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Mistletoe Therapy in Primary and Recurrent Inoperable Pancreatic Cancer (MISTRAL)

Primary Purpose

Pancreatic Cancer

Status
Completed
Phase
Phase 3
Locations
Sweden
Study Type
Interventional
Intervention
Mistletoe extract (Iscador Qu)
Placebo
Sponsored by
Karolinska University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer focused on measuring Primary diagnosis, Relapse

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Signed written informed consent

  • Age ≥ 18 years
  • Inoperable locally advanced or metastatic pancreatic cancer or relapse of pancreatic cancer.

    • Primary diagnosis: if histology is not clinically achievable diagnosis is to be confirmed according to local practice sufficient for diagnosis and choice of therapy (such as CA19-9 (=cancer antigen 19-9) and CT).
    • Relapse: histology (not required) or diagnosis according to local practice such as clinical signs and/or imaging and/or CA19-9.
  • ECOG ( Eastern Cooperative Oncology Group) performance status 0-2 (see table in section 12.14 )
  • Adequate negative pregnancy test and adequate contraception (where appropriate)

Exclusion Criteria:

Life expectancy less than 4 weeks

  • Pregnancy or breastfeeding
  • Neuroendocrine tumors of the pancreas (NET)
  • Current use of interferon, G-CSF (granulocyte colony-stimulating factor) and thymus preparations
  • Symptomatic brain edema due to brain metastases
  • Known hypersensitivity to mistletoe-containing products
  • Current use of mistletoe extract preparations in any form
  • Chronic granulomatous disease or active autoimmune disease or autoimmune disease with immunosuppressive treatment
  • Medical, psychiatric, cognitive or other conditions that may compromise the patient´s ability to understand the patient information, give informed consent, comply with the study protocol or complete the study (e.g. needle phobia).

Sites / Locations

  • Kathrin Wode

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Mistletoe extract (Iscador Qu)

Placebo

Arm Description

Fermented aqueous extract of Viscum album ssp album (L.) (mistletoe) = Iscador Qu, subcutaneous use 3 injections/week; dose escalation from 0,01mg - 20mg

isotonic saline solution, subcutaneous use 3 injections/week

Outcomes

Primary Outcome Measures

Overall survival (OS)
OS defined as time from randomization to death for any reason

Secondary Outcome Measures

Quality of Life questionnaire EORTC QLQ-C30
Evaluation according to EORTC QLQ-C30 Scoring Manual
Quality of Life questionnaire EORTC PAN -26
Evaluation according to EORTC PAN-26 Scoring Manual
Weight in kilograms, height in meters, BMI in kg/m^2
Body weight, Body Mass Index
Corticosteroid use in milligrams betamethasone per day and indication (appetite, chemotherapy, nausea, pain, general wellbeing, other: specified)
Corticosteroid use and indication
Number of visits of homecare team per week
Costs for supportive care
Use of oral nutrition support per week (number used per day)
Costs for supportive care
Use of symptom relieving medication in mg/day (painkillers, antiemetic and anxiolitic medication)
Costs for supportive care
Chemotherapy use (number of cycles first line, second line, ..) and dose reduction in%
Costs for supportive care
Number of parenteral nutrition infusions per week
Costs for supportive care
Days of unplanned inpatient care
Costs for inpatient care
Incidence of treatment-emergent adverse events (AE)
Safety

Full Information

First Posted
September 13, 2016
Last Updated
January 12, 2023
Sponsor
Karolinska University Hospital
Collaborators
University of Witten/Herdecke, Karolinska Institutet, Regional Cancer Centre Stockholm Gotland, Stiftelsen Konung Gustaf V:s Jubileumsfond för cancerforskning, Signe & Ane Gyllenbergs Stiftelse, Ekhagastiftelsen, Dagmar Ferbs Minnesfond, Cancerforskningsfonden i Norrland, Immunpathologisches Labor, University Tübingen, The Sjöberg Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02948309
Brief Title
Mistletoe Therapy in Primary and Recurrent Inoperable Pancreatic Cancer
Acronym
MISTRAL
Official Title
Mistletoe Therapy in Primary & Recurrent Inoperable Pancreatic Cancer. A Phase III Prospective Randomized Double Blinded Multicenter Parallel Group Placebo Controlled Clinical Trial on Overall Survival and Quality of Life
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
September 2022 (Actual)
Study Completion Date
September 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska University Hospital
Collaborators
University of Witten/Herdecke, Karolinska Institutet, Regional Cancer Centre Stockholm Gotland, Stiftelsen Konung Gustaf V:s Jubileumsfond för cancerforskning, Signe & Ane Gyllenbergs Stiftelse, Ekhagastiftelsen, Dagmar Ferbs Minnesfond, Cancerforskningsfonden i Norrland, Immunpathologisches Labor, University Tübingen, The Sjöberg Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In this study a mistletoe preparation (Iscador Qu) is added to standard therapy in inoperable pancreatic cancer in order to evaluate effect on overall survival and health-related quality of life. Half of participants will take subcutaneous injections with mistletoe in addition to standard therapy (palliative chemotherapy or best supportive care); the other half will receive a placebo and standard therapy.
Detailed Description
Extracts from European mistletoe (Viscum album L.) have been used as complementary cancer therapy since the 1920s. To date over 160 clinical studies on mistletoe in cancer therapy have been conducted with varying quality; the therapy is still controversial. Best evidence is found for increase of health-related quality of life (HRQoL) and reduction of side effects of conventional therapies (chemotherapy, radiation) in breast cancer patients. Mistletoe treatment is described as safe and well tolerated. There are some clinical studies supporting the use of mistletoe extract in the management of late stage cancer. Statistically significant effects on overall survival (OS) and HRQoL in pancreatic cancer patients have recently been shown in a randomized open label trial in Serbia investigating the addition of mistletoe extract to best supportive care. The results are questioned because patients knew what kind of treatment they received. Mistletoe extracts are usually administered subcutaneously. They contain a multitude of substances with immune modulatory and cytotoxic or - in animal studies - antitumorigenic, anti-metastatic and antiangiogenic effects. This trial investigates whether there is a beneficial effect of mistletoe extracts on OS and HRQoL in pancreatic cancer patients receiving standard treatment (palliative chemotherapy or best supportive care). Inclusion has started at 4 study centers (2 more centers are waiting for participation). And participants are randomized 1:1 to mistletoe treatment (Iscador Qu®) given in increasing dosage from 0,01mg to 20 mg or placebo injections subcutaneously 3 times /week. Stratification will be performed for received oncological treatment (palliative chemotherapy or best supportive care). At 7 visits in 9 months, participants fill in the validated EORTC QLQ-C30 (QLO=quality of life questionnaire) and PAN-26 (PAN=pancreas) quality of life questionnaires. Body weight, use of cancer-related medicines, substitution of nutrition, adverse events need of supportive care and inpatient care are measured. To be able to assess more dimensions of quality of life than possible with questionnaires, a qualitative sub-study with interviews on about 30 participants in this trial is performed in month 3. A 2nd substudy has been added november 2016 to elucidate the systemic effects of mistletoe therapy and to explore potential prognostic and predictive biomarkers (anticipated n=100).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
Primary diagnosis, Relapse

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
290 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mistletoe extract (Iscador Qu)
Arm Type
Experimental
Arm Description
Fermented aqueous extract of Viscum album ssp album (L.) (mistletoe) = Iscador Qu, subcutaneous use 3 injections/week; dose escalation from 0,01mg - 20mg
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
isotonic saline solution, subcutaneous use 3 injections/week
Intervention Type
Drug
Intervention Name(s)
Mistletoe extract (Iscador Qu)
Other Intervention Name(s)
Fermented aqueous extract of Viscum album ssp album (L.)
Intervention Description
1ml subcutaneous injection 3 times/week, dose escalation 0,01mg - 20mg
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Isotonic saline solution
Intervention Description
1ml subcutaneous injection 3 times/week
Primary Outcome Measure Information:
Title
Overall survival (OS)
Description
OS defined as time from randomization to death for any reason
Time Frame
End of study (estimated 3 years)
Secondary Outcome Measure Information:
Title
Quality of Life questionnaire EORTC QLQ-C30
Description
Evaluation according to EORTC QLQ-C30 Scoring Manual
Time Frame
At 7 visits during study (9 months)
Title
Quality of Life questionnaire EORTC PAN -26
Description
Evaluation according to EORTC PAN-26 Scoring Manual
Time Frame
At 7 visits during study (9 months)
Title
Weight in kilograms, height in meters, BMI in kg/m^2
Description
Body weight, Body Mass Index
Time Frame
At 7 visits during study (9 months)
Title
Corticosteroid use in milligrams betamethasone per day and indication (appetite, chemotherapy, nausea, pain, general wellbeing, other: specified)
Description
Corticosteroid use and indication
Time Frame
At 7 visits during study (9 months)
Title
Number of visits of homecare team per week
Description
Costs for supportive care
Time Frame
At 7 visits during study (9 months)
Title
Use of oral nutrition support per week (number used per day)
Description
Costs for supportive care
Time Frame
At 7 visits during study (9 months)
Title
Use of symptom relieving medication in mg/day (painkillers, antiemetic and anxiolitic medication)
Description
Costs for supportive care
Time Frame
At 7 visits during study (9 months)
Title
Chemotherapy use (number of cycles first line, second line, ..) and dose reduction in%
Description
Costs for supportive care
Time Frame
At 7 visits during study (9 months)
Title
Number of parenteral nutrition infusions per week
Description
Costs for supportive care
Time Frame
At 7 visits during study (9 months)
Title
Days of unplanned inpatient care
Description
Costs for inpatient care
Time Frame
At 7 visits during study (9 months)
Title
Incidence of treatment-emergent adverse events (AE)
Description
Safety
Time Frame
Through study completion (9 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed written informed consent Age ≥ 18 years Inoperable locally advanced or metastatic pancreatic cancer or relapse of pancreatic cancer. Primary diagnosis: if histology is not clinically achievable diagnosis is to be confirmed according to local practice sufficient for diagnosis and choice of therapy (such as CA19-9 (=cancer antigen 19-9) and CT). Relapse: histology (not required) or diagnosis according to local practice such as clinical signs and/or imaging and/or CA19-9. ECOG ( Eastern Cooperative Oncology Group) performance status 0-2 (see table in section 12.14 ) Adequate negative pregnancy test and adequate contraception (where appropriate) Exclusion Criteria: Life expectancy less than 4 weeks Pregnancy or breastfeeding Neuroendocrine tumors of the pancreas (NET) Current use of interferon, G-CSF (granulocyte colony-stimulating factor) and thymus preparations Symptomatic brain edema due to brain metastases Known hypersensitivity to mistletoe-containing products Current use of mistletoe extract preparations in any form Chronic granulomatous disease or active autoimmune disease or autoimmune disease with immunosuppressive treatment Medical, psychiatric, cognitive or other conditions that may compromise the patient´s ability to understand the patient information, give informed consent, comply with the study protocol or complete the study (e.g. needle phobia).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Annika Bergquist, Ass Prof
Organizational Affiliation
Gastrocentrum Karolinska University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Kathrin Wode
City
Stockholm
ZIP/Postal Code
14186
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The trial results will be submitted for publication in relevant medical journals
Citations:
PubMed Identifier
25142075
Citation
Troger W, Galun D, Reif M, Schumann A, Stankovic N, Milicevic M. Quality of life of patients with advanced pancreatic cancer during treatment with mistletoe: a randomized controlled trial. Dtsch Arztebl Int. 2014 Jul 21;111(29-30):493-502, 33 p following 502. doi: 10.3238/arztebl.2014.0493.
Results Reference
background
PubMed Identifier
23890767
Citation
Troger W, Galun D, Reif M, Schumann A, Stankovic N, Milicevic M. Viscum album [L.] extract therapy in patients with locally advanced or metastatic pancreatic cancer: a randomised clinical trial on overall survival. Eur J Cancer. 2013 Dec;49(18):3788-97. doi: 10.1016/j.ejca.2013.06.043. Epub 2013 Jul 24.
Results Reference
background
PubMed Identifier
18425885
Citation
Horneber MA, Bueschel G, Huber R, Linde K, Rostock M. Mistletoe therapy in oncology. Cochrane Database Syst Rev. 2008 Apr 16;2008(2):CD003297. doi: 10.1002/14651858.CD003297.pub2.
Results Reference
background
PubMed Identifier
19519890
Citation
Kienle GS, Glockmann A, Schink M, Kiene H. Viscum album L. extracts in breast and gynaecological cancers: a systematic review of clinical and preclinical research. J Exp Clin Cancer Res. 2009 Jun 11;28(1):79. doi: 10.1186/1756-9966-28-79.
Results Reference
background
PubMed Identifier
32917288
Citation
Wode K, Hok Nordberg J, Kienle GS, Elander NO, Bernhardson BM, Sunde B, Sharp L, Henriksson R, Fransson P. Efficacy of mistletoe extract as a complement to standard treatment in advanced pancreatic cancer: study protocol for a multicentre, parallel group, double-blind, randomised, placebo-controlled clinical trial (MISTRAL). Trials. 2020 Sep 11;21(1):783. doi: 10.1186/s13063-020-04581-y.
Results Reference
derived

Learn more about this trial

Mistletoe Therapy in Primary and Recurrent Inoperable Pancreatic Cancer

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