Literature DB >> 21518948

Treatment with β-blockers and reduced disease progression in patients with thick melanoma.

Vincenzo De Giorgi1, Marta Grazzini, Sara Gandini, Silvia Benemei, Torello Lotti, Niccolò Marchionni, Pierangelo Geppetti.   

Abstract

Preclinical evidence shows that β-adrenoceptor antagonists (β-blockers) inhibit tumor and metastasis progression in animal models of melanoma. We hypothesized that the use of β-blockers for concomitant diseases is associated with a reduced risk of progression of thick (Breslow thickness >1 mm) malignant melanoma. Two patient subgroups were identified from the medical records of 121 consecutive patients with a thick melanoma. Of these, 30 patients had been prescribed β-blockers for 1 year or more (treated subgroup), whereas the other 91 were untreated. After a median follow-up time of 2.5 years, tumor progression was observed in 3.3% of the treated subgroup and in 34.1% of the untreated subgroup. The Cox model on progression indicated a 36% (95% confidence interval, 11%-54%) (P = .002) risk reduction for each year of β-blocker use. No deaths were observed in the treated group, whereas in the untreated group 24 patients died. To our knowledge, the present study suggests for the first time that exposure to β-blockers for 1 year or more is associated with a reduced risk of progression of thick malignant melanoma, indicating the need for larger epidemiological studies and randomized clinical trials.

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Year:  2011        PMID: 21518948     DOI: 10.1001/archinternmed.2011.131

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  75 in total

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Authors:  Francesco Bertolini; Vikas P Sukhatme; Gauthier Bouche
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9.  Low Socioeconomic Status, Adverse Gene Expression Profiles, and Clinical Outcomes in Hematopoietic Stem Cell Transplant Recipients.

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10.  Prognostic significance of β2-adrenergic receptor expression in malignant melanoma.

Authors:  Akira Shimizu; Kyoichi Kaira; Keita Mori; Madoka Kato; Kimihiro Shimizu; Masahito Yasuda; Ayumi Takahashi; Tetsunari Oyama; Takayuki Asao; Osamu Ishikawa
Journal:  Tumour Biol       Date:  2015-11-23
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