Appendix cancer natural history, complications and prognosis: Difference between revisions

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==Overview==
==Overview==


*The majority of patients with appendix cancer may be initially asymptomatic. Most of appendix cancer cases are discovered after surgical or histological evaluation of a patient with acute appendicitis, or are an accidental finding in imaging studies for the other reasons. Early clinical features include periodical unspecific abdominal pain, bloating, and nausea. If left untreated, the majority of patients with appendix cancer may progress to develop peritoneal carcinomatosis and metastases. Prognosis is generally excellent and good in carcinoid tumors and adenocarcinomae respectively. Tumor size plays a crucial role in determining prognosis. Most of the appendiceal tumors are less than 2 cm in size and have a quite favorable prognosis since they barely metastasize.<ref>{{Cite journal
Because of the location and size of [[Vermiform appendix|appendix]], most of the [[Appendix cancer (patient information)|patients with appendix cancer]] may be initially [[asymptomatic]]. Early clinical features might include periodical unspecific [[abdominal pain]], [[bloating]], and [[Nausea and vomiting|nausea]]. Most of [[Vermiform appendix|appendix]] [[cancer]] cases are discovered after [[Surgery|surgical]] or [[Histology|histological]] evaluation of a patient with acute [[appendicitis]], or are an accidental finding in [[imaging studies]] for the other reasons. Around one percent of all [[appendectomy]] specimens are [[malignant]]. [[Vermiform appendix|Appendix]] [[cancer]] account for 0.5 percent of all intestinal neoplasms. If left untreated, the majority of patients with [[appendix cancer]] may progress to develop [[peritoneal carcinomatosis]] and [[metastasis]]. [[Prognosis]] is generally excellent and good in [[Carcinoid Tumor|carcinoid]] [[Tumor|tumors]] and [[adenocarcinoma]] respectively. [[Prognosis|Prognostic factors]] including tumor stage, [[tumor]] size, [[Histology|histologic]] as well [[Genetics|genetic]] characteristics of appendiceal tumors were discussed in details. 
==Natural History, Complications, and Prognosis==
 
===Natural History===
*The majority of patients with [[Vermiform appendix|appendix]] [[cancer]] may be initially [[asymptomatic]].
*Early clinical features might include periodical unspecific [[abdominal pain]], [[bloating]], and [[Nausea and vomiting|nausea]].
*Most of [[Vermiform appendix|appendix]] [[cancer]] cases are discovered after [[Surgery|surgical]] or [[Histology|histological]] evaluation of a patient with acute [[appendicitis]], or are an accidental finding in [[imaging studies]] for the other reasons.
*Around one percent of all [[appendectomy]] specimens are [[malignant]]. 
*Appendix cancer account for 0.5 percent of all intestinal [[neoplasm]]<nowiki/>s. 
*If left untreated, the majority of patients with appendix cancer may progress to develop [[peritoneal carcinomatosis]] and [[Metastasis|metastases]].
 
===Complications===
*Common complications of [[Vermiform appendix|appendix]] [[cancer]] include:
**[[Appendicitis|Acute appendicitis]]
*** Most of appendix [[adenocarcinoma]]<nowiki/>s present with [[Appendicitis|acute appendicitis]].
***However, majority of <nowiki/>[[Carcinoid Tumor|carcinoid]]<nowiki/>s are located in the distal one third of the [[Vermiform appendix|appendix]], hence rarely present with [[appendicitis]].
***Merely 10 percent of appendiceal [[Carcinoid Tumor|carcinoid]]<nowiki/>s are located at the base of [[Vermiform appendix|appendix]] and may tend to obstruction and [[appendicitis]].
**[[Pseudomyxoma peritonei]]
**[[Metastasis]]
**[[Carcinoid syndrome]]
***More commonly seen in [[midgut]] ([[Vermiform appendix|appendix]] and [[Small intestine|small bowel]]) [[Carcinoid Tumor|carcinoid]]<nowiki/>s.
***Almost always (90%) seen in [[Metastasis|metastatic]] disease, typically [[liver]] is the involved organ.
 
===Prognosis===
*
*
*Major [[Prognosis|prognostic]] factors are [[Cancer staging|tumor stage]], [[tumor]] size, [[Histology|histologic]] as well [[Genetics|genetic]] characteristics of appendiceal [[tumor]]<nowiki/>s. For [[TNM|TNM classification]] of [[tumor|t]]<nowiki/>[[tumor|umor]]<nowiki/>s of the [[Vermiform appendix|appendix]], [[Appendix cancer diagnostic study of choice|click here]].<ref name="WHO">Chapter 5: Tumours of the Appendix - IARC. https://www.iarc.fr/en/publications/pdfs-online/pat-gen/bb2/bb2-chap5.pdf Accessed on January 15, 2019</ref> 
 
*[[Prognosis]] is generally excellent and good in [[Carcinoid Tumor|carcinoid tumors]] and [[adenocarcinoma]]<nowiki/>s respectively.  
*The overall 5-year survival rate for adenocarcinoma of appendix is approximately 71% (see the Table below).<ref name="pmid9024720">{{cite journal| author=Modlin IM, Sandor A| title=An analysis of 8305 cases of carcinoid tumors. | journal=Cancer | year= 1997 | volume= 79 | issue= 4 | pages= 813-29 | pmid=9024720 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9024720  }}</ref>
*'''Tumor size''' plays a crucial role in determining prognosis.  
**Most of the appendiceal tumors are less than 2 cm in size and have a quite favorable prognosis since they barely metastasize.<ref name=":0">{{Cite journal
  | author = [[Irvin M. Modlin]], [[Kevin D. Lye]] & [[Mark Kidd]]
  | author = [[Irvin M. Modlin]], [[Kevin D. Lye]] & [[Mark Kidd]]
  | title = A 5-decade analysis of 13,715 carcinoid tumors
  | title = A 5-decade analysis of 13,715 carcinoid tumors
Line 18: Line 49:
  | doi = 10.1002/cncr.11105
  | doi = 10.1002/cncr.11105
  | pmid = 12569593
  | pmid = 12569593
}}</ref><ref>A poorer survival has been reported for the black patients with carcinoid tumors. <nowiki><ref name=":0"></nowiki>{{Cite journal
}}</ref><ref name=":1">A poorer survival has been reported for the black patients with carcinoid tumors. <nowiki><ref name=":0"></nowiki>{{Cite journal
  | author = [[Melinda A. Maggard]], [[Jessica B. O'Connell]] & [[Clifford Y. Ko]]
  | author = [[Melinda A. Maggard]], [[Jessica B. O'Connell]] & [[Clifford Y. Ko]]
  | title = Updated population-based review of carcinoid tumors
  | title = Updated population-based review of carcinoid tumors
Line 28: Line 59:
  | month = July
  | month = July
  | pmid = 15213627
  | pmid = 15213627
}}</ref> The overall 5-year survival rate for adenocarcinoma of appendix is approximately 71% (see the Table below). <ref name="pmid9024720">{{cite journal| author=Modlin IM, Sandor A| title=An analysis of 8305 cases of carcinoid tumors. | journal=Cancer | year= 1997 | volume= 79 | issue= 4 | pages= 813-29 | pmid=9024720 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9024720  }}</ref> Other prognostic factors such as histologic and genetic characteristics of appendiceal tumors are discussed in details below.
}}</ref>  
==Natural History, Complications, and Prognosis==
*The prognosis varies with the [[histology]] of tumor.
 
*[[Carcinoid Tumor|Carcinoid tumors]] are associated with a better [[prognosis]] among patients with appendiceal cancer.
===Natural History===
*Localized [[Carcinoid Tumor|carcinoid tumors]] are associated with the most favorable [[prognosis]].
*The symptoms of (disease name) usually develop in the first/ second/ third decade of life, and start with symptoms such as ___.  
*The presence of tubular pathology is also associated with a particularly good prognosis among patients with appendix adenocarcinoma.
*The symptoms of (disease name) typically develop ___ years after exposure to ___.
*Goblet cell carcinoids are generally more aggressive than other [[Carcinoid Tumor|carcinoid tumors]].
*If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
*According to surveillance, [[epidemiology]] and end results (SEER) database of the [[National Cancer Institute|national cancer institute]] five-year appendiceal  [[Carcinoid Tumor|carcinoid]] [[survival rate]]<nowiki/>s were as follows:
 
:* '''Tumor size <3 cm''' without regional nodal or distant [[Metastasis|metastas]]<nowiki/>es: 100 percent
===Complications===
:* '''Tumor size between 2 and 3 cm''' plus regional node [[Metastasis|metastases]] / tumor size ≥3 cm with or without regional nodal or distant [[Metastasis|metastases]]: 78 percent
*Common complications of appendix cancer include:
:* '''Distant metastasis:''' 32 percent
**Acute appendicitis
{| class="wikitable" style="border: 5px; font-size: 90%; margin: 5px; width: 300px" align="center"
**Pseudomyxoma pritonei
! style="padding: 5px 5px; background: #4479BA; font-weight: bold; text-align:center;" |{{fontcolor|#FFF|Five year survival rates}}
**?????????
 
===Prognosis===
*Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [--]%.
*Depending on the extent of the [tumor/disease progression] at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor/good/excellent.
*The presence of [characteristic of disease] is associated with a particularly [good/poor] prognosis among patients with [disease/malignancy].
*[Subtype of disease/malignancy] is associated with the most favorable prognosis.
*The prognosis varies with the [characteristic] of tumor; [subtype of disease/malignancy] have the most favorable prognosis.
 
{| style="border: 5px; font-size: 90%; margin: 5px; width: 300px" align="center"
! colspan="2" style="padding: 5px 5px; background: #4479BA; font-weight: bold; text-align:center;" |Five year survival rates
| valign="top" |
|+
|+
|-
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" | Carcinoid tumors
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |Carcinoid tumors
|-
|-
|  
|  
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:*Distant metastasis 51%*
:*Distant metastasis 51%*
|-
|-
|''* Shows that mucinous adenocarcinomae are less aggressive'' ''than nunmnucinous tumors''
|<small>''* Shows that mucinous adenocarcinomae are less aggressive'' ''than nunmnucinous tumors''</small>
|}
|}


* '''Poor prognostic factors''' for '''appendiceal adenocarcinoma''' are as follows:  
* '''Poor [[Prognosis|prognostic]] factors''' for '''appendiceal [[adenocarcinoma]]''' are as follows:  
** Advanced stage  
** Advanced [[Cancer staging|stage]]
**High grade
**High grade
** Nonmucinous histology  
** Non-mucinous [[histology]]
** Spread of the tumor beyond the left lower quadrant
** Spread of the [[tumor]] beyond the left lower quadrant
** Presence of malignant cells outside of the visceral peritoneum of the appendix
** Presence of [[malignant]] cells outside of the visceral [[peritoneum]] of the appendix
* '''Poor prognostic factors in the presence of'''  '''''pseudomyxoma peritonei''''' are as follows:   
 
** Abdominal distension
* '''Poor prognostic factors in the presence of'''  '''[[pseudomyxoma peritonei]]''' are as follows:   
** Weight loss
** [[Abdominal distension]]
** [[Weight loss]]
** High histological grade
** High histological grade
** Morphological evidence of invasion of underlying structures  
** Morphological evidence of invasion of underlying structures  


*'''Genetic prognostic markers of appendical cancers are as follows:'''
*'''[[Genetics|Genetic]] [[Prognosis|prognostic]] markers of appendiceal cancers''' are as follows:
**Genetic studies revolutionized cancer treatment, appendix cancer is not an exception.
**[[Genetics|Genetic]] studies revolutionized [[cancer]] treatment; [[Vermiform appendix|appendix]] [[cancer]] is not an exception.
**Traditionally appandiceal cancers were approached the same as colorectal cancers.  
**Traditionally appendiceal cancers were approached the same as [[colorectal cancer]]<nowiki/>s.  
**Recent genetic studies demonstrated that appendiceal tumors are clearly differ from colorectal cancers. <ref name="pmid22342786">&lt;/nowiki&gt;{{cite journal| author=Levine EA, Blazer DG, Kim MK, Shen P, Stewart JH, Guy C et al.| title=Gene expression profiling of peritoneal metastases from appendiceal and colon cancer demonstrates unique biologic signatures and predicts patient outcomes. | journal=J Am Coll Surg | year= 2012 | volume= 214 | issue= 4 | pages= 599-606; discussion 606-7 | pmid=22342786 | doi=10.1016/j.jamcollsurg.2011.12.028 | pmc=3768122 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22342786  }} </ref>
***Recent [[Genetics|genetic]] studies demonstrated that appendiceal tumors are clearly differ from [[colorectal cancer]]<nowiki/>s. <ref name="pmid22342786">&lt;/nowiki&gt;{{cite journal| author=Levine EA, Blazer DG, Kim MK, Shen P, Stewart JH, Guy C et al.| title=Gene expression profiling of peritoneal metastases from appendiceal and colon cancer demonstrates unique biologic signatures and predicts patient outcomes. | journal=J Am Coll Surg | year= 2012 | volume= 214 | issue= 4 | pages= 599-606; discussion 606-7 | pmid=22342786 | doi=10.1016/j.jamcollsurg.2011.12.028 | pmc=3768122 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22342786  }} </ref>
 
***Presence of mutated [[TP53]] and [[APC]] genes were significantly lower in appendiceal cancers compared to [[colorectal cancer]]<nowiki/>s.
**Presence of mutated TP53 and APC genes were significantly lower in appendiceal cancers compared to colorectal cancers.
** It has been shown that mutation profiles are associated with the patients’ [[prognosis]]. <ref name="pmid26821970">{{cite journal| author=Levine EA, Votanopoulos KI, Qasem SA, Philip J, Cummins KA, Chou JW et al.| title=Prognostic Molecular Subtypes of Low-Grade Cancer of the Appendix. | journal=J Am Coll Surg | year= 2016 | volume= 222 | issue= 4 | pages= 493-503 | pmid=26821970 | doi=10.1016/j.jamcollsurg.2015.12.012 | pmc=4808611 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26821970  }} </ref>
** It has been shown that mutation profiles are associated with the patients’ prognosis. <ref name="pmid26821970">{{cite journal| author=Levine EA, Votanopoulos KI, Qasem SA, Philip J, Cummins KA, Chou JW et al.| title=Prognostic Molecular Subtypes of Low-Grade Cancer of the Appendix. | journal=J Am Coll Surg | year= 2016 | volume= 222 | issue= 4 | pages= 493-503 | pmid=26821970 | doi=10.1016/j.jamcollsurg.2015.12.012 | pmc=4808611 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26821970  }} </ref>
*** [[Mutation]]<nowiki/>s in the [[TP53]] significantly decrease life expectancy in patients with appendix cancer.   
**Mutations in the TP53 significantly decrease life expectancy in patients with appendix cancer.   
*** Regardless of tumor grade, [[TP53]] mutations were associated with poorer outcomes.
** Regardless of tumor grade, Tp 53 mutations were associated with poorer outcomes.
*** Patients with [[GNAS complex locus|GNAS]] [[mutation]]<nowiki/>s had a [[life expectancy]] of 10 years after diagnosis.  
** Patients with GNAS mutations had a life expectancy of 10 years after diagnosis.  
*** Appendiceal [[tumor]]<nowiki/>s with [[GNAS complex locus|GNAS]] [[mutation]]<nowiki/>s rarely develop into high-grade tumors.
** Appendiceal tumors with GNAS mutations rarely develop into high-grade tumors.


==References==
==References==
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Latest revision as of 17:48, 22 February 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Soroush Seifirad, M.D.[2]


Overview

Because of the location and size of appendix, most of the patients with appendix cancer may be initially asymptomatic. Early clinical features might include periodical unspecific abdominal pain, bloating, and nausea. Most of appendix cancer cases are discovered after surgical or histological evaluation of a patient with acute appendicitis, or are an accidental finding in imaging studies for the other reasons. Around one percent of all appendectomy specimens are malignant. Appendix cancer account for 0.5 percent of all intestinal neoplasms. If left untreated, the majority of patients with appendix cancer may progress to develop peritoneal carcinomatosis and metastasis. Prognosis is generally excellent and good in carcinoid tumors and adenocarcinoma respectively. Prognostic factors including tumor stage, tumor size, histologic as well genetic characteristics of appendiceal tumors were discussed in details.

Natural History, Complications, and Prognosis

Natural History

Complications

Prognosis

  • Prognosis is generally excellent and good in carcinoid tumors and adenocarcinomas respectively.
  • The overall 5-year survival rate for adenocarcinoma of appendix is approximately 71% (see the Table below).[2]
  • Tumor size plays a crucial role in determining prognosis.
    • Most of the appendiceal tumors are less than 2 cm in size and have a quite favorable prognosis since they barely metastasize.[3][4]
  • The prognosis varies with the histology of tumor.
  • Carcinoid tumors are associated with a better prognosis among patients with appendiceal cancer.
  • Localized carcinoid tumors are associated with the most favorable prognosis.
  • The presence of tubular pathology is also associated with a particularly good prognosis among patients with appendix adenocarcinoma.
  • Goblet cell carcinoids are generally more aggressive than other carcinoid tumors.
  • According to surveillance, epidemiology and end results (SEER) database of the national cancer institute five-year appendiceal carcinoid survival rates were as follows:
  • Tumor size <3 cm without regional nodal or distant metastases: 100 percent
  • Tumor size between 2 and 3 cm plus regional node metastases / tumor size ≥3 cm with or without regional nodal or distant metastases: 78 percent
  • Distant metastasis: 32 percent
Five year survival rates
Carcinoid tumors
  • localized disease 94%
  • Regional disease 85%
  • Distant metastases 34%
  • Goblet cell 12.5%
  • Tubular tumors are benign clinically
Adenocarcinoma
Nonmucinus
  • Localized 95%
  • Distant metastasis 0%*
Mucinous adenocarcinoma
  • localized 80%
  • Distant metastasis 51%*
* Shows that mucinous adenocarcinomae are less aggressive than nunmnucinous tumors

References

  1. Chapter 5: Tumours of the Appendix - IARC. https://www.iarc.fr/en/publications/pdfs-online/pat-gen/bb2/bb2-chap5.pdf Accessed on January 15, 2019
  2. Modlin IM, Sandor A (1997). "An analysis of 8305 cases of carcinoid tumors". Cancer. 79 (4): 813–29. PMID 9024720.
  3. Irvin M. Modlin, Kevin D. Lye & Mark Kidd (2003). "A 5-decade analysis of 13,715 carcinoid tumors". Cancer. 97 (4): 934–959. doi:10.1002/cncr.11105. PMID 12569593. Unknown parameter |month= ignored (help)
  4. A poorer survival has been reported for the black patients with carcinoid tumors. <ref name=":0">Melinda A. Maggard, Jessica B. O'Connell & Clifford Y. Ko (2004). "Updated population-based review of carcinoid tumors". Annals of surgery. 240 (1): 117–122. PMID 15213627. Unknown parameter |month= ignored (help)
  5. </nowiki>Levine EA, Blazer DG, Kim MK, Shen P, Stewart JH, Guy C; et al. (2012). "Gene expression profiling of peritoneal metastases from appendiceal and colon cancer demonstrates unique biologic signatures and predicts patient outcomes". J Am Coll Surg. 214 (4): 599–606, discussion 606-7. doi:10.1016/j.jamcollsurg.2011.12.028. PMC 3768122. PMID 22342786.
  6. Levine EA, Votanopoulos KI, Qasem SA, Philip J, Cummins KA, Chou JW; et al. (2016). "Prognostic Molecular Subtypes of Low-Grade Cancer of the Appendix". J Am Coll Surg. 222 (4): 493–503. doi:10.1016/j.jamcollsurg.2015.12.012. PMC 4808611. PMID 26821970.

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