Table 2 Summary of the mouse TGI data used in this study.

From: Semi-mechanistic efficacy model for PARP + ATR inhibitors—application to rucaparib and talazoparib in combination with gartisertib in breast cancer PDXs

Study

PDX

PARP inhibitor (PARPi)

ATR inhibitor (ATRi) gartisertib

Treatment arms

1 N = 7

HBCx-9

rucaparib 50, 100 mg/kg

qd x35 days, BID x35 days

3 mg/kg qd x35 days

3 mg/kg (1won/1woff)x2 + 1won

1x PARPi monotherapy

1x ATRi monotherapy

5x combination

2 N = 7

HBCx-9

rucaparib 50 mg/kg

qd x28 days

10, 20 mg/kg once weekly x4

5, 10 mg/kg twice weekly x4

1, 3 mg/kg qd x28

1x PARPi monotherapy

2x ATRi monotherapy

6x combination

3 N = 8

HBCx-9

talazoparib 0.15 mg/kg

BID x28 days

10, 20 mg/kg once weekly x4

5, 10 mg/kg twice weekly x4

1, 3 mg/kg qd x28 days

3 mg/kg qd x7 days

1x PARPi monotherapy

2x ATRi monotherapy

7x combination

4 N = 9

HBCx-9

talazoparib 0.15 mg/kg

BID x6 or x8 weeks

20 mg/kg once weekly x6

20 mg/kg twice weekly x6 (*)

20 mg/kg three times a week x6 (*)

(*) Dose reduced to 10 mg/kg from Day 13

1x PARPi monotherapy

1x ATRi monotherapy

3x combination

PDX panel

N = 3

9 TNBC PDXs (*)

talazoparib 0.3 mg/kg

qd x28

10, 20 mg/kg twice weekly x4

1x PARPi monotherapy

1x ATRi monotherapy

1x combination

  1. N = number of mice per arm at the start of treatment for each study. Additional details, deviations and full list of PDXs(*) in Supplementary Methods 8.