Paclitaxel, cisplatin, and concurrent radiation for esophageal cancer

Citation
H. Safran et al., Paclitaxel, cisplatin, and concurrent radiation for esophageal cancer, CANCER INV, 19(1), 2001, pp. 1-7
Citations number
33
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER INVESTIGATION
ISSN journal
07357907 → ACNP
Volume
19
Issue
1
Year of publication
2001
Pages
1 - 7
Database
ISI
SICI code
0735-7907(2001)19:1<1:PCACRF>2.0.ZU;2-D
Abstract
Paclitaxel is an active agent for adenocarcinomas and squamous cell carcino mas of the esophagus and is a radiation sensitizer We sought to investigate the toxicity and complete response rate of paclitaxel, cisplatin, and conc urrent radiation for esophageal cancer Forty-one patients with esophageal c ancer were studied, 29 with adenocarcinomas and 12 with squamous cell cance rs. Twelve patients had tumor extension into the proximal stomach and/or ab dominal adenopathy Patients received paclitaxel 60 mg/m(2) by 3-hour intrav enous (IV) infusion, and cisplatin 25 mg/m(2) weekly on days 1, 8, 15, and 22. Radiation was administered concurrently to a total dose of 39.60 Gy, in 1.80 Gy fractions, for 22 treatments. Patients with medical or surgical co ntraindications to esophagectomy received 2 additional weeks of paclitaxel with a radiation boost to 50.4 Gy Neutropenia was the most common grade 3/4 toxicity occurring in 10 patients (24%). Only 2 patients (5%) had grade 4 esophagitis requiring parenteral nutrition. Twelve patients (29%) obtained a complete response. The 2-year progression-free and overall survival rates were 40% and 42%, respectively. Esophagitis was less severe than expected and prophylactic enteral feeding tubes were not necessary. Additional effec tive systemic treatments are needed to reduce the development of distant me tastases.