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Enneking Staging for Malignant and Benign Bone Tumour

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The Enneking (Musculoskeletal Tumor Society, MSTS) staging system is a widely used orthopaedic-oncology framework that stages both benign and malignant bone tumours. It combines histological grade (G), local anatomical extent (T), and metastasis (M) to predict behaviour and guide the surgical margin needed.

Core components

Factor Code Meaning
Grade G0 Benign histology
G1 Low-grade malignant
G2 High-grade malignant
Local extent T0 Intracapsular/intracompartmental; well contained
T1 Extracapsular but still intracompartmental
T2 Extracompartmental; has breached natural barriers
Metastasis M0 No regional or distant metastasis
M1 Regional or distant metastasis

Grade reflects cellular aggressiveness; T is assessed mainly with MRI/CT and describes whether the tumour remains within the bone or another anatomical compartment; M records spread, most often to lung.

Enneking staging tumour
Enneking staging tumour

Benign bone tumours

Benign lesions are staged 1–3 according to clinical and radiographic aggressiveness, rather than metastatic potential.

Stage Name Behaviour Typical management
1 Latent Well-defined, often asymptomatic, non-progressive or self-healing; intact cortex and sclerotic rim Observe; treat only if symptomatic or at risk of fracture
2 Active Slowly growing and symptomatic; may thin cortex but usually does not penetrate it Intralesional curettage, often with bone graft or adjuvant
3 Aggressive Locally destructive, indistinct margin, may breach cortex and extend into soft tissue; higher recurrence risk More extensive curettage with adjuvants or marginal/wide excision, selected by lesion and site

Examples: a small non-ossifying fibroma is commonly latent; an osteoid osteoma or aneurysmal bone cyst may be active; a giant cell tumour of bone is a classic aggressive benign lesion. Even stage 3 benign tumours usually do not metastasize, but they can recur locally.

Malignant bone tumours

For malignant tumours, Enneking stages are written with Roman numerals and use A/B to denote compartmental status.

Stage Grade Extent Metastasis Practical implication
IA G1 low grade T1 intracompartmental M0 Lower-risk localized disease
IB G1 low grade T2 extracompartmental M0 Low grade but locally advanced
IIA G2 high grade T1 intracompartmental M0 High grade, still contained
IIB G2 high grade T2 extracompartmental M0 Common presentation of osteosarcoma; high local aggressiveness
III G1 or G2 T1 or T2 M1 Any malignant tumour with metastasis; prognosis is substantially worse

Thus, I = low grade, II = high grade, and III = metastatic disease, while A = confined to the compartment and B = extension beyond it. A “skip lesion”—a separate tumour deposit in the same bone or across an adjacent joint—is generally treated as stage III disease.

Why it matters

The system helps surgeons choose an oncologically appropriate margin:

  • Intralesional curettage: through the lesion; suitable for many latent/active benign lesions.
  • Marginal excision: through the reactive zone/pseudocapsule; may be used for some aggressive benign lesions.
  • Wide en-bloc resection: removes the tumour with a cuff of normal tissue; typically required for malignant lesions.
  • Radical resection: removes the entire affected compartment; now less commonly used but conceptually part of the Enneking surgical-margin framework.

For example, a high-grade osteosarcoma that has broken through the femoral cortex into surrounding soft tissue but has no metastases is stage IIB; if lung metastases are present, it becomes stage III regardless of grade or local extent.

REFERENCES:

Davis JH. Anatomical classification and surgical considerations: primary spinal tumours an overview. SA orthop. j.  [Internet]. 2011  Jan [cited  2026  Oct  31] ;  10( 3 ): 26-30. Available from: http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S1681-150X2011000300003&lng=en.

Springfield D, Rosen G. Staging. In: Kufe DW, Pollock RE, Weichselbaum RR, et al., editors. Holland-Frei Cancer Medicine. 6th edition. Hamilton (ON): BC Decker; 2003. Available from: https://www.ncbi.nlm.nih.gov/books/NBK12389/

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