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Table 2 Absorbed doses in the tumour and normal organs in mice with subcutaneous PANC-1 xenografts treated with RICs

From: Radioimmunotherapy of PANC-1 human pancreatic cancer xenografts in NOD/SCID or NRG mice with Panitumumab labeled with Auger electron emitting, 111In or β-particle emitting, 177Lu

 

Absorbed Dose (Mean ± SD; Gy) a

Organ

Panitumumab-DOTA-[111In]In b

Panitumumab-MCP-[111In]In b

Panitumumab-DOTA-[177Lu]Lu c

Heart

1.9 ± 0.4

2.2 ± 0.1

2.5 ± 0.3

Lungs

2.5 ± 0.7

2.3 ± 0.3

4.0 ± 1.3

Liver

2.8 ± 0.6

6.1 ± 0.6

6.5 ± 0.9

Spleen

4.5 ± 1.4

7.5 ± 0.7

6.3 ± 1.1

Pancreas

1.4 ± 0.2

2.0 ± 0.3

5.3 ± 1.9

Stomach

1.2 ± 0.2

1.8 ± 0.1

0.9 ± 0.1

Intestine

1.5 ± 0.3

1.4 ± 0.2

0.6 ± 0.1

Kidneys

5.3 ± 0.7

5.2 ± 0.3

7.8 ± 1.1

Whole Body

1.7 ± 0.2

1.5 ± 0.1

1.3 ± 0.1

Tumour

8.8 ± 3.0

2.6 ± 0.3

11.6 ± 4.9

  1. aEstimated using \( D=\sum {\overset{\sim }{A}}_S\times {S}_{T\leftarrow S} \), where \( {\overset{\sim }{A}}_S \) is the time-integrated activity (Bq × sec) in the source organ (see Supplementary Fig. S2), and S is the Snyder factor for mouse organs (Bitar et al., 2007). The tumour dose was estimated using the sphere model in OLINDA/EXM dosimetry software and the tumour size (Stabin et al., 2005)
  2. bAbsorbed dose for NOD/SCID mice injected i.v. (tail vein) with three amounts (10 MBq; 10 μg; ~ 0.07 nmoles) of 111In-labeled RICs separated by 3 weeks
  3. cAbsorbed dose for NRG mice injected i.v. (tail vein) with a single amount (6 MBq; 10 μg; ~ 0.07 nmoles) of 177Lu-labeled RICs