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. 2019 Nov 13;7:299. doi: 10.1186/s40425-019-0800-0

Table 4.

Characterization of the responders to combined checkpoint blockade (n = 10)

Response Duration of response (months) Time to response (weeks) Treatment cycles (induction + maintenance) Gender Time to metastasis from primary tumor (months) Age at treatment onset (years) Available molecular/ genetic analysis ECOG LDH CRP Risk score Previous systemic treatment Previous liver-directed treatment Sites of metastasis AE ≥ grade 3 (CTCAE v5.0)
PR 14 5 4 + 0 female 9 46 mutated: GNAQ (Q209P) 0 normal normal low nivolumab (PD) TACE liver yes (colitis)
PR 9 10 1 + 0 female 92 54 mutated: GNAQ (Q209P), ALK, MET; wildtype: BRAF, NRAS, GNA11, BAP1 0 normal normal low none none lung yes (colitis)
PR 23 10 4 + 0 female 33 77 mutated: GNA11 0 elevated unknown low none chemo-saturation liver, mesenteric fat tissue yes (Guillain-Barré syndrome)
PR 55 13 3 + 0 male 408 67 mutated: GNAQ 0 normal elevated high none surgery liver, nodal yes (colitis, hypophysitis)
PR 65 19 4 + 0 female 168 60 mutated: GNAQ; wildtype: BRAF, NRAS, KIT, GNA11 0 elevated normal high none TACE liver, lung, ovarial, cervix, omentum no
CR 53 12 4 + 5 male unknown 59 unknown 0 unknown unknown low none surgery lung no
CR 50 12 4 + 16 male unknown 45 unknown 0 elevated elevated very high none none liver, bone, pelvic no
PR 26 13 3 + 0 female 14 67 unknown 0 elevated normal intermediate none SIRT liver, lung yes (uveitis)
PR 25 14 4 + 1 female 30 56 wildtype: BRAF, NRAS, KIT; expression PD-L1 20%; polysomia of chromosome 12 0 elevated elevated high none none liver, lung no
PR 11 31 4 + 27 female 53 73 wildtype: BRAF, KIT, KRAS, NRAS, NF1, CDKN2A, CDK4 0 elevated unknown intermediate none chemo-saturation liver, bone, nodal, renal no

Abbreviations: CR Complete response, PR Partial response, ECOG Eastern Cooperative Oncology Group, LDH Lactate dehydrogenase, CRP C-reactive protein, TACE Transarterial chemoembolization, SIRT Selective internal radiation therapy, AE Adverse event(s), CTCAE Common Terminology Criteria for Adverse Events