Table 2 Summary characteristics of the proteomic clusters of the muscle-invasive bladder cancer neoadjuvant chemotherapy cohort

From: Proteomic profiling identifies muscle-invasive bladder cancers with distinct biology and responses to platinum-based chemotherapy

Pre-NAC (TUR) cluster

CC1-Luminal

CC2-Nuclear

CC3-Basal

CC4-Stroma-rich

Number of patients in cluster (%)

42 (39%)

7 (7%)

20 (19%)

38 (35%)

Clinical features

Female, T2+

Small cell histology

Squamous, T3+

T2+

Enriched gene sets

Mitochondrial, metabolic

mRNA processing

Cornification, antibody-mediated immune responses

Collagen, antibody-mediated immune responses

MIBC transcriptomic subtype class concordance (%)

95%

57%

94%

11%

Immune

Cold

Medium

Hot (Monocytes, T & B cells)

Hot (T & B cells)

Stroma

Low

Low

Medium

High

CR+PR Response to NAC (%)

48%

57%

25%

31%

Post-NAC (RC) class switch using pre-NAC consensus cluster centroids (%)

61%

0%

42%

9.5%

Median overall survival (months)

113.5

66

15.6

52

Post-NAC (RC) cluster

PN-CC1

PN-CC2

PN-CC3

PN-CC4

Number of patients in cluster (%)

3 (6%)

15 (27%)

15 (27%)

22 (40%)

Enriched gene sets

mRNA processing and splicing

Keratinisation, RNA metabolism

ECM, antibody-mediate immune responses

Mitochondrial and metabolic processes

Immune

Low

Hot

Medium

Low

Stroma

Low

High

Medium

Low

Recurrences at last follow-up (%)

66%

60%

50%

66%

Median overall survival (months)

3

9

26

32

Approved druggable targets

MTOR, PARP1, PARP2

CD274, CTLA4

CTLA4, CD274

NECTIN4, ERBB2, EPCAM

  1. CR complete response, GSEA gene set enrichment analysis, MIBC muscle-invasive bladder cancer, NAC neoadjuvant chemotherapy, PR partial response, RC radical cystectomy, TUR transurethral resection.