Your browser doesn't support javascript.
loading
Cisplatin as second-line therapy in ovarian carcinoma treated initially with single-agent paclitaxel: a Gynecologic Oncology Group study.
Thigpen, J Tate; Blessing, John A; Olt, George; Lentz, Samuel S; Bell, Jeffrey.
Afiliação
  • Thigpen JT; Division of Oncology, Department of Medicine, University of Mississippi School of Medicine, Jackson, MS 39216-4505, USA. jthigpen@medicine.umsmed.edu
Gynecol Oncol ; 90(3): 581-6, 2003 Sep.
Article em En | MEDLINE | ID: mdl-13678728
ABSTRACT

OBJECTIVES:

The platinum compounds are the most active agents in the treatment of ovarian carcinoma. Phase II trials demonstrated the activity of paclitaxel in patients with disease clinically resistant to platinum-based front-line therapy, and phase III studies confirmed that a combination of paclitaxel plus a platinum was superior to cyclophosphamide plus a platinum. This study evaluated the activity of platinum in patients with bulky advanced disease treated with single-agent paclitaxel as front-line therapy on a Gynecologic Oncology Group protocol. Those patients who had persistent (stable) or progressive disease while receiving paclitaxel, or a recurrence of disease within 6 months of completing six cycles of paclitaxel therapy, received single-agent cisplatin.

METHODS:

Thirty-nine eligible patients with ovarian carcinoma persistent, progressive, or recurrent after initial treatment with paclitaxel 200 mg/m(2) over 24 h every 3 weeks received cisplatin 100 mg/m(2) every 3 weeks until disease progression or unacceptable toxicity.

RESULTS:

Among 37 patients evaluable for response, 8 complete (22%) and 13 partial (35%) responses resulted. Twelve (32%) patients exhibited stable disease, while 4 (11%) had increasing disease. Median progression-free survival was 11.0 months. Median survival was 15.0 months. All but two patients were clinically resistant to paclitaxel (progression during or within 6 months after completion of paclitaxel). Grade 2 or worse adverse effects among 39 patients evaluable for toxicity included neutropenia (23), thrombocytopenia (3), anemia (10), nausea and vomiting (23), azotemia (7), neurotoxicity (9), fever (2), and tinnitus (1).

CONCLUSION:

These data provide evidence that cisplatin is active as second-line therapy in patients clinically resistant to paclitaxel. The overall response rate is high (57%) with excellent progression-free and overall survival in the second-line setting.
Assuntos
Buscar no Google
Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Cisplatino / Paclitaxel / Recidiva Local de Neoplasia / Antineoplásicos Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2003 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Cisplatino / Paclitaxel / Recidiva Local de Neoplasia / Antineoplásicos Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2003 Tipo de documento: Article