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Cancer Research 67, 3970, April 15, 2007. doi: 10.1158/0008-5472.CAN-06-3822
© 2007 American Association for Cancer Research

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Clinical Research

Specific Growth Rate versus Doubling Time for Quantitative Characterization of Tumor Growth Rate

Esmaeil Mehrara1, Eva Forssell-Aronsson1, Håkan Ahlman2 and Peter Bernhardt1

Departments of 1 Radiation Physics and 2 Surgery, Göteborg University, Göteborg, Sweden

Requests for reprints: Esmaeil Mehrara, Department of Radiation Physics, Sahlgrenska University Hospital, Göteborg, SE-413 45 Sweden. Phone: 46-31-342-4023; Fax: 46-31-822-493; E-mail: e.mehrara{at}radfys.gu.se.

Doubling time (DT) is widely used for quantification of tumor growth rate. DT is usually determined from two volume estimations with measurement time intervals comparable with or shorter than DT. Clinical data show that the frequency distribution of DT in patients is positively skewed, with some very long DT values compared with the average DT. Growth rate can also be quantified using specific growth rate (SGR; %/d), equal to ln2/DT. The aim of this work was to compare DT and SGR as growth rate variables. Growth rate calculations were computer simulated for a tumor with DT of 100 days, measurement time interval of 1 to 200 days, and volume estimation uncertainty of 5% to 20%. Growth rate variables were determined and compared for previously published clinical data. The study showed that DT is not a suitable variable for tumor growth rate because (a) for short measurement time intervals, or high volume uncertainties, mean DT can either overestimate or underestimate the average growth rate; (b) DT is not defined if the consecutively estimated volumes are equal; and (c) the asymmetrical frequency distribution of DT makes it unsuitable for common statistical testing. In contrast, mean SGR and its equivalent DT give the correct values for average growth rate, SGR is defined for all tumor volume changes, and it has a symmetrical frequency distribution. SGR is also more accurate to use when discussing, for example, growth fraction, cell loss rate, and growth rate heterogeneities within the tumor. SGR should thus be used, instead of DT, to quantify tumor growth rate. [Cancer Res 2007;67(8):3970–5]




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Copyright © 2007 by the American Association for Cancer Research.