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PIONEERING CANCER RESEARCH
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Breast
BCM-3936
Model Details
Patient
PDX Model
Drug Studies
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-3936
Contact Model Developer
Model Contact
Model: BCM-3936
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-3936
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: 242
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
AFF1
chr4
87131211
87131211
T
G
c.3093T>G
gaT/gaG
p.D1031E
0.667
12
1
Missense Variant
Missense Variant
MODERATE
ENST00000395146.8
.
12
1
ENST00000395146.8
.
AKAP9
chr7
92085597
92085597
C
T
c.8935C>T
Cct/Tct
p.P2979S
0.979
115
115
Missense Variant
Missense Variant
MODERATE
ENST00000356239.8
Benign/Likely_benign
COSV104663065
0.996325000000
rs1063242
115
115
ENST00000356239.8
Benign/Likely_benign
COSV104663065
rs1063242
ALK
chr2
29193706
29193706
T
C
c.4381A>G
Atc/Gtc
p.I1461V
0.99
115
115
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV101201052
0.997594000000
rs1670283
115
115
ENST00000389048.8
Benign
COSV101201052
rs1670283
ALK
chr2
29193615
29193615
T
C
c.4472A>G
aAg/aGg
p.K1491R
0.626
115
51
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV66555753
0.349007000000
rs1881420
115
51
ENST00000389048.8
Benign
COSV66555753
rs1881420
ALK
chr2
29193500
29193500
G
C
c.4587C>G
gaC/gaG
p.D1529E
0.685
115
80
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV66569695
0.472160000000
rs1881421
115
80
ENST00000389048.8
Benign
COSV66569695
rs1881421
ALK
chr2
29320870
29320870
A
G
c.1427T>C
gTg/gCg
p.V476A
0.305
115
8
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV66568530
0.028229100000
rs35093491
115
8
ENST00000389048.8
Benign
COSV66568530
rs35093491
AMER1
chrX
64190069
64190069
G
A
c.3218C>T
cCa/cTa
p.P1073L
0.493
23
1
Missense Variant
Missense Variant
MODERATE
ENST00000374869.8
.
23
1
ENST00000374869.8
.
ANK1
chr8
41690309
41690309
G
T
c.4022C>A
tCg/tAg
p.S1341*
0.938
37
1
Nonsense Mutation
Nonsense Mutation
HIGH
ENST00000289734.13
.
37
1
ENST00000289734.13
.
ANK1
chr8
41723629
41723629
C
T
c.716G>A
gGc/gAc
p.G239D
0.068
37
1
Missense Variant
Missense Variant
MODERATE
ENST00000289734.13
COSV55881818
rs867799041
37
1
ENST00000289734.13
COSV55881818
rs867799041
ATR
chr3
142459302
142459302
C
T
c.7274G>A
cGa/cAa
p.R2425Q
0.18
101
24
Missense Variant
Missense Variant
MODERATE
ENST00000350721.9
Benign
COSV63383988
0.130080000000
rs2229032
101
24
ENST00000350721.9
Benign
COSV63383988
rs2229032
ATR
chr3
142562770
142562770
A
G
c.632T>C
aTg/aCg
p.M211T
0.97
101
91
Missense Variant
Missense Variant
MODERATE
ENST00000350721.9
Benign/Likely_benign
COSV63383325
0.545488000000
rs2227928
101
91
ENST00000350721.9
Benign/Likely_benign
COSV63383325
rs2227928
ATR
chr3
142558717
142558717
A
T
c.1792T>A
Tgg/Agg
p.W598R
0.112
101
1
Missense Variant
Missense Variant
MODERATE
ENST00000350721.9
.
101
1
ENST00000350721.9
.
ATRX
chrX
77682471
77682471
C
G
c.2785G>C
Gag/Cag
p.E929Q
0.512
91
73
Missense Variant
Missense Variant
MODERATE
ENST00000373344.10
Benign
rs3088074
91
73
ENST00000373344.10
Benign
rs3088074
AXIN2
chr17
65558473
65558473
G
A
c.148C>T
Cct/Tct
p.P50S
0.987
75
60
Missense Variant
Missense Variant
MODERATE
ENST00000307078.10
Benign
COSV61057354
0.474888000000
rs2240308
75
60
ENST00000307078.10
Benign
COSV61057354
rs2240308
BARD1
chr2
214809500
214809500
G
A
c.70C>T
Ccc/Tcc
p.P24S
0.5
85
52
Missense Variant
Missense Variant
MODERATE
ENST00000260947.9
Benign
COSV53608734
0.384797000000
rs1048108
85
52
ENST00000260947.9
Benign
COSV53608734
rs1048108
Total mutations showing: 242
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-3936
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
AC
6
Treatment
C188-9
6
Treatment
Docetaxel20
6
Treatment
Carboplatin
6
Control
Vehicle
Treatment
Carboplatin+C188-9
6
Treatment
AC+C188-9
5
Total arms showing: 8
F
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Treatment Results
Total treatment results showing: 8
F
P
1
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Treatment Arm
Treatment Duration
Monitoring Method
Monitor Duration
Tumor volume over time (%)
Response Category
Docetaxel20+C188-9
28
28
-42
PR
AC
28
28
152
PD
C188-9
28
28
322
PD
Docetaxel20
28
28
-59
PR
Carboplatin
28
28
182
PD
Vehicle
28
28
327
PD
Carboplatin+C188-9
28
28
258
PD
AC+C188-9
28
28
162
PD
Total treatment results showing: 8
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Histology Information for Model: BCM-3936
There are no histology images for this model.
Metastasis Information for Model: BCM-3936
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-3936
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
Reason Stopped
15
Cyclophosphamide,Doxorubicin
Neoadjuvant
44.21
44.38
62 days
Partial Response
Partial Response
Treatment Completed
25
Docetaxel
Adjuvant
44.61
44.79
66 days
Not Reported
Not Applicable
Treatment Completed
35
Radiation Therapy
Adjuvant
44.88
44.96
29 days
Not Reported
Not Applicable
Treatment Completed
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