Skip to main content
. 2022 May 16;14(10):2453. doi: 10.3390/cancers14102453

Table 1.

Recent advances in PARP inhibitor therapy, adapted from Gupta and colleagues [90].

Investigators Phase Patient Population Number of PDAC Patients Intervention Outcome Ref
Kauffman et al. II PDAC with gBRCA1/2 mutation following progression on gemcitabine 23 Olaparib 400mg PO BID ORR 22% PFS 4.6 months OS 9.8 months [91]
Shroff et al. II PDAC with any BRCA mutation, previously treated with 1-2 lines 19 Rucaparib 600mg PO BID ORR 16% [83]
Lowery et al. II PDAC with gBRCA mutation or PALB2 mutation, 1-2 prior lines of treatment 16 Veliparib PO BID PO PFS 1.7 months OS 3.1 months [85]
Golan et al. II PDAC with BRCA-appearing phenotype, first or second line 32 Olaparib PO BID PFS 14 weeks in Israel 25 weeks in the US [81]
Golan et al. III PDAC with gBRCA mutation that has not progressed on firstline platinum-based treatment 92 olaparib 62 placebo 3:2 olaparib versus placebo ORR 37% [80]
Reiss et al. II PDAC with g or s BRCA or PALB2 mutations that has not progressed on firstline platinum-based treatment 24 Rucaparib 600mg PO BID ORR 37% [82]
Chiorean et al. II PDAC including g or s BRCA or PALB2 mutations 108 1:1 veliparib + FOLFIRI versus FOLFIRI alone OS 5.1 vs 5.9 months PFS 2 months vs 3 months [92]
Pishvaian et al I/II PDAC with g or S BRCA or PALB2 mutations or relevant breast or ovarian family history 22 Veliparib + mFOLFOX6 OS 8.5 months PFS 3.7 months [93]