Ttc. Yip et al., PROGNOSTIC-SIGNIFICANCE OF DNA FLOW CYTOMETRIC ANALYSIS IN PATIENTS WITH NASOPHARYNGEAL CARCINOMA, Cancer, 83(11), 1998, pp. 2284-2292
BACKGROUND. Nasopharyngeal carcinoma (NPC) is a prevalent malignant tu
mor among Southern Chinese. Previously, the authors described the prog
nostic significance of a serum antibody assay to a recombinant Epstein
-Barr virus Bam HI-Z replication activator protein (ZEBRA) in NPC pati
ents with long term follow-up. In same series. METHODS. One hundred an
d forty-three archival biopsies from 110 NPC patients were deparaffini
zed and subjected to DNA-FCM analysis. DNA ploidy state and various pr
oliferative indices (PI) of the tumors were correlated with patient su
rvival and frequency of recurrence. RESULTS, Among the biopsies analyz
ed, 119 were histologically positive NPC and 24 were negative. Fifty-o
ne tumor biopsies that fulfilled the guideline criteria of the DNA Cyt
ometry Consensus Conference were correlated with the clinical manifest
ations of the patients. Among them, 43 tumors (84%) were DNA diploid a
nd 8 (16%) were aneuploid. TWO PI, S-phase fraction (SPF) and prolifer
ation fraction (PF), appear to be potentially useful prognostic indica
tors. For example, PF in patients who developed locoregional recurrenc
e (15.1%) and distant recurrence (16.4%) after radiation therapy both
were significantly higher than PF in patients who were in complete rem
ission (8.2%) (P = 0.0005 and P = 0.004, respectively). Significant di
fferences in SPF between patients with distant recurrence (10.6%) and
those in remission (5.7%) also was found (P = 0.005). Using Kaplan-Mei
er analysis, patients With high PF, high SPF, and aneuploid tumors had
significantly poorer 12-year survival rates (35%, 26%, and 28%, respe
ctively) than those patients with low PF, low SPF, and diploid tumors
(77%, 67%, and 59%, respectively) (P < 0.0009, P < 0.004, and P < 0.01
, respectively).CONCLUSIONS. Determination of tumor PI and DNA ploidy
state by DNA-FCM at diagnosis of NPC can be potentially useful in sele
cting a poor prognostic subgroup of NPC patients. These parameters may
enable oncologists to plan for more stringent treatment strategies su
ch as hyperfractionated and accelerated radiation therapy or concomita
nt chemoradiotherapy for these patients. (C) 1998 American Cancer Soci
ety.