Tumour assessment and staging: United Kingdom National Multidisciplinary Guidelines. (May 2016)

• Record Type: Journal Article
• Authors: Roland, N; Porter, G; Fish, B; Makura, Z
• Is Part Of: Journal of laryngology & otology. Volume 130(2016)Supplement 2
• Page Start: S53
• Page End: S58
• Publication Date: 2016-05
• Subjects: Otolaryngology -- Periodicals; 617.51
• DOI: 10.1017/S002221511600044X
• Languages: English
• ISSNs: 0022-2151

Abstract

Abstract: In general, the first decision to be made in a patient with a confirmed head and neck cancer is whether or not to treat the patient before deciding what form of management strategy is appropriate. There is no more important an aspect of head and neck cancer care than the initial evaluation of the patient and the patient's tumour. The practice requires specific expertise and judgement. The current tumour–node–metastasis system relies on morphology of the tumour (anatomical site and extent of disease) but the final decision on treatment hinges on a full assessment of the patient including physiological age and general condition. The aim of this paper is primarily to describe why and how we appraise a patient and their tumour. It addresses the general principles applicable to the topic of evaluation, classification and staging. In addition, the limitations and pitfalls of this process are described. Recommendations: All patients with head and neck cancer (HNC) should undergo tumour classification and staging prior to treatment. (R) Pre-therapeutic clinical staging of HNCs should be based on at least a C2 factor (evidence obtained by special diagnostic means, e.g. radiographic imaging (e.g. computed tomography, magnetic resonance imaging or ultrasound scan), endoscopy, biopsy and cytology). (R) Imaging to evaluate the primary site should be performed prior to biopsy to avoid the effect of upstaging from the oedema caused by biopsy trauma. (G) Panendoscopy is only recommended for symptomatic patients or patients with primary tumours known to have a significant risk of a second (synchronous) primary tumour. (G)