Ponatinib - Frontline for Chronic Myeloid Leukemia (CML) in Accelerated Phase (AP)
Study Details
Study Description
Brief Summary
The goal of this clinical research study is to learn if ponatinib can help to control Chronic Myeloid Leukemia (CML) in accelerated phase. The safety of this drug will also be studied.
Ponatinib is designed to block the function of BCR-ABL, which is the abnormal protein responsible for causing leukemia in certain cells.
Ponatinib may cause a blood clot to form in an artery or in a vein. Depending on the location of the clot, this could cause a heart attack, a stroke, severe damage to other tissue, or death. A blood clot may occur within 2 weeks after you start taking the drug. About 25% (1 in 4) of patients taking the drug form an abnormal clot. Blood clots can occur in patients that do not have other known risk factors for forming clots. If you develop a blood clot, you will need to stop taking ponatinib. In some cases, emergency surgery could be needed to remove the clot and restore blood flow.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
Phase 2 |
Detailed Description
Study Drug Administration:
You will take ponatinib by mouth 1 time every day while you are on study with about a cup (8 ounces) of water. You should not eat within 2 hours before or after taking the drug. You will complete a study diary in which you will record the date and time that you take the study drug each time. If you miss any doses, you will also note this in the study diary. Bring this diary to every study visit, as described below.
Study Visits:
The tests and procedures for this study have a wide range of time in which they can be done.
In general, your schedule of study visits will be as follows:
-
Weekly in Month 1
-
Monthly in Year 1
-
Three (3) to 4 times in Year 2
-
Two (2) to 3 times in every year after that
The study staff will help you schedule your study visits. The following tests and procedures will be performed:
-
Every 1-2 weeks for the first 4 weeks, then every 4-6 weeks for the first year, then every 3-4 months for the next year, then every 4-6 months after that, blood (about 1/2 tablespoon) will be drawn for routine tests.
-
Every 3 months for the first year, you will have an ECG.
-
Every 3 months for the first year, then every 6-12 months after that, you will have a physical exam.
-
Every 3-4 months for the first year, then every 6-12 months after that, blood (about 2 teaspoons) will be drawn to measure levels of leukemia cells in your body.
-
Every 3-4 months for the first year, then every 6-12 months for the next 2 years, then every 2-3 years after that, you will have a bone marrow aspirate for genetic testing and to check the status of the disease.
Length of Participation:
You may continue taking the study drug for up to 5 years. You will be taken off study early if intolerable side effects occur, if the disease gets worse, or if you are unable to follow study directions.
Your participation on the study will be over when you have completed the follow-up visit/call.
Follow-Up:
If you leave the study, you will be called or you will come to the clinic within 30 days to learn about any side effects or symptoms you may be having. If you are called, this call will last about 2-3 minutes.
This is an investigational study. Ponatinib is FDA approved to treat patients with certain types of leukemia. Its use in this study is investigational.
Up to 80 patients will take part in this study. All will be enrolled at MD Anderson.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Ponatinib 45 mg Ponatinib at a dose of 45 mg orally, once daily. If a dose is missed or vomited, the next dose should not be increased to account for missing a dose. Total duration of therapy 3 to 5 years. |
Drug: Ponatinib
Starting dose: 45 mg by mouth once daily.
Other Names:
|
Experimental: Ponatinib 30 mg Ponatinib at a dose of 30 mg orally, once daily. If a dose is missed or vomited, the next dose should not be increased to account for missing a dose. Total duration of therapy 3 to 5 years. |
Drug: Ponatinib
Starting dose: 45 mg by mouth once daily.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Number of Participants With Complete Cytogenetic Response (CCyR) [6 months]
Proportion of participants with previously-untreated accelerated phase CML attaining complete cytogenetic response (CCyR) at 6 months of treatment with Ponatinib classified according to suppression of the Philadelphia chromosome (Ph) by cytogenetics (FISH if cytogenetic analysis not informative, e.g., insufficient metaphases). CCyR defined as Ph positive 0%.
- Number of Participants With Complete Cytogenetic Response (CCyR) [Up to 24 months]
Proportion of participants with previously-untreated accelerated phase CML receiving treatment of Ponatinib achieving a Complete cytogenetic response (CCyR). Classified according to suppression of the Philadelphia chromosome (Ph) by cytogenetics (FISH if cytogenetic analysis not informative, e.g., insufficient metaphases. CCyR is defined as Ph positive 0%.
Secondary Outcome Measures
- Toxicity Profile: Most Common Grade 3-4 Non-Hematologic Adverse Events (AEs) Seen in More Than 1 Participant [3 months]
Time to toxicity monitoring defined as any grade 3 or 4 drug-related non-hematologic adverse event that has not resolved to grade 2 or less after 6 weeks of optimal therapeutic management, or drug-related toxicity of any grade that in the opinion of the investigator prevents further therapy with ponatinib. Time to toxicity monitored using the Bayesian method of Thall, et al.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Diagnosis of Ph-positive (by cytogenetics or FISH) or Bcr-ABL-positive (by PCR) CML with accelerated phase features at the time of diagnosis.
-
Patients must have received no or minimal prior therapy, defined as </=1 month of prior IFN-α (with or without ara-C) and/or an FDA-approved tyrosine kinase inhibitor (e.g, dasatinib, nilotinib). Prior use of hydroxyurea or anagrelide is allowed with no limitations.
-
Age >/=18 years
-
Eastern Cooperative Oncology Group (ECOG) performance of 0-2.
-
Adequate end organ function, defined as the following: total bilirubin <1.5x upper limit of normal (ULN), serum glutamate pyruvate transaminase (SGPT) <2.5x ULN,creatinine clearance (CrCl) >/= 30 mL/min at screening (calculation according to Cockcroft & Gault formula).
-
Patients must sign an informed consent indicating they are aware of the investigational nature of this study, in keeping with the policies of the hospital.
-
Women of pregnancy potential must practice an effective method of birth control during the course of the study, in a manner such that risk of failure is minimized. Prior to study enrollment, women of childbearing potential (WOCBP) must be advised of the importance of avoiding pregnancy during trial participation and the potential risk factors for an unintentional pregnancy. Postmenopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential. In addition, men enrolled on this study should understand the risks to any sexual partner of childbearing potential and should practice an effective method of birth control. Adequate forms of contraception are barrier methods (e.g., condoms, diaphragm), oral, depo provera, or injectable contraceptives, intrauterine devices, spermicidal jelly or foam, abstinence, and tubal ligation. Women and men must continue birth control for the duration of the trial & at least 3 months after the last dose of study drug.
-
**continued from above: All WOCBP MUST have a negative serum or urine pregnancy test within 7 days prior to first receiving investigational product. If the pregnancy test is positive, the patient must not receive investigational product and must not be enrolled in the study.
Exclusion Criteria:
-
NYHA cardiac class 3-4 heart disease
-
Cardiac Symptoms: Patients meeting the following criteria are not eligible: History of unstable angina, myocardial infarction, transient ischemic attack (TIA), stroke, peripheral arterial occlusive disease, venous thromboembolism or pulmonary embolism; Any history of clinically significant ventricular arrhythmias (such as ventricular tachycardia, ventricular fibrillation, or Torsades de pointes); Prolonged corrected QT interval (QTc) interval on pre-entry electrocardiogram (> 470 msec) on both the Fridericia and Bazett's correction; Symptomatic congestive heart failure within 3 months prior to first dose of ponatinib (NYHA class III or IV).
-
Patients with active, uncontrolled psychiatric disorders including: psychosis, major depression, and bipolar disorders.
-
Pregnant or breast-feeding women are excluded.
-
Patients with uncontrolled hypertension (defined as sustained stage 2 hypertension, i.e., systolic BP >/=160 mmHg or diastolic BP >/=100 mmHg).
-
Patients with history of pancreatitis.
-
Patients in late chronic phase (i.e., time from diagnosis to treatment >6 months), or blast phase are excluded. The definitions of CML phases are as follows: A. Early chronic phase: time from diagnosis to therapy </= 6 months; B. Late chronic phase: time from diagnosis to therapy > 6 months; C. Blastic phase: presence of 30% blasts or more in the peripheral blood or bone marrow; D. Accelerated phase CML: presence of any of the following features: Peripheral or marrow blasts 15% or more; Peripheral or marrow basophils 20% or more; Thrombocytopenia < 100 x 10(9)/L unrelated to therapy; Documented extramedullary blastic disease outside liver or spleen.
-
**continued from above: E. Clonal evolution defined as the presence of additional chromosomal abnormalities other than the Ph chromosome has been historically been included as a criterion for accelerated phase. However, patients with clonal evolution as the only criterion of accelerated phase have a significantly better prognosis, and when present at diagnosis may not impact the prognosis at all. Thus, patients with clonal evolution and no other criteria for accelerated phase will be eligible for this study.
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | University of Texas MD Anderson Cancer Center | Houston | Texas | United States | 77030 |
Sponsors and Collaborators
- M.D. Anderson Cancer Center
- Ariad Pharmaceuticals
Investigators
- Principal Investigator: Jorge Cortes, MD, M.D. Anderson Cancer Center
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 2012-0074
- NCI-2012-00572
Study Results
Participant Flow
Recruitment Details | Recruitment period: April 27, 2012 to May 12, 2015. All recruitment done at The University of Texas MD Anderson Cancer Center. |
---|---|
Pre-assignment Detail | Study terminated early. |
Arm/Group Title | Ponatinib 45 mg | Ponatinib 30 mg |
---|---|---|
Arm/Group Description | Ponatinib 45 mg orally, once daily. | Ponatinib 30 mg orally, once daily. |
Period Title: Overall Study | ||
STARTED | 43 | 8 |
COMPLETED | 0 | 0 |
NOT COMPLETED | 43 | 8 |
Baseline Characteristics
Arm/Group Title | Ponatinib 45 mg | Ponatinib 30 mg | Total |
---|---|---|---|
Arm/Group Description | Ponatinib 45 mg orally, once daily. | Ponatinib 30 mg orally, once daily. | Total of all reporting groups |
Overall Participants | 43 | 8 | 51 |
Age (years) [Median (Full Range) ] | |||
Median (Full Range) [years] |
52
|
42
|
43
|
Sex: Female, Male (Count of Participants) | |||
Female |
19
44.2%
|
5
62.5%
|
24
47.1%
|
Male |
24
55.8%
|
3
37.5%
|
27
52.9%
|
Region of Enrollment (Count of Participants) | |||
United States |
43
100%
|
8
100%
|
51
100%
|
Outcome Measures
Title | Number of Participants With Complete Cytogenetic Response (CCyR) |
---|---|
Description | Proportion of participants with previously-untreated accelerated phase CML attaining complete cytogenetic response (CCyR) at 6 months of treatment with Ponatinib classified according to suppression of the Philadelphia chromosome (Ph) by cytogenetics (FISH if cytogenetic analysis not informative, e.g., insufficient metaphases). CCyR defined as Ph positive 0%. |
Time Frame | 6 months |
Outcome Measure Data
Analysis Population Description |
---|
[Not Specified] |
Arm/Group Title | Ponatinib 45 mg | Ponatinib 30 mg |
---|---|---|
Arm/Group Description | Ponatinib 45 mg orally, once daily. Dose escalation to 30 mg possible for participants with adverse events. | Ponatinib 30mg orally, once daily. Dose escalation to 30 mg possible for participants with adverse events. |
Measure Participants | 42 | 8 |
Count of Participants [Participants] |
40
93%
|
3
37.5%
|
Title | Number of Participants With Complete Cytogenetic Response (CCyR) |
---|---|
Description | Proportion of participants with previously-untreated accelerated phase CML receiving treatment of Ponatinib achieving a Complete cytogenetic response (CCyR). Classified according to suppression of the Philadelphia chromosome (Ph) by cytogenetics (FISH if cytogenetic analysis not informative, e.g., insufficient metaphases. CCyR is defined as Ph positive 0%. |
Time Frame | Up to 24 months |
Outcome Measure Data
Analysis Population Description |
---|
[Not Specified] |
Arm/Group Title | Ponatinib 45 mg | Ponatinib 30 mg |
---|---|---|
Arm/Group Description | Ponatinib 45 mg orally, once daily. | Ponatinib 30 mg orally, once daily. |
Measure Participants | 42 | 8 |
Count of Participants [Participants] |
42
97.7%
|
6
75%
|
Title | Toxicity Profile: Most Common Grade 3-4 Non-Hematologic Adverse Events (AEs) Seen in More Than 1 Participant |
---|---|
Description | Time to toxicity monitoring defined as any grade 3 or 4 drug-related non-hematologic adverse event that has not resolved to grade 2 or less after 6 weeks of optimal therapeutic management, or drug-related toxicity of any grade that in the opinion of the investigator prevents further therapy with ponatinib. Time to toxicity monitored using the Bayesian method of Thall, et al. |
Time Frame | 3 months |
Outcome Measure Data
Analysis Population Description |
---|
One participant was not included in analysis. |
Arm/Group Title | Ponatinib 45 mg | Ponatinib 30 mg |
---|---|---|
Arm/Group Description | Ponatinib oral dose 45 mg daily. | Ponatinib oral dose 30 mg daily. |
Measure Participants | 43 | 8 |
Elevated Amylase |
2
4.7%
|
0
0%
|
Lipase Elevation |
15
34.9%
|
1
12.5%
|
Pancreatitis |
7
16.3%
|
2
25%
|
Abdominal Pain |
1
2.3%
|
0
0%
|
Hypertension |
3
7%
|
0
0%
|
Elevated alanine aminotransferase (ALT) |
2
4.7%
|
0
0%
|
Adverse Events
Time Frame | Adverse event collection minimally every 4 weeks for total duration of therapy up to one year, study collection period to be 3 to 5 years. | |||
---|---|---|---|---|
Adverse Event Reporting Description | ||||
Arm/Group Title | Ponatinib 45 mg | Ponatinib 30 mg | ||
Arm/Group Description | Ponatinib 45 mg orally, once daily. | Ponatinib 30 mg orally, once daily. | ||
All Cause Mortality |
||||
Ponatinib 45 mg | Ponatinib 30 mg | |||
Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
Total | / (NaN) | / (NaN) | ||
Serious Adverse Events |
||||
Ponatinib 45 mg | Ponatinib 30 mg | |||
Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
Total | 17/43 (39.5%) | 3/8 (37.5%) | ||
Blood and lymphatic system disorders | ||||
Anemia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Febrile neutropenia | 0/43 (0%) | 0 | 1/8 (12.5%) | 1 |
Cardiac disorders | ||||
Acute Coronary Syndrome | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Chest Pain | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Myocardial infarction | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Gastrointestinal disorders | ||||
abdominal pain | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Colitis | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Diarrhea | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Pancreatitis | 7/43 (16.3%) | 10 | 2/8 (25%) | 2 |
General disorders | ||||
Fever | 1/43 (2.3%) | 2 | 0/8 (0%) | 0 |
Non-Cardiac chest pain | 1/43 (2.3%) | 2 | 0/8 (0%) | 0 |
Infections and infestations | ||||
Infections and infestations-Other | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Lung Infection | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Pelvic infection | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Surgical and medical procedures - Other, Hysterectomy | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Urinary tract infection | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Metabolism and nutrition disorders | ||||
Hyperglycemia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Hypoglycemia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Nervous system disorders | ||||
Seizure | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Stroke | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Transient ischemic attacks | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Renal and urinary disorders | ||||
Acute kidney injury | 0/43 (0%) | 0 | 1/8 (12.5%) | 1 |
Vascular disorders | ||||
Hypertension | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Vaso-Occulusive diasease | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Bialteral superfical femoral artery occulsion | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Peripheral vascular disease | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Other (Not Including Serious) Adverse Events |
||||
Ponatinib 45 mg | Ponatinib 30 mg | |||
Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
Total | 35/43 (81.4%) | 6/8 (75%) | ||
Blood and lymphatic system disorders | ||||
Anemia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Febrile neutropenia | 0/43 (0%) | 0 | 1/8 (12.5%) | 1 |
Cardiac disorders | ||||
Acute Coronary Syndrome | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Cardiac Disorders other | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Chest Pain | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Myocardial Infarction | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Ear and labyrinth disorders | ||||
Tinnitus | 0/43 (0%) | 0 | 1/8 (12.5%) | 1 |
Endocrine disorders | ||||
Endocrine disorders | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Hypothyroidism | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Eye disorders | ||||
Dry eye | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Gastrointestinal disorders | ||||
Abdominal Pain | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Colitis | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Diarrhea | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Dyspepsia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Pancreatitis | 7/43 (16.3%) | 7 | 2/8 (25%) | 2 |
Pelvic infection | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
General disorders | ||||
Fever | 2/43 (4.7%) | 3 | 0/8 (0%) | 0 |
Non-cardiac chest pain | 1/43 (2.3%) | 2 | 0/8 (0%) | 0 |
Pain | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Infections and infestations | ||||
Infection other | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Urinary tract infection | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Injury, poisoning and procedural complications | ||||
Fracture | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Injury, poisoning and procedural complications | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Investigations | ||||
Increased Alanine aminotransferase | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Increased amylase | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Increased Aspartate aminotransferase | 1/43 (2.3%) | 2 | 0/8 (0%) | 0 |
Increased GGT | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Increased Lipase | 10/43 (23.3%) | 15 | 1/8 (12.5%) | 1 |
Weight gain | 3/43 (7%) | 3 | 1/8 (12.5%) | 1 |
Metabolism and nutrition disorders | ||||
Dehydration | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Hyperglycemia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Hypoglycemia | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Musculoskeletal and connective tissue disorders | ||||
Bone pain | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
decreased range of motion, joint | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Musculoskeletal and connective tissue disorder | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Nervous system disorders | ||||
Cognitive disturbance | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Dysesthesia | 0/43 (0%) | 0 | 1/8 (12.5%) | 1 |
Memory impairment | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Nervous system disorders | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Peripheral sensory neuropathy | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Stroke | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Transient ischemic attacks | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Psychiatric disorders | ||||
Anxiety | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Decreased libido | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Depression | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Renal and urinary disorders | ||||
Acute Kidney Injury | 0/43 (0%) | 0 | 1/8 (12.5%) | 1 |
Renal and urinary disorders | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Reproductive system and breast disorders | ||||
Reproductive system and breast disorders | 2/43 (4.7%) | 2 | 1/8 (12.5%) | 1 |
Respiratory, thoracic and mediastinal disorders | ||||
Lung infection | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Skin and subcutaneous tissue disorders | ||||
Dry Skin | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Erythroderma | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Skin and subcutaneous tissue disorder | 2/43 (4.7%) | 2 | 0/8 (0%) | 0 |
Skin hyperpigmentation | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Rash Acneiform | 1/43 (2.3%) | 1 | 0/8 (0%) | 0 |
Surgical and medical procedures | ||||
Surgical and medical procedures | 5/43 (11.6%) | 5 | 0/8 (0%) | 0 |
Vascular disorders | ||||
Hypertension | 3/43 (7%) | 3 | 0/8 (0%) | 0 |
Vascular disorders | 3/43 (7%) | 3 | 0/8 (0%) | 0 |
Limitations/Caveats
More Information
Certain Agreements
All Principal Investigators ARE employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
Results Point of Contact
Name/Title | Jorge Cortes, MD/Professor, Leukemia |
---|---|
Organization | The University of Texas (UT) MD Anderson Cancer Center |
Phone | 713-792-7734 |
CR_Study_Registration@mdanderson.org |
- 2012-0074
- NCI-2012-00572