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Modified Severity Weighted Assessment Tool

Physician-Reported Clinical Assessment

Calculate the mSWAT skin score for mycosis fungoides and Sezary syndrome from the percentage of body surface area with patches, plaques and tumours in 12 regions. Includes change from baseline and the consensus response thresholds.

About the mSWAT

Clinical Background

The Severity Weighted Assessment Tool (SWAT) was introduced by Stevens et al. (2002) to quantify the skin burden of mycosis fungoides by weighting the extent of patches, plaques and tumours, and it correlated closely with the percentage of body surface area involved and with the time to remission under phototherapy. The modified SWAT (mSWAT) replaced the original grid counting with twelve body regions carrying fixed shares of body surface area and raised the tumour weight from three to four; it was first used in the phase IIb vorinostat trial (Olsen et al. 2007) and was then adopted as the standard skin measure in the consensus statement of the International Society for Cutaneous Lymphomas, the United States Cutaneous Lymphoma Consortium and the EORTC Cutaneous Lymphoma Task Force (Olsen et al. 2011).

For each of the twelve regions (head 7%, neck 2%, anterior trunk 13%, arms 8%, forearms 6%, hands 5%, posterior trunk 13%, buttocks 5%, thighs 19%, legs 14%, feet 7% and groin 1% of body surface area), the percentage of total body surface area occupied by patches, by plaques and by tumours is recorded, with the patient's palm including the fingers taken as approximately 1% of body surface area. A patch is any size lesion without induration or significant elevation; a plaque is elevated or indurated; a tumour is a solid or nodular lesion of at least 1 cm with deep infiltration or vertical growth. The percentages for each lesion type are summed across the regions and multiplied by the weighting factors 1, 2 and 4, and the three weighted totals are added to give the mSWAT, from 0 to 400. The lesion areas within a region cannot exceed that region's share of body surface area.

Skin response in the consensus criteria is defined from the change in the mSWAT: a complete response is 100% clearance of skin lesions, a partial response is a 50% to 99% clearance from baseline without new tumours in patients whose skin disease was patches, plaques or erythroderma only, stable disease lies between a 25% increase and a 50% clearance, and progressive disease is an increase of 25% or more from baseline, the appearance of new tumours, or loss of a previous response. Trials such as MAVORIC (Kim et al. 2018) and ALCANZA (Prince et al. 2017) operationalise the partial response as a reduction of at least 50% in the mSWAT, and later reports describe this threshold as mSWAT 50, with mSWAT 90 for a 90% reduction. The calculator evaluates the 50%, 90% and 100% reductions and the 25% progression threshold from an optional baseline score; new tumours and biopsy findings must be judged clinically.

The mSWAT measures skin disease only and is combined with blood, lymph node and visceral assessments in the global response of the consensus. Estimating lesion areas by palm counts introduces observer variability, particularly for tumours and erythrodermic disease, and no dedicated psychometric validation of the modified tool has been published; its use rests on the consensus and on trial practice. The 2022 update of the recommendations (Olsen et al. 2022) retained the twelve regions and the weighting factors, defined erythroderma as involvement of at least 80% of body surface area, and aligned the response categories with the Lugano classification.

References

  1. Olsen EA, Whittaker S, Kim YH, Duvic M, Prince HM, Lessin SR, et al.. Clinical end points and response criteria in mycosis fungoides and Sezary syndrome: a consensus statement of the International Society for Cutaneous Lymphomas, the United States Cutaneous Lymphoma Consortium, and the Cutaneous Lymphoma Task Force of the European Organisation for Research and Treatment of Cancer. J Clin Oncol. 2011;29(18):2598-2607. doi:10.1200/JCO.2010.32.0630
  2. Olsen EA, Whittaker S, Willemze R, Pinter-Brown L, Foss F, Geskin L, et al.. Primary cutaneous lymphoma: recommendations for clinical trial design and staging update from the ISCL, USCLC, and EORTC. Blood. 2022;140(5):419-437. doi:10.1182/blood.2021012057
  3. Stevens SR, Ke MS, Parry EJ, Mark J, Cooper KD. Quantifying skin disease burden in mycosis fungoides-type cutaneous T-cell lymphomas: the severity-weighted assessment tool (SWAT). Arch Dermatol. 2002;138(1):42-48. doi:10.1001/archderm.138.1.42
  4. Olsen EA, Kim YH, Kuzel TM, Pacheco TR, Foss FM, Parker S, et al.. Phase IIb multicenter trial of vorinostat in patients with persistent, progressive, or treatment refractory cutaneous T-cell lymphoma. J Clin Oncol. 2007;25(21):3109-3115. doi:10.1200/JCO.2006.10.2434
  5. Kim YH, Bagot M, Pinter-Brown L, Rook AH, Porcu P, Horwitz SM, et al.. Mogamulizumab versus vorinostat in previously treated cutaneous T-cell lymphoma (MAVORIC): an international, open-label, randomised, controlled phase 3 trial. Lancet Oncol. 2018;19(9):1192-1204. doi:10.1016/S1470-2045(18)30379-6
  6. Prince HM, Kim YH, Horwitz SM, Dummer R, Scarisbrick J, Quaglino P, et al.. Brentuximab vedotin or physician's choice in CD30-positive cutaneous T-cell lymphoma (ALCANZA): an international, open-label, randomised, phase 3, multicentre trial. Lancet. 2017;390(10094):555-566. doi:10.1016/S0140-6736(17)31266-7
  7. Combalia A, Estrach T. The Modified Severity-Weighted Assessment Tool: a PASI/EASI system for mycosis fungoides. Actas Dermosifiliogr. 2018;109(8):745-746. doi:10.1016/j.adengl.2017.11.022

Development

The clinical calculators on this site are free to use. They were developed in partnership by the Centre for Medical and Surgical Dermatology and Dermi(opens in a new tab), a Toronto company that makes clinical imaging software for dermatology practices, which continues to maintain them.

Frequently Asked Questions about the mSWAT

The modified Severity Weighted Assessment Tool (mSWAT) is the physician-scored measure of skin tumour burden in mycosis fungoides and Sezary syndrome adopted by the ISCL, USCLC and EORTC consensus on clinical end points (Olsen et al. 2011). It records the percentage of body surface area occupied by patches, plaques and tumours in twelve body regions, weights the three lesion types by 1, 2 and 4, and ranges from 0 to 400.
For each of the twelve body regions the percentage of total body surface area covered by patches, by plaques and by tumours is estimated, using the patient's palm with fingers as about 1% of body surface area. The percentages for each lesion type are added across the regions, the patch total is multiplied by 1, the plaque total by 2 and the tumour total by 4, and the three products are summed. For example, 33% patches, 12% plaques and 2% tumours give 33 + 24 + 8, an mSWAT of 65.
A patch is a lesion of any size without induration or significant elevation above the surrounding skin; poikiloderma may be present. A plaque is a lesion of any size that is elevated or indurated, with or without crusting, ulceration or poikiloderma. A tumour is a solid or nodular lesion at least 1 cm in shortest diameter with evidence of deep infiltration or vertical growth. The weighting factors of 1, 2 and 4 reflect the increasing severity of the three lesion types.
mSWAT 50 denotes a reduction of at least 50% in the mSWAT from baseline, which is the skin partial response threshold of the consensus criteria provided no new tumours have appeared. A complete response requires 100% clearance of skin lesions, and progressive disease is an increase of 25% or more from baseline, new tumours, or loss of a previous response. mSWAT 90 is sometimes reported for a reduction of at least 90%.
No severity bands have been defined for the mSWAT. Clinical stage in mycosis fungoides is assigned from the TNMB classification, in which the T category depends on the percentage of body surface area involved and the presence of tumours or erythroderma, together with lymph node, visceral and blood findings. The mSWAT is used to quantify skin burden and to measure change over time rather than to stage the disease.

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