Glioblastoma WHO Grade IVPhase 3HIT-HGG-2013NCT03243461
International Cooperative Phase III Trial of the HIT-HGG Study Group (HIT-HGG-2013)
A Phase 3 study testing Temozolomide + Valproic Acid in people with Glioblastoma WHO Grade IV and Diffuse Midline Glioma Histone 3 K27M WHO Grade IV, run by University of Göttingen at 51 sites in Germany.
Trial summary
The HIT-HGG-2013 trial offers an innovative high-quality diagnostics and science program for children and adolescents >3 years, suffering from one of the following types of high grade gliomas: 1. glioblastoma WHO grade IV (GBM) 2. diffuse midlineglioma histone 3 K27M mutated WHO grade IV (DMG) 3. Read more about this study
- Who is it for?
- Ages 3 to 17 years
- Conditions the study is for
- Glioblastoma WHO Grade IV, Diffuse Midline Glioma Histone 3 K27M WHO Grade IV, Anaplastic Astrocytoma WHO Grade III
- What is being tested?
- Temozolomide + Valproic Acid
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 167 participants
- Where
- 51 sitesGermany
- Study dates
- 17 Jul 2018to 31 Dec 2023
- Phase
- Phase 3
- 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 3 to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Newly diagnosed, previously untreated diffuse paediatric high grade glioma with central neuropathological review including paedHGG (WHO grade IV) and anaplastic astrocytoma (WHO grade III).
- Newly diagnosed, previously untreated diffuse intrinsic pontine glioma with central neuroradiological review
- Newly diagnosed, previously untreated gliomatosis cerebri of all tumour grades with central neuroradiological review
- Patient ≥ 3 years and < 18 years of age at time of diagnosis
- Written informed consent of the patient and/or the patient's parents or legal guardian according to national laws
Who cannot join
- Pre-treatment of paedHGG (WHO grade IV), anaplastic astrocytoma (WHO grade III), diffuse intrinsic pontine glioma (as confirmed by neuroradiological review), and gliomatosis cerebri (as confirmed by neuroradiological review).
- Known hypersensitivity or contraindication to study drugs and/or dacarbazine
- Prior chemotherapy within the last 30 days before HIT-HGG-2013 treatment or radiotherapy which prevents adequate Performance of radiotherapy as outlined by the present protocol. This may mainly apply to patients with secondary high grade glioma after previous malignant brain tumour, e.g. medulloblastoma, ependymoma, craniopharyngeoma. If previous treatment does not prevent the adequate performance of the outlined Treatment protocol patients with secondary high grade glioma will be eligible for the present trial.
- Other (simultaneous) malignancies
- Pregnancy and / or lactation
- Patients who are sexually active refusing to use effective contraception (oral contraception, intrauterine devices, barrier method of contraception in conjunction with spermicidal jelly)
Show all 18Show fewer
- Current or recent (within 30 days prior to start of trial treatment) treatment with another investigational drug or participation in another investigational trial.
- Clinical (e.g. a constitutional mismatch repair deficiency score ≥ 3; Wimmer et al. 2014) and/or other hints (e.g. absent intratumoral immunohistochemical expression of at least one of the MLH1, MSH2, MSH6, or PMS2 mismatch repair proteins and/or high microsatellite instability) for an underlying biallelic (constitutional) mismatch repair deficiency (bMMRD/CMMRD) or a heterozygous mismatch repair deficiency (hereditary non-polyposis colon cancer syndrome/HNPCC syndrome/Lynch syndrome): These patients and their relatives should be offered human genetic counseling and rapid genetic diagnostics to confirm or rule out These conditions. These patients might not benefit from the present study treatment but maybe from other therapeutic strategies (Bouffet et al. 2016). Since patients with clinically suspected neurofibromatosis type 1 may display similar symptoms as in CMMRD, patients with clinically suspected neurofibromatosis type 1 should be also checked for CMMRD as suggested above.
- Very poor clinical condition as defined by demand of mechanical ventilation and/or demand for intravenous catecholamines and/or very severe neurological damage equivalent to a coma and/or tetraplegia with complete incapability for communication (deafness, blindness, mutism)
- Severe concomitant diseases (e.g. immune deficiency syndrome; known tumour predisposition syndromes which do not affect adequate performance of the trial represent no exclusion criterion a priori
- Known HIV positivity
- Known severe manifest hepatic disease including hepatic porphyria as well as personal or family history of severe hepatic dysfunction, especially drug-related
- Known severe pancreatic disease
- Known lethal hepatic dysfunction in a sibling during valproic acid treatment
- Known urea cycle defect
- Known mitochondrial diseases caused by genetic mutations within the gene coding for the enzyme polymerase gamma (POLG), e.g. Alpers-Huttenlocher syndrome, as well as suspected POLGrelated disorders in children under the age of two years
- Known severe coagulation disorders (in regards to thrombopenia see prerequisite for blood cell count before starting treatment)
- Valproic acid as antiepileptc drug for any pre-existing epilepsy (Exception: Valproic acid treatment due to tumour-related epilepsy will be tolerated, if the time interval between start of valproic acid treatment and trial enrolment is ≤ 8 weeks.
Trial locations and contacts
51 sites in 1 country.
51 sites in 1 country
Germany51 sites, 50 recruiting
- Recruiting
Universitätsklinik RWTH Aachen
Aachen
Udo Kontny, Prof. Dr.
- Recruiting
Klinikum Augsburg
Augsburg
Michael Frühwald, Prof.
- Recruiting
Charité Universitätsmedizin Berlin
Berlin
Pablo Hernaiz-Driever, PD Dr.
- Recruiting
HELIOS Klinikum Berlin Buch
Berlin
Patrick Hundsdörfer, PD Dr.
- Recruiting
Evangelisches Krankenhaus Bielefeld
Bielefeld
Norbert Jorch, Dr.
- Recruiting
Universitätsklinikum Bonn
Bonn
Gabriele Calaminus, Dr.
- Recruiting
Städtisches Klinikum Braunschweig gGmbH
Braunschweig
Torsten Ebeling, Dr.
- Recruiting
Klinikum Bremen-Mitte gGmbH
Bremen
Arnulf Pekrun, Prof.
- Recruiting
Kliniken der Stadt Köln gGmbH
Cologne
Stefan Balzer, Dr.
- Recruiting
Carl-Thiem-Klinikum Cottbus gGmbH
Cottbus
Georg Schwabe, PD Dr.
- Recruiting
Klinikum Dortmund gGmbH
Dortmund
Dominik Schneider, Prof. Dr.
- Recruiting
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Ralf Knöfler, Prof. Dr.
- Recruiting
Sana Kliniken Duisburg GmbH - Wedau Kliniken
Duisburg
Tanja Höll, Dr.
- Recruiting
HELIOS Klinikum Erfurt GmbH
Erfurt
Axel Sauerbrey, Prof. Dr.
- Recruiting
Universitätsklinikum Erlangen
Erlangen
Markus Metzler, Prof.
- Recruiting
Universitätsklinikum Essen
Essen
Regina Wieland, Dr.
- Recruiting
Universitätsklinikum Frankfurt
Frankfurt
Martina Becker, Dr.
- Recruiting
Universitätsklinikum Freiburg
Freiburg im Breisgau
Charlotte Niemeyer, Prof.
- Recruiting
Universitätsklinikum Gießen und Marburg GmbH
Giessen
Christine Mauz-Körholz, Prof. Dr.
- Recruiting
Universitätsmedizin Göttingen
Göttingen
Christof Kramm, Prof.
- Recruiting
Universitätsmedizin Greifswald
Greifswald
Holger Lode, Prof.
- Recruiting
Universitätsklinikum Halle
Halle
Toralf Bernig, Dr.
- Recruiting
Universitätsklinikum Hamburg
Hamburg
Uwe Kordes, Dr.
- Recruiting
Medizinische Hochschule Hannover
Hanover
Annette Sander, Dr.
- Recruiting
Angelika-Lautenschläger-Klinik
Heidelberg
Olaf Witt, Prof. Dr.
- Recruiting
SLK-Kliniken Heilbronn GmbH
Heilbronn
Monika Streiter
- Recruiting
Gemeinschaftskrankenhaus Herdecke
Herdecke
Alfred Längler, Prof. Dr.
- Recruiting
Universitätsklinikum des Saarlandes
Homburg
Norbert Graf, Prof.
- Recruiting
Universitätsklinikum Jena
Jena
Bernd Gruhn, Prof. Dr.
- Recruiting
Städtisches Klinikum Karlsruhe
Karlsruhe
Alfred Leipold, Dr.
- Recruiting
Gesundheit Nordhessen - Klinikum Kassel
Kassel
Michaela Nathrath, Prof.
- Recruiting
UKSH Kiel
Kiel
Alexander Claviez, PD Dr.
- Recruiting
Gemeinschaftsklinikum Mittelrhein gGmbH
Koblenz
Ümmügül Behr, Dr.
- Recruiting
HELIOS Klinikum Krefeld
Krefeld
Thomas Imschweiler
- Recruiting
Universitätsklinikum Leipzig
Leipzig
Lars Fischer, Dr.
- Recruiting
UKSH Campus Lübeck
Lübeck
Thorsten Langer, Prof. Dr.
- Recruiting
Universitätsklinikum Magdeburg A. ö. R.
Magdeburg
Antje Redlich, Dr.
- Recruiting
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Mainz
Jörg Faber, Prof. Dr.
- Recruiting
UMM Universitätsmedizin Mannheim
Mannheim
Matthias Dürken, PD Dr.
- Recruiting
Johannes Wesling Klinikum Minden
Minden
Bernhard Erdlenbruch, Prof.
- Recruiting
Technische Universität München / Klinikum Schwabing
München
Irene Teichert-von-Lüttichau, PD Dr.
- Recruiting
Universitätsklinikum Münster
Münster
Ronald Sträter, PD Dr.
- Recruiting
Klinikum Oldenburg gGmbH
Oldenburg
Hermann Müller, Prof.
- Recruiting
Universitätsklinikum Regensburg
Regensburg
Marcus Jakob, Dr.
- Active, not recruiting
Universitäts-Kinder- und Jugendklinik Rostock
Rostock
- Recruiting
ASKLEPIOS Klinik St. Augustin
Sankt Augustin
Harald Reinhard, PD Dr.
- Recruiting
HELIOS Kliniken Schwerin GmbH
Schwerin
Aram Prokop, Dr. Dr.
- Recruiting
Klinikum Stuttgart - Olgahospital
Stuttgart
Claudia Blattmann, PD Dr.
- Recruiting
Universitätsklinikum Tübingen
Tübingen
Martin Ebinger, PD Dr.
- Recruiting
Universitätsklinikum Ulm
Ulm
Klaus-Michael Debatin, Prof. Dr.
- Recruiting
Universitätsklinik Würzburg
Würzburg
Matthias Eyrich, Prof. Dr.
About this study
Official title: International Cooperative Phase III Trial of the HIT-HGG Study Group for the Treatment of High Grade Glioma, Diffuse Intrinsic Pontine Glioma, and Gliomatosis Cerebri in Children and Adolescents < 18 Years.(HIT-HGG-2013)
The HIT-HGG-2013 trial offers an innovative high-quality diagnostics and science program for children and adolescents >3 years, suffering from one of the following types of high grade gliomas:
- glioblastoma WHO grade IV (GBM)
- diffuse midlineglioma histone 3 K27M mutated WHO grade IV (DMG)
- anaplastic astrocytoma WHO grade III (AA)
- diffuse intrinsic pontine glioma (DIPG)
- gliomatosis cerebri (GC) For 1.-3. diagnosis has to be confirmed by neuropathological survey, for 4. and 5. diagnosis has to be confirmed by neuroradiological survey.
Read more
In addition to standard treatment (radiotherapy and temozolomide chemotherapy) the effect of valproic acid which is traditionally used for treatment of seizure disorder, will be investigated. The aim of the trial will be to investigate whether this drug may increase the effects of radio- and chemotherapy, resulting in a better survival of the treated patients. Scientific studies provided evidence for anti-tumoral effects of valproic acid: the drug seems to be a so-called histondeacetylase inhibitor (HDAC inhibitor), controlling important genetic processes of tumor growth.
Studies in cell culture, animals and first clinical trials in adults as well provided evidence for efficacy of valproic acid in the treatment of glioblastoma. Due to this we hope children and adolescents suffering from GBM, DMG, AA, DIPG und GC will benefit from the treatment, too.
The aim of the HIT-HGG-2013 trial will be to compare the effects of Valproic acid with data of the HIT-HGG-2007 trial (children and adolescents with same diseases, only treated with simultaneous temozolomide radiochemotherapy).
In the present study, it was originally planned to investigate the therapeutic efficiency and safety of valproic acid and the autophagy inhibitor chloroquine, both in addition to temozolomide therapy. Since distribution of Resochin junior (chloroquine phosphate) was terminated, recruitment of new patients was stopped on August 8, 2019. For continuation of the trial, the chloroquine arm was closed but the patients already recruited in this arm will be followed up.
Read the detailed description
Indication:
First-line treatment of high grade gliomas, diffuse intrinsic pontine glioma, and gliomatosis cerebri in paediatric patients < 18 years of age.
Background:
Based on published preclinical and clinical results regarding the potential therapeutic benefit of adult and pediatric high grade glioma patients receiving the histone deacetylase (HDAC) inhibitor valproic acid (VPA; Barker et al. 2013; Wolff et al. 2008, 2011; Felix et al. 2011; Su et al. 2011; Rokes et al. 2010; Masoudi et al. 2008; Guthrie et al. 2013; Weller et al. 2011) in addition to radiochemotherapy, the present trial is aimed to investigate if the addition of VPA to radiochemo- and maintenance therapy with temozolomide (Stupp et al. 2005; Cohen et al. 2011a, b) provides a survival advantage in comparison to radiochemo- and maintenance therapy with temozolomide alone. Therapeutic efficiency of VPA will be evaluated by comparison with a historical patient control from the previous trial HIT-HGG-2007 with temozolomide radiochemo- and maintenance therapy alone. Besides therapeutic efficiencies as indicated by event-free survival (EFS) and overall survival (OS) treatment-related toxicities will also be analysed.
Therapy:
TMZ and VPA will be studied as investigational medicinal products in the present trial.
- Trial treatment will be performed as follows: Surgery with best possible extent of tumour resection
- Start as soon as diagnosis is confirmed with VPA 10 mg/kg/d in two daily doses preferencially as NONRETARDED FORMULA (e.g. Valproat-neuraxpharm®, Valproat-neuraxpharm® Lösung, Ergenyl®, Ergenyl®-Lösung or Orfiril® Saft; however, any VPA preparation including generic drugs is allowed; the use of a retarded formula might be helpful in some case as indicated below), increase by 10 mg/kg/d once per week up until recommended target Serum level of 75-100 μg/ml (520-694 μmol/L) is reached. If target serum levels cannot be reached with non-retarded formula and/or side effects occur which might be connected to VPA, change to a retarded formula may be helpful to obtain sufficient VPA serum levels and/or reduce side effects. If VPA target serum levels are still not reached and/or side effects occur even with a retarded VPA formula, please contact the HIT-HGG study office.
After start of VPA induction with simultaneous radiochemotherapy:
- Fractionated, locoregional radiotherapy, total dose 54-60 Gy
- Simultaneous chemotherapy with oral temozolomide, 7 days per week at 75 mg/m2/d, starting at day 1 for the entire period of radiotherapy (at maximum 49 days; oral temozolomide treatment may be started in single cases at maximum 7 days before radiotherapy if the 49 days treatment period still fully covers radiotherapy).
- Please, use temozolomide capsules (for oral application) and temozolomide powder (for preparation of an intravenously applicable solution). Any temozolomide preparation including generic drugs is allowed except for patients who are not able to swallow capsules and in whom the use of an intravenous solution is no Option only Temodal® capsules must be used to generate a temozolomide suspension as described in the Appendix A.11. Parents have to be advised how to prepare the Temodal® suspension at the trial site. PLEASE NOTE: Capsules of generic temozolomide drugs other than Temodal® MUST NOT be opened and used for generating temozolomide suspension.
- Maintenance therapy with daily VPA and temozolomide four weeks after simultaneous radiochemotherapy initiation of a 5 day-course of oral temozolomide [150-200 mg/m2/d], repeated every 28 days for in total 12 courses VPA treatment is performed until day 28 of the 12th course of temozolomide.
- Treatment doses may vary according to available medication formulations and sizes. Thus, deviances of +/- 15% of the recommended doses may be acceptable if not stated otherwise.The starting points of treatment may also vary in single cases. Thus, deviances of +/- 7 days of the recommended time periods to start treatment may be acceptable if not stated otherwise.
Primary end point : Event-free survival
Biometry (regarding the primary objectives):
- Confirmatory statistical design:
- Difference between the treatment with additional VPA and the historic sample from the HIT-HGG-2007 study with respect to EFS. Rejection of H0 will be interpreted as a significant difference between VPA treatment and the historic sample. A directional interpretation will detect either a superiority of the VPA-treatment compared to the historic sample, or a superiority of the historic sample compared to the VPA Treatment sample. Statistical tests: adaptive Log-rank test / (conventional) Log-rank test Multiple Significance level α(overall) = 5% Power = 80% Assumed 6 months EFS-rates = 55% vs. 70% Multiple Testing: No Multiplicity Problem in this trial.
- Estimated sample sizes:
About 167 recruitments at final analysis
Patient recruitment will be performed for 5,4 years. Individual follow-up (including study treatment) is required for this protocol for at least 1 year and 30 days after study entry. Long-term follow-up is strongly recommended and will be organised according to national guidelines and recommendations.
Financial support:
Deutsche Kinderkrebsstiftung, Bonn, Germany
- Conditions
- Glioblastoma WHO Grade IV, Diffuse Midline Glioma Histone 3 K27M WHO Grade IV, Anaplastic Astrocytoma WHO Grade III, Diffuse Intrinsic Pontine Glioma, Gliomatosis Cerebri
- Being tested
- Temozolomide + Valproic Acid
- Keywords
- Glioblastoma, high grade glioma, brain tumor, Anaplastic astrocytoma, DIPG, Gliomatosis cerebri, Diffuse midline glioma, Valproic acid, Temozolomide
- Medical subject headings
- Diffuse Intrinsic Pontine Glioma, Neoplasms, Neuroepithelial, Glioblastoma, Glioma, Brain Neoplasms, Astrocytoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Temozolomide + Valproic AcidDrug
Valproic acid additionally to simultaneous radiochemotherapy with temozolomide
| Study group | Role | What they receive |
|---|---|---|
| Temozolomide + Valproic acid | Experimental | E.g. Valproat-neuraxpharm®, Valproat-neuraxpharm® Lösung, Ergenyl®, Ergenyl®-Lösung oder Orfiril® Saft (Valproic acid), [10 mg/kg/d] tablet oder juice, p.o., every day in parallel to simultaneous radiochemotherapy with cytostatic drug Temodal (Temozolomid): [75 mg/m2/d] during simultaneous radiochemotherapy (7 days a week, max. 49 days); [150-200 mg/m2/d] during consolidation therapy (for 5 days every 28 days, 12 cycles), tablets, p.o. (or powder for preparation of an intravenously applicable solution). Receives: Drug: Temozolomide + Valproic Acid |
What is being measured
The primary outcome is the main question the study is designed to answer.
Comparison of effects of valproine acid with respect to historical control group.
To confirm that the Event-Free Survival (EFS) in patients ≥ 3 years of age with paed HGG WHO grade IV, anaplastic astrocytoma WHO grade III (AAIII), DIPG, and gliomatosis cerebri differs for children treated with additional VPA compared to children in the historical HIT-HGG-2007 study sample.
Measured: 5.4 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Aug 2017
- Study start17 Jul 2018
- Primary completion31 Dec 2023 (estimated)
- Study completion31 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Glioblastoma WHO Grade IVStudies 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
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 167 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Göttingen
- Sponsor type
- University, hospital or other
- Collaborators
- Deutsche Kinderkrebsstiftung, Hannover Medical School
- Responsible party
- Principal investigator, Prof. Dr. Christof Kramm, University of Göttingen
- Investigators
- Christof Kramm, Prof., MD, Study chair, University of Göttingen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03243461
- Sponsor's protocol ID
- 01153
- Other IDs
- 2013-004187-56
- Acronym
- HIT-HGG-2013
- Status last verified
- Jun 2022
- First submitted
- 4 Aug 2017
- Last updated
- 6 Jun 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- International Cooperative Phase III Trial of the HIT-HGG Study Group for the Treatment of High Grade Glioma, Diffuse Intrinsic Pontine Glioma, and Gliomatosis Cerebri in Children and Adolescents < 18 Years.(HIT-HGG-2013)
- ClinicalTrials.gov ID
- NCT03243461
- Acronym / sponsor ID
- HIT-HGG-2013 / 01153
- Conditions
- Glioblastoma WHO Grade IV, Diffuse Midline Glioma Histone 3 K27M WHO Grade IV, Anaplastic Astrocytoma WHO Grade III, Diffuse Intrinsic Pontine Glioma, Gliomatosis Cerebri
- Keywords
- Glioblastoma, high grade glioma, brain tumor, Anaplastic astrocytoma, DIPG, Gliomatosis cerebri, Diffuse midline glioma, Valproic acid
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 167 participants (estimated)
- Lead sponsor
- University of GöttingenUniversity, hospital or other
- Collaborators
- Deutsche Kinderkrebsstiftung, Hannover Medical School
- Study start
- 17 Jul 2018 (actual)
- Primary completion
- 31 Dec 2023 (estimated)
- Study completion
- 31 Dec 2023 (estimated)
- First posted
- 9 Aug 2017 (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.
The HIT-HGG-2013 trial offers an innovative high-quality diagnostics and science program for children and adolescents >3 years, suffering from one of the following types of high grade gliomas:
- glioblastoma WHO grade IV (GBM)
- diffuse midlineglioma histone 3 K27M mutated WHO grade IV (DMG)
- anaplastic astrocytoma WHO grade III (AA)
- diffuse intrinsic pontine glioma (DIPG)
- gliomatosis cerebri (GC) For 1.-3. diagnosis has to be confirmed by neuropathological survey, for 4. and 5. diagnosis has to be confirmed by neuroradiological survey.
In addition to standard treatment (radiotherapy and temozolomide chemotherapy) the effect of valproic acid which is traditionally used for treatment of seizure disorder, will be investigated. The aim of the trial will be to investigate whether this drug may increase the effects of radio- and chemotherapy, resulting in a better survival of the treated patients. Scientific studies provided evidence for anti-tumoral effects of valproic acid: the drug seems to be a so-called histondeacetylase inhibitor (HDAC inhibitor), controlling important genetic processes of tumor growth.
Studies in cell culture, animals and first clinical trials in adults as well provided evidence for efficacy of valproic acid in the treatment of glioblastoma. Due to this we hope children and adolescents suffering from GBM, DMG, AA, DIPG und GC will benefit from the treatment, too.
The aim of the HIT-HGG-2013 trial will be to compare the effects of Valproic acid with data of the HIT-HGG-2007 trial (children and adolescents with same diseases, only treated with simultaneous temozolomide radiochemotherapy).
In the present study, it was originally planned to investigate the therapeutic efficiency and safety of valproic acid and the autophagy inhibitor chloroquine, both in addition to temozolomide therapy. Since distribution of Resochin junior (chloroquine phosphate) was terminated, recruitment of new patients was stopped on August 8, 2019. For continuation of the trial, the chloroquine arm was closed but the patients already recruited in this arm will be followed up.
Detailed description
Indication:
First-line treatment of high grade gliomas, diffuse intrinsic pontine glioma, and gliomatosis cerebri in paediatric patients < 18 years of age.
Background:
Based on published preclinical and clinical results regarding the potential therapeutic benefit of adult and pediatric high grade glioma patients receiving the histone deacetylase (HDAC) inhibitor valproic acid (VPA; Barker et al. 2013; Wolff et al. 2008, 2011; Felix et al. 2011; Su et al. 2011; Rokes et al. 2010; Masoudi et al. 2008; Guthrie et al. 2013; Weller et al. 2011) in addition to radiochemotherapy, the present trial is aimed to investigate if the addition of VPA to radiochemo- and maintenance therapy with temozolomide (Stupp et al. 2005; Cohen et al. 2011a, b) provides a survival advantage in comparison to radiochemo- and maintenance therapy with temozolomide alone. Therapeutic efficiency of VPA will be evaluated by comparison with a historical patient control from the previous trial HIT-HGG-2007 with temozolomide radiochemo- and maintenance therapy alone. Besides therapeutic efficiencies as indicated by event-free survival (EFS) and overall survival (OS) treatment-related toxicities will also be analysed.
Therapy:
TMZ and VPA will be studied as investigational medicinal products in the present trial.
- Trial treatment will be performed as follows: Surgery with best possible extent of tumour resection
- Start as soon as diagnosis is confirmed with VPA 10 mg/kg/d in two daily doses preferencially as NONRETARDED FORMULA (e.g. Valproat-neuraxpharm®, Valproat-neuraxpharm® Lösung, Ergenyl®, Ergenyl®-Lösung or Orfiril® Saft; however, any VPA preparation including generic drugs is allowed; the use of a retarded formula might be helpful in some case as indicated below), increase by 10 mg/kg/d once per week up until recommended target Serum level of 75-100 μg/ml (520-694 μmol/L) is reached. If target serum levels cannot be reached with non-retarded formula and/or side effects occur which might be connected to VPA, change to a retarded formula may be helpful to obtain sufficient VPA serum levels and/or reduce side effects. If VPA target serum levels are still not reached and/or side effects occur even with a retarded VPA formula, please contact the HIT-HGG study office.
After start of VPA induction with simultaneous radiochemotherapy:
- Fractionated, locoregional radiotherapy, total dose 54-60 Gy
- Simultaneous chemotherapy with oral temozolomide, 7 days per week at 75 mg/m2/d, starting at day 1 for the entire period of radiotherapy (at maximum 49 days; oral temozolomide treatment may be started in single cases at maximum 7 days before radiotherapy if the 49 days treatment period still fully covers radiotherapy).
- Please, use temozolomide capsules (for oral application) and temozolomide powder (for preparation of an intravenously applicable solution). Any temozolomide preparation including generic drugs is allowed except for patients who are not able to swallow capsules and in whom the use of an intravenous solution is no Option only Temodal® capsules must be used to generate a temozolomide suspension as described in the Appendix A.11. Parents have to be advised how to prepare the Temodal® suspension at the trial site. PLEASE NOTE: Capsules of generic temozolomide drugs other than Temodal® MUST NOT be opened and used for generating temozolomide suspension.
- Maintenance therapy with daily VPA and temozolomide four weeks after simultaneous radiochemotherapy initiation of a 5 day-course of oral temozolomide [150-200 mg/m2/d], repeated every 28 days for in total 12 courses VPA treatment is performed until day 28 of the 12th course of temozolomide.
- Treatment doses may vary according to available medication formulations and sizes. Thus, deviances of +/- 15% of the recommended doses may be acceptable if not stated otherwise.The starting points of treatment may also vary in single cases. Thus, deviances of +/- 7 days of the recommended time periods to start treatment may be acceptable if not stated otherwise.
Primary end point : Event-free survival
Biometry (regarding the primary objectives):
- Confirmatory statistical design:
- Difference between the treatment with additional VPA and the historic sample from the HIT-HGG-2007 study with respect to EFS. Rejection of H0 will be interpreted as a significant difference between VPA treatment and the historic sample. A directional interpretation will detect either a superiority of the VPA-treatment compared to the historic sample, or a superiority of the historic sample compared to the VPA Treatment sample. Statistical tests: adaptive Log-rank test / (conventional) Log-rank test Multiple Significance level α(overall) = 5% Power = 80% Assumed 6 months EFS-rates = 55% vs. 70% Multiple Testing: No Multiplicity Problem in this trial.
- Estimated sample sizes:
About 167 recruitments at final analysis
Patient recruitment will be performed for 5,4 years. Individual follow-up (including study treatment) is required for this protocol for at least 1 year and 30 days after study entry. Long-term follow-up is strongly recommended and will be organised according to national guidelines and recommendations.
Financial support:
Deutsche Kinderkrebsstiftung, Bonn, Germany
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Temozolomide + Valproic acid | Experimental | Drug: Temozolomide + Valproic AcidE.g. Valproat-neuraxpharm®, Valproat-neuraxpharm® Lösung, Ergenyl®, Ergenyl®-Lösung oder Orfiril® Saft (Valproic acid), [10 mg/kg/d] tablet oder juice, p.o., every day in parallel to simultaneous radiochemotherapy with cytostatic drug Temodal (Temozolomid): [75 mg/m2/d] during simultaneous radiochemotherapy (7 days a week, max. 49 days); [150-200 mg/m2/d] during consolidation therapy (for 5 days every 28 days, 12 cycles), tablets, p.o. (or powder for preparation of an intravenously applicable solution). |
Who may qualify
- Ages
- 3 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (5 listed)
- Newly diagnosed, previously untreated diffuse paediatric high grade glioma with central neuropathological review including paedHGG (WHO grade IV) and anaplastic astrocytoma (WHO grade III).
- Newly diagnosed, previously untreated diffuse intrinsic pontine glioma with central neuroradiological review
- Newly diagnosed, previously untreated gliomatosis cerebri of all tumour grades with central neuroradiological review
- Patient ≥ 3 years and < 18 years of age at time of diagnosis
- Written informed consent of the patient and/or the patient's parents or legal guardian according to national laws
Key exclusion criteria (18 listed)
- Pre-treatment of paedHGG (WHO grade IV), anaplastic astrocytoma (WHO grade III), diffuse intrinsic pontine glioma (as confirmed by neuroradiological review), and gliomatosis cerebri (as confirmed by neuroradiological review).
- Known hypersensitivity or contraindication to study drugs and/or dacarbazine
- Prior chemotherapy within the last 30 days before HIT-HGG-2013 treatment or radiotherapy which prevents adequate Performance of radiotherapy as outlined by the present protocol. This may mainly apply to patients with secondary high grade glioma after previous malignant brain tumour, e.g. medulloblastoma, ependymoma, craniopharyngeoma. If previous treatment does not prevent the adequate performance of the outlined Treatment protocol patients with secondary high grade glioma will be eligible for the present trial.
- Other (simultaneous) malignancies
- Pregnancy and / or lactation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Temozolomide + Valproic AcidValproic acid additionally to simultaneous radiochemotherapy with temozolomide | Drug | Temozolomide + Valproic acid |
Primary outcome
Comparison of effects of valproine acid with respect to historical control group.
Time frame: 5.4 years
To confirm that the Event-Free Survival (EFS) in patients ≥ 3 years of age with paed HGG WHO grade IV, anaplastic astrocytoma WHO grade III (AAIII), DIPG, and gliomatosis cerebri differs for children treated with additional VPA compared to children in the historical HIT-HGG-2007 study sample.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jun 2022.
- Individual participant dataSharing planned: No
Related trials for Glioblastoma WHO Grade IV
RecruitingObservational study
Leica Microsystems Sponsored PMCF Study to Collect and Confirm Clinical Data on the Performance of the GLOW400 Device When Used in Accordance With Its Intended Use
Suspected Grade III and IV Gliomas Requiring Surgical Intervention, Neurosurgical Procedure
Active, not recruitingPhase 2
Dabrafenib Combined With Trametinib After Radiation Therapy in Treating Patients With Newly-Diagnosed High-Grade Glioma
Anaplastic Astrocytoma, Anaplastic Astrocytoma, Not Otherwise Specified
RecruitingPhase 1
A Study of RNA-lipid Particle (RNA-LP) Vaccines for Newly Diagnosed Pediatric High-Grade Gliomas (pHGG) and Adult Glioblastoma (GBM)
Adult Glioblastoma, High Grade Glioma
RecruitingPhase 1/2
A Study of Zedoresertib (Debio 0123) in Combination With Temozolomide in Adult Participants With Recurrent or Progressive Glioblastoma and of Zedoresertib (Debio 0123) in Combination With Temozolomide and Radiotherapy in Adult Participants With Newly Diagnosed Glioblastoma
Glioblastoma IDH (Isocitrate Dehydrogenase) Wildtype, Astrocytoma, Grade III
Active, not recruitingPhase 2
A Study Testing the Effect of Immunotherapy (Ipilimumab and Nivolumab) in Patients With Recurrent Glioma With Elevated Mutational Burden
Astrocytoma, IDH-Mutant, Grade 4, Diffuse Glioma
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.
Christof Kramm, Prof., MD study chair
University of Göttingen
51 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Temozolomide + Valproic Acid in people with Glioblastoma WHO Grade IV and Diffuse Midline Glioma Histone 3 K27M WHO Grade IV, run by University of Göttingen at 51 sites in Germany.
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 5 inclusion and 18 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 6 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 51 sites in Germany. 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.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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 Christof Kramm, Prof., MD (49(0)551 39 63081, christof.kramm@med.uni-goettingen.de), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Comparison of effects of valproine acid with respect to historical control group. (time frame: 5.4 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 6 Jun 2022.