Source:http://linkedlifedata.com/resource/pubmed/id/11205920
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2001-2-1
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pubmed:abstractText |
The combination of weekly irinotecan (CPT-11) and monthly cisplatin has shown promising activity in advanced non-small cell lung cancer (NSCLC) in previous Phase I and II studies. However, same-day administration of these agents may better exploit their therapeutic synergy and minimize toxicities. This multicenter Phase II study was undertaken to evaluate the efficacy and safety of a combination of weekly CPT-11 and weekly cisplatin in patients with advanced NSCLC. Patients with chemotherapy-naive stage IIIB or IV NSCLC were treated with repeated cycles of therapy comprising weekly treatment with both cisplatin and CPT-11 for 4 weeks, followed by a 2-week rest. The starting doses of CPT-11 and cisplatin were 65 and 30 mg/m2, respectively. Treatment was continued until the occurrence of disease progression, unacceptable toxicity, or a maximum of six cycles. Fifty patients were enrolled. The median age was 59 years (range, 44-79 years). Eastern Cooperative Oncology Group performance status was 0 in 22 patients, 1 in 19 patients, and 2 in 9 patients. Seven and 43 patients had stages IIIB and IV disease, respectively. Five patients had brain metastasis. Patients received a median of three 6-week cycles (range, 1-6). The objective response rate was 36% (18 of 50; 95% confidence interval, 24-54%) and included 18 partial responses. Median time to tumor progression was 6.9 months (range, 0.6-15.2). The median survival was 11.6 months (range, 0.16-21.9 months), and the 1-year survival rate was 46%. Grade 3/4 nonhematological toxicities included vomiting (12%) and diarrhea (26%). Grade 3/4 hematological toxicities included anemia (14%), neutropenia (26%), and thrombocytopenia (14%). Relative dose intensities for CPT-11 and cisplatin were 89 and 62%, respectively. Weekly combined administration of CPT-11 and cisplatin achieved a promising overall response rate, median time to tumor progression, and median survival in patients with stage IIIB/IV NSCLC. The regimen was well tolerated, and the planned dose intensity was well maintained. Further evaluation of this combination in NSCLC is warranted.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1078-0432
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
68-73
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pubmed:dateRevised |
2006-4-24
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pubmed:meshHeading |
pubmed-meshheading:11205920-Adult,
pubmed-meshheading:11205920-Aged,
pubmed-meshheading:11205920-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:11205920-Camptothecin,
pubmed-meshheading:11205920-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:11205920-Cisplatin,
pubmed-meshheading:11205920-Disease Progression,
pubmed-meshheading:11205920-Dose-Response Relationship, Drug,
pubmed-meshheading:11205920-Drug Administration Schedule,
pubmed-meshheading:11205920-Female,
pubmed-meshheading:11205920-Humans,
pubmed-meshheading:11205920-Lung Neoplasms,
pubmed-meshheading:11205920-Male,
pubmed-meshheading:11205920-Middle Aged,
pubmed-meshheading:11205920-Neoplasm Staging,
pubmed-meshheading:11205920-Survival Analysis,
pubmed-meshheading:11205920-Treatment Outcome
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pubmed:year |
2001
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pubmed:articleTitle |
Weekly irinotecan and cisplatin in advanced non-small cell lung cancer: a multicenter phase II study.
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pubmed:affiliation |
Vanderbilt University, Nashville, Tennessee 37232, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Multicenter Study,
Clinical Trial, Phase II
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