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. 2022 Nov 11;10(11):2899. doi: 10.3390/biomedicines10112899

Table 1.

Patient characteristics and injected activity.

Participant Age [Years] Sex Primary First Diagnosis Status at Time of Study Disease State Mutational Status Treatment at Time of Study Injected Activity [MBq]
01 76 f Duodenum 2003 Omental and liver metastasis PD Exon 11 of cKit gene, TRP 557 ARG Sunitinib 179
02 72 f Ileum 2012 Liver metastases PD Exon 9 cKit gene Sunitinib 127
03 72 m Duodenum 2016 Liver and lung metastases SD Exon 9 cKit gene Sunitinib 214
04 83 f Stomach 2014 Liver metastases SD Exon 11 del557-558
Silent mutation PDGFRa P567P, CCA > CCG
Imatinib 158
05 50 f Stomach 2016 Local relapse, liver and peritoneal metastases PD Exon 18 D842V of PDGFRa gene None 169
06 55 m Ileum 2014 Liver metastasis PD Exon 11 of cKit gene, secondary exon 17 mutation Sunitinib 199
07 56 f Peritoneal 2015 Peritoneal and liver metastases PD Exon 11 of cKit gene, PDGF-R wild type Imatinib 177
08 56 f Stomach 2001 Liver, lung SD cKit-positive, specific mutation not assessed Nilotinib 161
09 56 m Small gut 2004 Liver, peritoneal metastases SD Exon 9 of cKit gene, PDGF-R wild type Imatinib 250

SD—stable disease, PD—progressive disease. Further data on safety, tolerability and pharmacokinetics in participants 1–6 were previously reported in [25].