Anal cancer

Changed by Bruno Di Muzio, 27 Mar 2020

Updates to Article Attributes

Body was changed:

Anal cancer is a relatively uncommon, accounting for less than 2% of large bowel malignancies, and most of the cases are made of squamous cell carcinoma. 

Epidemiology

It accounts for less than 2% of large bowel malignancies and 1-6% of anorectal tumours (~1.5% of all gastrointestinal tract malignancies in the United States 14). Commonly diagnosed between the ages of 45 and 75 years 16. 

There may be a slight malefemale predilection where its incidence has been reported to be approximately 0.5 per 100 000 in men and 1.0 per 100 000 in women 1. Its incidence is thought to be rising over the years 5,16.

Clinical presentation

Approximately 45% of patients may present with bleeding per rectum. Around 30% of patients may have pain and/or a sensation of a mass.

Pathology

Anal carcinoma typically originates between the anorectal junction above and the anal verge below. The vast majority of anal canal cancers are squamous cell cancers. See WHO classification of anal canal tumours.

  • ~85% squamous cell carcinoma
  • ~10% adenocarcinoma 
  • ~5% made of rarer tumours (e.g. melanoma, small cell carcinoma, and metastatic disease) 16
Risk factors

Both male and female 15:

  • HPV / HIV infection
  • HPV infection
    • ​strongly related to sexual activity
      • in particular, anal receptive intercourse 
    • more than 90% of patients presenting with metastatic SCC have been reported with detectable HPV 16
  • immunosuppression 
  • number of lifetime sexual partners, and receptive anal intercourse
  • smoking

In females: previous in situ or invasive cervical, vulvalvulva, or vaginal cancer 15

Lymphatic spread
  • tumour above dentate line: to pararectalmesorectal and paravertebralinternal iliac nodes 13,16
  • tumour below dentate line: to inguinalexternal iliac, inguinal, and femoraldeep inguinal nodes 13,16

Radiographic features

Imaging performed before treatment provides an assessment of the extent of local disease and nodal involvement. Accurate delineation of the disease in relation to the rest of the perineal anatomy is of paramount importance in initial imaging assessment. The size of the tumour is also considered a critical prognostic factor (see staging of anal cancer13.

Ultrasound

Endoanal ultrasound can sometimes be used in locoregional staging 6, particularly for small superficial lesions (T1 stage) 16. Some authors suggest that endoanal ultrasound can accurately determine the depth of penetration of the carcinoma into the sphincter complex and can be used to accurately gauge the response of these tumours to chemoradiation therapy 8.

MRI

MRI is the modality of choice in the assessment of locoregional disease and is performed with performed with a dedicated protocol: see MRI protocol for assessment of anal cancer.

Reported typical signal characteristics include 2:

  • T1: primary and recurrent tumours are usually of low to intermediate signal intensity relative to skeletal muscle
  • T2: primary and recurrent tumours are generally of high signal intensity relative to skeletal muscle

Nodal metastases have a signal intensity similar to that of the primary tumour.

PET-CT

Recent research suggests that there are groundsF-18 FDG PET-CT has been now used as an auxiliary imaging modality for using PET-CT routinelystaging in the workupmany countries. It has a high sensitivity for detection of anal cancerboth the primary lesion and the regional node involvement 16, asand it alters the initial staging sufficiently frequently 4.

Treatment and prognosis

Treatment is often with a combination of chemotherapy and radiotherapy (often given concurrently) and is usually curative in lower stages. Approximately

  • approximately 50-60% are thought to present with T1 to T2 lesions carrying a 5-year survival of 80-90% 3.

Some authors suggest a benefit of a salvage abdominoperineal resection (APR) for those patients with failed chemoradiation 10,12.

  • -<p><strong>Anal cancer</strong> is a relatively uncommon, accounting for less than 2% of large bowel malignancies, and most of the cases are made of squamous cell carcinoma. </p><h4>Epidemiology</h4><p>It accounts for less than 2% of large bowel malignancies and 1-6% of anorectal tumours (~1.5% of all gastrointestinal tract malignancies in the United States <sup>14</sup>).  </p><p>There may be a slight male predilection where its incidence has been reported to be approximately 0.5 per 100 000 in men and 1.0 per 100 000 in women <sup>1</sup>. Its incidence is thought to be rising over the years <sup>5</sup>.</p><h4>Clinical presentation</h4><p>Approximately 45% of patients may present with bleeding per rectum. Around 30% of patients may have pain and/or a sensation of a mass.</p><h4>Pathology</h4><p>Anal carcinoma typically originates between the <a href="/articles/anorectal-junction">anorectal </a><a href="/articles/anorectal-junction">junction</a> above and the anal verge below. The vast majority of anal canal cancers are squamous cell cancers. See <a href="/articles/who-classification-of-anal-canal-tumours">WHO classification of anal canal tumours</a>.</p><h5>Risk factors</h5><p>Both male and female <sup>15</sup>:</p><ul>
  • -<li>HPV / HIV infection</li>
  • +<p><strong>Anal cancer</strong> is a relatively uncommon, accounting for less than 2% of large bowel malignancies, and most of the cases are made of squamous cell carcinoma. </p><h4>Epidemiology</h4><p>It accounts for less than 2% of large bowel malignancies and 1-6% of anorectal tumours (~1.5% of all gastrointestinal tract malignancies in the United States <sup>14</sup>). Commonly diagnosed between the ages of 45 and 75 years <sup>16</sup>. </p><p>There may be a slight female predilection where its incidence has been reported to be approximately 0.5 per 100 000 in men and 1.0 per 100 000 in women <sup>1</sup>. Its incidence is thought to be rising over the years <sup>5,16</sup>.</p><h4>Clinical presentation</h4><p>Approximately 45% of patients may present with bleeding per rectum. Around 30% of patients may have pain and/or a sensation of a mass.</p><h4>Pathology</h4><p>Anal carcinoma typically originates between the <a href="/articles/anorectal-junction">anorectal </a><a href="/articles/anorectal-junction">junction</a> above and the anal verge below. The vast majority of anal canal cancers are squamous cell cancers. See <a href="/articles/who-classification-of-anal-canal-tumours">WHO classification of anal canal tumours</a>.</p><ul>
  • +<li>~85% squamous cell carcinoma</li>
  • +<li>~10% adenocarcinoma </li>
  • +<li>~5% made of rarer tumours (e.g. melanoma, small cell carcinoma, and metastatic disease) <sup>16</sup>
  • +</li>
  • +</ul><h5>Risk factors</h5><p>Both male and female <sup>15</sup>:</p><ul>
  • +<li>HIV infection</li>
  • +<li>HPV infection<ul>
  • +<li>​strongly related to sexual activity<ul><li>in particular, anal receptive intercourse </li></ul>
  • +</li>
  • +<li>more than 90% of patients presenting with metastatic SCC have been reported with detectable HPV <sup>16</sup>
  • +</li>
  • +</ul>
  • +</li>
  • -</ul><p>In females: previous <em>in situ</em> or invasive cervical, vulval or vaginal cancer <sup>15</sup>. </p><h5>Lymphatic spread</h5><ul>
  • -<li>tumour above dentate line: to pararectal and paravertebral nodes <sup>13 </sup>
  • +</ul><p>In females: previous <em>in situ</em> or invasive cervical, vulva, or vaginal cancer <sup>15</sup>. </p><h5>Lymphatic spread</h5><ul>
  • +<li>tumour above dentate line: mesorectal and internal iliac nodes <sup>13,16</sup>
  • -<li>tumour below dentate line: to inguinal and femoral nodes <sup>13</sup>
  • +<li>tumour below dentate line: external iliac, inguinal, and deep inguinal nodes <sup>13,16</sup>
  • -</ul><h4>Radiographic features</h4><p>Imaging performed before treatment provides an assessment of the extent of local disease and nodal involvement. Accurate delineation of the disease in relation to the rest of the perineal anatomy is of paramount importance in initial imaging assessment. The size of the tumour is also considered a critical prognostic factor (see <a href="/articles/anal-cancer-staging-1">staging of anal cancer</a>) <sup>13</sup>.</p><h5>Ultrasound</h5><p>Endoanal ultrasound can sometimes be used in locoregional staging <sup>6</sup>. Some authors suggest that endoanal ultrasound can accurately determine the depth of penetration of the carcinoma into the sphincter complex and can be used to accurately gauge the response of these tumours to chemoradiation therapy <sup>8</sup>.</p><h5>MRI</h5><p>MRI is the modality of choice in the assessment of locoregional disease and is performed with performed with a dedicated protocol: see <a href="/articles/mri-protocol-for-assessment-of-anal-cancer">MRI protocol for assessment of anal cancer</a>.</p><p>Reported typical signal characteristics include <sup>2</sup>:</p><ul>
  • +</ul><h4>Radiographic features</h4><p>Imaging performed before treatment provides an assessment of the extent of local disease and nodal involvement. Accurate delineation of the disease in relation to the rest of the perineal anatomy is of paramount importance in initial imaging assessment. The size of the tumour is also considered a critical prognostic factor (see <a href="/articles/anal-cancer-staging-1">staging of anal cancer</a>) <sup>13</sup>.</p><h5>Ultrasound</h5><p>Endoanal ultrasound can sometimes be used in locoregional staging <sup>6</sup>, particularly for small superficial lesions (<a href="/articles/anal-cancer-staging-1">T1 stage</a>) <sup>16</sup>. Some authors suggest that endoanal ultrasound can accurately determine the depth of penetration of the carcinoma into the sphincter complex and can be used to accurately gauge the response of these tumours to chemoradiation therapy <sup>8</sup>.</p><h5>MRI</h5><p>MRI is the modality of choice in the assessment of locoregional disease and is performed with a dedicated protocol: see <a href="/articles/mri-protocol-for-assessment-of-anal-cancer">MRI protocol for assessment of anal cancer</a>.</p><p>Reported typical signal characteristics include <sup>2</sup>:</p><ul>
  • -</ul><p>Nodal metastases have a signal intensity similar to that of the primary tumour.</p><h5>PET-CT</h5><p>Recent research suggests that there are grounds for using PET-CT routinely in the workup of anal cancer, as it alters the initial staging sufficiently frequently <sup>4</sup>.</p><h5>Treatment and prognosis</h5><p>Treatment is often with a combination of chemotherapy and radiotherapy (often given concurrently) and is usually curative. Approximately 50-60% are thought to present with T1 to T2 lesions carrying a 5-year survival of 80-90% <sup>3</sup>. Some authors suggest a benefit of a salvage abdominoperineal resection (APR) for those patients with failed chemoradiation <sup>10,12</sup>.</p>
  • +</ul><p>Nodal metastases have a signal intensity similar to that of the primary tumour.</p><h5>PET-CT</h5><p><a href="/articles/f-18-fluorodeoxyglucose">F-18 FDG PET-CT</a> has been now used as an auxiliary imaging modality for staging in many countries. It has a high sensitivity for detection of both the primary lesion and the regional node involvement <sup>16</sup>, and it alters the initial staging frequently <sup>4</sup>.</p><h5>Treatment and prognosis</h5><p>Treatment is often with a combination of chemotherapy and radiotherapy (often given concurrently) and is usually curative in lower stages.</p><ul><li>approximately 50-60% are thought to present with T1 to T2 lesions carrying a 5-year survival of 80-90% <sup>3</sup>.</li></ul><p>Some authors suggest a benefit of a salvage abdominoperineal resection (APR) for those patients with failed chemoradiation <sup>10,12</sup>.</p>

References changed:

  • 16. Jennifer S. Golia Pernicka, Shannon P. Sheedy, Randy D. Ernst, Bruce D. Minsky, Dhakshinamoorthy Ganeshan, Gaiane M. Rauch. MR staging of anal cancer: what the radiologist needs to know. (2019) Abdominal Radiology. 44 (11): 3726. <a href="https://doi.org/10.1007/s00261-019-02020-4">doi:10.1007/s00261-019-02020-4</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/31041496">Pubmed</a> <span class="ref_v4"></span>

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