Introduction: Adenoid cystic carcinoma of minor salivary glands (AdCCmSG) represents a ‘rarity in the rarity,’ posing a clinical challenge in lack of standardized, evidence-based recommendations. At present, AdCCmSG management is mostly translated from major salivary gland cancers (MSGCs). Ideally, AdCCmSG diagnostic-therapeutic workup should be discussed and carried out within a multidisciplinary, high-expertise setting, including pathologists, surgeons, radiation oncologists and medical oncologists. Areas Covered: The present review provides an overview of epidemiology and pathologic classification. Moreover, the most recent, clinically relevant updates in the treatment of AdCCmSG (Pubmed searches, specific guidelines) are critically discussed, aiming to a better understanding of this rare pathologic entity, potentially optimizing the care process, and offering a starting point for reflection on future therapeutic developments. Expert Opinion: The management of rare cancers is often hindered by limited data and clinical trials, lack of evidence-based guidelines, and hardly represented disease heterogeneity, which cannot be successfully tackled with a ‘one-size-fits-all’ approach. Our goal is to address these potential pitfalls, providing an easy-to-use, updated, multidisciplinary collection of expert opinions concerning AdCCmSG management as of today’s clinical practice. We will also cover the most promising future perspectives, based on the potential therapeutic targets highlighted within AdCCmSG’s molecular background.

Adenoid Cystic carcinoma of minor salivary glands (AdCCmSG): a multidisciplinary update / R. Romano, F. De Felice, A. Ferri, M. Della Monaca, R. Maroldi, L. Licitra, L.D. Locati, S. Alfieri. - In: EXPERT REVIEW OF ANTICANCER THERAPY. - ISSN 1473-7140. - 24:7(2024), pp. 567-580. [10.1080/14737140.2024.2357806]

Adenoid Cystic carcinoma of minor salivary glands (AdCCmSG): a multidisciplinary update

L. Licitra;
2024

Abstract

Introduction: Adenoid cystic carcinoma of minor salivary glands (AdCCmSG) represents a ‘rarity in the rarity,’ posing a clinical challenge in lack of standardized, evidence-based recommendations. At present, AdCCmSG management is mostly translated from major salivary gland cancers (MSGCs). Ideally, AdCCmSG diagnostic-therapeutic workup should be discussed and carried out within a multidisciplinary, high-expertise setting, including pathologists, surgeons, radiation oncologists and medical oncologists. Areas Covered: The present review provides an overview of epidemiology and pathologic classification. Moreover, the most recent, clinically relevant updates in the treatment of AdCCmSG (Pubmed searches, specific guidelines) are critically discussed, aiming to a better understanding of this rare pathologic entity, potentially optimizing the care process, and offering a starting point for reflection on future therapeutic developments. Expert Opinion: The management of rare cancers is often hindered by limited data and clinical trials, lack of evidence-based guidelines, and hardly represented disease heterogeneity, which cannot be successfully tackled with a ‘one-size-fits-all’ approach. Our goal is to address these potential pitfalls, providing an easy-to-use, updated, multidisciplinary collection of expert opinions concerning AdCCmSG management as of today’s clinical practice. We will also cover the most promising future perspectives, based on the potential therapeutic targets highlighted within AdCCmSG’s molecular background.
Adenoid Cystic carcinoma (AdCC); head and neck; histotype; minor salivary gland cancer (mSGC); radiation therapy; surgery; targeted therapy
Settore MEDS-09/A - Oncologia medica
2024
4-giu-2024
Article (author)
File in questo prodotto:
File Dimensione Formato  
Adenoid Cystic carcinoma of minor salivary glands AdCCmSG a multidisciplinary update.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Licenza: Creative commons
Dimensione 1.62 MB
Formato Adobe PDF
1.62 MB Adobe PDF Visualizza/Apri
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/2434/1198615
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 1
  • ???jsp.display-item.citation.isi??? 2
  • OpenAlex 1
social impact