Background Androgen deprivation therapy has some clinical activity in selected salivary gland cancer histotypes, with androgen receptor expression. Methods We 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. Results Seventeen 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. Conclusion We 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.

Clinical activity of androgen deprivation therapy in patients with metastatic/relapsed androgen receptor-positive salivary gland cancers / L.D. Locati, F. Perrone, B. Cortelazzi, S. Lo Vullo, P. Bossi, G. Dagrada, P. Quattrone, C. Bergamini, P. Potepan, E. Civelli, C. Fallai, S. Pilotti, L. Licitra. - In: HEAD & NECK. - ISSN 1043-3074. - 38:5(2016), pp. 724-731. [10.1002/hed.23940]

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

L. Licitra
Ultimo
2016

Abstract

Background Androgen deprivation therapy has some clinical activity in selected salivary gland cancer histotypes, with androgen receptor expression. Methods We 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. Results Seventeen 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. Conclusion We 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.
androgen deprivation therapy; androgen receptor; hormonal treatment; recurrent/metastatic salivary gland cancer
Settore MED/06 - Oncologia Medica
2016
Article (author)
File in questo prodotto:
File Dimensione Formato  
Clinical activity of androgen deprivation therapy in patients with metastatic relapsed AR‐.pdf

accesso riservato

Tipologia: Post-print, accepted manuscript ecc. (versione accettata dall'editore)
Dimensione 1.92 MB
Formato Adobe PDF
1.92 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Locati_et_al-2016-Head_&_Neck.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 144.97 kB
Formato Adobe PDF
144.97 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/484726
Citazioni
  • ???jsp.display-item.citation.pmc??? 36
  • Scopus 93
  • ???jsp.display-item.citation.isi??? 83
social impact