-effects models. The time to tumor doubling was calculated, and tumor weights in the treatment groups were compared, with adjustments for multiple comparisons being made with either Tukey’s or Dunnett’s procedure. Second-line therapies (with tamoxifen, letrozole, or fulvestrant) were initiated when tumors doubled in size under first-line therapies. The times for doubling of tumor volume were as follows: control, 3–4 weeks; tamoxifen alone, 16 weeks; tamoxifen alternating with letrozole, 17–18 weeks; tamoxifen plus letrozole, 18 weeks; letrozole alternating with tamoxifen, 22 weeks; letrozole alone, 34 weeks. First-line treatment with letrozole was superior to treatment with tamoxifen alone or with the two drugs combined (at week 16, both First-line letrozole therapy extends time for tumor progression in this model relative to the other treatment regimens tested. Accepted for publication 30 December 2015 Published 1 March 2016 Volume 2016:9 Pages 1077—1084 DOI https://doi.org/10.2147/OTT. S81087 Checked for plagiarism Yes Review by Single-blind Peer reviewers approved by Dr Jia Fan Peer reviewer comments 3 Editor who approved publication: Professor Daniele Santini School of Pharmaceutical Sciences, Jiangnan University, Wuxi, People’s Republic of China Abstract: The incidence rate of breast cancers in People’s Republic of China has increased in the last decade, and many cases are responsive to hormone therapies. The third-generation aromatase inhibitor letrozole inhibits estrogen production, and is more efficacious than the estrogen receptor inhibitor tamoxifen. In recent years, letrozole has been widely used to treat postmenopausal breast cancers in People’s Republic of China. Also, metastatic, premenopausal, and male breast cancers have been effectively treated by a combination of letrozole with cytotoxic, radiation, or other therapies. In this review, we provide a perspective and summary of recent advances in the use of letrozole for breast cancer in Chinese patients. Keywords: breast cancer, Chinese, letrozole Based on the diverse expression of estrogen receptor-α (ER-α), progesterone receptor, human epidermal growth factor receptor-2 (HER2), claudin, cytokeratin, and other molecular markers, a growing number of recognized biological subtypes of breast cancer have been identified, such as luminal A, luminal B, HER2, basal-like, and claudin-low.

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    Jun 2, 2007. ATLANTA—Postmenopausal women with breast cancer who switch from tamoxifen Nolvadex to letrozole Femara have a dramatically. Tamoxifen or Femara? I've been a BC survivor for 4 years, 8 months. I've been through a mastectomy, chemo and radiation. My onc started me on Tamoxifen. He said I'd. The combination of Zometa and Femara after surgery offered better disease-free survival than tamoxifen for premenopausal women diagnosed with early-stage, hormone.

    Femara (letrozole) (commonly misspelled as fimara, femarra, and femera) is a drug in a category known as aromatase inhibitors. These drugs block the formation of estrogen made in areas other than the ovaries. Since estrogen can act as a fuel for the growth of breast cancer, Femara helps to lower your risk of breast cancer recurrence and improves your chance of survival. Studies indicate that using hormone therapy for estrogen receptor-positive breast cancer decreases the risk of recurrence and increases survival. There are two primary types of hormone therapy for people with breast cancer. After menopause, whether natural menopause, surgical menopause, or ovarian suppression medications, the major source of estrogen in the body is that produced from the breakdown of androgens in other locations of the body. Aromatase inhibitors work to block this reaction which converts androgens to estrogens, thus blocking the formation of estrogen. Hormone therapy for breast cancer is a treatment for breast cancers that are sensitive to hormones. The most common forms of hormone therapy for breast cancer work by blocking hormones from attaching to receptors on cancer cells or by decreasing the body's production of hormones. Hormone therapy is only used for breast cancers that are found to have receptors for the naturally occurring hormones estrogen or progesterone. Hormone therapy for breast cancer is often used after surgery to reduce the risk that the cancer will return. Hormone therapy for breast cancer may also be used to shrink a tumor before surgery, making it more likely the cancer will be removed completely. If your cancer has spread to other parts of your body, hormone therapy for breast cancer may help control it. Hormone therapy for breast cancer is only used to treat cancers that are hormone sensitive (hormone receptor positive breast cancers).

    Tamoxifen or femara

    Breast Cancer Survival Femara Better Than Tamoxifen, Tamoxifen or Femara? -

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  6. Compare adjuvant letrozole vs tamoxifen administered for 5 years in postmenopausal women with operable, hormone receptor-positive breast cancer. Compare.

    • Letrozole or Tamoxifen in Treating Postmenopausal Women With..
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    • Femara vs Tamoxifen Comparison -.

    To determine the optimal way to use letrozole and tamoxifen, we studied their effects on a breast tumor xenograft model, MCF-7Ca, that is responsive to both. Nov 1, 2017. You are most likely to have anastrozole or letrozole for 5 years. Or you might have one of these drugs for 2 years followed by tamoxifen for 3. The international BIG 1-98 trial, started in 1998, compared Femara to tamoxifen after surgery in postmenopausal women diagnosed with hormone-receptor-positive.

     
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