𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prolonged administration of low dose infusional etoposide in patients with advanced malignancies. A phase I/II study

✍ Scribed by Dana S. Thompson; John D. Hainsworth; Kenneth R. Hande; Mary Holzmer; F. Anthony Greco


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
738 KB
Volume
73
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.

✦ Synopsis


Background:

Etoposide displays remarkable schedule dependency. to better define the optimal dose and schedule, the authors administered etoposide as a prolonged low daily dose infusion in patients with a variety of advanced malignancies.

Methods:

Between october 1989 and april 1992, 40 patients met inclusion criteria and were enrolled in this study; the initial dose of infusional etoposide was 25 mg/m2/day. doses were not escalated further, because it became evident that 25 mg/m2/day was the maximum tolerated dose (mtd) in most patients using this prolonged schedule. because the initial dose proved to be the mtd on this prolonged schedule, several patients received a starting dose of either 20 mg/m2/day or 18 mg/m2/day. this continuous infusion was administered for at least 21 days or until either the leukocyte count dropped to less than 2,000/mm3, platelets dropped to less than 75,000/mm3, or tumor progression occurred. plasma etoposide levels were obtained at random times during infusions at 25 mg/m2/day.

Results:

Duration of therapy ranged from 15-561 days. myelosuppression was the major toxic reaction, although it was mild in most patients and reduced compared with other schedules. myelosuppression correlated with the extent of prior treatment: minimally pretreated patients tolerated prolonged infusions with only mild hematologic toxic effects, whereas heavily pretreated patients experienced moderate myelosuppression. patients treated at an initial dose of 25 mg/m2/day had more myelosuppression than did those treated at 20 mg/m2/day. a leukocyte count of less than 1,000/mm3 developed in only 5 of 40 patients (12%) at any time during therapy. twenty-one patients required packed erythrocyte transfusions, and one required platelet transfusion. the mean serum etoposide concentration in patients receiving 25 mg/m2/day was 0.7 plus or minus 0.42 microgram/ml. objective responses were obtained in 5 of 10 patients with previously treated non-hodgkin's lymphoma and 2 of 3 patients with previously untreated extensive stage small cell lung cancer.

Conclusions:

Etoposide administered by continuous infusion can be given at 25 mg/m2/day for prolonged periods to most patients and is the mtd in previously treated patients. tumoricidal activity in selected tumor types is demonstrated with this dose. further study in neoplasms that considered "etoposide-sensitive" seems warranted.


πŸ“œ SIMILAR VOLUMES


Phase I dose and sequencing study of peg
✍ Paula M. Fracasso; Luis C. Rodriguez; Thomas J. Herzog; Carole L. Fears; Sherry πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 89 KB πŸ‘ 1 views

## Abstract ## BACKGROUND Pegylated liposomal doxorubicin (PEG‐LD) and docetaxel have single‐agent activity in several malignancies. The authors conducted a Phase I trial to evaluate the maximum tolerated dose (MTD), toxicities, and effect of dose sequencing of this combination in patients with ad

Phase I study of pegylated liposomal dox
✍ Paula M. Fracasso; Kristie A. Blum; Benjamin R. Tan; Carole L. Fears; Nancy L. B πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 71 KB πŸ‘ 2 views

## Abstract ## BACKGROUND Pegylated liposomal doxorubicin (PEG‐LD) and gemcitabine have single‐agent activity in breast and ovarian carcinoma patients. We conducted a Phase I trial to evaluate the maximum tolerated dose (MTD) and toxicities of this combination in patients with advanced malignancie

A phase I study of sequential administra
✍ Caio M. S. Rocha Lima; Carlo V. Catapano; Daniel Pacheco; Carol A. Sherman; Greg πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 114 KB πŸ‘ 1 views

## Abstract ## BACKGROUND Based on preclinical findings and on the clinical antitumor efficacy of sequential paclitaxel/topotecan and topotecan/etoposide, the authors sought to define the maximum tolerated doses (MTDs) and dose‐limiting toxicities (DLTs) associated with a sequential combination of