Melanoma, Neoplasm Metastasis
Conditions
Keywords
Immunotherapy, Adoptive Transfer, IL-2, Toxicity, Clinical Response, Breast Cancer
Brief summary
This experiment will test the safety and effectiveness of a treatment for melanoma in which certain lymphocytes (a type of white blood cell) are taken from the patient, grown in the laboratory, and returned after the patient's immune system has been weakened with immune-suppressing drugs. Some patients will also receive interleukin-2 (IL-2), a drug that may enhance the activity of the re-infused lymphocytes. Patients with metastatic melanoma (melanoma whose tumor has spread) who have been treated unsuccessfully with gp100 vaccination may participate in this study. They will undergo apheresis or a tumor biopsy, or both, to collect lymphocytes. In apheresis, whole blood is drawn through a needle in the arm. A machine separates the blood components and removes the white cells. The rest of the blood is returned to the donor through a needle in the other arm. A biopsy is a surgical procedure to remove a small piece of tumor tissue. Several weeks before the lymphocytes are collected, patients will receive injections of growth colony stimulating factor (G-CSF) every day for five days. This drug stimulates white cell production, permitting as many cells as possible to be obtained during collection. The lymphocytes will then be grown in larger numbers in the laboratory. Seven days before the cells are re-infused, the patient is admitted to the hospital and a catheter (small tube) is placed in a large vein in the chest or neck. Two drugs, cyclophosphamide and fludarabine, are given through the tube. These drugs suppress the immune system so that it will not interfere with the work of the reinfused lymphocytes. The lymphocytes are then injected through the catheter over a 30-minute period. After the infusion, patients who receive IL-2 will be given the drug in a high dose over a 15-minute period every eight hours for up to five days. Patients whose condition does not permit high-dose IL-2, such as those with a heart condition or lung problem, may receive a low-dose regimen, with the drug given as a shot under the skin of the thigh or abdomen for five days followed by a 2-day break, continuing for a total of six weeks. These patients receive a higher dose the first week and then half that dose the next five weeks. Blood and tissue samples will be taken before and during the study to evaluate the size of the tumor and assess treatment. If, 3-5 weeks after therapy is completed, the patient's tumor has stabilized or shrunk, the entire treatment, except for chemotherapy, may be repeated two more times.
Detailed description
Patients with metastatic melanoma who are human immunodeficiency virus (HIV) and Hepatitis B negative and who have previously progressed after receiving standard therapy will receive a nonmyeloablative but lymphocyte depleting preparative regimen consisting of cyclophosphamide and fludarabine and then will be treated by the adoptive transfer of lymphocytes reactive with shared antigens on their tumors. This study will evaluate the toxicity, immunologic effects and potential therapeutic role of this treatment.
Interventions
gp100 = gp100:209-217(210M) peptide - 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus gp100:209-217(210M) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections. MART-1 = MART-1:26-35(27L) peptide- 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus MART-1:26-35(27L) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections.
MART-1 = MART-1:26-35(27L) peptide- 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus MART-1:26-35(27L) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections.
125,000 IU/kg dose intravenous for 5 days for 6 weeks with 2 days rest per week. 720,000 IU/kg intravenous every 8 hours for a maximum of 12 doses.
MART-1 = MART-1:26-35(27L) peptide- 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus MART-1:26-35(27L) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections.
Abl cells IV = Lymphocytes 10\^9-10\^11 IV over 30 minutes on day 0, repeated in 14 to 21 days Abl cells IA = Lymphocytes 10\^9-10\^11 IA over 30 minutes on day 0, repeated in 14 to 21 days
5x25 mg/m\^2 intravenous
2x30 mg/kg, 2x60 mg/kg intravenous
Beginning on day 1 or 2, GCSF will be administered subcutaneously at a dose of 5mcg/kg/day (not to exceed 300 mcg/day. Filgrastim administration will continue daily until neutrophil count \> 1.0 x10\^9/L x 3 days or \> 5.0 x10\^9/L.
Sponsors
Study design
Eligibility
Inclusion criteria
* INCLUSION CRITERIA * Patients must have evaluable metastatic melanoma that is refractory to standard therapy. * Age greater than or equal to 16 years. * Patients of both genders must be willing to practice birth control for four months after receiving the preparative regimen. * Clinical performance status of Eastern Cooperative Oncology Group (ECOG) 0, 1 at entry to the trial and at the time of chemotherapy induction. * Absolute neutrophil count greater than 1000/mm\^3. * Platelet count greater than 100,000/mm\^3. * Hemoglobin greater than 8.0 g/dl. * Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) less than two times the upper limit of normal. * Serum creatinine less than or equal to 1.6 mg/dl. * Total bilirubin less than or equal to 1.6 mg/dl, except for patients with Gilbert's Syndrome who must have a total bilirubin less than 3.0 mg/dl. * More than four weeks must have elapsed since any prior therapy at the time the patient receives the preparative regimen. * Women of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects of the preparative chemotherapy on the fetus. * Life expectancy of greater than three months. * No steroid therapy required. * Seronegative for human immunodeficiency virus (HIV) antibody. (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who are HIV seropositive can have decreased immune competence and thus be less responsive to the experimental treatment and more susceptible to its toxicities.) * Seronegative for hepatitis B antigen. * Patients to receive high dose interleukin 2 (IL-2) must have no active systemic infections, coagulation disorders or other major medical illnesses of the cardiovascular, respiratory or immune system. * Patients who will receive high dose IL-2 as part of the phase I portion of this study or who will be randomized must be eligible to receive high dose IL-2. * Any patient receiving IL-2 must sign a durable power of attorney.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical Response | Every three to four weeks after the treatment, for up to 5 years. | Complete response (CR) is defined as the disappearance of all clinical evidence of disease. Partial response (PR) is a 50% or greater decrease in the sum of the products of perpendicular diameters of all measurable lesions for at least one month. No new lesions may appear, and none may increase. Minor response (MR) is a 25-49% decrease in the sum of the products of the perpendicular diameters of all measurable lesions. Appearance of new lesions following a PR or CR are considered relapses. Patients with progressive disease (PD) and no evidence of stable disease will be taken off study after receiving IL-2. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Adverse Events | 10.5 months | Here is the number of participants with adverse events. For a detailed list of adverse events see the adverse event module. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Cells IV + Cyclophosphamide 30mg/kg Phase 1 Cyclophosphamide Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x30mg/kg + Cells IV | 3 |
| Cells IV + Cyclophosphamide 60mg/kg Phase 1 Cyclophosphamide Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV | 3 |
| Cells IV + Low-Dose IV IL-2 (Initial) Phase 1 IL-2 Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (72,000 IU/kg q8h for a maximum of 15 doses) | 3 |
| Cells IV + High-Dose IV IL-2 (Initial) Phase 1 IL-2 Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) | 6 |
| Cells IV + MTD IL-2 Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) + G-CSF (to shorten time to neutrophil recovery) | 51 |
| Cells IA + MTD IL-2 (Prior Cells IV on 6) Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IA + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) Prior Cells IV + G-CSF | 4 |
| Cells IA + MTD IL-2 Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IA + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) + G-CSF | 7 |
| Cells IA + MTD IL-2 (MART-1 Reactive) Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IA + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) + G-CSF + MART-1:26-35(27L) Peptide 1mg/day (5-8 days) in patients with MART-1 reactive cells | 8 |
| Cells IV + MTD IL-2 no GCSF Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) without G-CSF (to determine if G-CSF has harmful effects when adoptively transferring lymphocytes following a nonmyeloablative chemotherapy regimen) | 6 |
| Cells IV + MTD IL-2 no GCSF (gp100 Reactive) Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) without G-CSF + gp100:209-217(210M) 1mg/day (2-8 days) in patients with gp100 reactive cells | 1 |
| Cells IV + MTD IL-2 no GCSF (MART-1 Reactive) Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) without G-CSF + MART-1:26-35(27L) Peptide 1mg/day (5-8 days) in patients with MART-1 reactive cells | 7 |
| Cells IV + SQ IL-2 w/GCSF Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + SQ IL-2 (125,000 IU/kg/dose for 5 days for six weeks with 2 days rest per week) + G-CSF (to shorten time to neutrophil recovery), reactivity not specified | 6 |
| Cells IV + SQ IL-2 w/GCSF (MART-1 Reactive) Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + SQ IL-2 (125,000 IU/kg/dose for 5 days for six weeks with 2 days rest per week) + G-CSF + MART-1:26-35(27L) Peptide 1mg/day (5-8 days) in patients with MART-1 reactive cells | 3 |
| Cells IV + SQ IL-2 w/GCSF (no Reactivity) Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + SQ IL-2 (125,000 IU/kg/dose for 5 days for six weeks with 2 days rest per week) + G-CSF in patients with no reactivity | 2 |
| Total | 110 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 | FG004 | FG005 | FG006 | FG007 | FG008 | FG009 | FG010 | FG011 | FG012 | FG013 | FG014 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Apheresis Period | not able to manufacture treatment cells | 60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Treatment Period | Death during treatment | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Treatment Period | Not treated | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
Baseline characteristics
| Characteristic | Cells IV + Cyclophosphamide 60mg/kg | Cells IV + Low-Dose IV IL-2 (Initial) | Cells IV + High-Dose IV IL-2 (Initial) | Cells IV + MTD IL-2 | Cells IA + MTD IL-2 (Prior Cells IV on 6) | Cells IA + MTD IL-2 | Cells IA + MTD IL-2 (MART-1 Reactive) | Cells IV + MTD IL-2 no GCSF | Cells IV + MTD IL-2 no GCSF (gp100 Reactive) | Cells IV + MTD IL-2 no GCSF (MART-1 Reactive) | Cells IV + SQ IL-2 w/GCSF | Cells IV + Cyclophosphamide 30mg/kg | Cells IV + SQ IL-2 w/GCSF (MART-1 Reactive) | Cells IV + SQ IL-2 w/GCSF (no Reactivity) | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants | 1 Participants |
| Age, Categorical Between 18 and 65 years | 3 Participants | 3 Participants | 5 Participants | 51 Participants | 4 Participants | 7 Participants | 8 Participants | 6 Participants | 1 Participants | 7 Participants | 6 Participants | 3 Participants | 3 Participants | 1 Participants | 108 Participants |
| Age Continuous | 52.3 years STANDARD_DEVIATION 4.5 | 42.3 years STANDARD_DEVIATION 13.3 | 37.8 years STANDARD_DEVIATION 14.7 | 41.9 years STANDARD_DEVIATION 12.7 | 38.0 years STANDARD_DEVIATION 14.3 | 39.7 years STANDARD_DEVIATION 11.1 | 41.8 years STANDARD_DEVIATION 11.6 | 49.0 years STANDARD_DEVIATION 10.3 | 62.0 years | 40.7 years STANDARD_DEVIATION 9.9 | 44.2 years STANDARD_DEVIATION 11.2 | 41.3 years STANDARD_DEVIATION 9.3 | 37.7 years STANDARD_DEVIATION 7.1 | 58.5 years STANDARD_DEVIATION 10.6 | 45.0 years STANDARD_DEVIATION 11.4 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants | 3 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 4 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 3 Participants | 3 Participants | 6 Participants | 48 Participants | 4 Participants | 7 Participants | 8 Participants | 6 Participants | 1 Participants | 6 Participants | 6 Participants | 3 Participants | 3 Participants | 2 Participants | 106 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 3 Participants | 3 Participants | 6 Participants | 50 Participants | 4 Participants | 7 Participants | 8 Participants | 6 Participants | 1 Participants | 7 Participants | 6 Participants | 3 Participants | 3 Participants | 2 Participants | 109 Participants |
| Region of Enrollment United States | 3 participants | 3 participants | 6 participants | 51 participants | 4 participants | 7 participants | 8 participants | 6 participants | 1 participants | 7 participants | 6 participants | 3 participants | 3 participants | 2 participants | 110 participants |
| Sex: Female, Male Female | 1 Participants | 1 Participants | 2 Participants | 22 Participants | 0 Participants | 2 Participants | 5 Participants | 1 Participants | 1 Participants | 1 Participants | 1 Participants | 1 Participants | 0 Participants | 0 Participants | 38 Participants |
| Sex: Female, Male Male | 2 Participants | 2 Participants | 4 Participants | 29 Participants | 4 Participants | 5 Participants | 3 Participants | 5 Participants | 0 Participants | 6 Participants | 5 Participants | 2 Participants | 3 Participants | 2 Participants | 72 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk | EG004 affected / at risk | EG005 affected / at risk | EG006 affected / at risk | EG007 affected / at risk | EG008 affected / at risk | EG009 affected / at risk | EG010 affected / at risk | EG011 affected / at risk | EG012 affected / at risk | EG013 affected / at risk |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — | — / — |
| other Total, other adverse events | 3 / 3 | 3 / 3 | 3 / 3 | 6 / 6 | 50 / 51 | 4 / 4 | 7 / 7 | 8 / 8 | 6 / 6 | 1 / 1 | 7 / 7 | 6 / 6 | 3 / 3 | 2 / 2 |
| serious Total, serious adverse events | 0 / 3 | 0 / 3 | 0 / 3 | 0 / 6 | 9 / 51 | 0 / 4 | 2 / 7 | 1 / 8 | 0 / 6 | 0 / 1 | 0 / 7 | 0 / 6 | 1 / 3 | 1 / 2 |
Outcome results
Clinical Response
Complete response (CR) is defined as the disappearance of all clinical evidence of disease. Partial response (PR) is a 50% or greater decrease in the sum of the products of perpendicular diameters of all measurable lesions for at least one month. No new lesions may appear, and none may increase. Minor response (MR) is a 25-49% decrease in the sum of the products of the perpendicular diameters of all measurable lesions. Appearance of new lesions following a PR or CR are considered relapses. Patients with progressive disease (PD) and no evidence of stable disease will be taken off study after receiving IL-2.
Time frame: Every three to four weeks after the treatment, for up to 5 years.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | No Response | 3 Participants |
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | No Response | 3 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | No Response | 3 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | No Response | 6 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | Complete Response | 3 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | Stable Disease | 1 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | Partial Response | 14 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | No Response | 32 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + MTD IL-2 | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Clinical Response | No Response | 4 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | No Response | 5 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IA + MTD IL-2 | Clinical Response | Complete Response | 1 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | Complete Response | 1 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | Partial Response | 1 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | Mixed Response | 1 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Clinical Response | No Response | 5 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | Partial Response | 1 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | No Response | 4 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | Complete Response | 1 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | Minor Response | 1 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | No Response | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | No Response | 5 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | Partial Response | 2 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | Partial Response | 3 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | No Response | 3 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | Partial Response | 1 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | Mixed Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Clinical Response | No Response | 2 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | Minor Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | No Response | 2 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | Stable Disease | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | Progressive Disease | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | Complete Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | Partial Response | 0 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Clinical Response | Mixed Response | 0 Participants |
Number of Participants With Adverse Events
Here is the number of participants with adverse events. For a detailed list of adverse events see the adverse event module.
Time frame: 10.5 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Abl Cells IV + Cyclophosphamide 30 mg/kg | Number of Participants With Adverse Events | 3 Participants |
| Abl Cells IV + Cyclophosphamide 60 mg/kg | Number of Participants With Adverse Events | 3 Participants |
| Abl Cells IV+Low Dose IV IL-2 (Initial) | Number of Participants With Adverse Events | 3 Participants |
| Abl Cells IV+High Dose IV IL-2 (Initial) | Number of Participants With Adverse Events | 6 Participants |
| Abl Cells IV + MTD IL-2 | Number of Participants With Adverse Events | 50 Participants |
| Abl Cells IA + MTD (Prior Cells IV on 6) | Number of Participants With Adverse Events | 4 Participants |
| Abl Cells IA + MTD IL-2 | Number of Participants With Adverse Events | 7 Participants |
| Abl Cells IA+MTD IL-2 (MART-1 Reactive) | Number of Participants With Adverse Events | 8 Participants |
| Abl Cells IV + MTD IL-2 no GCSF | Number of Participants With Adverse Events | 6 Participants |
| Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive) | Number of Participants With Adverse Events | 1 Participants |
| Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive) | Number of Participants With Adverse Events | 7 Participants |
| Abl Cells IV + SQ IL-2 With GCSF | Number of Participants With Adverse Events | 6 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive) | Number of Participants With Adverse Events | 3 Participants |
| Abl Cells IV + SQ IL-2 With GCSF (no Reactivity) | Number of Participants With Adverse Events | 2 Participants |