TY - JOUR
T1 - Systemic therapies for salivary gland cancer
T2 - Adenoid cystic carcinoma. REFCOR recommendations by the formal consensus method
AU - Ferrand, F. R.
AU - Even, C.
AU - Chabrillac, E.
AU - Thariat, J.
AU - Fakhry, N.
AU - Vergez, S.
AU - Bensadoun, R. J.
AU - Sarradin, V.
AU - Digue, L.
N1 - Publisher Copyright:
© 2023 Elsevier Masson SAS
PY - 2024/9/1
Y1 - 2024/9/1
N2 - Objective: To determine the therapeutic indications for systemic medical treatment in the management of adenoid cystic carcinoma (ACC) according to the clinical situation. Materials and methods: The French Network of Rare Head and Neck Tumors (REFCOR) formed a steering group, which drafted a narrative review of the literature published on Medline and proposed recommendations. The level of adherence to the recommendations was then assessed by a rating group, according to the formal consensus method. Results: ACCs are rare tumors and there is currently insufficient evidence to indicate chemotherapy at the localized stage. At the metastatic stage, progression is often slow. In case of oligometastatic ACC, local treatment should be discussed. The most often indolent nature of polymetastatic ACC can allow management by active surveillance. Molecular screening is recommended, for abnormalities potentially accessible to targeted therapy. Conclusion: ACCs are rare tumors for which there are currently few effective medical treatments. It is therefore recommended to include patients in clinical trials.
AB - Objective: To determine the therapeutic indications for systemic medical treatment in the management of adenoid cystic carcinoma (ACC) according to the clinical situation. Materials and methods: The French Network of Rare Head and Neck Tumors (REFCOR) formed a steering group, which drafted a narrative review of the literature published on Medline and proposed recommendations. The level of adherence to the recommendations was then assessed by a rating group, according to the formal consensus method. Results: ACCs are rare tumors and there is currently insufficient evidence to indicate chemotherapy at the localized stage. At the metastatic stage, progression is often slow. In case of oligometastatic ACC, local treatment should be discussed. The most often indolent nature of polymetastatic ACC can allow management by active surveillance. Molecular screening is recommended, for abnormalities potentially accessible to targeted therapy. Conclusion: ACCs are rare tumors for which there are currently few effective medical treatments. It is therefore recommended to include patients in clinical trials.
KW - Adenoid cystic carcinoma
KW - Chemotherapy
KW - Locally advanced stage
KW - Metastatic stage
KW - Systemic therapy
UR - http://www.scopus.com/inward/record.url?scp=85179171376&partnerID=8YFLogxK
U2 - 10.1016/j.anorl.2023.11.009
DO - 10.1016/j.anorl.2023.11.009
M3 - Article
C2 - 38061943
AN - SCOPUS:85179171376
SN - 1879-7296
VL - 141
SP - 286
EP - 291
JO - European Annals of Otorhinolaryngology, Head and Neck Diseases
JF - European Annals of Otorhinolaryngology, Head and Neck Diseases
IS - 5
ER -