Pancreatic CancerPAC-MAINNCT04112836
Pancreatic Cancer Malnutrition and Pancreatic Exocrine Insufficiency in the Course of Chemotherapy in Unresectable Pancreatic Cancer
An observational study of Pancreatic Cancer and Exocrine Pancreatic Insufficiency, run by Moscow Clinical Scientific Center at 8 sites in 6 countries.
Trial summary
Malnutrition and cachexia are common in patients with advanced pancreatic ductal adenocarcinoma (PDAC) and have a significant influence on the tolerance and response to treatments. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Pancreatic Cancer, Exocrine Pancreatic Insufficiency, Metastatic Pancreatic Cancer
- How many people
- 186 participants
- Where
- 8 sitesin 6 countries
- Study dates
- 15 Mar 2019to Aug 2020
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: patients with unresectable locally advanced or metastatic PDAC
Who may be able to join
- age ≥ 18 years;
- histological diagnosis of PDAC within one month from recruitment to the study;
- radiological diagnosis of the advanced stage not suitable for upfront surgical resection (either locally advanced or metastatic) within 5 weeks from recruitment to the study;
- data on the variables and the outcomes of interest are available;
- a written consent to participate in the study;
- being planned for chemotherapy;
- no past history of anticancer treatment.
Who cannot join
- poor performance status (Eastern Cooperative Oncology Group scale (ECOG) ≥ 3);
- pregnancy;
- surgery for PDAC in the past and developed progression.
Trial locations and contacts
8 sites in 6 countries.
Enrique de Madaria, MD, PhD contact
8 sites in 6 countries
Serbia2 sites, 2 recruiting
- Not yet recruiting
University Clinic "Dr. Dragisa Misovic-Dedinje"
Belgrade
Nikola Panic, MD, +381 11 3630600, nikola.panicmail@gmail.com
- Not yet recruiting
University of Belgrade
Belgrade
Nikola Panic, MD, +381 11 3630600, nikola.panicmail@gmail.com
Spain2 sites, 2 recruiting
- Not yet recruiting
Alicante University General Hospital
Alicante
Enrique de Madaria, MD, PhD, +34 965 933 468, madaria@hotmail.com
Maryana Bozhychko, MD, +34 965 933 468, maryanabozhychko@gmail.com
- Not yet recruiting
University Hospital of Santiago de Compostela
Santiago de Compostela
Daniel de la Iglesia Garcia, MD, +34981951364, danieldelaiglesiagarcia@hotmail.com
Italy1 site, 1 recruiting
- Recruiting
IRCCS San Raffaele Scientific Institute
Milan
Gabriele Capurso, MD, PhD, +39 02 26436548, gabriele.capurso@gmail.com
Romania1 site, 1 recruiting
- Recruiting
Clinical Emergency Hospital Bucharest
Bucharest
Vasile Sandru, MD, +0040728813095, drsandruvasile@gmail.com
Russia1 site, 1 recruiting
- Recruiting
A.S. Loginov Moscow Clinical Scientific Center
Moscow
Mariia Kiriukova, MD, +7 495 303 15 57, kiryukovam@yandex.ru
Turkey (Türkiye)1 site, 1 recruiting
- Recruiting
Istanbul University
Istanbul
Bartu Avci, +90 212 414 2000, bartuavci@ogr.iu.edu.tr
About this study
Malnutrition and cachexia are common in patients with advanced pancreatic ductal adenocarcinoma (PDAC) and have a significant influence on the tolerance and response to treatments. If timely identified, malnourished PDAC patients could be treated to increase their capacity to complete the planned treatments and therefore, possibly, improve their efficacy.
The aim of the study is to assess the impact of nutritional status, pancreatic exocrine insufficiency (PEI), and other clinical factors on patient outcomes in patients with advanced PDAC.
The nutritional status will be determined by means of Mini-Nutritional Assessment score and laboratory blood tests. PEI will be defined as the presence of typical symptoms and/or reduced fecal elastase. Analysis: chemotherapy dosing over the first 12 weeks of therapy (i.e. percent of chemotherapy received in the first 12 weeks, as defined above) PAC-MAIN will provide insights on the role of malnutrition and PEI in outcomes of PDAC.
Read the detailed description
Investigators hypothesize that malnutrition has an adverse impact on the clinical course of patients with advanced PDAC treated with chemotherapy.
Aims:
To investigate the association between the nutritional status and pancreatic exocrine function and the clinical outcomes of patients with advanced PDAC.
Study design:
The PAncreatic Cancer MAlnutrition and exocrine pancreatic INsufficiency in the course of chemotherapy in unresectable pancreatic cancer (PAC-MAIN) study is a non-profit, international, multicentre, prospective, observational, cohort study evaluating the effect of the nutritional status and pancreatic exocrine function on the main outcomes of patients with advanced PDAC. The study will be carried out in Russia, Turkey, Serbia, Romania, Italy, and Spain as a part of the Pancreas 2000 Educational Program. Pancreas 2000 is a post-graduate educational program that prepares young gastroenterologists, surgeons, radiologists, and other physicians for specialization in Pancreatology.
Patient-related:
- sex, race, age at diagnosis
- Mini-Nutritional Assessment (MNA) score
- sarcopenia (measured with computed tomography (CT) fat free mass is reduced; i.e. appendicular\L2 skeletal muscle mass index <7.2 kg/m2 (men) or <5.5 kg/m2 (women));
- cachexia (weight loss (WL)>5% in last 6 months, or WL>2% if body mass index (BMI) <20 kg/m² or sarcopenia);
- 12-item functional assessment of anorexia/cachexia therapy anorexia/cachexia subscale (FAACT-A/CS-12)
- a biliary stent
- a duodenal stent
- total and direct bilirubin
- ECOG status
- European Organization for Research and Treatment of Cancer (EORTC) QLQ-PAN26 scale
- Date of diagnosis, visit 1, visit 2 (3 months), and death/loss from follow up
- Check up on survival at 6m
Tumor-related:
- Tumor site documented by endoscopic ultrasound, CT, or magnetic resonance imaging (head, body, or tail)
- Stage according to the TNM classification
- Vessels involved
- Presence and site of metastatic disease
- Ascites
- CA-19-9
- Response evaluation criteria in solid tumors (RECIST) (for visit 2)
Nutritional parameters:
- Leucocytes (lymphocytes, neutrophils), neutrophil to lymphocytes ratio, erythrocytes, hemoglobin, hematocrit, platelets
- C-reactive protein, total protein, albumin, cholesterol, iron, transferrin, ferritin, magnesium, zinc
- International normalized ratio, activated partial thromboplastin time
- Blood fasting glucose, glycated hemoglobin
Pancreatic function and treatment:
- PEI, fecal elastase-1, pancreatic enzyme replacement therapy (PERT), date of starting PERT, the dosage of daily taken PERT
- Diabetes mellitus (DM), date of DM diagnosis, DM type, DM treatment
Treatment-related:
- Planned chemotherapy protocol Dosages of chemotherapy planned (mg/m2)
- Percent of standard chemotherapy dose delivered
- Percent of planned chemotherapy delivered
- Changes to the predefined schedule (dose reduction, schedule modifications, stop before planned)
- Date of treatment start and end
- Adverse events (National Cancer Institute toxicity scale for visit 2)
Description of the intervention (schedule of visits):
Visit 1 (screening, within 1 month from initial diagnosis). Patients will be informed about the study. Once patients agree with the inclusion in the study the investigators will evaluate the inclusion and exclusion criteria. Those patients who meet all the inclusion criteria and none of the exclusion criteria will be finally included in the study. In this visit, patients, tumor-related variables, and general patients' features will be recorded, and quality of life questionnaire will be administered. The researcher will record weight, height, body mass index (BMI), unplanned WL % for the last 6 months.
Each patient's baseline nutrition status will be evaluated using the MNA scores prior to starting chemotherapy. Patients will be classified as in the group with no nutritional risk, at risk of malnutrition, or malnourished.
Nutritional parameters and pancreatic function will be evaluated through blood tests and a fecal test.
Visit 2 (3 months after the first dose of planned chemotherapy). The researcher will record in the case report form (CRF) the planned chemotherapy, schedule, doses, dose reduction, and any adverse event. The same variables recorded at Visit 1 will be checked again.
Check up 3 (end of the study, 6 months). The researcher will record in the CRF the overall survival and time until progression.
Medication of the study:
The study is of observational nature, so a pre-planned treatment is not considered. However, the use of pancreatic enzyme replacement treatment will be recorded as well as data regarding the employed chemotherapy regimen.
Power size calculation:
The expected percent of chemotherapy delivered in well-nourished patients was based on a study that assessed the chemotherapy dose intensity in gastrointestinal malignancies included pancreaticobiliary disease during the firsts 8 weeks after the start of the chemotherapy23. Based on an expected percentage of chemotherapy delivered of 70% in well-nourished patients, with a type I error of 0.05 and a type II error of 0.20, a sample size of 93 patients per group will be required in case of a percentage difference of chemotherapy delivered of 20% between well-nourished and malnourished, 163 patients per group in case of a difference of 15% between both groups and 356 patients per group in case of 10% of difference.
Discussion:
Given the sparse overall scientific data on the subject, the investigators have designed a study that addresses the impact of patient's nutritional status and dietary intervention on the clinical course of patients with advanced PDAC treated with chemotherapy and is aimed at establishing whether it affects both tolerance and tumor response to medical therapy. PAC-MAIN will be the first study specifically investigating whether the nutritional status influences the possibility to complete planned chemotherapy in patients with advanced PDAC.
- Conditions
- Pancreatic Cancer, Exocrine Pancreatic Insufficiency, Metastatic Pancreatic Cancer, Chemotherapy, Malnutrition, Locally Advanced Malignant Neoplasm
- Keywords
- pancreatic cancer, locally advanced, metastatic, nutritional status, exocrine pancreatic insufficiency, chemotherapy, dose-intensity
- Medical subject headings
- Pancreatic Neoplasms, Exocrine Pancreatic Insufficiency, Malnutrition, Neoplasm Metastasis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Normal nutritional status | Patients, fulfilled inclusion criteria with Mini-Nutritional Assessment score of 24-30 points. | |
| Malnourished | Patients, fulfilled inclusion criteria with Mini-Nutritional Assessment score of fewer than 17 points. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percent of standard chemotherapy dose delivered
Drug doses will be expressed in weight-based, body surface area (BSA)-based, Area Under the Curve (AUC) units or flat dose, according to standard dosing practice for a given drug or combination. For each drug in a regimen, the sum of the doses delivered during the first 12 weeks of therapy will be divided by the sum of the expected doses based on published standard schedule and dosing. The mean percent dose delivered of all drugs in a regimen will be reported as 'percent of standard chemotherapy dose delivered.' The investigators will use percent of standard chemotherapy dose delivered to estimate the overall relative dose delivered.
Measured: 12 weeks after the diagnosis
Percent of planned chemotherapy delivered
Similarly, the sum of the doses delivered during the first 12 weeks of therapy will be divided by the sum of the expected doses based on each patient's starting chemotherapy dose, and the mean percent dose delivered for all drugs in a regimen will be reported as 'percent of planned chemotherapy delivered.' The investigators will use percent of planned chemotherapy dose delivered to quantify further dose reductions from starting dose and as an indicator of overall toxicity.
Measured: 12 weeks after the diagnosis
Secondary outcomes (6)
Percent of patients with chemotherapy-related toxicity in each group
Measured: 12 weeks after the diagnosis
Survival at 6 months
Measured: 12 weeks after the diagnosis, 6 months
Progression-free survival
Measured: 6 months
Quality of Life (EORTC) QLQ-PAN26 scale
The pancreatic cancer module is designed for patients at all disease stages undergoing surgical resection, palliative surgical intervention, endoscopic palliation or palliative chemotherapy (Fitzsimmons et al., 1999a,b). The module comprises 26 questions assessing pain, dietary changes, jaundice, altered bowel habit, emotional problems related to pancreatic cancer, and other symptoms (cachexia, indigestion, flatulence, dry mouth, taste changes). The answers range is the following: not at all - 1 point, a little - 2 points, quite a bit - 3 points, very much - 4 points. Minimum score is 26, maximum is 106. The higher total score represents the worse quality of life.
Measured: 12 weeks after the diagnosis
Number of hospitalizations
Measured: 12 weeks after the diagnosis
Factors associated with the percent of chemotherapy received
Measured: 12 weeks after the diagnosis
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Oct 2019
- Study start15 Mar 2019
- Primary completionJun 2020 (estimated)
- Study completionAug 2020 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Pancreatic CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 186 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Moscow Clinical Scientific Center
- Sponsor type
- University, hospital or other
- Collaborators
- University of Santiago de Compostela, University Clinic Dr Dragisa Misovic-Dedinje, University of Belgrade, Hospital General Universitario de Alicante, Istanbul University, European Institute of Oncology, IRCCS San Raffaele, Bucharest Emergency Hospital
- Responsible party
- Sponsor
- Investigators
- Mariia Kiriukova, MD, Study chair, Moscow Clinical Scientific Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04112836
- Sponsor's protocol ID
- 2/2019
- Acronym
- PAC-MAIN
- Status last verified
- Oct 2019
- First submitted
- 30 Sep 2019
- Last updated
- 16 Oct 2019
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Kiriukova M, de la Iglesia Garcia D, Panic N, Bozhychko M, Avci B, Maisonneuve P, de-Madaria E, Capurso G, Sandru V. Pancreatic Cancer Malnutrition and Pancreatic Exocrine Insufficiency in the Course of Chemotherapy in Unresectable Pancreatic Cancer. Front Med (Lausanne). 2020 Sep 3;7:495. doi: 10.3389/fmed.2020.00495. eCollection 2020.
PubMed 33015088
Study at a glance
From the registry record, last updated by the sponsor on 16 Oct 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pancreatic Cancer Malnutrition and Pancreatic Exocrine Insufficiency in the Course of Chemotherapy in Unresectable Pancreatic Cancer
- ClinicalTrials.gov ID
- NCT04112836
- Acronym / sponsor ID
- PAC-MAIN / 2/2019
- Conditions
- Pancreatic Cancer, Exocrine Pancreatic Insufficiency, Metastatic Pancreatic Cancer, Chemotherapy, Malnutrition, Locally Advanced Malignant Neoplasm
- Keywords
- pancreatic cancer, locally advanced, metastatic, nutritional status, exocrine pancreatic insufficiency, chemotherapy, dose-intensity
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 186 participants (estimated)
- Lead sponsor
- Moscow Clinical Scientific CenterUniversity, hospital or other
- Collaborators
- University of Santiago de Compostela, University Clinic Dr Dragisa Misovic-Dedinje, University of Belgrade, Hospital General Universitario de Alicante, Istanbul University, European Institute of Oncology, IRCCS San Raffaele, Bucharest Emergency Hospital
- Study start
- 15 Mar 2019 (actual)
- Primary completion
- Jun 2020 (estimated)
- Study completion
- Aug 2020 (estimated)
- First posted
- 2 Oct 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Malnutrition and cachexia are common in patients with advanced pancreatic ductal adenocarcinoma (PDAC) and have a significant influence on the tolerance and response to treatments. If timely identified, malnourished PDAC patients could be treated to increase their capacity to complete the planned treatments and therefore, possibly, improve their efficacy.
The aim of the study is to assess the impact of nutritional status, pancreatic exocrine insufficiency (PEI), and other clinical factors on patient outcomes in patients with advanced PDAC.
The nutritional status will be determined by means of Mini-Nutritional Assessment score and laboratory blood tests. PEI will be defined as the presence of typical symptoms and/or reduced fecal elastase. Analysis: chemotherapy dosing over the first 12 weeks of therapy (i.e. percent of chemotherapy received in the first 12 weeks, as defined above) PAC-MAIN will provide insights on the role of malnutrition and PEI in outcomes of PDAC.
Detailed description
Investigators hypothesize that malnutrition has an adverse impact on the clinical course of patients with advanced PDAC treated with chemotherapy.
Aims:
To investigate the association between the nutritional status and pancreatic exocrine function and the clinical outcomes of patients with advanced PDAC.
Study design:
The PAncreatic Cancer MAlnutrition and exocrine pancreatic INsufficiency in the course of chemotherapy in unresectable pancreatic cancer (PAC-MAIN) study is a non-profit, international, multicentre, prospective, observational, cohort study evaluating the effect of the nutritional status and pancreatic exocrine function on the main outcomes of patients with advanced PDAC. The study will be carried out in Russia, Turkey, Serbia, Romania, Italy, and Spain as a part of the Pancreas 2000 Educational Program. Pancreas 2000 is a post-graduate educational program that prepares young gastroenterologists, surgeons, radiologists, and other physicians for specialization in Pancreatology.
Patient-related:
- sex, race, age at diagnosis
- Mini-Nutritional Assessment (MNA) score
- sarcopenia (measured with computed tomography (CT) fat free mass is reduced; i.e. appendicular\L2 skeletal muscle mass index <7.2 kg/m2 (men) or <5.5 kg/m2 (women));
- cachexia (weight loss (WL)>5% in last 6 months, or WL>2% if body mass index (BMI) <20 kg/m² or sarcopenia);
- 12-item functional assessment of anorexia/cachexia therapy anorexia/cachexia subscale (FAACT-A/CS-12)
- a biliary stent
- a duodenal stent
- total and direct bilirubin
- ECOG status
- European Organization for Research and Treatment of Cancer (EORTC) QLQ-PAN26 scale
- Date of diagnosis, visit 1, visit 2 (3 months), and death/loss from follow up
- Check up on survival at 6m
Tumor-related:
- Tumor site documented by endoscopic ultrasound, CT, or magnetic resonance imaging (head, body, or tail)
- Stage according to the TNM classification
- Vessels involved
- Presence and site of metastatic disease
- Ascites
- CA-19-9
- Response evaluation criteria in solid tumors (RECIST) (for visit 2)
Nutritional parameters:
- Leucocytes (lymphocytes, neutrophils), neutrophil to lymphocytes ratio, erythrocytes, hemoglobin, hematocrit, platelets
- C-reactive protein, total protein, albumin, cholesterol, iron, transferrin, ferritin, magnesium, zinc
- International normalized ratio, activated partial thromboplastin time
- Blood fasting glucose, glycated hemoglobin
Pancreatic function and treatment:
- PEI, fecal elastase-1, pancreatic enzyme replacement therapy (PERT), date of starting PERT, the dosage of daily taken PERT
- Diabetes mellitus (DM), date of DM diagnosis, DM type, DM treatment
Treatment-related:
- Planned chemotherapy protocol Dosages of chemotherapy planned (mg/m2)
- Percent of standard chemotherapy dose delivered
- Percent of planned chemotherapy delivered
- Changes to the predefined schedule (dose reduction, schedule modifications, stop before planned)
- Date of treatment start and end
- Adverse events (National Cancer Institute toxicity scale for visit 2)
Description of the intervention (schedule of visits):
Visit 1 (screening, within 1 month from initial diagnosis). Patients will be informed about the study. Once patients agree with the inclusion in the study the investigators will evaluate the inclusion and exclusion criteria. Those patients who meet all the inclusion criteria and none of the exclusion criteria will be finally included in the study. In this visit, patients, tumor-related variables, and general patients' features will be recorded, and quality of life questionnaire will be administered. The researcher will record weight, height, body mass index (BMI), unplanned WL % for the last 6 months.
Each patient's baseline nutrition status will be evaluated using the MNA scores prior to starting chemotherapy. Patients will be classified as in the group with no nutritional risk, at risk of malnutrition, or malnourished.
Nutritional parameters and pancreatic function will be evaluated through blood tests and a fecal test.
Visit 2 (3 months after the first dose of planned chemotherapy). The researcher will record in the case report form (CRF) the planned chemotherapy, schedule, doses, dose reduction, and any adverse event. The same variables recorded at Visit 1 will be checked again.
Check up 3 (end of the study, 6 months). The researcher will record in the CRF the overall survival and time until progression.
Medication of the study:
The study is of observational nature, so a pre-planned treatment is not considered. However, the use of pancreatic enzyme replacement treatment will be recorded as well as data regarding the employed chemotherapy regimen.
Power size calculation:
The expected percent of chemotherapy delivered in well-nourished patients was based on a study that assessed the chemotherapy dose intensity in gastrointestinal malignancies included pancreaticobiliary disease during the firsts 8 weeks after the start of the chemotherapy23. Based on an expected percentage of chemotherapy delivered of 70% in well-nourished patients, with a type I error of 0.05 and a type II error of 0.20, a sample size of 93 patients per group will be required in case of a percentage difference of chemotherapy delivered of 20% between well-nourished and malnourished, 163 patients per group in case of a difference of 15% between both groups and 356 patients per group in case of 10% of difference.
Discussion:
Given the sparse overall scientific data on the subject, the investigators have designed a study that addresses the impact of patient's nutritional status and dietary intervention on the clinical course of patients with advanced PDAC treated with chemotherapy and is aimed at establishing whether it affects both tolerance and tumor response to medical therapy. PAC-MAIN will be the first study specifically investigating whether the nutritional status influences the possibility to complete planned chemotherapy in patients with advanced PDAC.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Normal nutritional status | – | –Patients, fulfilled inclusion criteria with Mini-Nutritional Assessment score of 24-30 points. |
| Malnourished | – | –Patients, fulfilled inclusion criteria with Mini-Nutritional Assessment score of fewer than 17 points. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- patients with unresectable locally advanced or metastatic PDAC
Key inclusion criteria (7 listed)
- age ≥ 18 years;
- histological diagnosis of PDAC within one month from recruitment to the study;
- radiological diagnosis of the advanced stage not suitable for upfront surgical resection (either locally advanced or metastatic) within 5 weeks from recruitment to the study;
- data on the variables and the outcomes of interest are available;
- a written consent to participate in the study;
Key exclusion criteria (3 listed)
- poor performance status (Eastern Cooperative Oncology Group scale (ECOG) ≥ 3);
- pregnancy;
- surgery for PDAC in the past and developed progression.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Percent of standard chemotherapy dose delivered
Time frame: 12 weeks after the diagnosis
Drug doses will be expressed in weight-based, body surface area (BSA)-based, Area Under the Curve (AUC) units or flat dose, according to standard dosing practice for a given drug or combination. For each drug in a regimen, the sum of the doses delivered during the first 12 weeks of therapy will be divided by the sum of the expected doses based on published standard schedule and dosing. The mean percent dose delivered of all drugs in a regimen will be reported as 'percent of standard chemotherapy dose delivered.' The investigators will use percent of standard chemotherapy dose delivered to estimate the overall relative dose delivered.
Percent of planned chemotherapy delivered
Time frame: 12 weeks after the diagnosis
Similarly, the sum of the doses delivered during the first 12 weeks of therapy will be divided by the sum of the expected doses based on each patient's starting chemotherapy dose, and the mean percent dose delivered for all drugs in a regimen will be reported as 'percent of planned chemotherapy delivered.' The investigators will use percent of planned chemotherapy dose delivered to quantify further dose reductions from starting dose and as an indicator of overall toxicity.
6 secondary outcomes
Percent of patients with chemotherapy-related toxicity in each group
Time frame: 12 weeks after the diagnosis
Survival at 6 months
Time frame: 12 weeks after the diagnosis, 6 months
Progression-free survival
Time frame: 6 months
Quality of Life (EORTC) QLQ-PAN26 scale
Time frame: 12 weeks after the diagnosis
Number of hospitalizations
Time frame: 12 weeks after the diagnosis
Factors associated with the percent of chemotherapy received
Time frame: 12 weeks after the diagnosis
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Oct 2019.
- Derived from this study: PubMed 33015088Kiriukova M, de la Iglesia Garcia D, Panic N, Bozhychko M, Avci B, Maisonneuve P, de-Madaria E, Capurso G, Sandru V. Pancreatic Cancer Malnutrition and Pancreatic Exocrine Insufficiency in the Course of Chemotherapy in Unresectable Pancreatic Cancer. Front Med (Lausanne). 2020 Sep 3;7:495. doi: 10.3389/fmed.2020.00495. eCollection 2020.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Enrique de Madaria, MD, PhD contact
Mariia Kiriukova, MD study chair
Moscow Clinical Scientific Center
8 sites in 6 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Pancreatic Cancer and Exocrine Pancreatic Insufficiency, run by Moscow Clinical Scientific Center at 8 sites in 6 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 16 Oct 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 8 sites in Serbia, Spain, Italy, Romania, Russia and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Gabriele Capurso, MD, PhD (+39 02 26436548, capurso.gabriele@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percent of standard chemotherapy dose delivered (time frame: 12 weeks after the diagnosis). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04112836, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2019.