PDX INSIGHTS
PIONEERING CANCER RESEARCH
Model Details

Patient Information for Model: BCM-3936

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)

GeneChrStartEndRefAltcDNA ChangeCodon ChangeProtein ChangeTVAF Gene Mutation Freq. Site Mutation Freq.Most Severe EffectAll EffectsMutation ImpactTranscript IDClinVar Clinical SignificanceCOSMIC IDgnomAD Non-Cancer AFdbSNP IDGene Mutation Freq.Site Mutation Freq.Transcript IDClinVar Clinical SignificanceCOSMIC IDdbSNP ID
AFF1chr48713121187131211TGc.3093T>GgaT/gaGp.D1031E0.667121Missense VariantMissense VariantMODERATEENST00000395146.8


.
121ENST00000395146.8.
AKAP9chr79208559792085597CTc.8935C>TCct/Tctp.P2979S0.979115115Missense VariantMissense VariantMODERATEENST00000356239.8
Benign/Likely_benign
COSV104663065
0.996325000000rs1063242
115115ENST00000356239.8Benign/Likely_benignCOSV104663065rs1063242
ALKchr22919370629193706TCc.4381A>GAtc/Gtcp.I1461V0.99115115Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV101201052
0.997594000000rs1670283
115115ENST00000389048.8BenignCOSV101201052rs1670283
ALKchr22919361529193615TCc.4472A>GaAg/aGgp.K1491R0.62611551Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV66555753
0.349007000000rs1881420
11551ENST00000389048.8BenignCOSV66555753rs1881420
ALKchr22919350029193500GCc.4587C>GgaC/gaGp.D1529E0.68511580Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV66569695
0.472160000000rs1881421
11580ENST00000389048.8BenignCOSV66569695rs1881421
ALKchr22932087029320870AGc.1427T>CgTg/gCgp.V476A0.3051158Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV66568530
0.028229100000rs35093491
1158ENST00000389048.8BenignCOSV66568530rs35093491
AMER1chrX6419006964190069GAc.3218C>TcCa/cTap.P1073L0.493231Missense VariantMissense VariantMODERATEENST00000374869.8


.
231ENST00000374869.8.
ANK1chr84169030941690309GTc.4022C>AtCg/tAgp.S1341*0.938371Nonsense MutationNonsense MutationHIGHENST00000289734.13


.
371ENST00000289734.13.
ANK1chr84172362941723629CTc.716G>AgGc/gAcp.G239D0.068371Missense VariantMissense VariantMODERATEENST00000289734.13

COSV55881818
rs867799041
371ENST00000289734.13COSV55881818rs867799041
ATRchr3142459302142459302CTc.7274G>AcGa/cAap.R2425Q0.1810124Missense VariantMissense VariantMODERATEENST00000350721.9
Benign
COSV63383988
0.130080000000rs2229032
10124ENST00000350721.9BenignCOSV63383988rs2229032
ATRchr3142562770142562770AGc.632T>CaTg/aCgp.M211T0.9710191Missense VariantMissense VariantMODERATEENST00000350721.9
Benign/Likely_benign
COSV63383325
0.545488000000rs2227928
10191ENST00000350721.9Benign/Likely_benignCOSV63383325rs2227928
ATRchr3142558717142558717ATc.1792T>ATgg/Aggp.W598R0.1121011Missense VariantMissense VariantMODERATEENST00000350721.9


.
1011ENST00000350721.9.
ATRXchrX7768247177682471CGc.2785G>CGag/Cagp.E929Q0.5129173Missense VariantMissense VariantMODERATEENST00000373344.10
Benign

rs3088074
9173ENST00000373344.10Benignrs3088074
AXIN2chr176555847365558473GAc.148C>TCct/Tctp.P50S0.9877560Missense VariantMissense VariantMODERATEENST00000307078.10
Benign
COSV61057354
0.474888000000rs2240308
7560ENST00000307078.10BenignCOSV61057354rs2240308
BARD1chr2214809500214809500GAc.70C>TCcc/Tccp.P24S0.58552Missense VariantMissense VariantMODERATEENST00000260947.9
Benign
COSV53608734
0.384797000000rs1048108
8552ENST00000260947.9BenignCOSV53608734rs1048108
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
Study Metadata
Study Design
Treatment Results





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 IdTreatmentTreatment SettingAge at StartAge at EndDurationClinical ResponsePathologic ResponseReason Stopped
15Cyclophosphamide,DoxorubicinNeoadjuvant44.2144.3862 daysPartial ResponsePartial ResponseTreatment Completed
25DocetaxelAdjuvant44.6144.7966 daysNot ReportedNot ApplicableTreatment Completed
35Radiation Therapy Adjuvant44.8844.9629 daysNot ReportedNot ApplicableTreatment Completed













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