PDX INSIGHTS
PIONEERING CANCER RESEARCH
Model Details

Patient Information for Model: BCM-2665

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)

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
A1CFchr105080674550806745CAc.1745G>TgGa/gTap.G582V0.071201Missense VariantMissense VariantMODERATEENST00000373997.8


.
201ENST00000373997.8.
ABI1chr102686078126860781CAc.83G>TcGg/cTgp.R28L0.0251Missense VariantMissense VariantMODERATEENST00000376142.6


.
51ENST00000376142.6.
ABL1chr9130854977130854977GTc.430G>TGgg/Tggp.G144W0.043551Missense VariantMissense VariantMODERATEENST00000318560.6


.
551ENST00000318560.6.
ABL1chr9130885592130885592CAc.3302C>AcCg/cAgp.P1101Q0.039552Missense VariantMissense VariantMODERATEENST00000318560.6

COSV100583563
.
552ENST00000318560.6COSV100583563.
ABL1chr9130885352130885352GTc.3062G>TcGg/cTgp.R1021L0.033551Missense VariantMissense VariantMODERATEENST00000318560.6

COSV100584237
.
551ENST00000318560.6COSV100584237.
ABL1chr9130885301130885301CAc.3011C>AcCt/cAtp.P1004H0.034551Missense VariantMissense VariantMODERATEENST00000318560.6


.
551ENST00000318560.6.
ABL1chr9130884503130884503GTc.2213G>TcGg/cTgp.R738L0.094551Missense VariantMissense VariantMODERATEENST00000318560.6


.
551ENST00000318560.6.
ABL1chr9130884488130884488CAc.2198C>AtCa/tAap.S733*0.086551Nonsense MutationNonsense MutationHIGHENST00000318560.6


.
551ENST00000318560.6.
ABL1chr9130878459130878459CAc.1315C>ACct/Actp.P439T0.082551Missense VariantMissense VariantMODERATEENST00000318560.6


.
551ENST00000318560.6.
ABL1chr9130878433130878433GTc.1289G>TtGg/tTgp.W430L0.091551Missense VariantMissense VariantMODERATEENST00000318560.6

COSV100583417
.
551ENST00000318560.6COSV100583417.
ABL1chr9130872913130872913GTc.961G>TGgg/Tggp.G321W0.088551Missense VariantMissense VariantMODERATEENST00000318560.6

COSV59331786
.
551ENST00000318560.6COSV59331786.
ABL1chr9130855056130855056GTc.509G>TaGg/aTgp.R170M0.095551Missense VariantMissense VariantMODERATEENST00000318560.6


.
551ENST00000318560.6.
ABL2chr1179107776179107776GTc.3491C>AcCt/cAtp.P1164H0.027111Missense VariantMissense VariantMODERATEENST00000502732.6


.
111ENST00000502732.6.
ABL2chr1179121663179121663GTc.892C>ACag/Aagp.Q298K0.025111Missense VariantMissense VariantMODERATEENST00000502732.6


.
111ENST00000502732.6.
ABL2chr1179121656179121656CAc.899G>TgGa/gTap.G300V0.015111Missense VariantMissense VariantMODERATEENST00000502732.6

COSV61015032
.
111ENST00000502732.6COSV61015032.
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
Study Metadata
Study Design
Treatment Results





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 IdTreatmentTreatment SettingAge at StartAge at EndDurationClinical ResponsePathologic ResponseReason Stopped
15Cyclophosphamide,DoxorubicinNeoadjuvant50.3750.5566 daysProgressive DiseaseNot ReportedTreatment Completed
25DocetaxelNeoadjuvant50.7250.8444 daysNot ReportedNo Response Treatment Completed
35Radiation Therapy Metastatic50.8550.918 daysNot ReportedNot Applicable
60CapecitabineMetastatic51.051.0829 daysDisease ProgressionNot ApplicableDisease Progression













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