Efficacy and Safety of Dronabinol in the Improvement of Chemotherapy-induced and Tumor-related Symptoms in Advanced Pancreatic Cancer

Arbeitsgemeinschaft medikamentoese Tumortherapie109 enrolled

Overview

Aim of this phase III trial is to investigate the efficacy and safety of dronabinol (orally administered tetrahydrocannabinol (THC)) as adjuvant therapy to first-line standard chemotherapy in patients with metastatic pancreatic cancer for improvement of chemotherapy- and tumor-related symptoms applicated by individual titration up to the maximum tolerated dose.

Patients with pancreatic cancer suffer from multiple symptoms related to the tumor itself or induced by the chemotherapy. The available supportive therapy is still not able to relief all symptoms that are caused by the malignancy itself as well as by the antineoplastic therapy. Additionally, anorexia and weight loss, that often result in increased morbidity and mortality in this patient population as well as in psycho-social burden and suffering in patients and their relatives, are unmet needs in pancreatic cancer patients. Therapeutic approaches focus on treating the malignancy itself, additional nutritional support and physical examination might prevent patients from further side effects such as sarcopenia. During the last decades a number of appetite-modulating drugs have been under clinical investigation. A number of studies focused on the endocannabinoid system, which is involved amongst others in appetite-modulating, antiemetic, analgesic and anti-inflammatory processes. As dronabinol is already used as magistral formulation, its beneficial effect has often been observed in these patients in the clinical routine, especially in patients with therapy-refractory nausea and emesis. Due to its broad efficacy it might be of benefit for patients suffering from malignancy. Thus, investigators want to evaluate the efficacy of dronabinol in the improvement of chemotherapy-induced and tumor-related symptoms in advanced pancreatic patients during systemic first-line chemotherapy. However, data on optimal dosage are conflicting yet. In detail, investigators want to study whether dronabinol has a positive influence on quality of life and whether symptoms caused by the tumor or by the chemotherapy itself might be palliated by dronabinol. Beneficial and potential harmful side effects and the personal perception of advanced pancreatic cancer patients will be documented.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

Interventions

Dronabinol in Oral Dosage FormDRUG

Titration period for 4 weeks: titration according to tolerability from 2.5 mg (3 x 1 droplet) up to 30 mg (3 x 12 droplets) per day; dose increased by 2.5 mg (3 x 1 droplet) every other day Maintenance period for 12 weeks: individually tolerated maximum dose (up to 30 mg ≙ 3 x 12 droplets) at end of titration period will be continued for maintenance treatment Tapering period for 2 weeks: dose is decreased every other day by 5 mg (3 x 2 droplets) Safety follow-up: 4 weeks after end of treatment

Placebo in Oral Dosage FormDRUG

Titration period for 4 weeks: titration according to tolerability from 3 x 1 droplet up to 3 x 12 droplets per day; dose increased by 3 x 1 droplet every other day Maintenance period for 12 weeks: individually tolerated maximum dose (up to 3 x 12 droplets) at end of titration period will be continued for maintenance treatment Tapering period for 2 weeks: dose is decreased every other day by 3 x 2 droplets Safety follow-up: 4 weeks after end of treatment

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Male and female subjects aged ≥18 * Patients with diagnosis of locally advanced, inoperable or metastatic pancreatic cancer, eligible for first-line chemotherapy with FOLFIRINOX or gemcitabine+Abraxane® * According to investigator life expectancy of \> 4 months at screening * Female patients must either be post-menopausal or surgically sterilized or use a highly effective method of birth control (hormonal contraceptives, intra-uterine devices, or diaphragms with spermicide) for the duration of the study and/or must have a negative pregnancy test (female patients with childbearing potential only) * Willing and able to provide written informed consent. * Written informed consent given prior to any trial-related procedure not part of the normal medical practice. Exclusion Criteria: * Patients who are members of the staff of the trial center, staff of the sponsor or CRO, the investigator him/herself or close relatives of the investigator. * Simultaneous participation in another interventional clinical trial, participation in another trial with less than 30 days or five half-lives of the IMP (whatever is longer) to screening, or previous participation in this trial. * Ineligible for chemotherapy treatment with FOLFIRINOX or gemcitabine+Abraxane® * Use of dronabinol or cannabis-based medicine with THC as constituent within 6 months before screening. A urine drug test will be performed during screening phase. * Use of marihuana within the last 4 weeks and unwillingness to abstain for the duration of the study. A urine drug test will be performed during screening phase. * Currently receiving chemotherapy or anticipated use of chemotherapy due to any condition not related to locally advanced or metastatic pancreatic cancer * History of or existing cardiac diseases or pathological findings (e.g. chronic insufficiency NYHA III/IV, severe arrhythmia, unstable angina pectoris, myocardial infarction within the past 6 months, significant QT-prolongation etc.), which in the opinion of the investigator might interfere with the safety or tolerability of the study treatment. An ECG has to be done to exclude pathological findings and must not be older than 3 months before screening or if none is available, has to be performed during the screening phase and assessed prior to randomization * Clinically relevant, severe pulmonary diseases, uncontrolled hypertension, or poorly controlled diabetes * History of or existing relevant CNS and/or psychiatric disorders (e.g. schizophrenia, psychosis, manic and/or depressive disorders, suicidal ideations, etc) which might interfere with the safety or tolerability of the study treatment. Patients with reactive depression are not excluded from participation. * Known current or past (within the last year prior to screening) alcohol, narcotics or drug abuse * Pregnancy or breast feeding * Known allergy to cannabinoids and other constituents of the investigational medicinal product * Intake of prohibited concomitant medication * Any other substantial medical condition that in the opinion of the investigator could create undue risk to the subject or could affect adherence with the trial protocol * Legal incapacity, limited legal capacity or any other condition which makes the subject unable to understand the subject information and informed consent form (ICF) * Patients unable or unwilling to waive driving motor vehicles or using machines especially during titration period * Unable or unwilling to comply with the protocol regulations

Locations (11)

IIIrd Medical Department, Private Medical University Hospital Salzburg

Salzburg, Salzburg, Austria

Klinikum Wels-Grieskirchen GmbH, Abteilung für Innere Medizin IV

Wels, Upper Austria, Austria

Hanusch Krankenhaus der Wiener Gebietskrankenkasse

Vienna, Vienna, Austria

KABEG-Klinikum Klagenfurt am Woerthersee, Abteilung f. Anaesthesie u. Intensivmedizin

Klagenfurt, Austria

LKH Hochsteiermark - Standort Leoben Abteilung für Innere Medizin und Hämatologie und internistische Onkologie

Leoben, Austria

Krankenhaus d. Barmherzigen Brüder, Abt. f. Innere Medizin

Sankt Veit an der Glan, Austria

Pyhrn-Eisenwurzen Klinikum Steyr, Interne Medizin II

Steyr, Austria

KH Zams, Innere Medizin, Internistische Onkologie u. Haematologie

Zams, Austria

Universitätsmedizin Göttingen Abt. f. Gastroenterologie, gastrointestinale Onkologie u. Endokrinologie

Göttingen, Germany

München Klinik Neuperlach

München, Germany

...and 1 more locations

Outcomes

Primary Outcomes

Standardized area under the curve of the European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30 symptom summary score over the on-treatment period.

The EORTC-QLQ-C30 is an integrated system for assessing the health-related quality of life (QoL) of cancer patients participating in international clinical trials. The validated QLQ-C30 summary score is calculated as mean score of the 13 of the 15 EORTC QLQ-C30 scales (v3.0), based on 27 of 30 items (the Financial Impact scale and Quality of Life score are not included). A high score for a symptom scale / item (fatigue, nausea and vomiting, pain, dyspnoea, insomnia, appetite loss, constipation, diarrhoea) represents a high level of symptomatology / problems. A high score for a functional scale (physical functioning, role functioning, cognitive functioning, emotional functioning, social functioning) represents a high / healthy level of functioning. Scores for individual items: "Not at All" = 1 point, "A Little" = 2 points, "Quite a Bit" = 3 points, "Very Much" = 4 points. A linear transformation is used to standardize the raw score, so that overall scores range from 0 to 100.

Time frame: Prior to treatment start until end of 16 weeks maintenance treatment

Secondary Outcomes

Standardized area under the curve of the European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30 symptom summary score over the maintenance period

The European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) is an integrated system for assessing the health-related quality of life (QoL) of cancer patients participating in international clinical trials. The validated QLQ-C30 summary score is calculated as mean score of items. A high score for a symptom scale / item (fatigue, nausea and vomiting, pain, dyspnoea, insomnia, appetite loss, constipation, diarrhoea) represents a high level of symptomatology / problems. Scores for individual items: "Not at All" = 1 point, "A Little" = 2 points, "Quite a Bit" = 3 points, "Very Much" = 4 points. A linear transformation is used to standardize the raw score, so that overall scores range from 0 to 100.

Time frame: After 4 weeks of treatment until week 16

Change of European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30 symptom summary score from baseline to summary score over the maintenance period

Time frame: From treatment start until week 16

Symptom scales of European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30

A high score for a symptom scale / item (fatigue, nausea and vomiting, pain, dyspnoea, insomnia, appetite loss, constipation, diarrhoea) represents a high level of symptomatology / problems. Scores for individual items: "Not at All" = 1 point, "A Little" = 2 points, "Quite a Bit" = 3 points, "Very Much" = 4 points. A linear transformation is used to standardize the raw score, so that overall scores range from 0 to 100.

Time frame: At baseline and 2-weekly until end of treatment at week 18

Global quality of life of the European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30

The European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) is an integrated system for assessing the health-related quality of life (QoL) of cancer patients participating in international clinical trials. The validated QLQ-C30 summary score is calculated as mean score of items. A high score for the global health status (overall health during the past week) and global QoL (overall quality of life during the past week) represents a high QoL. Scores: 1 - 7, 1 = very poor and 7 = excellent. A linear transformation is used to standardize the raw score, so that overall scores range from 0 to 100.

Time frame: At baseline and 2-weekly until end of treatment at week 18

Functional scales of the European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30

The European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) is an integrated system for assessing the health-related quality of life (QoL) of cancer patients participating in international clinical trials. A high score for a functional scale (physical functioning, role functioning, cognitive functioning, emotional functioning, social functioning) represents a high / healthy level of functioning. Scores for individual items: "Not at All" = 1 point, "A Little" = 2 points, "Quite a Bit" = 3 points, "Very Much" = 4 points. A linear transformation is used to standardize the raw score, so that overall scores range from 0 to 100.

Time frame: At baseline and 2-weekly until end of treatment at week 18

Mean change from baseline of the Glasgow Prognostic Score

Change of serum levels of the score-defining biomarkers C-reactive protein (CRP) and albumin. Prognostic scores; 0 (CRP ≥ 10 mg/l), 1 (CRP \> 10 mg/l and albumin ≥ 35 g/l), 2 CRP \> 10 mg/l and albumin \< 35g/l). Score 0 indicates good prognosis, score 1 intermediate prognosis and score 2 poor prognosis.

Time frame: At baseline and at end of treatment at week 16

Amount of concomitant medication taken

Special focus on antiemetic, psychotropic and pain medication

Time frame: From baseline until end of treatment at week 18

Mean time to critical weight-loss (5%)

Assessed with a standard scale

Time frame: From baseline until end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Lean body mass (LBM)

Mean change of Lean body mass (LBM = Fat free mass FFM) kg

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Total body water (TBW)

Mean change of Total body water (TBW) kg

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Fat mass (FM)

Mean change of Fat mass (FM) kg

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Body cell mass (BCM)

Mean change of Body cell mass (BCM) kg

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Extracellular mass (EM)

Mean change of Extracellular mass (ECM) kg

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Phase angle (PA)

Mean change of Phase angle (PA); Phase Angle has long been linked to nutritional status. This marker is fast becoming recognised as a global health marker in total body health assessment. A higher Phase Angle could mean an increase in muscle mass (body cell mass) or a decrease in fluid, either from recovery from infection or injury (a good thing!) or a decrease in fluid from dehydration (a bad thing!). A loss of fat could also increase Phase Angle. A lower Phase Angle could mean a loss of muscle mass (a bad thing), or an increase of fluid (rehydrating which is a good thing, or sign of inflammation or infection - a bad thing), or gaining fat (which could be a good or bad thing depending on your state of health). Phase Angle is a direct measurement, (not a calculation using equations) of the cell membrane.

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Resistance (Rz)

Mean change of Resistance (Rz), unit ohm; the resistance reflects the water or fluid in the body

Time frame: At baseline and at end of treatment at week 16

Mean changes from baseline for Bioelectrical Impedance Analysis (BIA) parameter Reactance(Xc)

Mean change of Reactance (Xc), unit ohm; reactance reflects the body cell mass.

Time frame: At baseline and at end of treatment at week 16

Mean change from baseline of muscle strength

To assess physical strength of patient's handgrip strength will be measured prior and after study treatment using a hydraulic hand dynamometer; mean value of three consecutive measurements will be documented

Time frame: At baseline and at end of treatment at week 16

Proportion of patients not adhering to individual baseline chemotherapy regimen

Percentage of patients who do not receive full dose of planned chemotherapy regimen and/or within scheduled time frame (interruption or delay)

Time frame: From baseline until end of treatment at week 18

Chemotherapeutic dose intensity over the treatment period of 18 weeks

The total amount of applied chemotherapy over the study treatment phase is documented

Time frame: From baseline until end of treatment at week 18

Frequency and severity of (serious) adverse events (S)AE

Assessed with Common Terminology Criteria for Adverse Events (NCI-CTCAE V5.0)

Time frame: From baseline until safety visit at week 22

Incidence of adverse drug reactions (ARs)

Frequency and severity of ARs

Time frame: From baseline until safety visit at week 22

Progression-free survival (PFS)

PFS in months; ; patients will be asked to agree on collection of data regarding PFS also after end of trial

Time frame: From treatment start until the date of first documented progression or death from any cause assessed up to week 22

Overall survival (OS)

OS in months; ; patients will be asked to agree on collection of data regarding PFS also after end of trial

Time frame: From treatment start until death from any cause assessed up to week 22

Efficacy and Safety of Dronabinol in the Improvement of Chemotherapy-induced and Tumor-related Symptoms in Advanced Pancreatic Cancer

Overview

Conditions

Interventions

Eligibility

Locations (11)

Outcomes

Primary Outcomes

Secondary Outcomes