TREATMENT OF RECURRENT AND OR METASTATIC SQUAMOUS-CELL HEAD AND NECK-CARCINOMA WITH A COMBINATION OF VINORELBINE, CISPLATIN, AND 5-FLUOROURACIL - A MULTICENTER PHASE-II TRIAL/
V. Gebbia et al., TREATMENT OF RECURRENT AND OR METASTATIC SQUAMOUS-CELL HEAD AND NECK-CARCINOMA WITH A COMBINATION OF VINORELBINE, CISPLATIN, AND 5-FLUOROURACIL - A MULTICENTER PHASE-II TRIAL/, Annals of oncology, 6(10), 1995, pp. 987-991
Purpose: Vinorelbine has been demonstrated to be active against squamo
us cell carcinomas of the head/neck (SCHNC) and lung. This multicenter
phase II trial was carried out to evaluate the activity and tolerabil
ity of the combination of vinorelbine, cisplatin, and fi-fluorouracil
given on an outpatient schedule in a series of 80 patients with recurr
ent SCHNC. Patients and methods: Eighty patients with recurrent and/or
metastatic SCHNC were treated with a combination of CDDP 80 mg/m(2) o
n day 1, 5-FU 600 mg/m(2) as a 4-hour infusion on days 2-5, and vinore
lbine 25 mg/m(2) on days 2+8. This cycle was repeated every 28 days. M
ost patients had oral cavity, larynx, or oropharynx carcinoma (88%). F
orty-seven had previously received surgery alone, two radiotherapy alo
ne, and 31 surgery plus radiotherapy. Seventy-two patients had locoreg
ional recurrency, and eight had distant metastases. Results: According
to an intent-to-treat analysis, complete response (CR) of a mean dura
tion of 12.7+ months was achieved in 13% of cases (95% CI 5%-21%), and
partial response of 8.3+ months in 45% of patients (95% CI 33%-56%),
for an overall response rate of 55% (95% CI 43%-65%). Nine patients (1
1%) showed no change, and 22 (28%) progressed. Five patients were not
evaluable for response and toxicity. CR were seen more frequently in p
atients pre treated with only surgery than in those who had also recei
ved radiotherapy (15% vs. 9%; p = 0.7). No statistically significant d
ifferences in response rate according to site of primary tumor were fo
und (p = 0.8, NS). The received dose intensities of 5-FU, CDDP, and VN
R were 90%, 99%, and 82%, respectively. The overall survival of the se
ries as a whole was 9.7+ months (range 4-27). Toxicity was generally a
cceptable. Grades 3 and 4 leukopenia were recorded in 11% and 5% of pa
tients, respectively. Noteworthy was the occurrence of pain at the tum
or site after vinorelbine administration in 5 patients. Conclusion: Th
e combination regimen of CDDP, 5-FU and vinorelbine is quite active in
the treatment of metastatic and/or recurrent SCHNC. This regimen shou
ld be tested as initial treatment in previously untreated patients and
compared to a standard regimen in recurrent SCHNC.