Trial of Intensive Chemotherapy With or Without Volasertib in Patients With Newly Diagnosed High-Risk Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML)

NCT ID: NCT02198482

Last Updated: 2018-02-28

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-02-29
• Study Completion Date: 2016-11-30

Brief Summary

Randomized Phase II Trial of Intensive Chemotherapy With or Without Volasertib (BI 6727) in Patients With Newly Diagnosed High-Risk Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML)

Detailed Description

The trial is a randomized, Phase II, open label multi-center trial in adult patients with newly diagnosed AML or high-risk MDS as defined in the inclusion/exclusion criteria.

An initial safety run-in study will be performed administering intensive induction therapy consisting of daunorubicin and cytarabine with the study drug volasertib administered prior or after chemotherapy, as well as consolidation therapy consisting of intermediate-dose cytarabine with the study drug volasertib administered prior or after chemotherapy. After establishing the volasertib dose, the randomized Phase II portion of the trial will begin:

Patients will be equally randomized to DA (daunorubicin, cytarabine), V-DA (volasertib administered prior to daunorubicin, cytarabine), and DA-V (volasertib administered after daunorubicin, cytarabine). All patients will receive a second induction cycle with reduced daunorubicin and cytarabine doses. Patients refractory to the first induction cycle and patients not achieving a CR/CRi after two induction cycles will be off-study and followed up.

Patients in CR/CRi after induction therapy will proceed to consolidation therapy. Consolidation will be stratified based on the genetic risk profile (according to ELN criteria) and patient-related factors (e.g., age, HCT-CI, comorbidities, patient wish). Patients with a favorable genetic risk profile and those patients considered ineligible for allogeneic HCT will receive repetitive cycles of consolidation according to initial randomization, either MiDAC, V-MiDAC (volasertib administered prior to cytarabine), or MiDAC-V (volasertib administered after cytarabine). All other patients are assigned to allogeneic HCT.

Conditions

Acute Myeloid Leukemia (AML); High-risk Myelodysplastic Syndrome (MDS)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Daunorubicin, Cytarabine (DA)

DA

Induction I:

• Daunorubicin 60 mg/m² i.v., d 1-3
• Cytarabine 100 mg/m² cont. i.v., d 1-7

Induction II:

• Daunorubicin 50 mg/m² i.v. d 1-3
• Cytarabine 100 mg/m² cont. i.v., d 1-5

Consolidation therapy:

Patients with genetic favourable risk and those patients not eligible for allogeneic HSCT due to comorbidities, high HCT-CI or patient wish will proceed to 3 cycles of age-adapted consolidation therapy with mitoxantrone and intermediate-dose cytarabine (MiDAC).

• Mitoxantrone Younger adults (18 to 60 yrs): 10 mg/m2 by i.v. on day 1. Elderly patients (>60 yrs): 8 mg/m2 by i.v. infusion on day 1.
• Intermediate-dose cytarabine:

Younger adults (18 to 60 yrs): 1500 mg/m2 q12h on days 1-3 Elderly patients (>60 yrs): 1000 mg/m2 q12h on days 1-3 An allogeneic HSCT is intended for patients with intermediate I/II and adverse-risk genetics. Optionally, one cycle of consolidation with MiDAC may be given prior to alloHSCT.

Group Type: ACTIVE_COMPARATOR

Cytarabine

Intervention Type: DRUG

Daunorubicin

Intervention Type: DRUG

Mitoxantrone

Intervention Type: DRUG

Volasertib, Daunorubicin, Cytarabine

VDA

Induction I

• Volasertib i.v., d1
• Daunorubicin 60 mg/m² i.v., d 2-4
• Cytarabine 100 mg/m² cont. i.v., d 2-8 Induction II
• Volasertib i.v., d1
• Daunorubicin 50 mg/m² i.v. d 2-4
• Cytarabine 100 mg/m² cont. i.v., d 2-6

Consolidation therapy:

Patients with genetic favourable risk and those patients not eligible for allogeneic HSCT will proceed to 3 cycles of age-adapted consolidation therapy with mitoxantrone and intermediate-dose cytarabine in combination with Volasertib (V-MiDAC).

• Volasertib i.v., d1
• Mitoxantrone Younger adults (18 to 60 yrs): 10 mg/m2 by i.v. on day 2. Elderly patients (>60 yrs): 8 mg/m2 by i.v. on day 2.
• Intermediate-dose cytarabine:

Younger adults (18 to 60 yrs): 1500 mg/m2 q12h on days 2-4 Elderly patients (>60 yrs): 1000 mg/m2 q12h on days 2-4 An allogeneic HSCT is intended for patients with intermediate I/II and adverse-risk genetics. Optionally, one cycle of consolidation with V-MiDAC may be given prior to alloHSCT.

Group Type: EXPERIMENTAL

Volasertib

Intervention Type: DRUG

Cytarabine

Intervention Type: DRUG

Daunorubicin

Intervention Type: DRUG

Mitoxantrone

Intervention Type: DRUG

Daunorubicin, Cytarabine, Volasertib

DAV

Induction I

• Volasertib i.v., d7
• Daunorubicin 60 mg/m² i.v., d 1-3
• Cytarabine 100 mg/m² i.v., d 1-7 Induction II
• Volasertib i.v., d5
• Daunorubicin 50 mg/m² i.v. d 1-3
• Cytarabine 100 mg/m² cont. i.v., d 1-5

Consolidation therapy:

Patients with genetic fav. risk and those patients not eligible for alloHSCT will proceed to 3 cycles of age-adapted consolidation therapy with mitoxantrone and intermediate-dose cytarabine in combination with Volasertib (MiDAC-V).

• Volasertib i.v., d4
• Mitoxantrone Younger adults (18 to 60 yrs): 10 mg/m2 by i.v. on day 1. Elderly patients (>60 yrs): 8 mg/m2 by i.v. on day 1.
• Intermediate-dose cytarabine:

Younger adults (18 to 60 yrs): 1500 mg/m2 q12h on days 1-3 Elderly patients (>60 yrs): 1000 mg/m2 q12h on days 1-3 An allogeneic HSCT is intended for patients with intermediate I/II and adverse-risk genetics. Optionally, one cycle of consolidation with MiDAC-V may be given prior to alloHSCT.

Group Type: EXPERIMENTAL

Volasertib

Intervention Type: DRUG

Cytarabine

Intervention Type: DRUG

Daunorubicin

Intervention Type: DRUG

Mitoxantrone

Intervention Type: DRUG

Interventions

Volasertib

Intervention Type: DRUG

Cytarabine

Intervention Type: DRUG

Daunorubicin

Intervention Type: DRUG

Mitoxantrone

Intervention Type: DRUG

Other Intervention Names

ARA-cell; Daunoplastin; Novantron

Eligibility Criteria

Inclusion Criteria

• Patients with confirmed diagnosis of acute myeloid leukemia (AML) or related precursor neoplasm, or acute leukemia of ambiguous lineage according to the current World Health Organization (WHO) classification, or patients with myelodysplastic syndrome (MDS) classified as refractory anemia with excess blasts-2 (RAEB-2)
• Consent for a genetic assessment in AMLSG central laboratory
• Patients considered eligible for intensive chemotherapy
• ECOG performance status of ≤ 2
• Age >= 18; there is no upper age limit
• No prior chemotherapy for acute leukemia except hydroxyurea for up to 5 days during the diagnostic screening phase; patients may have received prior therapy for myelodysplastic syndrome.
• Non-pregnant and non-nursing. Due to the teratogenic potential of volasertib in humans, pregnant or nursing patients may not be enrolled. Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within a sensitivity of at least 25 mIU/mL within 72 hours prior to registration. Women of child-bearing potential must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control - one highly effective method (e.g., IUD, hormonal, tubal ligation, or partner's vasectomy), and one additional effective method (e.g., latex condom, diaphragm, or cervical cap) for 6 months after therapy is stopped. "Women of childbearing potential" is defined as a sexually active mature woman who has not undergone a hysterectomy or who has had menses at any time in the preceding 24 consecutive months.
• Men must agree not to father a child and must use a latex condom during any sexual contact with women of childbearing potential while receiving therapy and for 6 months after therapy is stopped, even if they have undergone a successful vasectomy
• Signed written informed consent

Exclusion Criteria

• Patients with acute promyelocytic leukemia exhibiting t(15;17)(q22;q12); PML-RARA, or with variant translocations
• Prior treatment with volasertib or any other PLK1 inhibitor
• Performance status WHO >2 (see Appendix I)
• Patients with ejection fraction <50% by echocardiography within 14 days of day 1
• QTcF prolongation >470 ms or QT prolongation deemed clinically relevant by the investigator (e.g., congenital long QT syndrome). The QTcF will be calculated as the mean of 3 ECGs taken at screening.
• Any clinically significant, advanced or unstable disease or history of that may interfere with primary or secondary variable evaluations or put the patient at special risk, such as:

• creatinine >1.5x upper normal serum level;
• total bilirubin, AST or AP >2.5x upper normal serum level;
• heart failure NYHA III/IV,
• uncontrolled hypertension,
• unstable angina,
• serious cardiac arrhythmia;
• severe obstructive or restrictive ventilation disorder
• uncontrolled infection
• Patients with a "currently active" second malignancy other than non-melanoma skin cancers. Patients are not considered to have a "currently active" malignancy, if they have completed therapy and are considered by their physician to be at less than 30% risk of relapse within one year.
• Severe neurological or psychiatric disorder interfering with ability of giving an informed consent
• Known or suspected active alcohol or drug abuse
• Known positive for HIV, active HBV, HCV, or hepatitis A infection
• Hematologic disorder independent of leukemia
• No consent for registration, storage and processing of the individual disease characteristics and course as well as information of the family physician and/or other physicians involved in the treatment of the patient about study participation.
• No consent for biobanking.
• Current participation in any other interventional clinical study within 30 days before the first administration of the investigational product or at any time during the study
• Breast feeding women or women with a positive pregnancy test at Screening visit

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Ulm

OTHER

Sponsor Role: lead

Responsible Party

Prof. Dr. Hartmut Doehner

Prof. Dr.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hartmut Döhner, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

AMLSG Clinical Trials Office

Peter Paschka, MD

Role: STUDY_CHAIR

University Hospital Ulm

Locations

Hospital Aschaffenburg

Aschaffenburg, , Germany

Helios Hospital Bad Saarow

Bad Saarow, , Germany

Vivantes Hospital Am Urban

Berlin, , Germany

Vivantes Hospital Neukölln

Berlin, , Germany

Charite Berlin Campus Virchow Hospital

Berlin, , Germany

Knappschaftskrankenhaus Bochum-Langendeer

Bochum, , Germany

University Hospital Bonn

Bonn, , Germany

Community Hospital Braunschweig

Braunschweig, , Germany

Hospital Darmstadt

Darmstadt, , Germany

University Hospital Düsseldorf

Düsseldorf, , Germany

Hospital Essen, Protestant Hospital Essen-Werden

Essen, , Germany

Hospital Esslingen

Esslingen am Neckar, , Germany

Malteser Hospital St. Franziskus

Flensburg, , Germany

Hospital Frankfurt-Höchst

Frankfurt, , Germany

Medical Care Unit Osthessen

Fulda, , Germany

University Hospital Gießen

Giessen, , Germany

Wilhelm-Anton-Hospital Goch

Goch, , Germany

University Hospital Göttingen

Göttingen, , Germany

University Hospital Hamburg-Eppendorf

Hamburg, , Germany

Asklepios Hospital Altona

Hamburg, , Germany

Hospital Hanau

Hanau, , Germany

KRH Hospital Siloah-Oststadt-Heidehaus

Hanover, , Germany

Hannover Medical School

Hanover, , Germany

SLK-Hospital Heilbronn

Heilbronn, , Germany

Marienhospital Herne

Herne, , Germany

University Hospital des Saarlandes

Homburg/Saar, , Germany

Community Hospital Karlsruhe

Karlsruhe, , Germany

University Hospital Schleswig-Holstein

Kiel, , Germany

Caritas Hospital Lebach

Lebach, , Germany

Hospital Lippe-Lemgo

Lemgo, , Germany

University Hospital Magdeburg

Magdeburg, , Germany

University Hospital Johannes Gutenberg Mainz

Mainz, , Germany

Johannes Wesling Hospital Minden

Minden, , Germany

Stauferklinikum Schwäbisch-Gmünd

Mutlangen, , Germany

Hospital Schwabing

München, , Germany

Hospital rechts der Isar München

München, , Germany

Hospital Oldenburg

Oldenburg, , Germany

Hospital Passau

Passau, , Germany

Hospital Stuttgart

Stuttgart, , Germany

Diakonie Hospital Stuttgart

Stuttgart, , Germany

Hospital Traunstein

Traunstein, , Germany

Mutterhaus der Borromäerinnen

Trier, , Germany

Hospital Barmherzige Brüder Trier

Trier, , Germany

University Hospital Tübingen

Tübingen, , Germany

University Hospital Ulm

Ulm, , Germany

Countries

Germany

Other Identifiers

2014-000477-39

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

AMLSG 20-13

Identifier Type: -

Identifier Source: org_study_id