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Published online before print April 14, 2009
British Journal of Radiology 2009, doi:10.1259/bjr/72829563

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© 2009 The British Institute of Radiology

Full paper

The minimum number of target lesions that need to be measured to be representative of the total number of target lesions (according to RECIST)

M H S E DARKEH 1, C SUZUKI 2, M R TORKZAD 3

1 Department of Diagnostic Radiology, Karolinska University Hospital Solna and Karolinska Institute, Stockholm Sweden
2 Department of Diagnostic Radiology, Karolinska University Hospital Solna and Karolinska Institute, Stockholm Sweden. National Cancer Center East, Chiba, Japan; Department of Radiology, Keio University School of Medicine, Tokyo, Japan
3 Radiology Department, Uppsala University Hospital, Uppsala, Sweden and Institution for Molecular Medicine and Surgery, Karolinska Institute, Stockholm Sweden


   Abstract

Response evaluation criteria in solid tumors (RECIST) were introduced as a means to classify tumour response with no definition of the minimum number of lesions. This study was conducted in order to evaluate discrepancies between full assessments based on either all target lesions or fewer lesions. RECIST evaluation was performed on separate occasions based on between one and seven of the target lesions, with simultaneous assessment of non-target lesions. 99 patients were included. 38 patients demonstrated progressive disease, 61% of which was as a result of the appearance of new lesions or unequivocal progress in non-target lesions. 32 patients showed stable disease, with 8 having results that differed when 1–3 target lesions were measured. 22 cases were considered as having partial regression, with only 1 case differing when performing 1–3 target lesion assessments. Seven cases demonstrated complete response. The number of discordant cases increased gradually from measuring three lesions to one target lesion. The average number of available target lesions among those with discrepancies was 7.1, which was significantly higher than those demonstrating concordance (4.1 lesions; p<0.05). In conclusion, measuring fewer than four target lesions might cause discrepancies when more than five target lesions are present.







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