Literature DB >> 20883410

Tamoxifen vs. non-tamoxifen treatment for advanced melanoma: a meta-analysis.

Julieta Ruiz Beguerie1, Jin Xingzhong, Raúl P Valdez.   

Abstract

Although tamoxifen (TAM) is routinely used in advanced melanoma, it is still uncertain whether evidence exists to support this practice. This review assesses the benefits and harms of systemic therapy with TAM vs. without TAM on response and mortality in patients with advanced melanoma. MEDLINE, The Cochrane Database of Systemic Reviews, The Cochrane Central Register of Controlled Trials, EMBASE and LILACS were searched for randomized controlled trials comparing chemotherapy using and not using TAM in any dose, in patients of any age with advanced melanoma. References lists, databases of ongoing trials and conference proceedings were hand-searched. All included trials were evaluated for quality assessment. Primary outcomes were response and mortality. Secondary outcomes were hematologic and non hematologic toxicity, treatment-related mortality and quality of life. A meta-analysis was performed and results were presented as relative risk with 95% confidence interval. Nine randomized controlled trials met the inclusion criteria. Patients treated with TAM were more likely to respond, with a relative risk 1.36 (95% CI: 1.04-1.77, P = 0.02). However, there was no improvement in 1-year mortality. The incidence of hematologic toxicity was higher in the TAM group. Subgroup analyses showed that female patients were more likely to respond. Chemotherapies with TAM improve overall and partial response, but do not improve mortality in 1 year in advanced melanoma. Further use of TAM in melanoma should be done only in the context of clinical trials.
© 2010 The International Society of Dermatology.

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Year:  2010        PMID: 20883410     DOI: 10.1111/j.1365-4632.2010.04529.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  12 in total

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Journal:  Tumour Biol       Date:  2013-02-15

Review 2.  Giants and monsters: Unexpected characters in the story of cancer recurrence.

Authors:  Shai White-Gilbertson; Christina Voelkel-Johnson
Journal:  Adv Cancer Res       Date:  2020-05-04       Impact factor: 6.242

3.  Polymorphisms in apoptosis-related genes in cutaneous melanoma prognosis: sex disparity.

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Review 4.  Is Uveal Melanoma a Hormonally Sensitive Cancer? A Review of the Impact of Sex Hormones and Pregnancy on Uveal Melanoma.

Authors:  Manisha Miller; Lynn Schoenfield; Mohamed Abdel-Rahman; Colleen M Cebulla
Journal:  Ocul Oncol Pathol       Date:  2021-04-22

5.  CB1 and CB2 receptors are novel molecular targets for Tamoxifen and 4OH-Tamoxifen.

Authors:  Paul L Prather; FeAna FrancisDevaraj; Centdrika R Dates; Aleksandra K Greer; Stacie M Bratton; Benjamin M Ford; Lirit N Franks; Anna Radominska-Pandya
Journal:  Biochem Biophys Res Commun       Date:  2013-10-19       Impact factor: 3.575

6.  4-Hydroxytamoxifen induces autophagic death through K-Ras degradation.

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Review 8.  Estrogen Receptor β in Melanoma: From Molecular Insights to Potential Clinical Utility.

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Journal:  Front Endocrinol (Lausanne)       Date:  2016-10-26       Impact factor: 5.555

9.  Tamoxifen is a candidate first-in-class inhibitor of acid ceramidase that reduces amitotic division in polyploid giant cancer cells-Unrecognized players in tumorigenesis.

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Journal:  Cancer Med       Date:  2020-03-05       Impact factor: 4.452

10.  Oxidative stress contributes to the tamoxifen-induced killing of breast cancer cells: implications for tamoxifen therapy and resistance.

Authors:  Raie T Bekele; Ganesh Venkatraman; Rong-Zong Liu; Xiaoyun Tang; Si Mi; Matthew G K Benesch; John R Mackey; Roseline Godbout; Jonathan M Curtis; Todd P W McMullen; David N Brindley
Journal:  Sci Rep       Date:  2016-02-17       Impact factor: 4.379

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