The somatic affairs of BRAF: tailored therapies for advanced malignant melanoma and orphan non-V600E (V600R-M) mutations

被引:19
作者
Ponti, Giovanni [1 ]
Pellacani, Giovanni [2 ]
Tomasi, Aldo [1 ]
Gelsomino, Fabio [3 ]
Spallanzani, Andrea [3 ]
Depenni, Roberta [3 ]
Al Jalbout, Samer [2 ]
Simi, Lisa [4 ]
Garagnani, Lorella [5 ]
Borsari, Stefania [2 ]
Conti, Andrea [2 ]
Ruini, Cristel [2 ]
Fontana, Annalisa [3 ]
Luppi, Gabriele [3 ]
机构
[1] Univ Hosp Modena & Reggio Emilia, Dept Clin & Diagnost Med & Publ Hlth, Modena, Italy
[2] Univ Hosp Modena & Reggio Emilia, Dept Dermatol, Modena, Italy
[3] Univ Modena & Reggio Emilia, Dept Oncol, I-41100 Modena, Italy
[4] Univ Florence, Dept Clin Physiopathol, Florence, Italy
[5] Univ Modena & Reggio Emilia, Dept Pathol, I-41100 Modena, Italy
关键词
INHIBITION; DABRAFENIB; RESISTANCE; PIK3CA;
D O I
10.1136/jclinpath-2012-201345
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
BRAF V600R-M-D are uncommon mutations, not included in the experimental protocols of BRAF selective inhibitors. We report the evaluation of correlations among different types of BRAF somatic mutations in melanoma and their management with BRAF inhibitors. 21 patients with BRAF mutated metastatic melanoma were enrolled in the protocol with BRAF inhibitors for compassionate use at the University of Modena. Hot spot V600E mutations were found in 19 patients. V600R mutation and double (V600E -V600M) mutation were identified in two melanomas. In one case, V600K mutation was found. Two screening failures were noted. Mean progression free survival at follow-up of to 8 weeks, was 7.6 months. Five patients had a very short follow-up and the experimental protocol is still ongoing, so we cannot provide complete follow-up data. However, all of them are still under treatment and disease progression free. An objective response with few side effects was observed in all patients. in vitro studies with the aim of testing drug sensitivity.
引用
收藏
页码:441 / 445
页数:5
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