Metformin and Insulin to Pancreatic Cancer Related Diabetes (Type 3c)

Sponsor
Fudan University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05306028
Collaborator
(none)
20
1
8

Study Details

Study Description

Brief Summary

About 80% of patients with pancreatic adenocarcinoma have aberrant fasting blood glucose at the time of diagnosis. The consistent association between pancreatic cancer and diabetes mellitus has long been recognized and even been termed as "chicken and egg". Many reports have found that pancreatic cancer can result in diabetes, which is called type 3c diabetes. New-onset diabetes is commonly observed in pancreatic cancer patients and has been considered as a potential screening sign. Moreover, diabetes has been found as a predictor of poor outcome in pancreatic cancer.

Pancreatic cancer cells have a strong dependence on glucose and they are well-known for their sweet teeth. High glucose is associated with impaired immunologic reaction, intolerability to chemotherapy, radiotherapy and other major treatments, an increased risk of pancreatic surgery. Given the linkage between pancreatic cancer and diabetes or high blood glucose, a clinical trial is needed to validate the effect of metformin and insulin on regulating blood glucose in type 3c diabetes.

Condition or Disease Intervention/Treatment Phase
  • Drug: Metformin or insulin treatment
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Administration of Metformin and Insulin to Pancreatic Cancer Related Diabetes Mellitus (Type 3c)
Anticipated Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metformin or insulin treatment

Drug: Metformin or insulin treatment
For patients with new-onset diabetes Fasting blood glucose 7-10 mmol/L, metformin 2 g/day, BID, PO; Fasting blood glucose 10-14 mmol/L, metformin 1 g/day, BID, PO, Novolin 30R Penfil 12 U before breakfast, 8 U; Fasting blood glucose > 14 mmol/L, metformin 1 g/day, BID, PO, Novolin 30R Penfil 16 U before breakfast, 10 U; Adjusting insulin dosage according to the monitor of fasting blood glucose. For patients with history of diabetes Adjusting metformin or insulin dosage according to the monitor of fasting blood glucose.

Outcome Measures

Primary Outcome Measures

  1. Blood glucose control rate [1 week]

    Blood glucose control rate before and after anti-diabetic administration

Secondary Outcome Measures

  1. HbA1C control rate [1 week]

    HbA1C control rate before and after anti-diabetic administration

Other Outcome Measures

  1. Change in serum Carbohydrate Antigen 19-9 (CA19-9) From Baseline to Day 8. [1 week]

    Change of tumor biomarkers before and after anti-diabetic administration.Patients will collect CA19-9 values on the day of enrollment and on day 8.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Signed informed content obtained prior to treatment

  • Age ≥ 18 years and ≤ 80 years

  • Eastern Cooperative Oncology Group (ECOG) performance status 0-2

  • Patients must have histologically confirmed pancreatic adenocarcinoma

  • Fasting blood glucose ≥ 7.0 mmol/L(126 mg/dl)

  • The expected survival after surgery ≥ 3 months

Exclusion Criteria:
  • Active second primary malignancy or history of second primary malignancy

  • Patients who have received any form of anti-tumor therapy before surgery, including chemotherapy, radiotherapy, interventional chemoembolization, radiofrequency ablation, and molecular targeted therapy

  • Inflammation of the digestive tract, including pancreatitis, cholecystitis, cholangitis, etc

  • Total bilirubin (TBIL) > institutional upper limit of normal (ULN)

  • Pregnant or nursing women

  • Patients who are unwilling or unable to comply with study procedures

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Fudan University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xian-Jun Yu, Professor, Fudan University
ClinicalTrials.gov Identifier:
NCT05306028
Other Study ID Numbers:
  • PTCA199-2
First Posted:
Mar 31, 2022
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xian-Jun Yu, Professor, Fudan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2022