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Perioperative Intervention to Reduce Metastatic Processes in Pancreatic Cancer Patients Undergoing Curative Surgery (BC-PC)

Primary Purpose

Pancreatic Neoplasms

Status
Recruiting
Phase
Phase 2
Locations
Israel
Study Type
Interventional
Intervention
Propranolol and etodolac
Placebo
Sponsored by
Assaf-Harofeh Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pancreatic Neoplasms focused on measuring Beta-blocker, Propranolol, COX-2 inhibitor, Etodolac

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Newly diagnosed Stage I or II adenocarcinoma of the head, neck, or uncinated- process of the pancreas.
  • Surgically resectable disease (R0 or R1) by spiral CT chest and abdomen scan, No distant metastases
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1
  • Signed informed consent form
  • Willing and able to comply with study procedures
  • Men and women from age 20 up to age 80

Exclusion Criteria:

  • Patients with metastatic disease, known prior to surgery
  • Patients with history or concomitant malignant disease of any type (except for the current pancreatic cancer
  • Patients who were treated with chemotherapy in the last 10 years for any reason
  • Patients in whom surgical resection is planned without curative intent
  • Patients exhibiting levels Carbohydrate antigen (CA) 19-9 above 500
  • Patients with renal failure, measured by creatinine level >1.5
  • Patients with significant heart failure (NYHA functional class 3 or higher),
  • Patients with significant liver failure (known cirrhosis)
  • Patients suffering from active asthma
  • Patients with known allergy to any medication from the non-steroidal anti- inflammatory or beta-blockers drug group
  • Patients treated chronically with any type of a beta-adrenergic blocker or a cyclooxygenase (COX) inhibitor
  • Patients with bradycardia or second or third degree atrioventricular block (AV) block
  • Patients with a history of cerebrovascular accident (CVA) or established diagnosed transient ischemic attack (TIA)
  • Patients with prinzmetal's angina
  • Patients with right sided heart failure owing to pulmonary hypertension
  • Patients with significant diagnosed cardiomegaly
  • Patients with (current) pheochromocytoma
  • Patients with chronic Digoxin treatment
  • Patients with active peptic disease
  • Patients with peripheral vascular disease
  • Pregnant woman
  • Special population with impaired judgment
  • Patients currently actively participating in any other clinical trial
  • contraindication for Whipple procedure
  • Patients suffering from sick sinus syndrome
  • Patients with borderline resectable tumors, as defined by one of the following:

    • an infiltration >180° of the portal vein
    • abutment of the tumor to the superior mesenteric artery
    • infiltration of the superior mesenteric artery or the celiac trunk

Sites / Locations

  • Sheba Medical CenterRecruiting
  • Sourasky Medical Center
  • Asaf Harofeh Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Propranolol and etodolac

Placebo

Arm Description

Both study medications will be given orally for an intervention phase of 35 days as follows. Etodolac:400mg PO bid for the entire intervention period,Propranolol:20 mg PO bid for 5 preoperative days, 80 mg PO bid on the day of surgery and the following morning, 40 mg PO bid for following 6.5 days, and 20 mg PO bid for next 22 days.

Same schedule as in the active comparator arm

Outcomes

Primary Outcome Measures

Rate of cancer recurrence
Data regrading post-surgical recurrence will be recorded at 1,3,6,12,18,24,36,48, and 60 following surgery
Biomarkers in extracted tumor tissue samples
Epithelial-to-mesenchymal-transition ( EMT) status and natural-killer cell, macrophage, T-cell, and B-cell infiltration levels into tumor tissue (as assessed by messenger RNA profiling of tissue samples.
Biomarkers in blood samples
Cytokine levels in blood samples (interleukin-6, interleukin-10, C-reactive protein, interferon-gamma, and vascular endothelial growth factor and additional exploratory analysis of other cytokines)

Secondary Outcome Measures

Number of patients with treatment related adverse events
According to the Clavien-Dindo classification system (7 grades of events depicting the severity of the event)
Depression, Anxiety, Global distress
Assessed by changes on the brief symptom inventory 18 questionnaire (this questionnaire assess all three scales for depression, anxiety and global distress)
Fatigue
4 items related to fatigue in the 36 item short-form survey questionnaire.

Full Information

First Posted
January 23, 2019
Last Updated
November 19, 2019
Sponsor
Assaf-Harofeh Medical Center
Collaborators
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03838029
Brief Title
Perioperative Intervention to Reduce Metastatic Processes in Pancreatic Cancer Patients Undergoing Curative Surgery
Acronym
BC-PC
Official Title
Perioperative Use of a Beta-adrenergic Blocker and a COX-2 Inhibitor in Patients Undergoing Surgery With Primary Pancreatic Cancer: Intervention Aiming to Reduce Pro-metastatic Processes
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Recruiting
Study Start Date
November 20, 2019 (Anticipated)
Primary Completion Date
January 2026 (Anticipated)
Study Completion Date
January 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assaf-Harofeh Medical Center
Collaborators
Sheba Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In Israel, of the ~1000 patients diagnosed annually with pancreatic cancer (PC), approximately 250 (25 percent) will be eligible for curative surgery, of which 80 percent will succumb to post-surgical metastatic disease. A reduction in post-surgical metastatic disease will save dozens of patients in Israel annually, and tens-of thousands-around the world. The short perioperative period (days to weeks around surgery) is characterized by stress-inflammatory responses, including catecholamines (CAs, e.g., adrenaline) and prostaglandins (PGs, e.g., prostaglandin-E2) release, and induce deleterious pro-metastatic effects. Animal studies implicated excess perioperative release of CAs and PGs in facilitating cancer progression by affecting the malignant tissue, its local environment, and anti-metastatic immune functions. Congruently, our animal studies indicate that combined use of the beta-adrenergic blocker, propranolol, and the prostaglandins inhibitor, etodolac - but neither drug separately - efficiently prevented post-operative metastatic development. We recently conducted two clinical trials in three medical centers in Israel, recruiting breast (n=38) and colorectal (n=34) cancer patients, assessing the safety and short-term efficacy of perioperative propranolol and etodolac treatment. Drugs were well tolerated, without severe adverse events. Importantly, molecular/biological analyses of the excised primary tumor indicated that drug treatment caused promising anti-metastatic transformations, as well as improvements in immune and inflammatory indices. These included (i) decreased tumor cell capacity to migrate, (ii) reduced pro-metastatic capacity of the malignant tissue, and (iii) improvement in immune infiltrating into the tumor (Paper published in Clinical Cancer Research, 2017). Herein, we propose to conduct a double-blind placebo-controlled two-arm Phase II clinical trial in 210 pancreatic cancer patients undergoing curative surgery in Israel. A perioperative 35-day drug treatment will be initiated 5 days before surgery. Primary outcomes will include (i) 1-year disease-free-survival (DFS), and 5-year overall survival (OS); and (ii) biological markers in blood samples, and in the excised tumor tissue. Secondary outcomes will include safety indices and psychological measures of depression, anxiety, distress, and fatigue.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Neoplasms
Keywords
Beta-blocker, Propranolol, COX-2 inhibitor, Etodolac

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Propranolol and etodolac
Arm Type
Active Comparator
Arm Description
Both study medications will be given orally for an intervention phase of 35 days as follows. Etodolac:400mg PO bid for the entire intervention period,Propranolol:20 mg PO bid for 5 preoperative days, 80 mg PO bid on the day of surgery and the following morning, 40 mg PO bid for following 6.5 days, and 20 mg PO bid for next 22 days.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Same schedule as in the active comparator arm
Intervention Type
Drug
Intervention Name(s)
Propranolol and etodolac
Other Intervention Name(s)
Deralin and etopan
Intervention Description
A perioperative combined drug regimen
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Rate of cancer recurrence
Description
Data regrading post-surgical recurrence will be recorded at 1,3,6,12,18,24,36,48, and 60 following surgery
Time Frame
From the date of surgery until malignant disease is identified, assessed up to 60 months post-surgery
Title
Biomarkers in extracted tumor tissue samples
Description
Epithelial-to-mesenchymal-transition ( EMT) status and natural-killer cell, macrophage, T-cell, and B-cell infiltration levels into tumor tissue (as assessed by messenger RNA profiling of tissue samples.
Time Frame
An average of one year following surgery
Title
Biomarkers in blood samples
Description
Cytokine levels in blood samples (interleukin-6, interleukin-10, C-reactive protein, interferon-gamma, and vascular endothelial growth factor and additional exploratory analysis of other cytokines)
Time Frame
An average of one year following surgery
Secondary Outcome Measure Information:
Title
Number of patients with treatment related adverse events
Description
According to the Clavien-Dindo classification system (7 grades of events depicting the severity of the event)
Time Frame
30 days following surgery
Title
Depression, Anxiety, Global distress
Description
Assessed by changes on the brief symptom inventory 18 questionnaire (this questionnaire assess all three scales for depression, anxiety and global distress)
Time Frame
At baseline and at 30 days post-surgery
Title
Fatigue
Description
4 items related to fatigue in the 36 item short-form survey questionnaire.
Time Frame
At baseline and at 30 days post-surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newly diagnosed Stage I or II adenocarcinoma of the head, neck, or uncinated- process of the pancreas. Surgically resectable disease (R0 or R1) by spiral CT chest and abdomen scan, No distant metastases Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1 Signed informed consent form Willing and able to comply with study procedures Men and women from age 20 up to age 80 Exclusion Criteria: Patients with metastatic disease, known prior to surgery Patients with history or concomitant malignant disease of any type (except for the current pancreatic cancer Patients who were treated with chemotherapy in the last 10 years for any reason Patients in whom surgical resection is planned without curative intent Patients exhibiting levels Carbohydrate antigen (CA) 19-9 above 500 Patients with renal failure, measured by creatinine level >1.5 Patients with significant heart failure (NYHA functional class 3 or higher), Patients with significant liver failure (known cirrhosis) Patients suffering from active asthma Patients with known allergy to any medication from the non-steroidal anti- inflammatory or beta-blockers drug group Patients treated chronically with any type of a beta-adrenergic blocker or a cyclooxygenase (COX) inhibitor Patients with bradycardia or second or third degree atrioventricular block (AV) block Patients with a history of cerebrovascular accident (CVA) or established diagnosed transient ischemic attack (TIA) Patients with prinzmetal's angina Patients with right sided heart failure owing to pulmonary hypertension Patients with significant diagnosed cardiomegaly Patients with (current) pheochromocytoma Patients with chronic Digoxin treatment Patients with active peptic disease Patients with peripheral vascular disease Pregnant woman Special population with impaired judgment Patients currently actively participating in any other clinical trial contraindication for Whipple procedure Patients suffering from sick sinus syndrome Patients with borderline resectable tumors, as defined by one of the following: an infiltration >180° of the portal vein abutment of the tumor to the superior mesenteric artery infiltration of the superior mesenteric artery or the celiac trunk
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Oded Zmora, MD
Phone
+97289779202
Email
ozmora@post.tau.ac.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oded Zmora, MD
Organizational Affiliation
Asaf Harofeh Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheba Medical Center
City
Tel Hashomer
ZIP/Postal Code
45858
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Talia Golan, MD
Email
Talia.Golan@sheba.health.gov.il
Facility Name
Sourasky Medical Center
City
Tel-Aviv
ZIP/Postal Code
6423906
Country
Israel
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ido Nachmany, MD
Email
idon@tlvmc.gov.il
Facility Name
Asaf Harofeh Medical Center
City
Tsrifin
ZIP/Postal Code
70300
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Oded Zmora, MD
Phone
+97289779202
Email
ozmora@post.tau.ac.il

12. IPD Sharing Statement

Citations:
PubMed Identifier
29800703
Citation
Haldar R, Shaashua L, Lavon H, Lyons YA, Zmora O, Sharon E, Birnbaum Y, Allweis T, Sood AK, Barshack I, Cole S, Ben-Eliyahu S. Perioperative inhibition of beta-adrenergic and COX2 signaling in a clinical trial in breast cancer patients improves tumor Ki-67 expression, serum cytokine levels, and PBMCs transcriptome. Brain Behav Immun. 2018 Oct;73:294-309. doi: 10.1016/j.bbi.2018.05.014. Epub 2018 May 22.
Results Reference
result
PubMed Identifier
28490464
Citation
Shaashua L, Shabat-Simon M, Haldar R, Matzner P, Zmora O, Shabtai M, Sharon E, Allweis T, Barshack I, Hayman L, Arevalo J, Ma J, Horowitz M, Cole S, Ben-Eliyahu S. Perioperative COX-2 and beta-Adrenergic Blockade Improves Metastatic Biomarkers in Breast Cancer Patients in a Phase-II Randomized Trial. Clin Cancer Res. 2017 Aug 15;23(16):4651-4661. doi: 10.1158/1078-0432.CCR-17-0152. Epub 2017 May 10.
Results Reference
result

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Perioperative Intervention to Reduce Metastatic Processes in Pancreatic Cancer Patients Undergoing Curative Surgery

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