Study of Palbociclib in MLL-rearranged Acute Leukemias

NCT02310243

Last updated date
Study Location
Klinikum Augsburg
Augsburg, , 86156, Germany
Contact
1-800-718-1021

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Eligibility Criteria
condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18 + years
Inclusion Criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

- Patients with confirmed diagnosis of acute leukemia with MLL rearrangement according to the 2008 WHO Classification

- Patients with MLL-rearranged leukemia who are refractory to standard induction therapy and not immediate candidates for allogeneic HSCT (bridge to transplant is allowed)

- Patients with MLL-rearranged leukemia who relapsed after standard first-line treatment and are not immediate candidates for allogeneic HSCT (bridge to transplant is allowed)

- Patients with newly diagnosed MLL-rearranged leukemia who are not eligible for intensive first-line therapy

- Genetic/histologic/immunohistologic assessment in one of the central laboratories

- Age ≥ 18 years, no upper age limit

- WHO performance status of ≤ 2

- No prior chemotherapy two weeks before study entry except hydroxyurea to control hyperleukocytosis

- Non-pregnant and non-nursing. Women of child-bearing potential must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 72 hours prior to registration (WOCBP 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 months).

- Female patients in the reproductive age and male patients must agree to avoid getting pregnant or to father a child while on therapy and for three months after the last dose of therapy.

- Women of child-bearing potential must either commit to continued abstinence from heterosexual intercourse or begin one acceptable method of birth control (IUD, tubal ligation, or partner's vasectomy). Hormonal contraception is an inadequate method of birth control.

- Men must agree not to father a child and must use a latex condom during any sexual contact with WOCBP while receiving therapy and for three months after therapy is stopped, even if they have undergone successful vasectomy.

- Signed written informed consent

Exclusion Criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
Show details


- Prior treatment with palbociclib


- Performance status > 2 according to WHO criteria


- Organ insufficiency: creatinine > 1.5 x upper normal serum level; bilirubin, AST, or
AP > 2.5 x 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
cancer. 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 neurologic or psychiatric disorder interfering with ability of giving informed
consent


- Known or suspected active alcohol or drug abuse


- Known positivity for HIV, active HAV, HBV, or HCV infection


- Bleeding disorder unrelated to leukemia


- Uncontrolled CNS involvement (treatment for CNS-involvement prior to inclusion is
allowed)


- QTc > 470 msec (based on the mean value of triplicate ECGs), family or personal
history of long or short QT syndrome, Brugada syndrome, or known history of QTc
prolongation or Torsade de Pointes


- Uncontrolled electrolyte disorders that can aggravate the effects of a QTc-prolonging
drug (e.g., hypocalcemia, hypokalemia, hypomagnesemia)


- No consent for registration, storage, and processing of individual disease
characteristics, information on the course of the disease, and information obtained
from the family physician and/or other physicians involved in the treatment of the
patient about study participation


- No consent for biobanking

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Acute Myeloid Leukemia, Acute Lymphoblastic LeukemiaStudy of Palbociclib in MLL-rearranged Acute Leukemias
NCT02310243
  1. Augsburg,
  2. Bad Saarow,
  3. Berlin,
  4. Berlin,
  5. Braunschweig,
  6. Düsseldorf,
  7. Essen,
  8. Flensburg,
  9. Fulda,
  10. Giessen,
  11. Hannover,
  12. Heidelberg,
  13. Karlsruhe,
  14. Kiel,
  15. Lebach,
  16. Magdeburg,
  17. Mainz,
  18. Oldenburg,
  19. Tübingen,
  20. Ulm,
  21. Freiburg,
  22. Bonn,
  23. Berlin,
  24. Hamburg,
ALL GENDERS
18 Years+
years
MULTIPLE SITES
Advanced Information
Descriptive Information
Brief Title  ICMJE Study of Palbociclib in MLL-rearranged Acute Leukemias
Official Title  ICMJE Phase Ib/IIa Study of Palbociclib in MLL-rearranged Acute Leukemias AMLSG 23-14/Palbo-AL-1
Brief Summary

Diagnosis: Acute myeloid leukemia; Acute lymphoblastic leukemia Age ? 18 years, no upper age limit Study drug: Palbociclib Phase Ib/IIa, open-label

  • Phase Ib: Based on previous experience with 125 mg palbociclib once daily for 21 days followed by 7 days of rest in patients with breast cancer, liposarcoma, non-small cell lung cancer, hepatocellular carcinoma, ovarian cancer, mantle-cell lymphoma, and glioblastoma, this regimen will be chosen for the first dose to be evaluated in the phase Ib. Based on a 3 + 3 modified Fibonacci design, the tolerable dose of palbociclib for the phase IIa is defined.
  • Phase IIa: single-agent palbociclib using the tolerable dose defined in the phase Ib part of the study is administered once daily for 21 days followed by 7 days of rest. Based on the optimal two-stage design of Simon, 21 patients are treated in the first stage. If results are positive, 29 additional patients will be recruited into the second stage of the study. An efficacy of the investigational therapy will be rejected in the first stage of 21 treated patients if two or less patients achieve complete remission (CR), CR with incomplete blood count recovery (CRi), partial remission (PR), or anti-leukemic effect (ALE). If three or more patients achieve CR, CRi, PR, or ALE during this first stage, the trial is intended to be continued in the second stage with a total sample size of 50 patients.

Start of recruitment: July 2015 End of recruitment: July 2017 End of study (last patient out): July 2018 The treatment duration of an individual patient is estimated to be 2-6 months, but may be unlimited in patients with sustained response ("case-by-case decision").

Observation time per patient after entry into the study (incl. treatment) is at least 12 months.

Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 1
Phase 2
Study Design  ICMJE Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE
  • Acute Myeloid Leukemia
  • Acute Lymphoblastic Leukemia
Intervention  ICMJE Drug: Palbociclib
oral, once daily (125mg, 100mg or 75mg) for 21 days
Other Name: PD-0332991-00
Study Arms  ICMJE Experimental: Palbociclib

Phase1b: 125 mg palbociclib once daily for 21 days followed by 7 days of rest; this regimen will be chosen for the first dose to be evaluated.

phase IIa: single-agent palbociclib using the tolerable dose defined in the phase Ib part of the study is administered once daily for 21 days followed by 7 days of rest.

Intervention: Drug: Palbociclib
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Recruiting
Estimated Enrollment  ICMJE
 (submitted: December 5, 2014)
50
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE July 2019
Estimated Primary Completion Date July 2019   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Patients with confirmed diagnosis of acute leukemia with MLL rearrangement according to the 2008 WHO Classification
  • Patients with MLL-rearranged leukemia who are refractory to standard induction therapy and not immediate candidates for allogeneic HSCT (bridge to transplant is allowed)
  • Patients with MLL-rearranged leukemia who relapsed after standard first-line treatment and are not immediate candidates for allogeneic HSCT (bridge to transplant is allowed)
  • Patients with newly diagnosed MLL-rearranged leukemia who are not eligible for intensive first-line therapy
  • Genetic/histologic/immunohistologic assessment in one of the central laboratories
  • Age ? 18 years, no upper age limit
  • WHO performance status of ? 2
  • No prior chemotherapy two weeks before study entry except hydroxyurea to control hyperleukocytosis
  • Non-pregnant and non-nursing. Women of child-bearing potential must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 72 hours prior to registration (WOCBP 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 months).
  • Female patients in the reproductive age and male patients must agree to avoid getting pregnant or to father a child while on therapy and for three months after the last dose of therapy.
  • Women of child-bearing potential must either commit to continued abstinence from heterosexual intercourse or begin one acceptable method of birth control (IUD, tubal ligation, or partner's vasectomy). Hormonal contraception is an inadequate method of birth control.
  • Men must agree not to father a child and must use a latex condom during any sexual contact with WOCBP while receiving therapy and for three months after therapy is stopped, even if they have undergone successful vasectomy.
  • Signed written informed consent

Exclusion Criteria:

  • Prior treatment with palbociclib
  • Performance status > 2 according to WHO criteria
  • Organ insufficiency: creatinine > 1.5 x upper normal serum level; bilirubin, AST, or AP > 2.5 x 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 cancer. 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 neurologic or psychiatric disorder interfering with ability of giving informed consent
  • Known or suspected active alcohol or drug abuse
  • Known positivity for HIV, active HAV, HBV, or HCV infection
  • Bleeding disorder unrelated to leukemia
  • Uncontrolled CNS involvement (treatment for CNS-involvement prior to inclusion is allowed)
  • QTc > 470 msec (based on the mean value of triplicate ECGs), family or personal history of long or short QT syndrome, Brugada syndrome, or known history of QTc prolongation or Torsade de Pointes
  • Uncontrolled electrolyte disorders that can aggravate the effects of a QTc-prolonging drug (e.g., hypocalcemia, hypokalemia, hypomagnesemia)
  • No consent for registration, storage, and processing of individual disease characteristics, information on the course of the disease, and information obtained from the family physician and/or other physicians involved in the treatment of the patient about study participation
  • No consent for biobanking
Sex/Gender  ICMJE
Sexes Eligible for Study:All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE
Listed Location Countries  ICMJE Germany
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT02310243
Other Study ID Numbers  ICMJE AMLSG 23-14
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Peter Paschka, University of Ulm
Study Sponsor  ICMJE University of Ulm
Collaborators  ICMJE
  • Pfizer
  • National Center for Tumor Diseases, Heidelberg
Investigators  ICMJE Not Provided
PRS Account University of Ulm
Verification Date April 2019

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP