A RANDOMIZED TRIAL OF HYBRID ADMINISTRATION OF CYCLOPHOSPHAMIDE, DOXORUBICIN, AND VINCRISTINE (CAV) CISPLATIN AND ETOPOSIDE (PVP) VERSUS SEQUENTIAL ADMINISTRATION OF CAV-PVP FOR THE TREATMENT OF PATIENTS WITH SMALL-CELL LUNG-CARCINOMA - RESULTS OF LONG-TERM FOLLOW-UP
H. Ueoka et al., A RANDOMIZED TRIAL OF HYBRID ADMINISTRATION OF CYCLOPHOSPHAMIDE, DOXORUBICIN, AND VINCRISTINE (CAV) CISPLATIN AND ETOPOSIDE (PVP) VERSUS SEQUENTIAL ADMINISTRATION OF CAV-PVP FOR THE TREATMENT OF PATIENTS WITH SMALL-CELL LUNG-CARCINOMA - RESULTS OF LONG-TERM FOLLOW-UP, Cancer, 83(2), 1998, pp. 283-290
BACKGROUND. In an attempt to determine the efficacy of cyclophosphamid
e, doxorubicin, and vincristine (CAV)/cisplatin and etoposide (PVP) hy
brid chemotherapy (HYB), a rapidly alternating chemotherapy, in patien
ts with small cell lung carcinoma (SCLC), the authors conducted a rand
omized study to compare HYB with CAV-PVP sequential chemotherapy (SEQ)
. METHODS. Patients in the HYB group received the 3-drug CAV combinati
on on Day 1 and the 2-drug PVP combination on Day 8, repeated every 4
weeks for up to 6 cycles. Patients in the SEQ group received 3 cycles
each of CAV and PVP sequentially every 4 weeks, delivered on Days 1 an
d 8. All responding patients with limited disease (LD) received thorac
ic irradiation (50 gray) after chemotherapy. RESULTS. Between April 19
88 and October 1992, 129 patients were evaluated fully. There were no
significant differences in the treatment outcome between patients in t
he HYB and SEQ groups in terms of the complete response rate (59% for
LD patients and 21% for extensive disease [ED] patients in the HYB gro
up vs. 45% for LD patients and 16% for ED patients in the SEQ group),
or median survival time (17.9 months for LD patients and 9.7 months fo
r ED patients in the HYB group vs. 20.6 months for LD patients and 12.
2 months for ED patients in the SEQ group). CONCLUSIONS. Hybrid CAV-PV
P therapy is effective for the treatment of SCLC, but appears to be no
better than sequential therapy with the same regimen. (C) 1998 Americ
an Cancer Society.