pancreatic cancer

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Pancreatic cancer Pancreatic cancer chemotherapy chemotherapy Jarosław Reguła M.D. Jarosław Reguła M.D. Department of Gastroenterology, Institute Department of Gastroenterology, Institute of Oncology, Warsaw, Poland of Oncology, Warsaw, Poland

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Pancreatic cancer chemotherapy Jarosław Reguła M.D. Department of Gastroenterology, Institute of Oncology, Warsaw, Poland. Pancreatic cancer. 10-th common cancer 4-th cause of cancer death Overall 5-year survival – ca. 4%. general status (Karnofsky) - PowerPoint PPT Presentation

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Page 1: Pancreatic cancer

Pancreatic cancerPancreatic cancerchemotherapychemotherapy

Jarosław Reguła M.D.Jarosław Reguła M.D.

Department of Gastroenterology, Institute of Oncology, Department of Gastroenterology, Institute of Oncology, Warsaw, PolandWarsaw, Poland

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Pancreatic cancerPancreatic cancer

• 10-th common cancer10-th common cancer

• 4-th cause of cancer death4-th cause of cancer death

• Overall 5-year survival – ca. 4%Overall 5-year survival – ca. 4%

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Diagnosis establishedDiagnosis established

general status (Karnofsky)general status (Karnofsky)

supportive caresupportive care TNM stagingTNM staging

palliation palliation

surgery alonesurgery alone

surgery + adjuvant therapysurgery + adjuvant therapy

chemotherapychemotherapy

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Combined therapyCombined therapy

• Neo-adjuvant therapy = before surgeryNeo-adjuvant therapy = before surgery

• Adjuvant Adjuvant = after surgery = after surgery

• Sequential or concomittant (eg. CTH & RTH)Sequential or concomittant (eg. CTH & RTH)

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T staging

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T3 –locally advanced

Extends beyond pancreas but no involvement of celiac axis or superior mesenteric artery

Potentially resectable in expert centres

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T4

Involvement of celiac axis or superior mesenteric artery

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No or N1 (number of lymph nodes involved does not need to be defined

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Stage groups

Stage 0 Tis N0M0

Stage I A T1 N0M0 potentially resectableStage I B T2 N0M0

Stage II A T3 N0M0 usually potentially resectableStage II B T1-3 N1M0

Stage III T4 N0-1 M0 locally advanced, not resectable due to CA or SMA involvement

Stage IV T1-4 N0-1 M1 metastatic

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ResectionResection• RR classification classification ( (rresidual tumouresidual tumour))

– R0R0:: tumour resected macroscopically and tumour resected macroscopically and microscopically completely microscopically completely

– R1R1: : tumour resected completely macroscopically tumour resected completely macroscopically but incompletely microscopically but incompletely microscopically

– R2R2: : resection incomplete macroscopicallyresection incomplete macroscopically

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Stage I/II patients

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Neoptolemos NEJM, 2004

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ESPAC-3ESPAC-3• The largest ever trial on adjuvant therapy in The largest ever trial on adjuvant therapy in

pancreatic cancerpancreatic cancer

• 1100 patients in 17 European counties1100 patients in 17 European counties

• Arm A: Arm A: 5-FU/folinic acid5-FU/folinic acid

• Arm B: Arm B: gemcitabine day 1,8,15 every 28 daysgemcitabine day 1,8,15 every 28 days

• Results areResults are awaited awaited

Page 24: Pancreatic cancer

Clear benefit from adjuvant chemotherapy after resection

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Standard adjuvant therapiesStandard adjuvant therapies

• USA – adjuvantUSA – adjuvant chemoradiotherapy chemoradiotherapy • Europe – adjuvantEurope – adjuvant chemotherapy chemotherapy

Debate continuesDebate continues

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Advanced disease - usual survivalAdvanced disease - usual survival• Localized disease Localized disease – ca. 1 year– ca. 1 year

• Metastatic disease Metastatic disease – ca. 6 months – ca. 6 months

• Endpoints:Endpoints:– Overall survivalOverall survival– Quality of lifeQuality of life– Clinical benefit response (CBR): (pain, KPS, Clinical benefit response (CBR): (pain, KPS,

weight)weight)

Page 27: Pancreatic cancer

Main agents for chemotherapyMain agents for chemotherapy

• 5-FU – 5-FU – 600 mg/m2 weekly600 mg/m2 weekly

• Gemcitabine – Gemcitabine – 1000 mg/m2 weekly for 7 1000 mg/m2 weekly for 7 weeks (1 week off) + wekly 3 weeks with 1 weeks (1 week off) + wekly 3 weeks with 1 week offweek off

Page 28: Pancreatic cancer

5-FU vs gemcitabine5-FU vs gemcitabine

5-FU5-FU GemcitabineGemcitabineSurvival (median)Survival (median) 4,4 mo 4,4 mo 5,6 mo5,6 mo12 month survival12 month survival 2% 2% 18%18%CBRCBR 4,8% 4,8% 23,8%23,8%

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FDR GemcitabineFDR Gemcitabine• Increasing time of infusion holding the dose Increasing time of infusion holding the dose

rate constantrate constant

• Conflicting resultsConflicting results

• Most administer the drug in a standard wayMost administer the drug in a standard way

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Capecitabine (Xeloda)Capecitabine (Xeloda)• OrallyOrally• Pro-drug of 5-FUPro-drug of 5-FU

• Combination Combination Gemcitabine+capecitabine Gemcitabine+capecitabine vs vs gemcitabine gemcitabine for patients Karnofsky status 90-100 pointsfor patients Karnofsky status 90-100 points overall survival benefit overall survival benefit

10,4 monts vs 7,4 months 10,4 monts vs 7,4 months

Herrmann 2007

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Targeted therapiesTargeted therapies• EGFR inhibitors:EGFR inhibitors:

– ErlotinibErlotinib– cetuximabcetuximab

• VEGF inhibitorsVEGF inhibitors– BevacuzimabBevacuzimab

• OthersOthers

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Real life (Institute of Oncology, Real life (Institute of Oncology, Warsaw)Warsaw)

• Resectable tumour:Resectable tumour:- adjuvant chemotherapy (gemcitabine) – - adjuvant chemotherapy (gemcitabine) –

standard dosingstandard dosing- adjuvant radiochemotherapy as research - adjuvant radiochemotherapy as research

programmeprogramme• Palliative therapyPalliative therapy

• Gemcitabine (standard) until progression or toxicityGemcitabine (standard) until progression or toxicity• Gemcitabine + Xeloda (non standard approachGemcitabine + Xeloda (non standard approach

• Second lineSecond line• FAM (5-FU+ adriamycin + mitomycin)FAM (5-FU+ adriamycin + mitomycin)• Clinical trials with anti-EGFRClinical trials with anti-EGFR

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SummarySummary

• Proper staging is crucial for planning therapyProper staging is crucial for planning therapy

• Selection of patients for a given therapy is difficultSelection of patients for a given therapy is difficult

• Resectable patients should have adjuvant therapyResectable patients should have adjuvant therapy

(gemcitabine) providing good general (gemcitabine) providing good general

statusstatus

• Palliative therapy (gemcitabine monotherapy)Palliative therapy (gemcitabine monotherapy)

• Numerous trials existNumerous trials exist

Page 36: Pancreatic cancer

Question 1Question 1Tumour extending beyond pancreas, not Tumour extending beyond pancreas, not

inflitrating CA or SMA is:inflitrating CA or SMA is:

• 1) T11) T1

• 2) T22) T2

• 3) T33) T3

• 4) T44) T4

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Question 2Question 2T4N1M0 is unresectable due toT4N1M0 is unresectable due to::

• 1) metastatic disease1) metastatic disease

• 2) involvement of SMA or CA2) involvement of SMA or CA

• 3) lymph node involvement3) lymph node involvement

• 4) Karnofsky status 30%4) Karnofsky status 30%

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Question 3Question 3::

Capecitabine isCapecitabine is

• 1) oral gemcitabine1) oral gemcitabine

• 2) oral 5FU2) oral 5FU

• 3) oral cetuximab3) oral cetuximab

• 4) oral oxaliplatine4) oral oxaliplatine