The rule of fives, a simple way to stratify risk for primary gastrointestinal stromal tumors (GIST)
© Maki; licensee BioMed Central Ltd. 2012
Received: 20 August 2012
Accepted: 3 October 2012
Published: 5 October 2012
The current AJCC version 7 staging system is a lugubrious means to classify gastrointestinal stromal tumors with respect to their risk and need for adjuvant systemic therapy. The rule of fives, suggested here, is a means to quickly assess whether a given gastrointestinal stromal tumor is low vs intermediate-high risk.
KeywordsGastrointestinal stromal tumor GIST Staging Adjuvant therapy
Risk stratification for primary gastrointestinal stromal tumors (GISTs) has evolved with the understanding of the disease, spurred by its demonstration as a specific sarcoma subtype. GISTs most commonly contain an activating mutation in KIT, or much less commonly in PDGFRA; even rarer forms of GIST have other genetic alterations. Risk stratification is critical, since three years of adjuvant imatinib is now considered a standard of care for patients with intermediate to high risk primary GIST.
Risk criteria were first published in 2001 and were amended as more was learned about the importance of mitotic rate, anatomic primary site, and size, in large part due to large case series developed by Miettinen, Lasota and colleagues [1, 2]. These factors have been incorporated into a nomogram , risk heat map and detailed staging system , and have been incorporated into the most recent (7th) edition of the American Joint Committee on Cancer (AJCC) staging manual.
The nomenclature for staging involves a number of details that may be difficult to remember for an uncommon tumor. The collective data suggest a simple way to deduce low risk vs. intermediate-high risk GISTs. The “rule of fives” states that intermediate to high risk gastric GISTs are both more than 5 cm in size and have more than 5 mitoses (mit) per 50 high powered fields (hpf). Conversely, nonCXgastric GISTs are high grade if they are either more than 5 cm in size or have more than 5 mit/50 hpf. With this simple “and/or” construct, all the GISTs with over 50% risk of recurrence are captured, as are an intermediate risk group of 5–10 cm small bowel GIST with low mitotic rate (24% recurrence risk, Miettinen prognostic group 3a).
This rule is particularly useful to highlight the situation of a common but surprisingly low risk GIST, i.e. those gastric GISTs that are >5 cm and have a low mitotic rate. Since the recurrence risk of these GISTs is 12% or less per Miettinen and colleagues [1, 2], these patients are potentially good candidates for observation alone after primary surgery.
Further nuances will arise as exact mutation rate and KIT or PDGFRA mutation status are incorporated into staging. However, exon 9 KIT mutations (~15% of GIST) are nearly exclusively found in a small bowel primary site, and uncommon PDGFRA mutations are usually associated with a gastric primary site. As a result, future patient staging efforts should not prove unduly cumbersome, and can build on this simple rule.
The author was solely responsible for the content of this manuscript, including literature search, data interpretation, and writing.
Role of the funding source
There is no relevant research support to report.
- Miettinen M, Makhlouf H, Sobin LH, Lasota J: Gastrointestinal stromal tumors of the jejunum and ileum: a clinicopathologic, immunohistochemical, and molecular genetic study of 906 cases before imatinib with long-term follow-up. Am J Surg Pathol. 2006, 30: 477-489. 10.1097/00000478-200604000-00008View ArticlePubMed
- Miettinen M, Sobin LH, Lasota J: Gastrointestinal stromal tumors of the stomach: a clinicopathologic, immunohistochemical, and molecular genetic study of 1765 cases with long-term follow-up. Am J Surg Pathol. 2005, 29: 52-68. 10.1097/01.pas.0000146010.92933.deView ArticlePubMed
- Gold JS, Gonen M, Gutierrez A, Broto JM, Garcia-del-Muro X, Smyrk TC, Maki RG, Singer S, Brennan MF, Antonescu CR: Development and validation of a prognostic nomogram for recurrence-free survival after complete surgical resection of localised primary gastrointestinal stromal tumour: a retrospective analysis. Lancet Oncol. 2009, 10: 1045-1052. 10.1016/S1470-2045(09)70242-6PubMed CentralView ArticlePubMed
- Joensuu H, Vehtari A, Riihimaki J, Nishida T, Steigen SE, Brabec P, Plank L, Nilsson B, Cirilli C, Braconi C: Risk of recurrence of gastrointestinal stromal tumour after surgery: an analysis of pooled population-based cohorts. Lancet Oncol. 2012, 13: 265-274. 10.1016/S1470-2045(11)70299-6View ArticlePubMed
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