Higher or Lower Dose Cladribine, Cytarabine, and Mitoxantrone in Treating Medically Less Fit Patients With Newly Diagnosed Acute Myeloid Leukemia or Myeloid Neoplasm
Study Details
Study Description
Brief Summary
This randomized pilot trial studies how well higher or lower dose cladribine, cytarabine, and mitoxantrone work in treating medically less fit patients with newly diagnosed acute myeloid leukemia or myeloid neoplasm. Drugs used in chemotherapy, such as cladribine, cytarabine, and mitoxantrone, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether giving cladribine, cytarabine, and mitoxantrone at higher or lower dose may work better in treating patients with newly diagnosed acute myeloid leukemia.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
PRIMARY OBJECTIVES:
- To evaluate the feasibility of randomizing medically less fit adults with newly diagnosed acute myeloid leukemia (AML) or analogous myeloid neoplasms to either intensive or non-intensive induction and post remission chemotherapy.
EXPLORATORY OBJECTIVES:
-
To evaluate the attitude of patients and physicians toward randomization and explore reasons for treatment preference.
-
To evaluate whether the ability to assess fitness for intensive chemotherapy can be improved by an augmented treatment-related mortality (TRM) score that includes additional (co-morbidity) factors, and to compare the ability of physicians and the prediction algorithm(s) to assess the likelihood of early death.
-
To compare, within the limits of a pilot study, response, duration of response, and survival between patients receiving intensive and those receiving non-intensive chemotherapy.
-
To describe the impact of treatment intensity on quality of life of patients undergoing chemotherapy for newly diagnosed AML.
-
To describe the impact of treatment intensity on medical resource utilization and care cost of patients undergoing chemotherapy for newly diagnosed AML.
OUTLINE: Patients agreeable to randomization are randomized to 1 of 2 treatment arms. Patients not agreeable to randomization receive treatment based on their preference.
ARM I (HIGHER-DOSE):
INDUCTION: Patients receive granulocyte colony-stimulating factor (G-CSF) subcutaneously (SC) on days 0-5, higher dose cladribine intravenously (IV) over 2 hours on days 1-5, higher dose cytarabine IV over 2 hours on days 1-5, and higher dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity.
CONSOLIDATION: Patients who achieve complete response (CR)/CR with incomplete count recovery (CRi) with up to 2 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity.
ARM II (LOWER-DOSE):
INDUCTION: Patients receive G-CSF SC on days 0-5, lower dose cladribine IV over 2 hours on days 1-5, lower dose cytarabine IV over 1 hour on days 1-5, and lower dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity.
CONSOLIDATION: Patients who achieve complete response (CR)/CR with incomplete count recovery (CRi) with up to 6 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up periodically for 5 years.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Arm I (higher-dose) INDUCTION: Patients receive G-CSF SC on days 0-5, higher dose cladribine IV over 2 hours on days 1-5, higher dose cytarabine IV over 2 hours on days 1-5, and higher dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve CR/CRi with up to 2 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. |
Drug: Cladribine
Given IV
Other Names:
Drug: Cytarabine
Given IV
Other Names:
Biological: Granulocyte Colony-Stimulating Factor
Given SC
Other Names:
Drug: Mitoxantrone Hydrochloride
Given IV
Other Names:
Other: Quality-of-Life Assessment
Ancillary studies
Other Names:
Other: Questionnaire Administration
Ancillary studies
|
| Experimental: Arm II (lower-dose) INDUCTION: Patients receive G-CSF SC on days 0-5, lower dose cladribine IV over 2 hours on days 1-5, lower dose cytarabine IV over 1 hour on days 1-5, and lower dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve CR/CRi with up to 6 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
Drug: Cladribine
Given IV
Other Names:
Drug: Cytarabine
Given IV
Other Names:
Biological: Granulocyte Colony-Stimulating Factor
Given SC
Other Names:
Drug: Mitoxantrone Hydrochloride
Given IV
Other Names:
Other: Quality-of-Life Assessment
Ancillary studies
Other Names:
Other: Questionnaire Administration
Ancillary studies
|
Outcome Measures
Primary Outcome Measures
- Feasibility Defined as Proportion of Patients Willing to be Randomized to Either Intensive or Non-intensive Induction and Post Remission Chemotherapy [At end of enrollment]
Randomizing patients to either intensive or non-intensive induction and post remission chemotherapy will be considered feasible if the true proportion of patients willing to be randomized is 60% or higher.
Other Outcome Measures
- Event-free Survival [Up to 5 years]
Will be determined by peripheral blood count and bone marrow evaluation and categorized according to criteria recommended by International Working Groups.
- Medical Complications [Up to 5 years]
Information on medical complications (e.g. need for intensive care unit (ICU) level care, length of ICU stay, neutropenic fever, documented infections, bleeding, reasons for hospitalization) will be collected from the medical records from the University of Washington Medical Center (UWMC) and Seattle Cancer Care Alliance (SCCA).
- Medical Resource Utilization [Up to 5 years]
Information on use of medical resources (e.g. platelet transfusions; days of IV antimicrobial therapy, total hospital length of stay) will be collected from the medical records from the University of Washington Medical Center (UWMC) and Seattle Cancer Care Alliance (SCCA).
- Overall Survival [Up to 5 years]
Will be assessed for all patients. Will be determined by peripheral blood count and bone marrow evaluation and categorized according to criteria recommended by International Working Groups.
- Quality of Life as Measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30 [Up to 12 months]
Will be measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30. Exploratory, descriptive, and observational methods will be used.
- Relapse-free Survival [Up to 5 years]
Will be determined by peripheral blood count and bone marrow evaluation and categorized according to criteria recommended by International Working Groups.
- Response [Up to 5 years]
The differences in anti-leukemic efficacy between patients treated with lower-intensity chemotherapy and those treated with higher-intensity chemotherapy will be estimated. Exploratory, descriptive, and observational methods will be used.
- Fitness for Intensive Chemotherapy as Measured by a Treatment-related Mortality (TRM) Score That Includes Additional Co-morbidity Factors [Up to 12 months]
The ability of physicians and the prediction algorithm(s) to assess the likelihood of early death will be compared.
- Duration of Response [Up to 5 years]
Will be evaluated.
- Care Costs [Up to 5 years]
The costs associated with inpatient and outpatient management will be calculated using electronic billing information from the University of Washington Medical Center (UWMC) and Seattle Cancer Care Alliance (SCCA). Costs will be converted from charges using departmental cost-to-charge ratios. Descriptive information identifying major cost drivers and total/subset costs per phase of treatment will be reported.
- Attitude of Patients Toward Randomization [Up to 12 months]
Will be determined by a patient preference survey. Exploratory, descriptive, and observational methods will be used.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Diagnosis of untreated "high-grade" myeloid neoplasm (>= 10% myeloid blasts by morphology in bone marrow and/or peripheral blood) or AML other than acute promyelocytic leukemia (APL) with t(15;17)(q22;q12) or variants according to the 2016 World Health Organization (WHO) classification; patients with acute leukemias of ambiguous lineage are eligible; outside diagnostic material is acceptable as long as peripheral blood and/or bone marrow slides are reviewed at the study institution and cytogenetic/molecular information is available
-
Treatment-related mortality (TRM) score >= 13.1 as calculated with simplified model
-
The use of hydroxyurea before enrollment is permitted; hydroxyurea should be discontinued prior to start of study treatment. Patients with symptoms/signs of leukostasis, white blood cell (WBC) > 100,000/uL, or acute symptoms felt related to their high-grade myeloid neoplasm can be treated with leukapheresis or may receive up to 1 dose of cytarabine (up to 500 mg/m^2) anytime prior to study day 1
-
Patients may have received treatment (e.g. azacitidine/decitabine, lenalidomide, growth factors) for antecedent low-grade myeloid neoplasm
-
Left ventricular ejection fraction (LVEF) >= 45%, assessed within 3 months prior to registration, e.g. by multigated acquisition (MUGA) scan or echocardiography, or other appropriate diagnostic modality
-
Women of childbearing potential and men must agree to use adequate contraception beginning at the signing of the consent until at least 4 weeks after the last dose of study drug
-
Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
-
Myeloid blast crisis of chronic myeloid leukemia (CML), unless patient is not considered candidate for tyrosine kinase inhibitor treatment
-
Concomitant illness associated with a likely survival of < 1 year
-
Active systemic fungal, bacterial, viral, or other infection, unless disease is under treatment with anti-microbials and/or controlled or stable; patients with fever thought to be likely secondary to leukemia are eligible; known hypersensitivity to any study drug
-
Known hypersensitivity to any study drug used in this trial
-
Pregnancy or lactation
-
Concurrent treatment with any other anti-leukemia agent
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Fred Hutch/University of Washington Cancer Consortium | Seattle | Washington | United States | 98109 |
Sponsors and Collaborators
- University of Washington
- National Cancer Institute (NCI)
Investigators
- Principal Investigator: Anna Halpern, Fred Hutch/University of Washington Cancer Consortium
Study Documents (Full-Text)
More Information
Publications
None provided.- 9759
- NCI-2016-02051
- 9759
- P30CA015704
- RG9217016
Study Results
Participant Flow
| Recruitment Details | |
|---|---|
| Pre-assignment Detail |
| Arm/Group Title | Arm I (Higher-dose) | Arm II (Lower-dose) |
|---|---|---|
| Arm/Group Description | INDUCTION: Patients receive G-CSF SC on days 0-5, higher dose cladribine IV over 2 hours on days 1-5, higher dose cytarabine IV over 2 hours on days 1-5, and higher dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve CR/CRi with up to 2 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. | INDUCTION: Patients receive G-CSF SC on days 0-5, lower dose cladribine IV over 2 hours on days 1-5, lower dose cytarabine IV over 1 hour on days 1-5, and lower dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve CR/CRi with up to 6 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. |
| Period Title: Overall Study | ||
| STARTED | 20 | 30 |
| COMPLETED | 20 | 30 |
| NOT COMPLETED | 0 | 0 |
Baseline Characteristics
| Arm/Group Title | ARM I (HIGHER-DOSE) | ARM II (LOWER-DOSE) | Total |
|---|---|---|---|
| Arm/Group Description | ARM I (HIGHER-DOSE): INDUCTION: Patients receive granulocyte colony-stimulating factor (G-CSF) subcutaneously (SC) on days 0-5, higher dose cladribine intravenously (IV) over 2 hours on days 1-5, higher dose cytarabine IV over 2 hours on days 1-5, and higher dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve complete response (CR)/CR with incomplete count recovery (CRi) with up to 2 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. | ARM II (LOWER-DOSE): INDUCTION: Patients receive G-CSF SC on days 0-5, lower dose cladribine IV over 2 hours on days 1-5, lower dose cytarabine IV over 1 hour on days 1-5, and lower dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve complete response (CR)/CR with incomplete count recovery (CRi) with up to 6 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. | Total of all reporting groups |
| Overall Participants | 20 | 30 | 50 |
| Age (years) [Median (Full Range) ] | |||
| Median (Full Range) [years] |
71.5
|
72
|
72
|
| Sex: Female, Male (Count of Participants) | |||
| Female |
8
40%
|
9
30%
|
17
34%
|
| Male |
12
60%
|
21
70%
|
33
66%
|
| Race (NIH/OMB) (Count of Participants) | |||
| American Indian or Alaska Native |
0
0%
|
0
0%
|
0
0%
|
| Asian |
0
0%
|
2
6.7%
|
2
4%
|
| Native Hawaiian or Other Pacific Islander |
0
0%
|
1
3.3%
|
1
2%
|
| Black or African American |
0
0%
|
2
6.7%
|
2
4%
|
| White |
19
95%
|
25
83.3%
|
44
88%
|
| More than one race |
0
0%
|
0
0%
|
0
0%
|
| Unknown or Not Reported |
1
5%
|
0
0%
|
1
2%
|
| Secondary Disease (Count of Participants) | |||
| De Novo |
10
50%
|
15
50%
|
25
50%
|
| Secondary |
10
50%
|
15
50%
|
25
50%
|
| ELN Risk Category (Count of Participants) | |||
| Favorable |
1
5%
|
3
10%
|
4
8%
|
| Intermediate |
5
25%
|
6
20%
|
11
22%
|
| Adverse |
9
45%
|
17
56.7%
|
26
52%
|
| No Classifiable |
5
25%
|
4
13.3%
|
9
18%
|
Outcome Measures
| Title | Feasibility Defined as Proportion of Patients Willing to be Randomized to Either Intensive or Non-intensive Induction and Post Remission Chemotherapy |
|---|---|
| Description | Randomizing patients to either intensive or non-intensive induction and post remission chemotherapy will be considered feasible if the true proportion of patients willing to be randomized is 60% or higher. |
| Time Frame | At end of enrollment |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title | All Patients Enrolled |
|---|---|
| Arm/Group Description | Total number of patients enrolled |
| Measure Participants | 50 |
| Patients/physician pairs agreed to be randomized |
3
15%
|
| Patients/physician pairs not agreed to be randomized |
47
235%
|
| Title | Event-free Survival |
|---|---|
| Description | Will be determined by peripheral blood count and bone marrow evaluation and categorized according to criteria recommended by International Working Groups. |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Medical Complications |
|---|---|
| Description | Information on medical complications (e.g. need for intensive care unit (ICU) level care, length of ICU stay, neutropenic fever, documented infections, bleeding, reasons for hospitalization) will be collected from the medical records from the University of Washington Medical Center (UWMC) and Seattle Cancer Care Alliance (SCCA). |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Medical Resource Utilization |
|---|---|
| Description | Information on use of medical resources (e.g. platelet transfusions; days of IV antimicrobial therapy, total hospital length of stay) will be collected from the medical records from the University of Washington Medical Center (UWMC) and Seattle Cancer Care Alliance (SCCA). |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Overall Survival |
|---|---|
| Description | Will be assessed for all patients. Will be determined by peripheral blood count and bone marrow evaluation and categorized according to criteria recommended by International Working Groups. |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Quality of Life as Measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30 |
|---|---|
| Description | Will be measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30. Exploratory, descriptive, and observational methods will be used. |
| Time Frame | Up to 12 months |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Relapse-free Survival |
|---|---|
| Description | Will be determined by peripheral blood count and bone marrow evaluation and categorized according to criteria recommended by International Working Groups. |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Response |
|---|---|
| Description | The differences in anti-leukemic efficacy between patients treated with lower-intensity chemotherapy and those treated with higher-intensity chemotherapy will be estimated. Exploratory, descriptive, and observational methods will be used. |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Fitness for Intensive Chemotherapy as Measured by a Treatment-related Mortality (TRM) Score That Includes Additional Co-morbidity Factors |
|---|---|
| Description | The ability of physicians and the prediction algorithm(s) to assess the likelihood of early death will be compared. |
| Time Frame | Up to 12 months |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Duration of Response |
|---|---|
| Description | Will be evaluated. |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Care Costs |
|---|---|
| Description | The costs associated with inpatient and outpatient management will be calculated using electronic billing information from the University of Washington Medical Center (UWMC) and Seattle Cancer Care Alliance (SCCA). Costs will be converted from charges using departmental cost-to-charge ratios. Descriptive information identifying major cost drivers and total/subset costs per phase of treatment will be reported. |
| Time Frame | Up to 5 years |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Attitude of Patients Toward Randomization |
|---|---|
| Description | Will be determined by a patient preference survey. Exploratory, descriptive, and observational methods will be used. |
| Time Frame | Up to 12 months |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
Adverse Events
| Time Frame | AEs were collected for the duration that each patient remained on protocol. If a subject decided to terminate the study early AEs continued to be collected for up to 4 weeks after the treatment was given or until they started a new anti-leukemia therapy, whichever occurred first. | |||
|---|---|---|---|---|
| Adverse Event Reporting Description | Only grade ≥3 adverse events other than hematologic toxicities were recorded, graded, and reported as appropriate. | |||
| Arm/Group Title | ARM I (HIGHER-DOSE): | ARM II (LOWER-DOSE): | ||
| Arm/Group Description | ARM I (HIGHER-DOSE): INDUCTION: Patients receive granulocyte colony-stimulating factor (G-CSF) subcutaneously (SC) on days 0-5, higher dose cladribine intravenously (IV) over 2 hours on days 1-5, higher dose cytarabine IV over 2 hours on days 1-5, and higher dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve complete response (CR)/CR with incomplete count recovery (CRi) with up to 2 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. | ARM II (LOWER-DOSE): INDUCTION: Patients receive G-CSF SC on days 0-5, lower dose cladribine IV over 2 hours on days 1-5, lower dose cytarabine IV over 1 hour on days 1-5, and lower dose mitoxantrone IV over 60 minutes on days 1-3. Treatment repeats every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients who achieve complete response (CR)/CR with incomplete count recovery (CRi) with up to 6 courses of Induction receive G-CSF, cladribine, and cytarabine as in Induction. Courses repeat every 6 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. | ||
All Cause Mortality |
||||
| ARM I (HIGHER-DOSE): | ARM II (LOWER-DOSE): | |||
| Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
| Total | 16/20 (80%) | 25/30 (83.3%) | ||
Serious Adverse Events |
||||
| ARM I (HIGHER-DOSE): | ARM II (LOWER-DOSE): | |||
| Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
| Total | 9/20 (45%) | 14/30 (46.7%) | ||
| Blood and lymphatic system disorders | ||||
| Intracranial Hemorrhage | 2/20 (10%) | 2 | 1/30 (3.3%) | 1 |
| Febrile Neutropenia | 6/20 (30%) | 8 | 7/30 (23.3%) | 13 |
| Cardiac disorders | ||||
| Atrial Fibrillation | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Right Ventricular Dysfunction | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Pericardial Effusion | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Gastrointestinal disorders | ||||
| Colonic Pseudo-Obstruction | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| General disorders | ||||
| Multi-organ failure | 1/20 (5%) | 1 | 2/30 (6.7%) | 2 |
| Generalized Edema | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Infections and infestations | ||||
| Lung Infection | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Sepsis | 1/20 (5%) | 1 | 2/30 (6.7%) | 2 |
| Metabolism and nutrition disorders | ||||
| Nausea | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Anorexia | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Nervous system disorders | ||||
| Encephalopathy | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Psychiatric disorders | ||||
| Delirium | 2/20 (10%) | 2 | 0/30 (0%) | 0 |
| Renal and urinary disorders | ||||
| Acute Kidney Injury | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Respiratory, thoracic and mediastinal disorders | ||||
| Respiratory Failure | 2/20 (10%) | 2 | 4/30 (13.3%) | 5 |
| Pneumonitis | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Hypoxia | 0/20 (0%) | 0 | 1/30 (3.3%) | 2 |
| Vascular disorders | ||||
| Hypotension | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Vascular Access Complication | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
Other (Not Including Serious) Adverse Events |
||||
| ARM I (HIGHER-DOSE): | ARM II (LOWER-DOSE): | |||
| Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
| Total | 16/20 (80%) | 30/30 (100%) | ||
| Blood and lymphatic system disorders | ||||
| Epistaxis | 0/20 (0%) | 0 | 2/30 (6.7%) | 2 |
| Febrile Neutropenia | 9/20 (45%) | 10 | 15/30 (50%) | 21 |
| Tumor Lysis Syndrome | 3/20 (15%) | 3 | 1/30 (3.3%) | 1 |
| Cardiac disorders | ||||
| Atrial Fibrillation | 2/20 (10%) | 3 | 1/30 (3.3%) | 1 |
| Edema Limbs, Volume Overload | 2/20 (10%) | 2 | 2/30 (6.7%) | 2 |
| Cardiac Troponin I Increased | 3/20 (15%) | 4 | 2/30 (6.7%) | 2 |
| Hypertension | 1/20 (5%) | 1 | 1/30 (3.3%) | 1 |
| Hypotension | 1/20 (5%) | 1 | 3/30 (10%) | 3 |
| Paroxysmal Atrial Tachycardia | 1/20 (5%) | 1 | 1/30 (3.3%) | 1 |
| Pericardial Effusion | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Pericarditis | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Restrictive Cardiomyopathy | 0/20 (0%) | 0 | 2/30 (6.7%) | 2 |
| Ear and labyrinth disorders | ||||
| Blood Clot, Right Ear | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Eye disorders | ||||
| Optic Nerve Disorder | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Gastrointestinal disorders | ||||
| Nausea | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| General disorders | ||||
| Generalized Edema | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Infections and infestations | ||||
| Bacteremia | 5/20 (25%) | 5 | 4/30 (13.3%) | 6 |
| Catheter Related Infection | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Lung Infection | 1/20 (5%) | 1 | 4/30 (13.3%) | 5 |
| Soft Tissue Infection | 2/20 (10%) | 2 | 3/30 (10%) | 3 |
| Urinary Tract Infection | 2/20 (10%) | 3 | 4/30 (13.3%) | 4 |
| Mucositis | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Investigations | ||||
| AST/ALT Elevation | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Blood Bilirubin Increased | 2/20 (10%) | 2 | 1/30 (3.3%) | 1 |
| Ejection Fraction Decreased | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Metabolism and nutrition disorders | ||||
| Alkalosis | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Anorexia | 1/20 (5%) | 1 | 1/30 (3.3%) | 1 |
| Hyperglycemia | 3/20 (15%) | 3 | 2/30 (6.7%) | 2 |
| Hypokalemia | 1/20 (5%) | 1 | 1/30 (3.3%) | 2 |
| Hyponatremia | 1/20 (5%) | 1 | 1/30 (3.3%) | 1 |
| Nervous system disorders | ||||
| Headache | 2/20 (10%) | 2 | 2/30 (6.7%) | 2 |
| Psychiatric disorders | ||||
| Delirium | 2/20 (10%) | 2 | 1/30 (3.3%) | 1 |
| Renal and urinary disorders | ||||
| Acute Kidney Injury | 1/20 (5%) | 2 | 2/30 (6.7%) | 2 |
| Respiratory, thoracic and mediastinal disorders | ||||
| Dyspnea | 1/20 (5%) | 1 | 1/30 (3.3%) | 1 |
| Bronchopulmonary Hemorrhage | 1/20 (5%) | 1 | 0/30 (0%) | 0 |
| Hypoxia | 4/20 (20%) | 5 | 9/30 (30%) | 9 |
| Pleural Effusion | 0/20 (0%) | 0 | 1/30 (3.3%) | 1 |
| Pulmonary Edema | 2/20 (10%) | 3 | 8/30 (26.7%) | 8 |
| COPD Exacerbation | 2/20 (10%) | 2 | 1/30 (3.3%) | 1 |
| Skin and subcutaneous tissue disorders | ||||
| Rash Maculo-Papular | 4/20 (20%) | 4 | 4/30 (13.3%) | 4 |
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 | Anna Halpern, MD |
|---|---|
| Organization | University of Washington |
| Phone | 206-606-1978 |
| halpern2@uw.edu |
- 9759
- NCI-2016-02051
- 9759
- P30CA015704
- RG9217016