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Breast
BCM-2665
Model Details
Patient
PDX Model
Drug Studies
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-2665
Contact Model Developer
Model Contact
Model: BCM-2665
Model Contact: Michael Lewis
Institution: BCM Breast PDX Program
Email:
mtlewis@bcm.edu
Patient Information
Clinical Timeline
Color Keys:
Positive
Negative
N/A
Clinical Information at Collection
Clinical Biomarkers/Mutations at Collection
Pathology Information at Collection
Model Information for Model: BCM-2665
Model Details - Initial Implantation of Patient Tissue
Biomarkers & Mutations
Model Details - Acceptable Conditions for Passaging
Mutations (Cancer Gene Census List)
Show/Hide Columns
The number of models in this collection with mutations in the listed gene;
may include models that are not publicly available for distribution.
The number of models in this collection with mutations at the listed site;
may include models that are not publicly available for distribution.
Total mutations showing: 2303
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
Download
Gene
Filter by Gene
Chr
Filter by Chr
Start
End
Ref
Alt
cDNA Change
Codon Change
Protein Change
TVAF
Gene Mutation Freq.
Site Mutation Freq.
Most Severe Effect
All Effects
Mutation Impact
Transcript ID
ClinVar Clinical Significance
COSMIC ID
gnomAD Non-Cancer AF
dbSNP ID
Gene Mutation Freq.
Site Mutation Freq.
Transcript ID
ClinVar Clinical Significance
COSMIC ID
dbSNP ID
A1CF
chr10
50806745
50806745
C
A
c.1745G>T
gGa/gTa
p.G582V
0.071
20
1
Missense Variant
Missense Variant
MODERATE
ENST00000373997.8
.
20
1
ENST00000373997.8
.
ABI1
chr10
26860781
26860781
C
A
c.83G>T
cGg/cTg
p.R28L
0.02
5
1
Missense Variant
Missense Variant
MODERATE
ENST00000376142.6
.
5
1
ENST00000376142.6
.
ABL1
chr9
130854977
130854977
G
T
c.430G>T
Ggg/Tgg
p.G144W
0.043
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
.
55
1
ENST00000318560.6
.
ABL1
chr9
130885592
130885592
C
A
c.3302C>A
cCg/cAg
p.P1101Q
0.039
55
2
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
COSV100583563
.
55
2
ENST00000318560.6
COSV100583563
.
ABL1
chr9
130885352
130885352
G
T
c.3062G>T
cGg/cTg
p.R1021L
0.033
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
COSV100584237
.
55
1
ENST00000318560.6
COSV100584237
.
ABL1
chr9
130885301
130885301
C
A
c.3011C>A
cCt/cAt
p.P1004H
0.034
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
.
55
1
ENST00000318560.6
.
ABL1
chr9
130884503
130884503
G
T
c.2213G>T
cGg/cTg
p.R738L
0.094
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
.
55
1
ENST00000318560.6
.
ABL1
chr9
130884488
130884488
C
A
c.2198C>A
tCa/tAa
p.S733*
0.086
55
1
Nonsense Mutation
Nonsense Mutation
HIGH
ENST00000318560.6
.
55
1
ENST00000318560.6
.
ABL1
chr9
130878459
130878459
C
A
c.1315C>A
Cct/Act
p.P439T
0.082
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
.
55
1
ENST00000318560.6
.
ABL1
chr9
130878433
130878433
G
T
c.1289G>T
tGg/tTg
p.W430L
0.091
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
COSV100583417
.
55
1
ENST00000318560.6
COSV100583417
.
ABL1
chr9
130872913
130872913
G
T
c.961G>T
Ggg/Tgg
p.G321W
0.088
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
COSV59331786
.
55
1
ENST00000318560.6
COSV59331786
.
ABL1
chr9
130855056
130855056
G
T
c.509G>T
aGg/aTg
p.R170M
0.095
55
1
Missense Variant
Missense Variant
MODERATE
ENST00000318560.6
.
55
1
ENST00000318560.6
.
ABL2
chr1
179107776
179107776
G
T
c.3491C>A
cCt/cAt
p.P1164H
0.027
11
1
Missense Variant
Missense Variant
MODERATE
ENST00000502732.6
.
11
1
ENST00000502732.6
.
ABL2
chr1
179121663
179121663
G
T
c.892C>A
Cag/Aag
p.Q298K
0.025
11
1
Missense Variant
Missense Variant
MODERATE
ENST00000502732.6
.
11
1
ENST00000502732.6
.
ABL2
chr1
179121656
179121656
C
A
c.899G>T
gGa/gTa
p.G300V
0.015
11
1
Missense Variant
Missense Variant
MODERATE
ENST00000502732.6
COSV61015032
.
11
1
ENST00000502732.6
COSV61015032
.
Total mutations showing: 2303
F
P
1
2
3
4
5
6
7
8
9
10
N
E
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CNV
PDX Validation
In order to validate the identity of Baylor College of Medicine patient-derived xenograft (PDX) models, short tandem repeat (STR) testing is performed at the Cytogenetics and Cell Authentication core facility at MDACC. STR testing is performed on tissue from the initial tumor grown in the mouse (transplant generation 1 - TG1) and from a patient sample when possible. Thereafter, STR testing is performed every five transplant generations (TG5, TG10, TG15, and TG20). In the case that a PDX model is transplanted from viably frozen tissue to restart the model, the PDX Core will test the first outgrowth to confirm identity and every five transplant generations thereafter. In addition to STR, we assess clinical biomarkers and histology every 5th transplant generation. Finally, RNAseq gene expression profiles are evaluated periodically to ensure consistency with previous results and to evaluate phenotypic drift. If a significant change in PDX biology is noted, we identify the last known stable stock and re-start the model.
Drug Studies for Model: BCM-2665
Treatment Response Across All Studies
CR <=-95% to -100%
PR <-30% to >-95%
SD >=-30% to +20%
PD >=+20%
NA
Drug Study: VFoundation
Study Metadata
Study ID:
VFoundation
Study Type:
Efficacy
Study Description:
Dosing Initiation Timepoint:
Randomization and treatment began after average tumor size in cohort reached 150 mm³
Number of Arms:
10
Mouse Strain:
PI:
Mike Lewis
Study Title:
VFoundation Study
Treatments:
AC, AC+C188-9, C188-9, Carbo, Carbo+C188-9, Doc20, Doc20+C188-9, Pac, Pac+C188-9
Study Duration:
Transplant Site
Transplant Material:
Study Design
Total arms showing: 8
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Study Description
Arm Type
Treatment Arms
Number of Mice
Dose (mg/kg)
Concentration (mg/ml)
Vehicle
Route
Dosing Schedule
Treatment
Docetaxel20+C188-9
6
Treatment
C188-9
6
Treatment
AC
6
Treatment
Docetaxel20
6
Treatment
Carboplatin
6
Treatment
Carboplatin+C188-9
6
Control
Vehicle
Treatment
AC+C188-9
5
Total arms showing: 8
F
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Treatment Results
Total treatment results showing: 8
F
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Treatment Arm
Treatment Duration
Monitoring Method
Monitor Duration
Tumor volume over time (%)
Response Category
Docetaxel20+C188-9
28
77
102
PD
C188-9
28
77
583
PD
AC
28
77
234
PD
Docetaxel20
28
77
35
PD
Carboplatin
28
77
256
PD
Carboplatin+C188-9
28
77
419
PD
Vehicle
28
77
560
PD
AC+C188-9
28
77
196
PD
Total treatment results showing: 8
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Histology Information for Model: BCM-2665
There are no histology images for this model.
Metastasis Information for Model: BCM-2665
Patient
PDX
Abdomen
Adrenal gland
Bone
Bone (de novo)
Bones
Brain
CTC
Chest
Chest wall
Contralateral Breast
Dura
Fallopian Tubes
Head
Kidney
LMD
Liver
Lung
Lymph node
Lymph nodes
Neck
None
Ovary
Pancreas
Pericardium
Peritoneal cavity
Peritoneum
Pleura
Pleural effusion
Shoulder
Skin
Spine
Spleen
Thoracic Spine
Thymus
medistinal and right hilar
Patient Treatment Information for Model: BCM-2665
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
Reason Stopped
15
Cyclophosphamide,Doxorubicin
Neoadjuvant
50.37
50.55
66 days
Progressive Disease
Not Reported
Treatment Completed
25
Docetaxel
Neoadjuvant
50.72
50.84
44 days
Not Reported
No Response
Treatment Completed
35
Radiation Therapy
Metastatic
50.85
50.9
18 days
Not Reported
Not Applicable
60
Capecitabine
Metastatic
51.0
51.08
29 days
Disease Progression
Not Applicable
Disease Progression
Please wait...