Clinical activity of androgen deprivation therapy in patients with metastatic/relapsed androgen receptor-positive salivary gland cancers

被引:91
作者
Locati, Laura D. [1 ]
Perrone, Federica [2 ]
Cortelazzi, Barbara [2 ]
Lo Vullo, Salvatore [3 ]
Bossi, Paolo [1 ]
Dagrada, Gianpaolo [2 ]
Quattrone, Pasquale [4 ]
Bergamini, Cristiana [1 ]
Potepan, Paolo [5 ]
Civelli, Enrico [5 ]
Fallai, Carlo [6 ]
Pilotti, Silvana [2 ]
Licitra, Lisa [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Head & Neck Med Oncol Unit, Milan, Italy
[2] Fdn IRCCS Ist Nazl Tumori, Lab Expt Mol Pathol, Dept Pathol, Milan, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Clin Epidemiol & Trial Org Unit, Milan, Italy
[4] Fdn IRCCS Ist Nazl Tumori, Dept Pathol, Milan, Italy
[5] Fdn IRCCS Ist Nazl Tumori, Dept Radiol, Milan, Italy
[6] Fdn IRCCS Ist Nazl Tumori, Dept Radiotherapy 2, Milan, Italy
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2016年 / 38卷 / 05期
关键词
androgen deprivation therapy; hormonal treatment; androgen receptor; recurrent; metastatic salivary gland cancer; DUCT CARCINOMA; PROSTATE-CANCER; EXPRESSION;
D O I
10.1002/hed.23940
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
BackgroundAndrogen deprivation therapy has some clinical activity in selected salivary gland cancer histotypes, with androgen receptor expression. MethodsWe retrospectively analyzed patients with androgen receptor-expressing recurrent/metastatic salivary gland cancer, treated with androgen deprivation therapy. Protein expression of androgen receptor and ErbB family members was investigated. Progression-free survival (PFS) and overall survival (OS) were the main endpoints. ResultsSeventeen patients were identified. No significant toxicities were reported. Overall response rate was 64.7%; 3-year PFS and 5-year OS were 11.8% and 19.3%, respectively. Androgen receptor overexpression may be sustained by gain of chromosome X (58%) and TP53 mutation (44%). No association between response to androgen deprivation therapy and epidermal growth factor receptor (EGFR), human epidermal growth factor receptor (HER)2, HER3 expression, PIK3CA mutations, or phosphatase and tensin homolog (PTEN) deletion was identified. ConclusionWe confirm the activity of androgen deprivation therapy in androgen receptor-expressing recurrent/metastatic salivary gland cancers. The hypothesis that an androgen receptor increased gene copy number may represent a possible mechanism of primary resistance should be further investigated. (c) 2015 Wiley Periodicals, Inc. Head Neck 38: 724-731, 2016
引用
收藏
页码:724 / 731
页数:8
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