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12/15/2011 1 Welcome to the 6 th Annual Welcome to the 6 Annual Pancreatic Cancer Awareness Day November 12, 2011

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Page 1: Welcometothe6Welcome to the 6 Annual Pancreatic Cancer Awareness Day … · 2011. 11. 12. · pancreas, duodenum, +/‐ portion of stomach, gallbladder Typical hospital length of

12/15/2011

1

Welcome to the 6th AnnualWelcome to the 6 Annual Pancreatic Cancer Awareness Day

November 12, 2011

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Program AgendaWelcome from the Executive Director

John Chabot, MD

Mission and Goals from the Administrative Director

Francine Castillo, MS

Topics: 

I.  Surgical Options and Post‐operative Lifestyle Changes

Beth Schrope, MD, PhD (Surgery)

II. Genetics & Prevention 

Harold Frucht, MD (Genetics & Prevention)

III. Pancreatic Cysts 

John Allendorf, MD (Surgery)f, ( g y)

IV. The W’s and H’s of Drug Therapy in Pancreatic Cancer: How Can We Move Forward?

Wasif Saif, MD (Medical Director, The Pancreas Center)

V. Epidemiology of Pancreatic Cancer: What We Know About Risk and Prevention

Jeanine Genkinger, PhD, MHS (Epidemiology)

Q & A Session

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Mission

To decrease the societal and individual burden of pancreatic disease by establishing and maintaining a center of excellence dedicated to providing outstanding research and medical care to patients with pancreatic disease

100 Day Plan (Feb 1, 2008)Clinical Research

Imminent Changes:• Receptionist 2/4

• Dr Fine outpt practice 2/18•Obesity Center final operational 

flow agreement

ImplementTissue Banking

Continue and ExpandResearchMeetings

Imminent Changes:•Clinical Research Manager

Victoria Serrano 3/14Develop standards & ensure compliance for all researchinitiatives Liaison to HICCC

Fundraising/Marketing

Lustgarten Site VisitFeb 14

Mirzaand Dean visit

Data Collection&

Analysis

Continue to collectvolume numbers

and revenues acrossall departments

Have RN/NP help developsmooth patient flow process:

Temp RNs thru July 08Catherine & Rishikka

Break into three centers lead

Research MeetingsDr  Fine Dr Su

Dr FruchtPromote investigator 

driven studies

Continue to recruit forHigh Risk Prevention

Protocols:1: S‐MRCP vs S‐EUS 

for pancreatic cancer screening inhigh‐risk individuals

2: Utilizing S‐MRCP & arginine Testing to compare exocrine/endocrine function following 

Surgical resection for pancreatic

Fulfill staffing needs in 3 areas:• Secretarial

• Precerting and Credentialing• Financial Counseling

initiatives. Liaison to HICCC

Continue collaborationw/ other researchers

Dr. Wendy ChungDr.RotterdamDr. Lucas Dr. Verna

and ean visitFeb 28

Preliminary Proof of new comprehensiveMulitdept website

Comprehensive fundraising folder

High Risk program brochure 

Develop patientsatisfaction survey, pinpoint areas in 

need of improvement

Scanning HHQs & other clinicaldata directly into database

by mid level managers:Endocrine/Thyroid/Mesothel.

PancreasObesity

Design and developHigh Risk Prevention Room/

Patient resource room

Surgical resection for pancreatic adenocarcinoma

3: Comparing S‐MRCP with e‐PFT in patients w/abdominal pain or

symptoms of pancreatic insufficiency following surgical

resection for pancreaticadenocarcinoma

4: Studying the frequency ofdistal/multifocal PanIN lesions in locally‐recurrent pancreatic cancer5: Determining the frequency of

BRCA genetic mutations in Ashkenazi 

Jewish pancreatic cancer patients

EMR Implementation• In compliance

with university guidelines

GI Research FellowDr Caroline HwangJuly 2008 – July 2009

The Pancreas Centercomprehensive 

booklet

Purchase equipmentFor uniform study #s

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Long Term Goals

Marketing NetworkingClinical NYPH/HICCC

Research

Develop pancreas center affiliations

in suburbanhospitals

Fundraising forcharities

Encourage new donors

Develop true multi‐disciplinary practice with

open schedulingacross all depts.

Increase space on IP 8Develop a 

robust clinicaltrial organization

Hire Pathologist Solely for Pancreas Center

Have largesttumor bank in

countryRollout GI MED and MED ONC on EMR

Participate inindustry trials

Develop financial model depictingNYP growth

Work with survivors/

family membersin the community to

organize local 

Participate inspeaking

engagements

MED ONC on EMR NYP growth from PC activities

fundraising eventsand “walks”

GetNIH grants

Long(er) Term Goals!

Clinical Research Awareness

Continue to improve patient access/patient satisfaction

Auto‐islet Transplant

Grow CYST Program

Dedicated psychosocial support outpatient program on site

Pre‐surgical diabetes teaching video

SPORE grant!

Expand translational research to improve patient outcomes 

Add to clinical trials/continue collaboration with other 

institutions

Complete stool study

Build mainstream media outlets

PC Awareness outreach in minority communities

Build internet presence/blog

Pancreas Center Endowment!!!!

Expand referral physician base out of tri‐state area

Build international reputation

Create lost to follow up protocol

Collaboration for pain management

……………………….

Complete stool study

Funding for new lab equipment

Recruit up and coming basic science researchers dedicated to 

the pancreas

……………………………

Develop psychosocial program for families

Collaborate with American Cancer Society

……………………………..

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570589600

700

Pancreas Center New Patient Volume

159

184

281

386

200

300

400

500

44

92

136159

0

100

2002 2003 2004 2005 2006 2007 2008 2009 2010

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Th P C t TThe Pancreas Center Team 

The Pancreas Center

Vasudha Dhar, MD (Interventional Endoscopy)Tomas Gonda (Interventional Endoscopy)Claudia Kipp, PA (Interventional Endoscopy) Charles Lightdale, MD (Interventional Endoscopy)

John Allendorf, MD (Surgery)Laurie Budd, RN (Surgery)John Chabot, MD (Surgery)Nicole Goetz, DNP(Surgery)G b i l i (S )

Charles Lightdale, MD (Interventional Endoscopy)John Poneros, MD (Interventional Endoscopy) Amrita Sethi, MD (Interventional Endoscopy)Tim Wang, MD, PhD (GI/Basic Science Research)

Kyung Chu, NP (Medical Oncology)Robert Fine, MD (Medical Oncology)Wasif Saif, MD (Medical Oncology)William Sherman, MD (Medical Oncology)

Helen Remotti, MD (Pathology)Heidi Rotterdam, MD (Pathology)David Leung, MD (Nuclear Medicine)

( d l )

Gabriela Harrington (Surgery)James A. Lee, MD (Surgery)Beth Schrope, MD, PhD (Surgery)Yanghee Woo, MD (Surgery)

The Muzzi Mirza Pancreatic Cancer Prevention and Genetics Program

Harold Frucht, MD (Program Director )Wendy Chung, MD (Genetics)Fay Kastrinos, MD (Research)Michael Rasiej, MD (Radiology)Ashley Dikos (Administrative Manager)Jason Chu (Part Time Research Admin)Leonora Mui, MD (Radiology)

Jeffrey Newhouse, MD (Radiology)Martin Prince, MD (Radiology ) 

Mary Sciutto, MD (Dept of Psychiatry)

Jason Chu (Part Time Research Admin)Lauren Khanna, MD (Research)Elana Levinson, MS (Genetics Counselor)Aimee Lucas, MD (Research)Vilma Rosario (Part Time Research Admin)Eizabeth Verna, MD Research)

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The Pancreas CenterDivision of GI Endocrine Surgery Administrative 

SupportFrancine Castillo, MS(Administrative Director/Division Administrator)Bonnie Badenchini (Administrative Manager)Maureen Benjamin (Billing Manager General Surgery)Sarah Cambria (New Patient Coordinator,  NP Admin Asst)

Division of Hematology Oncology Administrative Support

Nancy Amalbert (Divisional Administrator)Jennifer Arroyo (Practice Manager)Kristina Howard (Admin Asst)Kindra Matthews (Admin Asst)

( )Colina Chapman Williams (Admin Asst)Kimone Crossley (Data Manager)Tyrina Jones (Medical Assistant)Alba Munoz (Financial Coordinator General Surgery)Priscilla Novas (New Patient Coordinator,  NP Admin Asst)Ana Rosario (Admin Asst)  Quanda Tarleton (Medical Assistant)Allison Villacis (Data Manager) Rodelyn Zapanta (Admin Asst) 

Division of Digestive and Liver Diseases Administrative Support

Misc Administrative StaffBryan Dotson (NYP Public Relations Office)Jada Fabrizio (Office of External Affairs )Bradley Jobling (Pancreas Center/Surgery Social Networking)Kristen Mahood (Assistant VP of Development)Juan Mejia (Service Line Director, Digestive Diseases)Marilyn Mullins (Development Officer)Amy Pietzak (NYP Public Relations Office)Kathleen Propp (NYP Marketing)Christine Rein (Office of External Affairs Events Coord)Deb Schwartz (Director, Office of External Affairs)Stephanie Sheeler (Office of External Affairs Events Coord)

i Shi h ( b i l )pp

Ana Ignat (Divisional Administrator)Clarissa  Alvino (MA)Yandreily Arroyo (Admin Asst)Carolyn Baldwin (Call Center)George DeJesus (Admin Asst)Jacqueline Infante (Practice Manager)Evelyn Martinez‐Garcia (Admin Asst)Camelia Salajeanu  (Billing)Yaniria Perez (Reception)Beatriz Valladres (Call Center)Connie Zapata (Practice Manager)

Ju‐Mei Shieh (Pancreas Center Website Developer)Jennifer Turvey (Office of External Affairs)

Herbert Irving Comprehensive Cancer Center Translational ResearchMary Ann Kral (Executive Director for Clinical Research) Mary Ann Kiernan (Regulatory Compliance Specialist) Frances Brogran (Research Nurse ‐ Dr. Wasif Saif) Kyung Chu, NP (Research Nurse ‐ Dr. William Sherman) 

Basic Science ResearchGloria Su, PhD Dario Garcia‐Carracedo, PhD Xiaojun Li  Wanglong Qiu, MD, PhD Ken Olive, PhD 

Kelly Mowatt (Study Coordinator ‐ Dr Robert Fine) Dawn Tsushima, RN (Research Nurse ‐ Dr Robert Fine) Sarah Zelonis (Study Coordinator ‐ Dr Wasif Saif) 

Pancreas Center Research StaffJoseph Dinorcia, MD (Research Fellow)Irene Epelboym (Research) Jeanine Genkinger( Epidemiology)Minna Lee (Research)Qiongfen Li  (Research – Autoislet) Megan Winner, MD (Research Fellow) 

Mike BadgleyMarina FurmanovJennifer JongenPaul ObersteinBarbara Orelli, PhDCarmine PalermoStephen SastraDafydd Thomas, PhDYilong Hung Robert Fine, MD Richard Dinnen, PhD Yuehua Mao,MD 

NYP Ancillary Care TeamAnne Ammons, RD (Nutrition) Fran Hellar, LCSW (Inpt Social Work) Angela Lloyd, LCSW (Social Work) Tina Sapienza, LCSW (Social Work)

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Bob BrownBob BrownPatient Speaker

Click to View Bob Brown's Story on Youtube

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SURGICAL OPTIONS &OS O SPOST‐OPERATIVE LIFESTYLE 

CHANGES

Beth Schrope, MD, PhDDepartment of SurgeryDepartment of Surgery

Columbia University Medical Center/ New York‐Presbyterian University

Pancreatic Surgery

Who gets surgery?

Types of procedures

Post‐operative lifestyle implications

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Who is Eligible for Surgery?

Localized diseaseLocalized diseaseAssess with MRI, PET scan

Acceptable medical riskCardiovascular clearance

Preoperative chemo or radiationFor “locally advanced” disease

The Neighborhood

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Whipple Procedure

Removal of the head of the pancreas, duodenum, +/‐portion of stomach, gallbladder

Typical hospital length of stay 7 – 14 days

Over 100 Whipplesperformed at CUMC in 2010, 22% with vascular reconstruction

Distal Pancreatectomy

Removal of the body and tail of pancreas and possiblytail of pancreas and possibly spleen

Option for laparoscopic procedure

Typical hospital length of stay 5 – 9 days

Requires certainRequires certain vaccinations (for loss of spleen)

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Central Pancreatectomy

Removal of a portion of the body of pancreasbody of pancreas 

Reserved for benign and low grade malignant lesions (islet cell tumors)

Typical hospital length of stay 5 – 9 days

Goal to preserve as muchGoal to preserve as much pancreatic function as possible*

Total Pancreatectomy

Removal of entire pancreas, duodenum, gallbladder, +/‐spleen

Typical hospital length of stay 10 – 14 days

All patients become insulin dependent diabetics*

Reserved for high cancer‐risk individuals

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Postoperative Expectations

Hospital length of stay

Pain

Resumption of diet / gastric ileus

Bl d it i / t lBlood sugar monitoring / control

Pain Management

Immediate postoperative pain

l dPCA ‐> oral pain medications

Non‐narcotics – Toradol, Lyrica, Tramadol

Chronic pain

Oral pain medications narcotic NSAIDs otherOral pain medications – narcotic, NSAIDs, other

Narcotic patch

Nerve blocks

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Post‐pancreatectomy Diet

Reduce the size of your meals

Restrict dietary fat

Consider dietary supplements

Have nourishing snacks within easy reach

Don't worry if you have days when you can't eat at all

Try to drink plenty of fluids

Pancreatic Digestive InsufficiencySymptoms

Diarrhea

Bloating

Foul‐smelling stool

Hair loss, dry skin

Difficulty gaining weightDifficulty gaining weight

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Digestive Medications

Pancreatic enzymes (take at each meal)Creon

Zenpep

Pancrease

Promotility agentsReglan (metoclopramide)

ErythromycinErythromycin

Antiulcer agents

Constipation regimen

Diabetes

ALL surgical patients experience elevated blood psugar after surgery

Insulin drip after surgery improves healing

Long term risk of diabetes 10 – 12% in patients with pnormal blood sugar before surgery (after Whipple)

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Quality of Life

Questionnaires from patients who have undergone Whipple report good quality of life,undergone Whipple report good quality of life, comparable scores to healthy controls (79 ‐ 81 vs. 83 ‐ 86)

Diabetes is not a ‘guarantee’ and is a controllable consequence

Digestive and nutritional issues are easily controlled with medications and food choices

GENETICS & PREVENTIONGENETICS & PREVENTION

Harold Frucht, MDDirector The Muzzi Mirza Pancreatic Cancer Prevention &Director, The Muzzi Mirza Pancreatic Cancer Prevention & 

Genetics Program

Associate Professor, Division of GI MedicineColumbia University Medical Center/New York‐Presbyterian Hospital 

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15% of patients with pancreatic cancer have a familial aggregation or an inherited predisposition15% of patients with pancreatic cancer have a familial aggregation or an inherited predisposition

Number of FDRs (w/ Pancreatic Cancer)

Incidence (per 100,000 in theUS Population)

Increased Risk (by Number of FDR)

General U.S. (reference) 9 ‐

1 41 4.6 x

2 58 6.4 x

3 or more 288 32.0 xSource: Klein AP, et al., Cancer Research 2004; 64; 2634‐2638

Mutation Relative Risk

Breast cancer BRCA1, BRCA2 10

FAMMM P16 15‐65

Peutz‐Jeghers Syndrome STK11 130

HNPCC MLH1, MSH2 2

H di i i T i 50Hereditary pancreatitis Trypsinogen 50

Familial Polyposis APC 5

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2 or more FDR with pancreatic cancer

1 FDR with pancreas cancer, ≤ 50 years old

2 or more second degree relatives with pancreatic 

cancer, one at an early age

History, physical exam,  family history, genetic testing

Average Risk:

‐1 family member with PC at > 55 years old 

Moderate Risk 

‐ ≥ 2 1st, 2nd or 3rd °with PC‐ 1 1st °at < 55 years old

High Risk 

‐ ≥ 3 1st, 2nd or 3rd°with PC 

Basic blood tests, additional testing if symptoms

‐ 1  1 at < 55 years old ‐ Not high risk

MRI or EUS

Any abnormal testing: EUS  (if not already done)

‐ ≥ 2 1st° with PC 

‐ ≥ 1 1st & 1 2nd° with PC, 1 at < 55 years old

EUS and MRI

Verna EC, et al, Pancreatic cancer screening in a prospective cohort of high‐risk patients: a comprehensive strategy of imaging and genetics. Clin Cancer Res. 2010 Oct 15;16(20):5028‐37

No malignant or pre‐malignant disease identified

Surveillance (based on further risk stratification)

Malignant or pre‐malignant disease diagnosed or suspected

Consider Surgery

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Genetic Counseling / TestingGenetic Counseling / Testing&&

Screening / PreventionScreening / Prevention

Probable HNPCC/FAMMM

History Suggestive of Inherited Pancreatic Cancer

Genetic test of anaffected individualaffected individual

Positive Negative

Genetic testing of family members

Continued high risk cancer screening of the individual and all 

family members

Cancer screening as recommended for 

the general population

PositiveNegative

Positivefor cancer

Surgery

Negative

Calvert & Frucht, Ann Int Med, 2002:137;603‐613

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Genetic Testing

EUS

CA 19‐9, OGTT

MRI/MRCP

ERCP

Laparoscopic Distal Pancreatectomy

Total Pancreatectomy

Ongoing Research Ongoing Research 

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Potentially the same methodology for Colon & Pancreas cancer screening?

Exfoliated cells ducts bowel stool

Extract crude DNA from stool samples

Analysis for abnormalities

Our Study Results

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TO MAKE AN APPOINTMENTTO MAKE AN APPOINTMENTPLEASE CALL:PLEASE CALL:

212212 305305 9337 9337 212212--305305--9337 9337

PANCREATIC CYSTSPANCREATIC CYSTS

John Allendorf, MD 

Assistant Professor of Surgery

Director of Endocrine Surgery Fellowship

Columbia University Medical Center/ New York‐Presbyterian Hospital 

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Differential Diagnosis

Inflammatory ‐‐ Pseudocyst

NeoplasticSerous cystadenoma

Mucinous lesionsMucinous cystadenoma

IPMNSide Branch IPMN

Main Duct IPMNMain Duct IPMN

Cystic degeneration of endocrine neoplasms

Diagnostic Workup

History

Physical exam

Fluid AnalysisCytologyPhysical exam

Imaging

CT

MRI/MRCP

EUS

BiochemistryCEA (192 ng/mL)Amylase

Mutational analysis

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Pseudocyst

Inflammatory

Hi t f P titiHistory of Pancreatitis

Fluid 

Inflammatory cells

Debris

High amylase

Low CEA

Serous Cystadenoma

Asymptomatic, may icause pain

Palpable mass

Central scar, calcification

Microcystic on EUS

Low amylaseLow amylase

Low CEA

Benign

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Mucinous Cystadenoma

Often asymptomatic

YYoung women

Usually located in tail

Unilocular or few septations

Low Amylase

High CEA

Ovarian type stromaOvarian type stroma

Malignant potential

Sidebranch IPMN

Asymptomatic or pancreatitis

Both genders

Not limited to the tail

Fluid analysis

High amylase

High CEAHigh CEA

Malignant potential

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Main Duct IPMN

Pancreatitis

Fishmouth ampulla

M cinMucin

High amylase

High CEA 

Malignant potential

Management

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Pseudocyst

Natural history

Ob tiObservation

Drainage

External

InternalEndoscopic 

SurgicalSurgical 

Endoscopic Internal Drainage

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Serous Cystadenoma

Observation

Resection

Symptoms

Size

Diagnostic uncertainty

Mucinous Cystadenoma

Resection

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Main Duct IPMN

Risk of malignancy (70%)

ResectionAffected portion of duct

Frozen section

May require total pancreatectomy

ObservationPoor surgical candidatesPoor surgical candidates

Advanced age

International consensus Guidelines (Sendai criteria)

Sidebranch IPMN

Risk of malignancy vs risk of morbidity

ResectionSymptomatic

>3cm

Mural nodules

Young age

ObservationSurveillance

Interval

Modality

? Practical

International consensus Guidelines (Tanaka, et al)

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Pancreatic Cyst Surveillance Program

500 patients in the registry

Program of active surveillanceProgram of active surveillance

MRI

EUS

Natural history

Patient quality of lifePatient quality of life

Mutational analysis of cyst fluid

Summary

Systematic approach

History, imaging, fluid analysis

Distinguish inflammatory from neoplastic

Weigh the risks and benefits of intervention

Symptoms

Risk of malignant degeneration

Risk of surgical complications and diabetesRisk of surgical complications and diabetes

Design an intervention tailored to the patient

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THE W’S AND H’S OF DRUG THERAPY IN PANCREATIC CANCER:

HOW CAN WE MOVE FORWARD?

Wasif Saif, MD

Professor of Clinical Medicine

Director of the Clinical Section GI Oncology 

Medical Director, Pancreas Center

Columbia University Medical Center/New York‐Presbyterian Hospital

Outline

Are there any different types of pancreatic cancer?

What are the known risk factors?What are the known risk factors? 

What are the common symptoms and signs?

How do we diagnose pancreatic cancer?

How do we treat pancreatic cancer?

What is the prognosis? 

Wh t C I d t I Odd ?What Can I do to Improve my Odds?

What are the novel drugs offered @ CU Pancreas Center?

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Types of Pancreatic Cancer

There are two types of cells in the pancreas: exocrine cells and endocrine cells.

Th ll l h diff f i

EXOCRINE95% of pancreatic cancers are classified as

exocrine tumors because they begin in the

exocrine cells that produce enzymes to aid

in digestion. 

ENDOCRINE5% are endocrine tumors, also called

neuroendocrine or islet cell tumors. 

Islet cells of the pancreas produce hormones

including insulin, glucagon and

These cells also have different functions. 

somatostatin. 

Endocrine tumors may be benign or

malignant and tend to be slower growing

than exocrine tumors. 

Pain : 80%

Mid epigastric 43%

Signs and Symptoms of Pancreatic CancerThere aren’t any noticeable signs or symptoms in the early stages of PC Signs of PC, when present, are like the signs of many other illnesses

Mid epigastric 43%

Upper abdominal               23%

Lower abdominal               18%     

Left upper quadrant          13%   

Jaundice : 47%

Weight loss: 60%

New onset of D. mellitus

Para‐neoplastic Syndromes

Weight loss

Trousseau’s syndrome

Depressive Symptoms

Courvoisier’s sign

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Causes of Pancreatic Cancer

SporadicSporadic ~65 ‐ 80%

Known genetic syndromes ~5%Hereditary Pancreatitis, HNPCC Lynch II Variant, BRCA2, FAMMM, Peutz‐Jeghers Syndrome

Familial pancreatic cancer~10% or more

How Do We Diagnose Pancreatic Cancer?

Blood TestsSerum chemistries, CBC, LFTs

Serum CA19‐9 and in some cases CEA

Other tests, such as fecal fat, stool trypsin, trypsinogen, amylase, and lipase may be evaluated to determine pancreas function and need for pancreatic enzyme supplementation.

Diagnostic ImagingDiagnostic ImagingCT scan of chest, abdomen, and pelvis

EUS

ERCP/MRCP

PET scan in certain cases

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How Do We Treat Pancreatic Cancer?

Resectable PC

Stages I‐IIB15‐20%

SurgeryAdjuvant Chemoradiotherapy

Inoperable PC

Locally AdvancedStage III 30‐40%

MetastaticStage IV40‐50%

ChemoradiationCh th

ChemotherapyN l Th ti

Inoperable PC

Locally AdvancedStage III 30‐40%

MetastaticStage IV40‐50%

j pyAdjuvant Chemotherapy

ChemotherapyNovel Therapeutics

Novel TherapeuticsSupportive Care

Adj t th i t t t ft t t d t di l

After Surgery: Adjuvant Therapy For Pancreatic Cancer

Adjuvant therapy is treatment after surgery to try and prevent disease relapse

As most patients after surgery will have the disease relapse in other places, the 

cancer must have spread prior to surgery

Tumors smaller than 10 million cells cannot be seen, so we cannot detect 

“micrometastatic” disease

Standards of care vary depending on which side of the Atlantic you’re on:

North America (GITSG, RTOG): chemo‐radiation followed by 

chemotherapy

Europe (ESPAC‐1, CONKO, ESPAC‐3): chemotherapy alone

The critical thing is that SOMETHING is better than NOTHING

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Neoadjuvant Therapy

Goals:Increase the resectability rateIncrease the resectability rateSee who needs radiation therapyDetermine why therapy failsIncrease the survival and cure rate of pancreatic cancer patients

LA Pancreatic Cancer

OPTIONS:Chemo‐XRT XRT (radiation therapy)Chemotherapy followed by Chemo‐XRT

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Treatment For Patients With Advanced Pancreatic Cancer

A Timeline For Slow Progress

Pre‐1996 Many drugs tested, nothing workedy g , g

1996 Gemcitabine FDA approved

1996‐2005 Many drugs tested, no drug or drug combination is better than Gemcitabine

2005 Tarceva FDA approved

2005 Capecitabine + Gemcitabine better than Gemcitabine

2006 G i bi O li l i d FDR G i bi b h2006 Gemcitabine + Oxaliplatin and FDR Gemcitabine not better than Gemcitabine

2006 Gemcitabine + Bevacizumab not better than Gemcitabine

2007 Gemcitabine + Cetuximab not better than Gemcitabine

2010 FOLFORINOX better than Gemcitabine

Li J, Saif MW. JOP. 2009 Mar 9;10(2):109‐17

PrognosisEstimated new cases and deaths from pancreatic cancer in the United States in 2010:

New cases: 43,140Deaths: 36,800

Functional Stage Description Median Survival (m)

Resectable Tumor confined to pancreas or extends beyond pancreas but without involvement of 

15‐19 

4th leading cause of cancer mortality (6%)

CA or SMA + Regional LAD

LA Tumor involves CA or SMA 6‐10 

Met/Adv Distant Mets 3‐6 

Staley CA, Pancreas 1996

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When Would Chemotherapy Not Be Appropriate?

If you are staying in bed greater than 50% of the time after you wake up

This may be a sign that your cancer is so advanced  that chemotherapy will likely do more harm than good

Hospice care and relief of symptoms should be the primary focus of your care

What Can I Do To Improve My Odds?

Participate in a CLINICAL TRIAL

Select the option that you feel is the best in conjunction with your doctors

When you require highly specialized care of a multi‐disciplinary nature, seek care in an i i i h h i l dinstitution where these teams are in place and functioning to work together on a daily basis

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CUMC PC Research

Treatment Options At The Pancreas Center

Resected LA , Borderline  Advanced disease

* HyperAcute  Vaccine* GTX

1st‐line 

2nd‐line 

3rd‐line• CO 1.01• MM398 vs

GTX GTX + Xeloda‐XRT

3 line

• Gemcitabine ± IPI-926• Gemcitabine ± GS6624• GTX• GTX vs. Gem-Erlotinib

• MM398 vs. 5FU/LV

Pipeline• NUC1031• NV-196

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EPIDEMIOLOGY OF PANCREATIC CANCER: WHAT WE KNOW ABOUT 

RISK AND PREVENTION?

Jeanine Genkinger, PhD, MHS

Department of Epidemiology

Columbia University

Mailman School of Public Health

2011 Estimated US Cancer Cases*

30% Breast

14% Lung & bronchus

Men822,300

Women774,370

Prostate 29%

Lung & bronchus 14% g

9% Colon & rectum

6% Uterine corpus

5% Thyroid 

4% Non‐Hodgkinlymphoma

4% Melanomaof skin

Lung & bronchus 14%

Colon & rectum 9%

Urinary bladder 6%

Melanoma of skin 5%

Kidney  5%

Non‐Hodgkin 

lymphoma 4%

*Excludes basal and squamous cell skin cancers and in situ carcinomas except urinary bladder.Source: American Cancer Society, 2011.

3%       Kidney 

3% Ovary

3% Pancreas

19% All Other Sites

lymphoma  4%

Oral Cavity 3%

Leukemia 3%

Pancreas 3%

All Other Sites 19%

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2011 Estimated US Cancer Deaths*

26% Lung & bronchus

15% Breast

Men300,430

Women271,520

Lung & bronchus 28%

Prostate  11%

9% Colon & rectum

7% Pancreas

6% Ovary 

4% Non‐hodgkin lymphoma 

3% Leukemia

3% Uterine corpus

Colon & rectum  8%

Pancreas 6%

Liver & Intrahepatic bile 4%

Leukemia 4%

Esophagus 4%

Urinary Bladder  4%

*Excludes basal and squamous cell skin cancers and in situ carcinomas except urinary bladder.Source: American Cancer Society, 2011.

2% Liver & intrahepatic bile   duct

2% Brain & other nervous   system

Non‐hodgkin lymphoma 3%

Kidney & renal pelvis 3%

Lifetime Risk1.41% of men and women born today will be diagnosed with cancer of the pancreas at some time during their lifetime. 

OR

1 in 71 men and women will be diagnosed with cancer of the pancreas during1 in 71 men and women will be diagnosed with cancer of the pancreas during their lifetime. 

Comparison: 

BREAST CANCER: 12.15% of women born today will be diagnosed at some time during their lifetime.

1 in 8 women will be diagnosed with cancer of the breast during their lifetime.g g

COLORECTAL CANCER:5.12% of men and women born today will be diagnosed with cancer of the colon and rectum at some time during their lifetime. 

1 in 20 men and women will be diagnosed with cancer of the colon and rectum during their lifetime.

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Risk Factors for Pancreatic Cancer

Non‐modifiable Factors

Age (60‐80 yrs of age)

Race 

Sex

Family History/Genetics

(Lowenfels AB, J Cell Biochem 2005)

Incidence Rates by Race/Ethnicity and Gender

Race/Ethnicity Male Female

All Races 55.0 per 100,000 men 41.0 per 100,000 women

White 54.4 per 100,000 men 40.2 per 100,000 women

Black 67.7 per 100,000 men 51.2 per 100,000 women

Asian/Pacific Islander  45.4 per 100,000 men 34.6 per 100,000 women

American Indian/AlaskaAmerican Indian/Alaska Native a

42.7 per 100,000 men 40.0 per 100,000 women

Hispanic b 39.9 per 100,000 men 28.4 per 100,000 women

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Risk or Preventive Factors for Pancreatic Cancer

Modifiable Factors:Smoking 

Alcohol

Obesity – BMI 

Physical Inactivity?

Dietary Factors?Sugar‐sweetened beverages

Red and processed meats 

Vitamin D

Fruits and Vegetables

Pooled Multivariate Adjusted Relative Risks (95% CI) for Pancreatic Cancer According to BMI at Baseline

00.2

0.40.6

0.81

1.21.4

1.61.8

2

Re

lati

ve

Ris

k (

95

% C

I

1.16(0.96-1.40)

1.47(1.23-1.75)

1.00(REF)

1.07(0.92-1.25)

1.18(1.03-1.36)

overweight obese0

0 1 2 3 4 5 6

Categories of Body Mass Index

Genkinger et al, CEBP

<21 21-22.9 23-24.9 25-29.9 > 30

BMI is calculated from your height and weight. BMI is an estimate of body fat

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Multivariate Adjusted Pooled Relative Risks (RR) and 95% Confidence Intervals (CI) for Pancreatic Cancer 

According to Alcohol Intake

1.40

0 40

0.60

0.80

1.00

1.20

Relative Risks Females

Males

Total1.00(REF)

1.02(0 91 1 14)

0.91(0 9 1 04)

0.96(0 82 1 14)

1.22(1 03 1 4 )

0.00

0.20

0.40

Alcohol Intake (g/day)

R

0 1-4.9 15-29.95-14.9 >30

(REF) (0.91-1.14) (0.79-1.04) (0.82-1.14) (1.03-1.45)

Genkinger et al, CEBP, 2009

1 drink/day

>2 drinks/day

Risk or Preventive Factors for Pancreatic Cancer

Modifiable Factors:Smoking 

Alcohol

Obesity – BMI 

Physical Inactivity?

Dietary Factors?Sugar sweetened beveragesSugar‐sweetened beverages

Red and processed meats 

Vitamin D

Fruits and Vegetables

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Risk Factors for Pancreatic Cancer

Health History FactorsHealth History Factors

Chronic pancreatitis

Diabetes

Periodontal Disease?

Allergies/Asthma?

(Lowenfels AB, J Cell Biochem 2005)

Recommendations

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World Cancer Research Fund/ American Institute for Cancer Research 

RecommendationsBe as lean as possible without becoming underweight.

h ll f l dBe physically active for at least 30 minutes every day.

Limit consumption of energy‐dense foods (foods high in fats and/or 

added sugars and/or low in fiber) and avoid sugary drinks.

Eat more of a variety of vegetables, fruits, whole grains, and pulses 

(beans).

Limit consumption of red meats (such as beef, pork and lamb) and avoid 

http://www.wcrf.org/cancer_research/expert_report/recommendations.php

processed meats (such as sausage, bacon).

If consumed at all, limit alcoholic drinks to 2 for men and 1 for women a 

day.

Limit consumption of salty foods and foods processed with salt (sodium).

Don’t use supplements to protect against cancer.

American Cancer SocietyRecommendations

Stay away from tobacco.

Stay at a healthy weight.

Get moving with regular physical activity.

Eat healthy with plenty of fruits and vegetables.

Limit how much alcohol you drink (if you drink at all).

Protect your skin.

Know yourself, your family history, and your risks.

Have regular check‐ups and cancer screening tests.

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Screening Guidelines  

No current recommended screening guidelines for pancreatic cancerp

USPTF recommends

Biennial screening mammography for women aged 50 to 74 years. 

Pap smear/HPV screening for cervical cancer in women who have been sexually active and have a cervix.

Fecal occult blood testing, sigmoidoscopy, or colonoscopy, for colorectal cancer in adults, beginning at age 50 years and 

continuing until age 75 years.

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American Heart Association Recommendations

Learn how many calories you are eating and drinkingIncrease amount and intensity of physical activity (at least 30 mins/day)Eat a variety of nutritious foods from all the food groups.

E t t i t i h f d (f it t bl fi d h l i f d )Eat nutrient rich foods (fruits, vegetables, unrefined whole‐grain foods)Eat fish at least twice a week

Eat less of the nutrient‐poor foods. Reduce consumption of high calorie and low nutrient foods and beverages

Cut back on beverages and foods with added sugars.Choose lean meats/poultry without skin and prepare them without saturated/trans fat.Cut back on foods containing partially hydrogenated vegetable oils to reduce trans fatCut back on foods high in dietary cholesterol. Eat less than 300 mg of cholesterol/day Choose and prepare foods with little or no salt. Eat less than1,500 mg of sodium/daySelect fat‐free, 1 percent fat, and low‐fat dairy products.

Alcohol : If you drink alcohol, drink in moderation. Smoking: Don’t smoke tobacco — and stay away from tobacco smoke.

Online Resources

American Cancer Society: http://www.cancer.org/

National Cancer Institute: http://www cancer gov/National Cancer Institute: http://www.cancer.gov/

Pancreatic Cancer Action Network: http://www.pancan.org/

Lustgarten Foundation: http://www.lustgarten.org/

Live Strong Foundation: http://www.livestrong.org/

Your Disease Risk: http://www.yourdiseaserisk.wustl.edu/english/index.htm

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Question & Answer Session

Thank You For Attending!

212.305.9467www.pancreascenter.com

www.nyp.org