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. 2020 Jul 3;123(6):965–972. doi: 10.1038/s41416-020-0975-7

Table 2.

Clinicopathological characteristics in patients with and without hyperprogressive disease.

HPD patients (n = 30) Non-HPD patients (n = 106) HPD rate (%) P value
Age (years) <70 13 42 23.6 0.72
≥70 17 64 21.0
Sex Male 25 82 23.4 0.48
Female 5 24 17.2
Performance status 0–1 23 97 19.2 0.026
2–3 7 9 43.8
BMI (kg/m2) <20 11 52 17.5 0.23
≥20 19 54 26.0
Histology* Differentiated 20 71 22.0 0.92
Undifferentiated 10 34 22.7
History of gastrectomy Yes 15 67 18.3 0.19
No 15 39 27.8
Number of previous chemotherapy regimens 2 18 58 23.7 0.76
3 7 32 17.9
≥4 5 16 23.8
Liver metastasis Yes 23 31 42.6 <0.001
No 7 75 8.5
Lung metastasis Yes 2 10 16.7 0.64
No 28 96 22.6
Lymph node metastasis Yes 12 62 16.2 0.073
No 18 44 29.0
Peritoneum metastasis Yes 10 31 24.4 0.67
No 20 75 21.1
NLR <2.4 14 53 20.9 0.75
≥2.4 16 53 23.2
CRP (mg/dL)* <1.0 18 80 18.4 0.080
≥1.0 12 25 32.4
PD-L1 TPS <1 24 77 23.8 0.42
≥1 6 29 17.1
PD-L1 CPS <1 14 36 28.0 0.20
≥1 16 70 18.6
PD-L1 CPS <5 22 62 26.2 0.14
≥5 8 44 15.4
PD-L1 CPS <10 27 77 26.0 0.048
≥10 3 29 9.4
MMR Proficient 27 88 23.5 0.35
Deficient 3 18 14.3

*Data not available for one patient.

HPD hyperprogressive disease, BMI body mass index, NLR neutrophil-to-lymphocyte ratio, CRP C-reactive protein, PD-L1 programmed death-ligand 1, TPS tumour-positive score, CPS combined positive score, MMR mismatch repair.