TY - JOUR
T1 - Continuous versus alternating combination chemotherapy for advanced small cell carcinoma of the lung
AU - Østerlind, Kell
AU - Hansen, Heine H.
AU - Hirsch, Fred R.
AU - Hansen, Mogens
AU - Rørth, Mikael
AU - Sörenson, Sverre
AU - Dombernowsky, Per
PY - 1983/12/1
Y1 - 1983/12/1
N2 - In a 2-year period, 146 patients with small cell carcinoma of the lung, staged as having extensive disease, were randomized to receive either continuous chemotherapy consisting of (a) 1-(2-chkxoethyl-3-cyck)hexyl-1-nitrosourea, cyclophosphamide, methotrexate, and vincristine followed by (b) 4’-demethylepipodophyllotoxin 9-[4,6-0-(R) ethylidene-ß-D-glucopyranoside] and doxorubicin at progression of disease or a regimen of (a) alternating with (b). Seventy-six patients received the continuous regimen; 70 patients received alternating treatment. Response rates were 68 and 72%, respectively. The median duration of response was 16 weeks in patients receiving continuous treatment compared to 28 weeks in patients receiving alternating treatment (p < 0.05). No survival time difference was observed between the groups, median survival being 36 and 38 weeks, respectively. Four patients became long-term survivors (5.6+, 5.5+, 5.1, and 4.7+ years). All received alternating therapy. Six toxic deaths were observed among patients receiving continuous therapy compared to only one death among those in the alternating regimen. In conclusion, alternating combination chemotherapy leads to prolonged duration of remission. Duration of survival is not prolonged in uncured patients, but an increased possibility of long-term disease-free survival cannot be precluded.
AB - In a 2-year period, 146 patients with small cell carcinoma of the lung, staged as having extensive disease, were randomized to receive either continuous chemotherapy consisting of (a) 1-(2-chkxoethyl-3-cyck)hexyl-1-nitrosourea, cyclophosphamide, methotrexate, and vincristine followed by (b) 4’-demethylepipodophyllotoxin 9-[4,6-0-(R) ethylidene-ß-D-glucopyranoside] and doxorubicin at progression of disease or a regimen of (a) alternating with (b). Seventy-six patients received the continuous regimen; 70 patients received alternating treatment. Response rates were 68 and 72%, respectively. The median duration of response was 16 weeks in patients receiving continuous treatment compared to 28 weeks in patients receiving alternating treatment (p < 0.05). No survival time difference was observed between the groups, median survival being 36 and 38 weeks, respectively. Four patients became long-term survivors (5.6+, 5.5+, 5.1, and 4.7+ years). All received alternating therapy. Six toxic deaths were observed among patients receiving continuous therapy compared to only one death among those in the alternating regimen. In conclusion, alternating combination chemotherapy leads to prolonged duration of remission. Duration of survival is not prolonged in uncured patients, but an increased possibility of long-term disease-free survival cannot be precluded.
UR - http://www.scopus.com/inward/record.url?scp=0021047387&partnerID=8YFLogxK
M3 - Article
C2 - 6315227
AN - SCOPUS:0021047387
SN - 0008-5472
VL - 43
SP - 6085
EP - 6089
JO - Cancer Research
JF - Cancer Research
ER -