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. 2021 Apr 28;5:33. doi: 10.1038/s41698-021-00171-6

Table 1.

Characteristics of the patients treated in WINTHER trial investigated with DDPP.

Study ID Age Sex Cancer site Prior lines PFS months DNA—list of molecular alterations (Foundation Medicine report)a Drug_given
203 67 F GI/NE 1 60.0+ No mutation Everolimus
148 82 M GI/NE 2 11.6 BCOR N1652fs*34; CDKN1B E126fs*1 Everolimus
6 64 F UP 1 8.1 TSC1 splice site 913 + 1G > T; BRCA1 truncation, intron 11; CDKN2A/B loss; DNMT3A R882H; LRP1B loss Everolimus
117 34 M HN 2 1.9 TSC2 S1431L; TP53 G245S; BCOR K374fs*19; SMARCA4 R1135W Everolimus
227 56 M LS 4 1.7 STK11 F354L; STK11 F354L; TERT promoter —124C > T Everolimus
90 74 M HN 2 1.3 PIK3CA Q546R; EP300 D1154fs*30; NOTCH1 L1746fs*40 Everolimus
83 59 M HN 4 8.8 MTOR L2209V; ETV6 trunc intron 5; CIC S333fs*36; MLL2 G3698 fs*51 Axitinib
223 65 F HN 3 7.1 CCND1 T2861 Axitinib
259 53 F HN 4 6.2 PDGFRA amp Axitinib
25 65 M HN 2 5.3 TP53 I195F; KDM6A L725fs*4; MSH6 K1358fs*2; NFE2L2 R18Q Axitinib
88 56 M Lung 1 2.9 DNMT3A R635P; KRAS G12C; TP53 Y220C; MLL2 T1246M Axitinib
149 54 F CRC 5 7.4 KRAS G12V; ARID1A SPLICE SITE 2733-1G > A Trametinib
100 43 M Lung 2 6.6 BRAF A598_T599insT; IDH1 R132C Trametinib
118 78 F Lung 3 3.1 KRAS G12C; CDKN2A/B loss; TP53 V157F, Y220 fs*27; MUTYH G382D Trametinib
156 71 F Lung 2 14.3 EGFR E746_A750del, T790M; CDKN2A/B loss; CTNNB1 S33F; MYC amplification; SMAD4 P186fs*6; STAG2 splice site 1535-12_1630del108 Afatinib + cetuximab
235 60 F Lung 1 11.3 ERBB2 A775_G776insYVMA Afatinib
136 79 M Lung 3 0.4 ERBB3 amp; MET splice site 3028 + 1G > A; STK11 Q100* ATM L2450fs*11; BRCA1 E23fs*17; CDK4 amp; CDKN2A/B loss; MDM2 amp; APC I1307K; KDM5C truncation; MAP3K1 S1475* Afatinib
237 47 M HN 6 19.3 CCND1 amp; FGFR2 amp; CDKN2A/B loss; FGF19 amp; FGF4 amp; BAP1 trunc exon 3; FGF3 amp; MAGI2 Q1077*; PBRM1 E1155fs*17 NCT01004224 BGJ398
247 67 M Esophagus 2 1.6 FGFR2 amp; CDKN2A/B loss; TP53 W91*; ASXL1 splice site 472-2A > G NCT02052778 TAS-120
228 38 M CRC 5 0.7 FGFR1 amp; TP53 C176F; APC E1322*, R213*; SMAD4 loss; SOX9 V163fs*21 NCT02052778 TAS-120
183 66 M CRC 2 61.0+ RBB3; V104M; MAP2K1; E203K; CDKN2A/B loss; FBXW7 R465C; PIK3CA E39K; PIK3R1 R348*, R639*; PTEN R233*, splice site 801 + 2T > G; TP53 R158H, R273H; APC R1450*, R499*; ARID1A P1115fs*46, Q1306fs*17; ATRX Q2422*; CDH1 D433N; EP300 R2263*; FAM123B R631*; FAT1 A4305V; FLCN H429fs*39; MSH6 L1330fs*12, S279fs*12

Pembrolizumab

(TMB: 74.8)

(MSI: +)

294 57 M HN 1 1.7 BRCA2 K3408*

Nivolumab

(TMB: 0)

(MSI: −)

270 76 F CRC 3 0.9 FLT4 amp; FLT3 amp equivocal; BARD1 C53fs*5; MYC amp; PARK2 loss exons 3–5; TP53 R175H; APC T1556fs*3; BCL2L1 amp; CDK8 amp; ETV6 rearrangement intron 5; FAM123B R497*; GATA6 amp equivocal; KDM6A-Y215*; MUTYH-Y165C; NOTCH1 Q2123*

Atezolizumab

(TMB: 10.4)

(MSI: −)

Foundation Medicinea10; ID 203, PFS 60+ and OS60+ are censored values, updated from the WINTHER trial Supplemental Table 3, Abbreviations: GI gastrointestinal, NE neuroendocrine, HN head and neck, UP unknown primary, LS liposarcoma, TMB tumor mutation burden, MSI microsatellite instability, amp amplification, del deletion, trunc truncation.