POSTOPERATIVE RADIOTHERAPY WITH CONCURRENT CISPLATIN APPEARS TO IMPROVE LOCOREGIONAL CONTROL OF ADVANCED, RESECTABLE HEAD-AND-NECK-CANCERS - RTOG-88-24
M. Alsarraf et al., POSTOPERATIVE RADIOTHERAPY WITH CONCURRENT CISPLATIN APPEARS TO IMPROVE LOCOREGIONAL CONTROL OF ADVANCED, RESECTABLE HEAD-AND-NECK-CANCERS - RTOG-88-24, International journal of radiation oncology, biology, physics, 37(4), 1997, pp. 777-782
Citations number
28
Categorie Soggetti
Oncology,"Radiology,Nuclear Medicine & Medical Imaging
Purpose: Despite aggressive surgery and postoperative radiation therap
y, only 30% of patients who have advanced, potentially resectable carc
inomas of the head and neck survive for 5 years. In the hope of improv
ing this situation we studied the effect of postoperative radiotherapy
delivered concurrently with cisplatin, Methods and Materials: Patient
s who had Stage IV tumors and/or involved surgical margins received 60
Gy in 30 fractions over 6 weeks plus 100 mg/m(2) of cisplatin on radi
otherapy days 1, 23 and 43, Fifty-two patients participated in this tr
ial and 51 were evaluated. Forty-three (84%) patients had pathologic T
3 or T4 disease, 43 (84%) had Stage IV disease, and 27 (53%) had histo
logically involved surgical margins. Results: Severe and life-threaten
ing toxicities occurred in 20% and 12% of patients, respectively; the
most common drug-related toxicities were leukopenia, anemia, nausea, a
nd vomiting. Seventeen patients (43%) remain alive with no evidence of
disease, Four patients (8%) died with no evidence of neoplastic disea
se, and one patient has died of a second independent malignancy, By ac
tuarial analysis at 3 years, 48% of patients are alive, 81% have locor
egional control of disease, and 57% are free of distant metastases. Co
nclusions: Based on comparison with similar patients treated in a prio
r Radiation Therapy Oncology Group/Intergroup trial (RTOG), we conclud
e that postoperative radiotherapy with concurrent cisplatin may improv
e locoregional control rates and should be prospectively tested, (C) 1
997 Elsevier Science Inc.