Background: Recently, commercial software tools have become available for dosimetry evaluations in clinical settings. The aim of this study was to compare a commercial dosimetry workstation (PLANETâDose) and the dosimetry approach (GE Dosimetry Toolkit® and OLINDA/EXM® V1.0) currently used in our department for quantification of the absorbed dose in organs at risk after peptide receptor radionuclide therapy with 177Lu-DOTATATE.Methods: First, an evaluation on phantom, with data acquisition at 5 time points, was performed to determine the SPECT calibration factor variations over time and to compare the Time Integrated Activity Coefficients (TIACs) and absorbed doses obtained with the two tools. Then, the two tools were used for dosimetry evaluation in 21 patients with neuroendocrine tumours after the first and second injection of 7.2 ± 0.2 GBq of 177Lu-DOTATATE (40 dosimetry analyses with each software). SPECT/CT images were acquired at 4h, 24h, 72h and 192h after 177Lu-DOTATATE injection and were reconstructed using the Xeleris software (General Electric). The liver, spleen and kidney masses, TIACs and absorbed doses were calculated using i) GE Dosimetry Toolkit® (DTK) and OLINDA/EXM® V1.0 and ii) the Local Deposition Method (LDM) or Dose voxel-Kernel convolution (DK) on PLANETâDose. Results: With the phantom, the 3D calibration factors showed a slight variation (0.8% and 3.3%) over time and TIACs of 225.19h and 217.52h were obtained with DTK and PLANETâDose, respectively. In patients, the mean of the relative standard deviations was -1% for the organ masses, 5.6%, for the TIACs, and 4.4% for the absorbed doses. The Lin’s concordance correlation coefficient was 0.99 and the Bland-Altman plot analysis estimated that the difference of absorbed dose values between methods ranged from -0.58 Gy to 0.84 Gy for approximately 95% of the 40 dosimetry analyses. A difference of 2.2% was obtained between the absorbed doses to organs at risk calculated with LDM and DK (PLANETâDose). Conclusions: The absorbed doses to organs at risk obtained with the new workstation are concordant with those calculated with the currently used software and in agreement with the literature. These results validate the use of PLANETâDose in clinical routine for patient dosimetry after targeted radiotherapy with 177Lu-DOTATATE.