MULTIDISCIPLINARY
CASE
DISCUSSION
Research Medical Center’s
Liver and Pancreas Institute Conference
Panel of Physicians
Cates, Joe MD
Farber, Michael MD
Freilich, Brad MD
Jafri, Syed MD
Mikhitarian, Kaidi MD
Singh, Jaswinder MD
PATIENT J.P.
 58 year old Asian male
 Past Medical History:
 Chronic Hepatitis B
 Hypertension
 Type II diabetes mellitus
 Osteoarthritis
 Fatty liver
 No previous surgical history.
 No significant family history.
 Patient was a smoker and quit at age 42. He is a social drinker.
PATIENT PRESENTATION
 October 2013 seen in PCP office with acute onset of sever right
upper quadrant pain with radiation to the right scapular and shoulder
area, mild nausea without emesis. Labs and CT ordered.
 Complete metabolic profile (10/7/2013):
 ALT: 67 iu/L
 Glucose: 234 mg/dL
 Lipase: 81 u/L
 CT Abdomen (10/8/2013) revealed several heterogeneously
enhancing lesions present in the liver, the largest measuring 7 cm in
size, suspicious for multifocal hepatocellular carcinoma. Small
periportal and peripancreatic lymph nodes. Borderline splenomegaly.
Small amount of abdominal ascites.
 US guided liver biopsy performed (10/15/2013) confirmed
hepatocellular carcinoma.
Liver, core biopsy:
- Moderately differentiated HCC
Liver, core biopsy:
- Moderately differentiated HCC
DIAGNOSIS
 Child Pugh score A, Barcelona B
 Stage III moderately differentiated hepatocellular carcinoma
LIVER MRI WITH EOVIST PRIOR TO STARTING TREATMENT
LABS PRIOR TO STARTING Y-90 THERAPY
 11/11/2013
 Total Bili: 0.9 mg/dL
 Direct Bili: 0.2 mg/dL
 AST: 47 U/L
 ALT: 79 U/L
 ALK Phos: 105 U/L
 Alpha-Fetoproteins: 106.6 ng/mL
TREATMENT APPROACH FOR J.P.
 Due to his multifocal bi-lobed disease he was not a candidate for
a liver transplant or surgery.
 11/14/13 Y-90 radioembolization of right hepatic artery. (#1)
 12/17/2013 Chemoembolization of left hepatic artery.
 2/5/2014 Started on Sorafenib ( 2 tabs in a.m. and 2 tabs in p.m.)
 4/2/2014 Y-90 radioembolization of right hepatic artery. (#2)
 October 2014 Sorafenib stopped and enrolled in a Phase I gene
therapy trial under Dr. Freilich’s care.
MRI OF THE ABDOMEN AND PELVIS POST FIRST Y-90 TREATMENT
LABS PRIOR TO STARTING GENE THERAPY
 7/17/2014
 Total Bili: 1.1 mg/dL
 Direct Bili: 0.4 mg/dL
 AST: 56 U/L
 ALT: 82 U/L
 Alk Phos: 145 U/L
 Alpha-Fetoprotein: 92.7 ng/mL
LIVER MRI WITH EOVIST PRIOR TO STARTING GENE THERAPY
DEVELOPMENT OF COMPLICATIONS
 11/21/2014 Port-A-Cath removed due to infection; Staphylococcus aureus.
 2/7/2015 Presented to emergency department with complaint of severe right
abdominal pain and right chest pain with radiation to the back associated with
shortness of breath and dizziness with a fever as high as 38.3.
 2/7/2015 CT of the abdomen and chest showed abnormalities that included
small right pleural effusion associated with a large collection of fluid around
the necrotic lesion in his liver, abutting the right hemidiaphragm.
 2/12/2015 underwent bronchoscopy, thracoscopy, right thoracotomy and
decortication due to development of staph aureus empyema and necrotic
hepatocellular tumor that spread to the right pleural space; a wedge biopsy of
the liver was done at that time.
CT OF ABDOMEN AND PELVIS DEMONSTRATING NECROTIC MASS
Liver, tumor resection:
- Residual moderately differentiated HCC
Liver, tumor resection:
- Residual moderately differentiated HCC
CT OF THE ABDOMEN AND PELVIS DEMONSTRATING GENE
THERAPY AND SURGICAL CHANGES
MOST RECENT LAB RESULTS
 3/2015
 Total Bili: 0.6 mg/dL
 Direct Bili: 0.2 mg/dL
 AST: 56 U/L
 ALT: 43 U/L
 ALK Phos: 377 U/L
 Alpha-Fetoprotein: 3.1 ng/mL
LI-RAD EXAMPLE CASE #1
LI-RAD EXAMPLE CASE #2
LI-RAD CASE EXAMPLES
 Example Case #1
 Cirrhotic liver, F4 fibrosis on elastography
 17 mm lesion with arterial phase enhancement, washout, pseudocapsule
 HCC LI-RADS 5
 Example Case #2
 HCC LI-RADS 5V
PATIENT V.B.
 75 year old African American female
 Past Medical History:
 Hypertension
 Degenerative joint disease/ osteoarthritis
 Hyperlipidemia
 Gastroesophageal reflux disease (GERD)
 Hypothyroidism
 Previous Surgeries:
 Right leg surgery as a child
 Right lens implant
 Family History:
 Sister with uterine cancer
 First cousin with breast cancer
 Brother and children with diabetes
PATIENT PRESENTATION
 In October 2013 she went to her PCP complaining of abdominal pain, upper back pain,
decreased appetite, a 10-15 pound weight loss and jaundice that had been ongoing for two
weeks. CT and labs were ordered.
 Comprehensive Metabolic Panel (10/11/2013):
 Creatinine: 1.09 mg/dL
 Total Bilirubin: 6.3 mg/dL
 Alkaline Phosphatase: 418 U/L
 AST: 435 U/L
 ALT: 758 U/L
 CA 19-9: 261.6 Units/mL
 CT of the Abdomen and pelvis (10/14/2013) revealed dilation of the biliary tree and pancreatic
duct and distention of the gallbladder secondary to a mass of the head of the pancreas
measuring 4.7 cm.
 Underwent EUS with FNA and ERCP with biliary sphincterotomy and placement of stent
(10/16/2013) that showed a focal 4 x 3.5 cm irregular hypoechoic fullness of the head of the
pancreas, showing malignant cells surrounding peripancreatic lymphadenopathy. EUS stage
T3 N1 M0
EUS
Pancreatic head mass, FNA:
- Positive for malignant cells;
compatible with adenocarcinoma
Pancreatic head mass, FNA:
- Positive for malignant cells;
compatible with adenocarcinoma
CT OF THE ABDOMEN AND PELVIS PRE NEOADJUVANT
THERAPY 10/14/2013
NEOADJUVANT APPROACH FOR V.B.
 Based on EUS staging, pathology and imaging V.B. was
determined to be borderline resectable and it was decided to
place her on Neoadjuvant Chemotherapy concurrent with
Radiation.
 11/12/13 Started Neoadjuvant chemotherapy with Gemzar
 11/19/13 Started radiation in combination with Gemzar
chemotherapy
 12/3/13 Stopped chemotherapy treatment (completed 4 cycles)
 12/24/13 Ended radiation treatment (completed 5 weeks)
CT OF THE ABDOMEN AND PELVIS POST
NEOADJUVANT THERAPY
RE-STAGING FOR V.B.
 1/20/14 CT of the Abdomen and pelvis was done to determine
patient’s resectability for surgery candidacy.
 1/29/14 Whipple procedure performed by Dr. Cates.
CT OF THE ABDOMEN AND PELVIS POST WHIPPLE RECOVERY
DIAGNOSIS
 EUS FNA pathology:
 Pancreatic adenocarcinoma
 Surgical pathology:
 Tumor site: cannot be determined
 Additional sites involved by tumor: none identified
 Histologic type: other, no residual tumor
 Histologic grade: cannot be assessed secondary to therapeutic effect
 Tumor size: cannot be determined; no residual tumor
 Microscopic tumor extension: no evidence of primary tumor
 Margins: margins uninvolved by invasive carcinoma
 Treatment effect: present, no residual tumor (complete response, grade 0)
 Stage: T0 N0 M0
Whipple resection:
- No residual carcinoma identified
- Negative lymph nodes (0/17)
ADJUVANT TREATMENT
 Due to complications with her Whipple recovery, the patient did
not receive any adjuvant chemotherapy.
 The patient is doing well with no evidence of pancreatic
adenocarcinoma recurrence at this time.

4.11.15 GI Symposium

  • 1.
    MULTIDISCIPLINARY CASE DISCUSSION Research Medical Center’s Liverand Pancreas Institute Conference Panel of Physicians Cates, Joe MD Farber, Michael MD Freilich, Brad MD Jafri, Syed MD Mikhitarian, Kaidi MD Singh, Jaswinder MD
  • 2.
    PATIENT J.P.  58year old Asian male  Past Medical History:  Chronic Hepatitis B  Hypertension  Type II diabetes mellitus  Osteoarthritis  Fatty liver  No previous surgical history.  No significant family history.  Patient was a smoker and quit at age 42. He is a social drinker.
  • 3.
    PATIENT PRESENTATION  October2013 seen in PCP office with acute onset of sever right upper quadrant pain with radiation to the right scapular and shoulder area, mild nausea without emesis. Labs and CT ordered.  Complete metabolic profile (10/7/2013):  ALT: 67 iu/L  Glucose: 234 mg/dL  Lipase: 81 u/L  CT Abdomen (10/8/2013) revealed several heterogeneously enhancing lesions present in the liver, the largest measuring 7 cm in size, suspicious for multifocal hepatocellular carcinoma. Small periportal and peripancreatic lymph nodes. Borderline splenomegaly. Small amount of abdominal ascites.  US guided liver biopsy performed (10/15/2013) confirmed hepatocellular carcinoma.
  • 4.
    Liver, core biopsy: -Moderately differentiated HCC
  • 5.
    Liver, core biopsy: -Moderately differentiated HCC
  • 6.
    DIAGNOSIS  Child Pughscore A, Barcelona B  Stage III moderately differentiated hepatocellular carcinoma
  • 7.
    LIVER MRI WITHEOVIST PRIOR TO STARTING TREATMENT
  • 10.
    LABS PRIOR TOSTARTING Y-90 THERAPY  11/11/2013  Total Bili: 0.9 mg/dL  Direct Bili: 0.2 mg/dL  AST: 47 U/L  ALT: 79 U/L  ALK Phos: 105 U/L  Alpha-Fetoproteins: 106.6 ng/mL
  • 11.
    TREATMENT APPROACH FORJ.P.  Due to his multifocal bi-lobed disease he was not a candidate for a liver transplant or surgery.  11/14/13 Y-90 radioembolization of right hepatic artery. (#1)  12/17/2013 Chemoembolization of left hepatic artery.  2/5/2014 Started on Sorafenib ( 2 tabs in a.m. and 2 tabs in p.m.)  4/2/2014 Y-90 radioembolization of right hepatic artery. (#2)  October 2014 Sorafenib stopped and enrolled in a Phase I gene therapy trial under Dr. Freilich’s care.
  • 12.
    MRI OF THEABDOMEN AND PELVIS POST FIRST Y-90 TREATMENT
  • 14.
    LABS PRIOR TOSTARTING GENE THERAPY  7/17/2014  Total Bili: 1.1 mg/dL  Direct Bili: 0.4 mg/dL  AST: 56 U/L  ALT: 82 U/L  Alk Phos: 145 U/L  Alpha-Fetoprotein: 92.7 ng/mL
  • 15.
    LIVER MRI WITHEOVIST PRIOR TO STARTING GENE THERAPY
  • 16.
    DEVELOPMENT OF COMPLICATIONS 11/21/2014 Port-A-Cath removed due to infection; Staphylococcus aureus.  2/7/2015 Presented to emergency department with complaint of severe right abdominal pain and right chest pain with radiation to the back associated with shortness of breath and dizziness with a fever as high as 38.3.  2/7/2015 CT of the abdomen and chest showed abnormalities that included small right pleural effusion associated with a large collection of fluid around the necrotic lesion in his liver, abutting the right hemidiaphragm.  2/12/2015 underwent bronchoscopy, thracoscopy, right thoracotomy and decortication due to development of staph aureus empyema and necrotic hepatocellular tumor that spread to the right pleural space; a wedge biopsy of the liver was done at that time.
  • 17.
    CT OF ABDOMENAND PELVIS DEMONSTRATING NECROTIC MASS
  • 18.
    Liver, tumor resection: -Residual moderately differentiated HCC
  • 19.
    Liver, tumor resection: -Residual moderately differentiated HCC
  • 20.
    CT OF THEABDOMEN AND PELVIS DEMONSTRATING GENE THERAPY AND SURGICAL CHANGES
  • 21.
    MOST RECENT LABRESULTS  3/2015  Total Bili: 0.6 mg/dL  Direct Bili: 0.2 mg/dL  AST: 56 U/L  ALT: 43 U/L  ALK Phos: 377 U/L  Alpha-Fetoprotein: 3.1 ng/mL
  • 23.
  • 25.
  • 26.
    LI-RAD CASE EXAMPLES Example Case #1  Cirrhotic liver, F4 fibrosis on elastography  17 mm lesion with arterial phase enhancement, washout, pseudocapsule  HCC LI-RADS 5  Example Case #2  HCC LI-RADS 5V
  • 27.
    PATIENT V.B.  75year old African American female  Past Medical History:  Hypertension  Degenerative joint disease/ osteoarthritis  Hyperlipidemia  Gastroesophageal reflux disease (GERD)  Hypothyroidism  Previous Surgeries:  Right leg surgery as a child  Right lens implant  Family History:  Sister with uterine cancer  First cousin with breast cancer  Brother and children with diabetes
  • 28.
    PATIENT PRESENTATION  InOctober 2013 she went to her PCP complaining of abdominal pain, upper back pain, decreased appetite, a 10-15 pound weight loss and jaundice that had been ongoing for two weeks. CT and labs were ordered.  Comprehensive Metabolic Panel (10/11/2013):  Creatinine: 1.09 mg/dL  Total Bilirubin: 6.3 mg/dL  Alkaline Phosphatase: 418 U/L  AST: 435 U/L  ALT: 758 U/L  CA 19-9: 261.6 Units/mL  CT of the Abdomen and pelvis (10/14/2013) revealed dilation of the biliary tree and pancreatic duct and distention of the gallbladder secondary to a mass of the head of the pancreas measuring 4.7 cm.  Underwent EUS with FNA and ERCP with biliary sphincterotomy and placement of stent (10/16/2013) that showed a focal 4 x 3.5 cm irregular hypoechoic fullness of the head of the pancreas, showing malignant cells surrounding peripancreatic lymphadenopathy. EUS stage T3 N1 M0
  • 29.
  • 30.
    Pancreatic head mass,FNA: - Positive for malignant cells; compatible with adenocarcinoma
  • 31.
    Pancreatic head mass,FNA: - Positive for malignant cells; compatible with adenocarcinoma
  • 32.
    CT OF THEABDOMEN AND PELVIS PRE NEOADJUVANT THERAPY 10/14/2013
  • 33.
    NEOADJUVANT APPROACH FORV.B.  Based on EUS staging, pathology and imaging V.B. was determined to be borderline resectable and it was decided to place her on Neoadjuvant Chemotherapy concurrent with Radiation.  11/12/13 Started Neoadjuvant chemotherapy with Gemzar  11/19/13 Started radiation in combination with Gemzar chemotherapy  12/3/13 Stopped chemotherapy treatment (completed 4 cycles)  12/24/13 Ended radiation treatment (completed 5 weeks)
  • 34.
    CT OF THEABDOMEN AND PELVIS POST NEOADJUVANT THERAPY
  • 35.
    RE-STAGING FOR V.B. 1/20/14 CT of the Abdomen and pelvis was done to determine patient’s resectability for surgery candidacy.  1/29/14 Whipple procedure performed by Dr. Cates.
  • 36.
    CT OF THEABDOMEN AND PELVIS POST WHIPPLE RECOVERY
  • 37.
    DIAGNOSIS  EUS FNApathology:  Pancreatic adenocarcinoma  Surgical pathology:  Tumor site: cannot be determined  Additional sites involved by tumor: none identified  Histologic type: other, no residual tumor  Histologic grade: cannot be assessed secondary to therapeutic effect  Tumor size: cannot be determined; no residual tumor  Microscopic tumor extension: no evidence of primary tumor  Margins: margins uninvolved by invasive carcinoma  Treatment effect: present, no residual tumor (complete response, grade 0)  Stage: T0 N0 M0
  • 38.
    Whipple resection: - Noresidual carcinoma identified - Negative lymph nodes (0/17)
  • 39.
    ADJUVANT TREATMENT  Dueto complications with her Whipple recovery, the patient did not receive any adjuvant chemotherapy.  The patient is doing well with no evidence of pancreatic adenocarcinoma recurrence at this time.