Indian Journal of Pathology and Microbiology
Home About us Instructions Submission Subscribe Advertise Contact e-Alerts Ahead Of Print Login 
Users Online: 710
Print this page  Email this page Bookmark this page Small font sizeDefault font sizeIncrease font size


 
  Table of Contents    
GUEST EDITORIAL  
Year : 2018  |  Volume : 61  |  Issue : 3  |  Page : 311-312
HER2 as a prospective novel biomarker in squamous cell carcinomas of the head and neck


1 Department of Pathology and Cytopathology, University Hospital “S. Giovanni di Dio e Ruggi D'Aragona”, Salerno, Italy
2 Department of Medicine and Surgery, University of Salerno, Salerno, Italy

Click here for correspondence address and email

Date of Web Publication13-Jul-2018
 

How to cite this article:
DAntonio A, Caputo A. HER2 as a prospective novel biomarker in squamous cell carcinomas of the head and neck. Indian J Pathol Microbiol 2018;61:311-2

How to cite this URL:
DAntonio A, Caputo A. HER2 as a prospective novel biomarker in squamous cell carcinomas of the head and neck. Indian J Pathol Microbiol [serial online] 2018 [cited 2018 Dec 11];61:311-2. Available from: http://www.ijpmonline.org/text.asp?2018/61/3/311/236601




Head-and-neck squamous cell carcinomas (HNSCC) represent the seventh most common cancer by incidence (686,000/year, worldwide) and ninth by mortality (375,000/year).[1] Despite advances in prevention, diagnosis, and therapy, the 5-year survival rate of patients affected by HNSCC is only 40%–60%, a number that has remained disturbingly stable for the past few decades.[2]

Together with efforts aimed at early diagnosis, the identification of a molecular marker able to pave the way for a novel therapeutic approach can be an effective way toward reducing the high mortality of HNSCC. HER2 may represent such a marker, and its role as a biomarker in HNSCC is being studied,[3] with one related study being published in this issue.[4]

Although data regarding the association between HER2 expression and the tumor-node-metastasis (TNM) stage is not conclusive, it is still possible that HER2 expression might be useful clinically. For example, it may identify a different subtype of HNSCC which may have its own therapeutic options, molecular pathogenesis, or prognosis.

For example, in some studies, HER2 has been shown to correlate with other clinicopathological parameters, such as disease-free survival.[5],[6] This may represent a different biologic behavior displayed by HNSCC's with HER2 overexpression. Such different biologic behavior is supported by other observations, for example, that HER2-positive clones tend to be selected – and sometimes enriched – in metastases.[7]

As for therapeutic implications, it has been observed that HER2 positivity may play a role in chemo-radioresistance of HNSCC.[4] If confirmed by further studies, such finding may make HER2 an important and clinically relevant prognostic marker independent from the TNM stage and histological grade.

Different therapies may be employed in HER2-positive HNSCC, the most obvious of which – HER2 inhibitors – is currently being studied in clinical trials. However, even if HER2-positive HNSCC's were not responsive to HER2-inhibitor therapy, identifying them may still shed light on the molecular pathogenesis of a subtype of HNSCC and thus possibly lead to a different therapy, more effective or safer than the current regimens.

For example, some studies have proposed a role for HER2 overactivation in the mechanism behind resistance to cetuximab treatment.[8] In parallel, some evidence suggests that HER2 inhibitors may be synergistic with EGFR-targeted therapy in treating HNSCC, possibly by overcoming such resistance.[9]

Another important point raised in the article in this issue is the possibility that subdividing HNSCC by location may provide more significant results.[4] Aggregating all squamous cell carcinomas of the head and neck into the HNSCC group may not render justice to some peculiar subtypes which may have independent molecular pathogenesis, response to therapies and prognosis.

In conclusion, efforts aimed at reducing the mortality of HNSCC are direly needed. A novel biomarker such as HER2 may represent the fruit of such efforts, and more studies aimed at clarifying its role as a biomarker in HNSCC are awaited.



 
   References Top

1.
Thompson LD, Brennan P, Pinto LF. Head and neck cancers. In: Stewart BW, Wild CP, editors. World Cancer Report 2014. Lyon: IARC Press; 2014. p. 422-30.  Back to cited text no. 1
    
2.
Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin 2018;68:7-30.  Back to cited text no. 2
[PUBMED]    
3.
Pollock NI, Grandis JR. HER2 as a therapeutic target in head and neck squamous cell carcinoma. Clin Cancer Res 2015;21:526-33.  Back to cited text no. 3
[PUBMED]    
4.
HER2-neu expression in head and neck squamous cell cancers and its clinicopathological correlation: Results from an Indian Cancer Center. Indian J Pathol Microbiol 2018.  Back to cited text no. 4
    
5.
Cavalot A, Martone T, Roggero N, Brondino G, Pagano M, Cortesina G, et al. Prognostic impact of HER-2/neu expression on squamous head and neck carcinomas. Head Neck 2007;29:655-64.  Back to cited text no. 5
    
6.
Tse GM, Yu KH, Chan AW, King AD, Chen GG, Wong KT, et al. HER2 expression predicts improved survival in patients with cervical node-positive head and neck squamous cell carcinoma. Otolaryngol Head Neck Surg 2009;141:467-73.  Back to cited text no. 6
[PUBMED]    
7.
Wei Q, Sheng L, Shui Y, Hu Q, Nordgren H, Carlsson J, et al. EGFR, HER2, and HER3 expression in laryngeal primary tumors and corresponding metastases. Ann Surg Oncol 2008;15:1193-201.  Back to cited text no. 7
    
8.
Yonesaka K, Zejnullahu K, Okamoto I, Satoh T, Cappuzzo F, Souglakos J, et al. Activation of ERBB2 signaling causes resistance to the EGFR-directed therapeutic antibody cetuximab. Sci Transl Med 2011;3:99ra86.  Back to cited text no. 8
[PUBMED]    
9.
Wheeler DL, Huang S, Kruser TJ, Nechrebecki MM, Armstrong EA, Benavente S, et al. Mechanisms of acquired resistance to cetuximab: Role of HER (ErbB) family members. Oncogene 2008;27:3944-56.  Back to cited text no. 9
[PUBMED]    

Top
Correspondence Address:
Antonio DAntonio
Department of Pathology and Cytopathology, University Hospital “S. Giovanni di Dio e Ruggi D'Aragona”, Salerno
Italy
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/IJPM.IJPM_236_18

Rights and Permissions




 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Email Alert *
    Add to My List *
* Registration required (free)  


    References

 Article Access Statistics
    Viewed861    
    Printed45    
    Emailed0    
    PDF Downloaded209    
    Comments [Add]    

Recommend this journal