## Abstract ## BACKGROUND. The safety and efficacy of the fully human antibody panitumumab was evaluated in patients with metastatic colorectal cancer refractory to available therapies. ## METHODS. This phase 2 openβlabel, multicenter study of panitumumab enrolled patients with metastatic colore
Trimetrexate in untreated and previously treated patients with metastatic breast cancer: A cancer and leukemia group b study
β Scribed by Dawson, Nancy A. ;Costanza, Mary E. ;Korzun, Ann H. ;Clamon, Gerald H. ;Pollak, Michael ;Vogelzang, Nicholas J. ;Carey, Robert W. ;Norton, Larry
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 554 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
β¦ Synopsis
Twenty-two patients with previously untreated metastatic breast cancer and nineteen patients with refractory metastatic breast cancer were treated with trimetrexate (TMTX). Patients received TMTX 8 mg/m2/day if previously treated or 12 mg/m2/day if previously untreated, both given by intravenous bolus days 1-5, every 21 days. None of the patients previously treated for metastatic disease responded to TMTX. There was one partial responder among the 22 patients with previously untreated metastatic disease. The primary toxicity was hematologic and occurred more frequently in patients with a pleural effusion, low serum protein or albumin, or poor performance status. There were three toxic deaths. The study for previously untreated patients required cyclophosphamide, doxorubicin, and 5-fluorouracil (CAF) after 4 cycles of TMTX. This study design for previously untreated patients allows the Cancer and Leukemia Group B (CALGB) to prospectively evaluate the activity of new agents in "chemotherapy-sensitive" metastatic breast cancer.
π SIMILAR VOLUMES
Ifosfamide (1.25 g/m2 intravenously/day x 5) with mesna (20% of the ifosfamide dose x six doses on each day of ifosfamide therapy) was administered to 46 previously treated patients with non-Hodgkin's lymphoma of which 31 were eligible and evaluable. A 29% response rate (9/31) was observed (2 CR and
## Abstract Ifosfamide (1Β·25 g/m^2^ intravenously/day Γ 5) with mesna (20 per cent of the ifosfamide dose Γ six doses on each day of ifosfamide therapy) was administered to 46 previously treated patients with nonβHodgkin's lymphoma of which 31 were eligible and evaluable. A 29 per cent response rat
## Abstract Ifosfamide (2.0 g/m^2^ intravenously/day Γ 3) with mesna (400 mg/m^2^ intravenously q 4 h daily Γ 3) was combined with mitoxantrone (14 mg/m^2^ intravenously Γ 1) and given on a 3 week schedule to patients with previously treated nonβHodkgin's lymphoma. In 45 eligible/evaluable patients