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Table 1 Clinical details and pathological characteristics of tumor specimens used for generating the PDX WHIM lines, as determined and further described in a previous publication [11]

From: Identifying biomarkers of breast cancer micrometastatic disease in bone marrow using a patient-derived xenograft mouse model

  

Patient details

  

Xenograft details

Pt ID

Receptor status

Subtype

Source of tissue

Sites of metastasis

Survival (months)

WHIM line

Mouse ID

Receptor status

Site of metastases

262

ER+/HER2-

Luminal-B

Breast

BN, CNS

37

11

11E 1221

ER+/HER2-

None

303

ER-/HER2-

Claudin-low

Breast

PL, PC

12

12

12A 1282

ER-/HER2-

L

12A1291

L

12C1363

ER-/HER2-

H

12C1264

None

12C 1375

None

12C 1376

None

270

ER-/HER2-

Basal

Chest wall

BR, CT, L, H, BN

44+ b

13

13A 1204

ER-/PR-

None

7192

ER-/HER2-

Claudin-low

Breast

None

37+ b

17

17A 1384

ER-/HER2-

H, N

17B 1139

ER-/HER2-

H

17B 1141

L

17B1188

L, H

17B29

L, H, S

17C1180

ER-/HER2-

L

17C1182

L, H, S, K

319

ER+/HER2-

Luminal-B

Skin

CT, N

97

23

23C 1832

 

None

23C 1833

ER+/HER2-

None

23C 1834

 

None

  1. Individual mice used for bone marrow analysis are designated by: WHIM line number - passage number – unique mouse ID
  2. Abbreviations: PDX patient-derived xenograft, WHIM Washington University Human in Mouse ER estrogen receptor, HER2 human epidermal growth factor receptor 2, BR breast, CNS brain, BN bone, L lung, CT cutaneous, PL pleura, PC pericardium, N nodes, H liver, S spleen, K kidney, PR progesterone receptor
  3. bAlive at last follow up