Laryngeal cancer

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https://en.wikipedia.org/wiki/Cancer_of_the_larynx
Laryngeal cancer
Other namesCancer of the larynx, laryngeal carcinoma
Tumor Laryngis-01.jpg
Larynx cancer - endoscopic view
Specialty Oncology
Deaths94,800 (2018) [1]

Laryngeal cancers are mostly squamous-cell carcinomas, reflecting their origin from the epithelium of the larynx.

Cancer can develop in any part of the larynx. The prognosis is affected by the location of the tumour. For the purposes of staging, the larynx is divided into three anatomical regions: the glottis (true vocal cords, anterior and posterior commissures); the supraglottis ( epiglottis, arytenoids and aryepiglottic folds, and false cords); and the subglottis.

Most laryngeal cancers originate in the glottis, with supraglottic and subglottic tumours being less frequent.

Laryngeal cancer may spread by: direct extension to adjacent structures, metastasis to regional cervical lymph nodes, or via the blood stream. The most common site of distant metastases is the lung. Laryngeal cancer occurred in 177,000 people in 2018, and resulted in 94,800 deaths (an increase from 76,000 deaths in 1990). [1] [2] Five-year survival rates in the United States are 60.3%. [3]

Signs and symptoms

The symptoms of laryngeal cancer depend on the size and location of the tumour. Symptoms may include the following: [4] [5]

Adverse effects of treatment can include changes in appearance, difficulty eating, dry mouth, or loss of voice that may require learning alternate methods of speaking. [6]

Risk factors

The most important risk factor for laryngeal cancer is smoking. Death from laryngeal cancer is 20 times more likely for the heaviest smokers than for their non-smoking peers. [7] Heavy chronic consumption of alcohol, particularly alcoholic spirits, is also a significant risk factor. When present in combination, the usages of alcohol and tobacco appear to have a synergistic effect. Other reported risk factors include being of low socioeconomic status, male sex, or age greater than 55 years.[ citation needed]

Occupational exposure to environmental factors such as wood dust, paint fumes, and certain chemicals used in the metalworking, petroleum, plastics, and textile industries [8] is also believed to be a risk factor for laryngeal cancers. Infections by some strains of Papillomaviridae carry some risk of laryngeal carcinoma. [9]

People with a history of head and neck cancer are known to be at higher risk (about 25%) of developing a second, separate cancer of the head, neck, or lung. This is likely due to chronic exposure to the carcinogenic effects of alcohol and tobacco. In this situation, a field change effect may occur, where the epithelial tissues start to become diffusely dysplastic with a reduced threshold for malignant change. This risk may be reduced by quitting alcohol and tobacco.[ citation needed]

Diagnosis

Larynx and nearby structures
Cavitas nasi: Nasal cavity
Cavis orum: oral cavity
Glottis: Larynx
Plica vocalis: Vocal cords
Trachea
Oesophagus: Esophagus

Diagnosis is made by the doctor on the basis of a medical history, physical examination, and special investigations which may include a chest x-ray, CT or MRI scans, and tissue biopsy. The examination of the larynx requires some expertise, which may require specialist referral.[ citation needed]

The physical exam includes a systematic examination of the whole patient to assess general health and to look for signs of associated conditions and metastatic disease. The neck and supraclavicular fossa are palpated to feel for cervical adenopathy, other masses, and laryngeal crepitus. The oral cavity and oropharynx are examined under direct vision. The larynx may be examined by indirect laryngoscopy using a small angled mirror with a long handle (akin to a dentist's mirror) and a strong light. Indirect laryngoscopy can be highly effective, but requires skill and practice for consistent results. For this reason, many specialist clinics now use fibre-optic nasal endoscopy where a thin and flexible endoscope, inserted through the nostril, is used to clearly visualise the entire pharynx and larynx. Nasal endoscopy is a quick and easy procedure performed in clinic. Local anaesthetic spray may be used.[ citation needed]

If there is a suspicion of cancer, biopsy is performed, usually under general anaesthetic. This provides histological proof of cancer type and grade. If the lesion appears to be small and well localised, the surgeon may undertake excision biopsy, where an attempt is made to completely remove the tumour at the time of first biopsy. In this situation, the pathologist will not only be able to confirm the diagnosis, but can also comment on the completeness of excision, i.e., whether the tumour has been completely removed. A full endoscopic examination of the larynx, trachea, and esophagus is often performed at the time of biopsy.[ citation needed]

For small glottic tumours further imaging may be unnecessary. In most cases, tumour staging is completed by scanning the head and neck region to assess the local extent of the tumour and any pathologically enlarged cervical lymph nodes.

The final management plan will depend on the site, stage (tumour size, nodal spread, distant metastasis), and histological type. The overall health and wishes of the patient must also be taken into account. A prognostic multigene classifier has been shown to be potentially useful for the distinction of laryngeal cancer of low or high risk of recurrence and might influence the treatment choice in future. [10]

Staging

Laryngeal tumours are classified according to the guidelines set by academic organisations such as the National Comprehensive Cancer Network (NCCN) . [11] Overall classification, also known as " staging", can help predict treatment options for patients. [12] Staging consists of three separate evaluations. The first is of the tumour/cancer itself ("T"). [12] The second is the extent to which adjacent lymph nodes are involved in the tumour/cancer's spread ("N"). [12] The third is the presence or absence of any distant metastases ("M). [12] The specific “staging” criteria for laryngeal cancer, as utilised in the NCCN’s 2019 Guidelines for Head and Neck Cancers, [13] are:

T

TX: Unable to assess

Tis: Carcinoma in situ

Supraglottis

T1: Tumour present in only one subsite of the supraglottis. Vocal cords have normal mobility.

T2: Tumour invades mucosa. There is no fixation of the larynx.

T3: Tumour causes fixation of the vocal cords, with or without invasion of neighbouring areas.

T4:

Glottis

T1: Tumour only involves the vocal cords. Vocal cords have normal mobility.

  • T1A - One vocal cord
  • T1B - Both vocal cords

T2: Tumour meets at least one of the following criteria:

  • extends to supra- or sub-glottis
  • impairs vocal cord mobility

T3: Tumour meets at least one of the following criteria:

T4: Same as “Supraglottis”

Subglottis

T1: Tumour is only in the subglottis

T2: Tumour involves both subglottis and vocal cords (regardless of cord mobility)

T3: Same as “ Glottis

T4: Same as “ Supraglottis

N

If Using Clinical (Non-Pathological) Diagnosis

NX: Unable to assess

N0: No involvement of neighbouring lymph nodes

N1: Tumour meets ALL of the following criteria:

  • involves single lymph node
  • involved lymph node on the same side of the body as tumour
  • involved lymph node less than 3 cm in “greatest dimension”
  • lacks extension beyond the lymph node

N2: Tumour meets ANY of the following criteria

  • N2A – Same as N1, except size can be between 3-6 cm
  • N2B – Same as N2A, except lymph nodes can be multiple, and there is no minimum size
  • N2C – Same as N2B, except lymph nodes can be on any side of the body

N3: Tumour meets ANY of the following criteria:

  • N3A – Same as N1, except size is greater than 6 cm
  • N3B – Tumour obviously extends beyond the lymph node border (regardless of number, size, or location of lymph nodes)

If Using Pathological Diagnosis

NX: Same as “Clinical Diagnosis – NX”

N0:  Same as “Clinical Diagnosis – N0”

N1:  Same as “Clinical Diagnosis – N1”

N2: Tumour meets ANY of the following criteria

  • N2A – Same as “Clinical Diagnosis – N2A”, except tumour can extend beyond the involved lymph node
  • N2B – Same as “Clinical Diagnosis – N2B”
  • N2C – Same as “Clinical Diagnosis – N2C”

N3: Tumour meets ANY of the following criteria:

  • N3A – Same as “Clinical Diagnosis – N3A”
  • N3B – Any provable presence of tumour extension beyond the lymph node

M

M0: No evidence of distant metastasis

M1: Evidence of distant metastasis

Treatment

Larynx, removed
At right: Fingertip,
At the bottom: Holder

Specific treatment depends on the location, type, and stage of the tumour. [14] Treatment may involve surgery, radiotherapy, or chemotherapy, alone or in combination. [14]

Surgical Treatment

Surgical treatment may involve partial or full removal of the tumour. [15] Neighbouring tissues and structures may or may not be removed, depending on their involvement in the tumour’s structure and spread. [16] Full removal of the larynx may be necessary in some cases.

Adjunct Treatment

Adjunct treatment, most commonly the administration of chemotherapy or radiotherapy, may be necessary. [16] Chemotherapy or radiotherapy may be necessary singly, in combination with each other, or in combination with surgery. [13] Adjunct treatment may be necessary prior to surgical treatment, alongside surgical treatment, or after surgical treatment. Clinical decision-making can be difficult in circumstances where the patient is unable to access necessary adjunct treatment.

Multi-Disciplinary Treatment

Often, successful treatment of and recovery from laryngeal cancer will involve expertise outside of the realms of surgery or oncology. Physical therapists, occupational therapists, speech therapists, psychiatrists, psychologists, oral/maxillofacial surgeons,   dentists, neurologists, neurosurgeons, and endocrinologists may all become involved in the care of patients with laryngeal cancer.

Epidemiology

Incidence is five in 100,000 (12,500 new cases per year) in the US. [17] The American Cancer Society estimated that 9,510 men and women (7,700 men and 1,810 women) would be diagnosed with and 3,740 men and women would die of laryngeal cancer in 2006.[ citation needed]

According to the GLOBOCAN 2018 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer, there were 177,422 new cases of laryngeal cancer worldwide in 2018 (1.0% of the global total.) Among worldwide cancer deaths, 94,771 (1.0%) were due to laryngeal cancer. [18]

In 2019, it is estimated that there will be 12,410 new laryngeal cancer cases in the United States, (3.0 per 100,000). [19] The number of new cases decreases every year at a rate of 2.4%, [19] and this is believed to be related to decreased cigarette smoking in the general population. [20]

Laryngeal cancer is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that laryngeal cancer affects fewer than 200,000 people in the US. [21]

See also

References

  1. ^ a b "Larynx Cancer Factsheet" (PDF). Global Cancer Observatory. Retrieved 8 November 2019.
  2. ^ GBD 2013 Mortality and Causes of Death, Collaborators (17 December 2014). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013". Lancet. 385 (9963): 117–71. doi: 10.1016/S0140-6736(14)61682-2. PMC  4340604. PMID  25530442.
  3. ^ "SEER Stat Fact Sheets: Larynx Cancer". NCI. Retrieved 22 January 2020.
  4. ^ Laryngeal cancer at Mount Sinai Hospital
  5. ^ DeVita, Hellman, and Rosenberg's Cancer: Principles & Practice of Oncology 10th edition ISBN  9781451192940
  6. ^ "Cancer of the Larynx - Causes, Symptoms, Treatment, Diagnosis - MedBroadcast.com". Retrieved 2018-01-25.
  7. ^ Ridge JA, Glisson BS, Lango MN, et al. "Head and Neck Tumors" in Pazdur R, Wagman LD, Camphausen KA, Hoskins WJ (Eds) Cancer Management: A Multidisciplinary Approach. 11 ed. 2008.
  8. ^ "Laryngeal Cancer". Retrieved April 7, 2019.
  9. ^ Rodrigo Torrente, ,M. Haigentz Jr, FG.Dikkers, A. Rinaldo, R.P. Takes, J. Olofsson, A.Ferlito (April 2011). "Human papillomavirus infections in laryngeal cancer". Head & Neck. Head Neck. 33 (4): 581–6. doi: 10.1002/hed.21421. PMID  20848441. S2CID  30274997.CS1 maint: multiple names: authors list ( link)
  10. ^ Mirisola V, Mora R, Esposito AI, Guastini L, Tabacchiera F, Paleari L, Amaro A, Angelini G, Dellepiane M, Pfeffer U, Salami A (August 2011). "A prognostic multigene classifier for squamous cell carcinomas of the larynx". Cancer Letters. 307 (1): 37–46. doi: 10.1016/j.canlet.2011.03.013. PMID  21481529.
  11. ^ "National Comprehensive Cancer Network".
  12. ^ a b c d M. Amin, S. Edge, F. Greene, et al, “AJCC Cancer Staging Manual”, New York: Springer, 2017
  13. ^ a b National Comprehensive Cancer Network, "Guidelines for Head and Neck Cancers," 2019
  14. ^ a b National Comprehensive Cancer Network, "Evidence Blocks for Head and Neck Cancers," 2019.
  15. ^ K. I. Nibu, R. Hayashi, T. Asakage, et al, Japanese Clinical Practice Guideline for Head and Neck Cancer, vol. 44, Elsevier Ireland Ltd, 2017, pp. 375-380.
  16. ^ a b V. Grégoire, J. L. Lefebvre, L. Licitra, et al, "Squamous cell carcinoma of the head and neck: EHNS-ESMO-ESTRO clinical practice guidelines for diagnosis, treatment and follow-up," Annals of Oncology, vol. 21, no. SUPPL. 5, 5 2010
  17. ^ Samuel W. Beenken, MD. "Laryngeal Cancer (Cancer of the larynx)". Armenian Health Network, Health.am. Retrieved 2007-03-22.
  18. ^ Bray, Freddie; Ferlay, Jacques; Soerjomataram, Isabelle; Siegel, Rebecca L.; Torre, Lindsey A.; Jemal, Ahmedin (2018-09-12). "Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries". CA: A Cancer Journal for Clinicians. Wiley. 68 (6): 394–424. doi: 10.3322/caac.21492. ISSN  0007-9235. PMID  30207593. S2CID  52188256.
  19. ^ a b "Cancer Stat Facts: Larynx Cancer". Retrieved 2019-08-09.
  20. ^ "What Are the Key Statistics About Laryngeal and Hypopharyngeal Cancers?".
  21. ^ "Annual Report on the Rare Diseases and Conditions Research". National Institutes of Health. Retrieved 2007-03-22.

External links

Classification
D
External resources