Mosaic Window

MOSAIC Window is a curated subset of the groundbreaking MOSAIC dataset, available through K Pro. It includes spatial omics and multimodal data from 60 patients across five cancer types:

  • BLCA (Bladder Cancer): 15 patients

  • OV (Ovarian Cancer): 15 patients

  • GBM (Glioblastoma): 10 patients

  • DLBCL (Diffuse Large B-cell Lymphoma): 10 patients

  • MESO (Mesothelioma): 10 patients

This unique resource enables researchers to explore tumor biology at near single-cell resolution, providing detailed insight into tumor and immune cell interactions.

MOSAIC Window Patient Details

BLCA (15 patients):

  • Stage II and III urothelial carcinoma (one squamous cell carcinoma)

  • Derived from upfront cystectomies

  • Most patients receiving complete lymph node dissection

  • Some treated with adjuvant chemotherapy, chemotherapy, or immune checkpoint inhibitors (ICI) at relapse, with or without radiotherapy

OV (15 patients):

  • FIGO stage II to IV high grade serous carcinoma

  • 7 baseline, 2 post-NACT, 6 relapse lesions

  • Treated by upfront or post-NACT interval debulking surgeries and chemotherapy

  • Additional treatments: Bevacizumab, PARP inhibitors, and ICI in first or later lines

GBM (10 patients):

  • Glioblastoma as per WHO 2021 definition, all IDH wildtype

  • 6 unmethylated and 4 methylated MGMT promoter samples

  • Obtained from baseline surgery before standard adjuvant therapy

  • 1 to 3 brain tumor sites, tumor sizes 27 to 80mm diameter

  • 5 patients received Bevacizumab at relapse

DLBCL (10 patients):

  • Ann Arbor stage III or IV

  • 3 Activated B-cell-like type (ABC), 6 Germinal center B-cell group (GCB), 1 unknown subtype

  • Obtained at baseline before R-CHOP therapy

  • Targeted interventions at relapse

MESO (10 patients):

  • Stage I to III pleural mesotheliomas

  • 5 epithelioid, 5 biphasic

  • 9 baseline biopsies/surgeries, 1 post-NACT sample

  • 4 patients treated by NACT (1 partial response, 3 progressive diseases)

  • 4 patients received anti-PD-1 ICI at relapse (monotherapy or combination with anti-CTLA4)

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