Table 3 Summary of disease characteristics and PARP inhibitor treatment characteristics for BRCAm patients in receipt of a PARP inhibitor (n = 9).

From: Oncologist-led BRCA ‘mainstreaming’ in the ovarian cancer clinic: A study of 255 patients and its impact on their management

Disease stage

PARP inhibitor received

Number of cycles dispensed

Days on PARP inhibitor

Reason for discontinuation

Age at date of initiation on PARP inhibitor

Post third-line chemotherapy, platinum sensitive

Olaparib

8

210

Disease progression

59

Post third-line chemotherapy, platinum sensitive

Olaparib

7*

206

Disease progression

52

Post second-line chemotherapy, platinum sensitive^

Niraparib

4*

181

Disease progression

66

Post third-line chemotherapy, platinum sensitive

Olaparib

1

1

Disease progression

57

Post third-line chemotherapy, platinum sensitive

Olaparib

2

35

Disease progression

63

Post third-line chemotherapy, platinum sensitive

Olaparib

1 (ongoing)

Ongoing

N/A - ongoing

47

Post second-line chemotherapy, platinum sensitive^

Niraparib

3*

147

Disease progression

52

Post second-line chemotherapy, platinum resistant^

Rucaparib

2* (ongoing)

Ongoing

N/A - ongoing

77

Post third-line chemotherapy, platinum sensitive

Olaparib

1*

<7

Unacceptable toxicities

80

  1. ^patients accessed PARP inhibitor through Early Access Programs and/or Compassionate Use Programs initiated by sponsoring company (all other patients accessed PARP inhibitor via the NHS, as per NICE guidelines).
  2. *patients received dose interruption and/or modification in order to manage adverse events/toxicities.