Resectable Pancreatic Carcinoma
Conditions
Keywords
pancreatectomy, Transfusion
Brief summary
This clinical trial tests the the feasibility of testing a red blood cell transfusion threshold for improved quality of life for patients undergoing a pancreatectomy for pancreatic cancer. Pancreatectomy can be associated with significant blood loss. Blood loss can result in clinically important anemia causing fatigue. Pancreatic cancer itself can be associated with malnutrition and fatigue. Having a red blood cell transfusion threshold that results in a more liberal use of transfusions may improve quality of life for patients undergoing a pancreatectomy for pancreatic cancer.
Detailed description
PRIMARY OBJECTIVE: I. The primary objective for this pilot study is protocol adherence for the transfusion study we propose for pancreatectomy patients. SECONDARY OBJECTIVES: I. Determine the feasibility of collecting and processing of all data that will be collected in the full study. II. Specific emphasis will be given to findings from Patient Reported Outcomes Measurement Information System (PROMIS)-29 to determine its sensitivity to changes in health related quality of life (HRQOL) that occur in the perioperative period after pancreatectomy. OUTLINE: Patients are randomized to 1 of 2 arms. ARM I: Patients undergo red blood cell transfusion if hemoglobin (Hgb) is less than 7 g/dL while on study. ARM II: Patients undergo red blood cell transfusion if Hgb is less than 9 g/dL while on study. Patients undergo computed tomography (CT) scan, x ray imaging, and blood sample collection throughout the study.
Interventions
BIOLOGICALArm I Packed Red Blood Cell Transfusion (Hgb < 7 g/dL)
Receive conservative transfusion strategy (Hgb \< 7 g/dL)
BIOLOGICALArm II Packed Red Blood Cell Transfusion (Hgb < 9 g/dL)
Receive liberal transfusion strategy (Hgb \< 9 g/dL)
PROCEDUREComputed Tomography
Undergo CT scan
PROCEDUREX-Ray Imaging
Undergo x-ray imaging
PROCEDUREBiospecimen Collection
Undergo blood sample collection
OTHERSurvey Administration
Ancillary studies
PROCEDUREPancreatectomy
surgical removal of all or part of pancreas
Sponsors
Jonsson Comprehensive Cancer Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Male or female \>= 18 years of age at Visit 1 * Documentation of a pancreatic cancer diagnosis as evidenced by one or more clinical features meeting the following criteria: * CT evidence of a mass in the pancreas consistent with cancer * Tissue diagnosis of cancer either before surgery or from the resected specimen * Preoperative evaluation suggestive that pancreatic resection is feasible * Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study
Exclusion criteria
* Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study * Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data * Patients who are unable to receive or who refuse blood products * Patients involved in an autologous pre-donation program * Patients found to have metastatic disease upon entry into abdomen-having been randomized, these patients will be removed from the study and replaced with another patient * Patients found to not have cancer during the operation- If the resected lesion proves not to be cancer, the patient will remain as an enrolled patient but not evaluable and replaced by another patient * Established severe cardiovascular disease with estimated 5-year survival \<10% based on Framingham risk score * Unstable angina or recent myocardial infarction (MI)/stroke within 6 months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of Protocol adherence | Up to 36 months post surgery | Will be measured as the proportion of patients who are enrolled in the study and do not experience major protocol |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Health related quality of life | At preoperative visit, post operative period, months 1, 3, 6, 9, 12, 24, 27, 30, 33, 36 | Will be assessed by Patient Reported Outcomes Measurement Information System (PROMIS)-29 v2.1. PROMIS, uses a T-score metric in which 50 is the mean of a relevant reference population and 10 is the standard deviation (SD) of that population. a higher T-score represents more of the concept being measured. For negatively-worded concepts like fatigue, a higher T-score represents greater fatigue and a lower T-score represents less fatigue. For positively-worded concepts like physical function, a higher T-score reflects higher (better) physical function and a lower T-score reflects lower (worse) physical function. For NIH Toolbox performance tests of cognitive, motor, and sensory function, a higher score indicates better performance. |
| Incidence of significant individual adverse events | Up to 36 months post operative | Will include major adverse cardiovascular events (MACE), surgical site infection (SSI), surgical site occurrence (SSO), clinically-relevant postoperative pancreatic fistula (CR-POPF), hemorrhage, pneumonia, urinary tract infection (UTI), reoperation, readmission, and mortality. Safety and tolerability data will be summarized by treatment group. Adverse events will be tabulated by treatment group and will include the number of patients for whom the event occurred, the rate of occurrence, and the severity and relationship to study drug. |
| Length of stay in hospital and intensive care unit (ICU) | through study completion, an average of 1 year | — |
| Proportion of patients transfused | Up to hospital discharge or post operative day 28 | — |
| Number of blood products received | Up to hospital discharge or post operative day 28 | — |
Countries
United States
Outcome results
None listed