PREDICTORS OF SURVIVAL FOLLOWING RELAPSE OR PROGRESSION OF SMALL-CELLLUNG-CANCER - SOUTHWEST-ONCOLOGY-GROUP STUDY 8605 REPORT AND ANALYSISOF RECURRENT DISEASE DATA-BASE
Ks. Albain et al., PREDICTORS OF SURVIVAL FOLLOWING RELAPSE OR PROGRESSION OF SMALL-CELLLUNG-CANCER - SOUTHWEST-ONCOLOGY-GROUP STUDY 8605 REPORT AND ANALYSISOF RECURRENT DISEASE DATA-BASE, Cancer, 72(4), 1993, pp. 1184-1191
Background. Survival after relapse or progression of small cell lung c
ancer (SCLC) is poor. The Southwest Oncology Group (SWOG) initiated a
study of modulation of cyclophosphamide (Cy) resistance in this popula
tion. At study closure, the value of testing new regimens in previousl
y treated patients was being debated nationally: Is there an independe
nt impact of treatment over favorable prognostic factors? Thus, the au
thors analyzed the SWOG recurrent SCLC data base. Methods. A 12-hour i
nfusion of cytosine arabinoside (ara-C) was used as a potential repair
inhibitor of Cy-induced DNA damage in patients with relapsed SCLC. A
data base of successive SWOG studies in recurrent SCLC was formed. The
independent contribution to survival of prognostic factors, type of p
rior chemotherapy (CT), time from diagnosis, and type of CT on relapse
were then assessed.Results. There were 3 partial responses observed i
n 67 patients, with substantial myelotoxicity. The median survival was
2.5 months, and 16% lived beyond 6 months. The multivariate analysis
of the recurrent SCLC data base found that a normal lactate dehydrogen
ase (LDH) and second-line treatment with etoposide plus cisplatin (EP)
, if not initially treated with either alternating or complex multidru
g regimens, were the only independent predictors of improved survival.
The 2-year survival of this subset was 20%. Conclusions. The Cy/ara-C
program cannot be recommended for patients with recurrent SCLC. Howev
er, EP independently contributed to improved survival in patients with
out complex prior CT and a normal LDH. This finding supports future tr
ials of new approaches in certain subsets of SCLC patients with limite
d prior treatment.