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. 2022 Dec 8;128(5):877–885. doi: 10.1038/s41416-022-02086-w

Table 2.

Characteristics of the patients included in the secondary analysis.

Non-platinum-based 1LTa (N = 28) Platinum-based 3- and 4-agents 1LTb (N = 40) Platinum-based 2 agents 1LTc (N = 9)
Age at diagnosis (years), median (range) 61 (38–75) 57 (35–72) 66 (51–72)
Gender, N (%)
 Female 19 (68) 17 (42) 4 (44)
 Male 9 (32) 23 (58) 5 (56)
ECOG PS at diagnosis, N (%)
 0 20 (71) 23 (60) 3 (33)
 1 7 (25) 15 (40) 4 (44)
 2 1 (4) 0 2 (23)
 NA 0 2 0
Liver metastases at diagnosis, N (%)
 Yes 22 (79) 31 (77) 7 (78)
 No 6 (21) 9 (23) 2 (22)
gBRCA PV status, N (%)
 gBRCA1 7 (25) 9 (23) 3 (33)
 gBRCA2 21 (75) 31 (77) 5 (56)
 gBRCA 1 + 2 0 0 1 (11)

1LT first-line therapy, PS performance status, NA not available, gBRCA germline BRCA, PV pathogenic variant.

a25 patients were treated with Nab-paclitaxel plus gemcitabine (AG) [4], 2 with AG-based therapy within a clinical trial [25, 26], 1 with Nab-Paclitaxel plus Fluorouracil and Irinotecan (Nab-FOLFIRI) within a clinical trial [27].

b22 patients received FOLinic acid, Fluorouracil, IRINotecan and OXaliplatin (FOLFIRINOX) [5], modified FOLFIRINOX (mFOLFIRINOX) [21] or FOLinic acid, Fluorouracil, Oxaliplatin and IRInotecan (FOLFOXIRI) [22], 14 PAXG [6], 2 Cisplatin, Epirubicin, Capecitabine and Gemcitabine (PEXG) [23], 2 Cisplatin plus AG.

c5 patients were treated with Gemcitabine plus Oxaliplatin (GEMOX) [24], 4 with FOLFOX [9].