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Forty-nine consecutive previously untreated patients with extensive stage small cell bronchogenic carcinoma were treated with cyclophosphamide 1,000 mg/m2, doxorubicin 50 mg/m2, etoposide (VP-16-213) 125 mg/m2, and vincristine 1.4 mg/m2 (maximum 2 mg) as induction chemotherapy. Thirty-four patients were given high-intensity therapy, receiving these drugs on both Days 1 and 8 of two or three 21-day induction courses. Fifteen other patients were treated with moderate intensity, receiving these drugs only on Day 1 of two 21-day induction courses. The number and intensity of induction courses were determined by the time of entry into the study. There were 31 complete or partial remissions among the 33 evaluable patients treated with high-intensity therapy (94 percent), including eight complete remissions (24 percent), whereas there were 11 responses (73 percent) including three complete responses (20 percent) among the 15 patients treated with moderate-intensity therapy. There was no marked tendency for the patients in the high-intensity group to have a more favorable response to the induction chemotherapy (p = 0.22), and survival experience was very similar in the two groups (p = 0.92). Overall median survival was 12 months. Within the high-intensity group, there was no significant difference between patients receiving two or three courses of induction therapy with respect to response (p = 0.97) or survival (p = 0.32). There were six induction deaths in the high-intensity induction group (18 percent) and one induction death in the moderate-intensity group (7 percent) (p = 0.59). In addition to the expected hematologic and infectious complications, there were unexpectedly high frequencies of mucositis, reversible congestive heart failure, and severe peripheral neuropathy in patients treated with high-intensity induction. Only two patients, both in the high-intensity group, were alive and free of disease at 24 months. Increasing the intensity of induction chemotherapy with these drugs did not significantly improve response or survival in extensive stage small cell bronchogenic carcinoma.
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
February 1985,
Journal of clinical oncology : official journal of the American Society of Clinical Oncology,
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
March 1984,
The American journal of medicine,
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
September 1983,
Cancer treatment reviews,
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
August 1980,
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M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
January 1980,
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M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
January 1983,
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M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
January 1977,
Cancer treatment reports,
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
August 1980,
International journal of radiation oncology, biology, physics,
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
February 1983,
Onkologie,
M Brower, and
D C Ihde, and
A Johnston-Early, and
P A Bunn, and
M H Cohen, and
D N Carney, and
R W Makuch, and
M J Matthews, and
P A Radice, and
J D Minna
March 1983,
Seminars in oncology,
