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.