SNPMiner Trials: Mutation Report
Report for Mutation D835V
 Developed by Shray Alag, 2019.
SNP Clinical Trial Gene 
There is one clinical trial. 
Clinical Trials
      This phase II trial studies how well ponatinib hydrochloride works in treating patients with
      cancer that has spread to other parts of the body (metastatic), has failed previous treatment
      (refractory), and has one of several alterations, or mutations, in its deoxyribonucleic acid
      (DNA) sequence. Ponatinib hydrochloride may stop the growth of cancer cells by blocking some
      of the enzymes needed for cell growth. It is not yet known whether a patient's genetic
      alterations may affect how well ponatinib hydrochloride works.
    
NCT02272998  Malignant Neoplasm  Drug: ponatinib hydrochloride  Other: laboratory biomarker analysis 
-  Patients with known ponatinib-resistant gene alterations
               -  PDGFRA D842V mutation
               -  cKIT D816V mutation
               -  FLT3 D835V/Y/H/F or Y842C mutations
               -  FGFR3 K652E mutation
          -  Major surgery (e.g. --- D842V ---  --- D816V ---  --- D835V --- 
  Primary Outcomes 
 Description: The proportion of responses for the purposes of the decision rule will be calculated out of all eligible patients who receive any treatment. Assuming the number of responses is binomially distributed, 95% binomial confidence intervals will also be calculated for the estimate of the proportion of responses.
 Measure: Overall response, defined as the number of patients who achieve any response according to disease type in the first 6 courses of treatment
 Time: Up to 6 months
  Secondary Outcomes 
 Description: Frequency and severity of adverse events will be collected and summarized by descriptive statistics. The maximum grade for each type of toxicity will be recorded for each patient, and frequency tables will be reviewed to determine toxicity patterns for each of the cohorts as well as across cohorts. In addition, all adverse event data that is graded as 3, 4, or 5 will be reviewed and classified as either "unrelated" or "unlikely to be related" to study treatment in the event of an actual relationship developing.
 Measure: Incidence of toxicity, defined as adverse events that are classified as either possibly, probably, or definitely related to study treatment per National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0
 Time: Up to 30 days after last dose of study drug
 Description: Collected and summarized by descriptive statistics. In addition, the proportion of patients who go off treatment due to adverse reactions or even those who refuse further treatment for lesser toxicities that inhibit their willingness to continue participation on the trial will be captured.
 Measure: Tolerability of the regimen, assessed by the number of patients who required dose modifications and/or dose delays
 Time: Up to 30 days after last dose of study drug
 Description: Kaplan-Meier curves will be used to estimate the survival distribution.
 Measure: Overall survival
 Time: The time from treatment initiation to death, assessed up to 52 weeks
 Description: Kaplan-Meier curves will be used to estimate the survival distribution.
 Measure: Progression free survival
 Time: The time from treatment initiation to progression or death, assessed up to 52 weeks
 Description: Calculated by the number of patients who have achieve a response and/or are progression-free and alive at 6 months divided by the total number of evaluable patients. Exact binomial 95% confidence intervals for CBR will be calculated.
 Measure: Clinical benefit rate (CBR)
 Time: 6 months
  Other Outcomes 
 Description: Correlative gene and protein markers will be summarized univariately in a quantitative manner and also summarized by clinical outcome group (e.g. response vs. no response). Graphical analyses will be largely used to assess potential patterns and relationships; e.g. side-by-side boxplots to assess differences in continuous marker levels between those with vs. without the clinical improvement (e.g. response vs. no response). Overall, hypothesis testing will largely be avoided given the sample size limitations.
 Measure: Correlative gene and protein markers
 Time: Up to 3 years (time of progression)
HPO Nodes
Genes 762
CDKN1A  CDKN1B  CDKN1C  CDKN2A  HFE  CDKN2B  CDKN2C  GDF5  TSR2  CDKN2D  H19-ICR  TMEM67  RPL26  RPL27  TREX1  ASXL1  ERBB2  SCN11A  POU6F2  ERCC2  RPL35A  ERCC3  BRIP1  ERCC4  ABL1  ERCC5  CEBPA  ERCC6  PDE6D  GCM2  CEL  PDGFB  PDGFRA  PDGFRL  MNX1  PDGFRB  LEMD3  ENPP1  CTSC  ESR1  HLA-DRB1  SLC26A4  MAX  APC2  RPS7  TMC6  TMEM216  TRPS1  ACTB  RPS10  MC1R  MC2R  BLNK  RPS14  RPS15A  ACTG2  ETV6  TCIRG1  DNAJC21  EVC  HMBS  L2HGDH  RPS17  MCM4  RPS19  RPS20  TSC1  TSC2  EWSR1  EXT1  EXT2  RPS24  RPS26  RPS27  ACVR1  EYA1  RPS28  RPS29  MAGT1  ACVRL1  MDH2  MDM2  ADA  HNF4A  ADAR  TRIP13  LYST  PICALM  ALX4  F13A1  TERF2IP  PHF21A  F13B  RYR1  MAP3K1  AXIN1  TBC1D24  AXIN2  BAP1  CHRNG  TWIST1  MEN1  TNFRSF4  FANCA  FANCC  FANCD2  FANCE  TYR  GFI1B  FAH  MET  TYROBP  FANCB  FANCF  FANCG  SERPINA1  ARID1B  SAMD9L  AP2S1  MGAT2  DLC1  ICOS  DMRT3  SFTPA2  PIGA  MGMT  MBTPS2  CLCNKB  HOXD13  PIK3CA  PIK3R1  ACAN  FDPS  HPGD  JAG1  RNASEH2C  RECQL4  SCN4A  HACE1  RAD54B  NR0B1  MITF  AHCY 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RPGRIP1L  KRT16  CARMIL2  NRAS  SRD5A3  KRT17  SASH1  RASA1  RHBDF2  SH2B3  USB1  RB1  TCOF1  NRTN  DOCK8  DYNC2H1  CALR  GPR35  SLC26A2  NTHL1  NTRK1  MYO1H  NUMA1  DVL1  ASCC1  DVL3  NSD1  LAMA3  AGGF1  GPR143  CASP8  B3GALT6  LAMB3  CASP10  GJC2  NR4A3  CASR  LAMC2  FANCL  RELA  OCA2  TDGF1  NUP214  OCRL  AIP  REST  RET  MLLT10  RUNX1  WRAP53  CBFB  ECE1  GPC6  DLL1  TEK  CBL  TERC  ECM1  AAGAB  TERT  OGG1  TFAP2A  DICER1  WDPCP  PALB2  EDN1  LETM1  OPCML  MSTO1  EDN3  EDNRB  TFE3  ZFPM2  RFWD3  KRIT1  KIF7  SIX6  TG  RAD50  ESCO2  VANGL2  RMRP  TBX18  TGFBR2  POLR1D  SLC22A18  TGIF1  MSH6  COL18A1  USP8  RASGRP1  LIG4  SEMA3D  GTF2E2  KLLN  RNASEL  THPO  SF3B1  HMGA2  ALX1  LMNA  RNF6  CD19  MS4A1  MTMR14  EGFR  LMO1  DCLRE1C  ABCA5  LZTS1  LMX1B  CD27  TRIM28  CD28  VANGL1  CCBE1  SBDS  FANCI  BRD4  SLC25A13  MRAP  ARMC5  LPP  SLC49A4  CHEK2  TREM2  TNFRSF13C  FIBP  LRRC8A  ELANE  TNFRSF13B  LRP5  CD70  SPRED1  CD79A  CD79B  CD81  SLC45A2  PRKN  PARN  HABP2  TAF15  PAX3  EIF2AK4  PAX4  RPL35  PAX6  GREM1  PAX7  SPRTN  TNFRSF1B  BUB3  KAT6B  HBB  PDCD10  RNF139  SH2D1A  ENG  CDH1  EPCAM  RSPO1  NNT  RPL5  TNPO3  CD96  EP300  DISP1  TOP2A  TP53  RPL10  RPL11  SMAD4  RPL15  CDK4  RPL18   hr>