L. Deandres et al., RANDOMIZED TRIAL OF NEOADJUVANT CISPLATIN AND FLUOROURACIL VERSUS CARBOPLATIN AND FLUOROURACIL IN PATIENTS WITH STAGE IV-M0 HEAD AND NECK-CANCER, Journal of clinical oncology, 13(6), 1995, pp. 1493-1500
Purpose: A randomized trial was designed to compare cisplatin (CDDP) a
nd fluorouracil (FU) versus carboplatin (CBDCA) and FU as neoadjuvant
treatment in stage IV-MO head and neck cancer to assess whether CBDCA-
FU is better than CDDP-FU with regard to response and toxicity, Patien
ts cmd Methods: Patients were randomized to receive CDDP 100 mg/m(2) i
ntravenously on day 1 and FU 5,000 mg/m(2) over a 120-hour continuous
infusion, or CBDCA 400 mg/m(2) over a 24-hour continuous infusion on d
ay 1 and FU with the same schedule, Both regimens were repeated every
21 days, The patients received three courses of chemotherapy, excludin
g those who foiled to achieve a partial response (PR) after the second
course, Complete responders were treated with radiotherapy, The remai
ning patients underwent surgery if the tumor was resectable. Results:
Interim analysis was performed when 95 patients were included, The tri
al was stopped due to significantly better results in the control arm,
Differences in response (P = .04) were favorable to CDDP-FU. Hematolo
gic toxicity predominated in the CBDCA-FU arm (P < .001). Mucositis an
d vomiting predominated in the CDDP-FU arm (P = .03, P < .001, respect
ively), Favorable outcomes (complete response [CR] plus any grade of t
oxicity and PR plus grade 0 to 3 toxicity) predominated in the CDDP-FU
arm (P = .02). Only the treatment assigned was associated with respon
se (P = .02) and favorable outcomes (P = .009) in the logistic regress
ion analysis. In the CDDP-FU arm, disease-free and overall survival we
re significantly better, Cox regression analysis showed that only trea
tment association with disease-free survival remains significant, Conc
lusion: Our results indicate that CDDP-FU is more effective than CBDCA
-FU as neoadjuvant treatment in stage IV-MO head and neck cancer. (C)
1995 by American Society of Clinical Oncology.