Irinotecan plus carboplatin in patients with extensive-disease small-cell lung cancer

This study was designed to evaluate the efficacy and safety of irinotecan in combination with carboplatin in previously untreated, extensive-disease small-cell lung cancer (ED-SCLC). Patients with histologically or cytologically confirmed ED-SCLC received irinotecan (60 mg/m 2 on days 1, 8, and 15)...

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Published inMedical oncology (Northwood, London, England) Vol. 28; no. 1; pp. 342 - 350
Main Authors Kim, Young Saing, Park, Se Hoon, Kyung, Sun Young, Sym, Sun Jin, Lee, Sang Pyo, Park, Jeong Woong, Jung, Sung Hwan, Park, Jinny, Cho, Eun Kyung, Lee, Jae Hoon, Shin, Dong Bok
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.03.2011
Springer Nature B.V
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Abstract This study was designed to evaluate the efficacy and safety of irinotecan in combination with carboplatin in previously untreated, extensive-disease small-cell lung cancer (ED-SCLC). Patients with histologically or cytologically confirmed ED-SCLC received irinotecan (60 mg/m 2 on days 1, 8, and 15) plus carboplatin (AUC 5 on day 1) every 4 weeks. Treatment was repeated until disease progression, unacceptable toxicity, or up to 6 cycles. Forty-four patients were enrolled. In an intent-to-treat analysis, the overall response rate (RR) was 75% (8 complete responses and 25 partial responses). The median progression-free (PFS) and overall survival (OS) were 5.6 and 8.7 months, respectively. The principle toxicities were neutropenia and diarrhea. Grade 3–4 neutropenia occurred in 30% of the patients and 7% of patients presented with febrile neutropenia. Grade 3–4 diarrhea occurred in 21% of the patients. A subgroup consisting of patients ≥65 years of age had outcomes similar to the younger group <65 years of age. The objective RR was 72% in the patients <65 years of age and 77% in the patients ≥65 years of age ( P  = .738). The median PFS and OS (<65 years vs. ≥65 years) were 5.3 vs. 5.6 months ( P  = .835) and 9.0 vs. 8.7 months ( P  = .648), respectively. The combination of irinotecan and carboplatin is active and tolerable in patients with ED-SCLC. This regimen could be considered as a treatment option for patients of advanced age.
AbstractList This study was designed to evaluate the efficacy and safety of irinotecan in combination with carboplatin in previously untreated, extensive-disease small-cell lung cancer (ED-SCLC). Patients with histologically or cytologically confirmed ED-SCLC received irinotecan (60 mg/m(2) on days 1, 8, and 15) plus carboplatin (AUC 5 on day 1) every 4 weeks. Treatment was repeated until disease progression, unacceptable toxicity, or up to 6 cycles. Forty-four patients were enrolled. In an intent-to-treat analysis, the overall response rate (RR) was 75% (8 complete responses and 25 partial responses). The median progression-free (PFS) and overall survival (OS) were 5.6 and 8.7 months, respectively. The principle toxicities were neutropenia and diarrhea. Grade 3-4 neutropenia occurred in 30% of the patients and 7% of patients presented with febrile neutropenia. Grade 3-4 diarrhea occurred in 21% of the patients. A subgroup consisting of patients ≥ 65 years of age had outcomes similar to the younger group <65 years of age. The objective RR was 72% in the patients <65 years of age and 77% in the patients ≥ 65 years of age (P = .738). The median PFS and OS (<65 years vs. ≥ 65 years) were 5.3 vs. 5.6 months (P = .835) and 9.0 vs. 8.7 months (P = .648), respectively. The combination of irinotecan and carboplatin is active and tolerable in patients with ED-SCLC. This regimen could be considered as a treatment option for patients of advanced age.
This study was designed to evaluate the efficacy and safety of irinotecan in combination with carboplatin in previously untreated, extensive-disease small-cell lung cancer (ED-SCLC). Patients with histologically or cytologically confirmed ED-SCLC received irinotecan (60 mg/m 2 on days 1, 8, and 15) plus carboplatin (AUC 5 on day 1) every 4 weeks. Treatment was repeated until disease progression, unacceptable toxicity, or up to 6 cycles. Forty-four patients were enrolled. In an intent-to-treat analysis, the overall response rate (RR) was 75% (8 complete responses and 25 partial responses). The median progression-free (PFS) and overall survival (OS) were 5.6 and 8.7 months, respectively. The principle toxicities were neutropenia and diarrhea. Grade 3–4 neutropenia occurred in 30% of the patients and 7% of patients presented with febrile neutropenia. Grade 3–4 diarrhea occurred in 21% of the patients. A subgroup consisting of patients ≥65 years of age had outcomes similar to the younger group <65 years of age. The objective RR was 72% in the patients <65 years of age and 77% in the patients ≥65 years of age ( P  = .738). The median PFS and OS (<65 years vs. ≥65 years) were 5.3 vs. 5.6 months ( P  = .835) and 9.0 vs. 8.7 months ( P  = .648), respectively. The combination of irinotecan and carboplatin is active and tolerable in patients with ED-SCLC. This regimen could be considered as a treatment option for patients of advanced age.
This study was designed to evaluate the efficacy and safety of irinotecan in combination with carboplatin in previously untreated, extensive-disease small-cell lung cancer (ED-SCLC). Patients with histologically or cytologically confirmed ED-SCLC received irinotecan (60 mg/m^sup 2^ on days 1, 8, and 15) plus carboplatin (AUC 5 on day 1) every 4 weeks. Treatment was repeated until disease progression, unacceptable toxicity, or up to 6 cycles. Forty-four patients were enrolled. In an intent-to-treat analysis, the overall response rate (RR) was 75% (8 complete responses and 25 partial responses). The median progression-free (PFS) and overall survival (OS) were 5.6 and 8.7 months, respectively. The principle toxicities were neutropenia and diarrhea. Grade 3-4 neutropenia occurred in 30% of the patients and 7% of patients presented with febrile neutropenia. Grade 3-4 diarrhea occurred in 21% of the patients. A subgroup consisting of patients ≥65 years of age had outcomes similar to the younger group <65 years of age. The objective RR was 72% in the patients <65 years of age and 77% in the patients ≥65 years of age (P = .738). The median PFS and OS (<65 years vs. ≥65 years) were 5.3 vs. 5.6 months (P = .835) and 9.0 vs. 8.7 months (P = .648), respectively. The combination of irinotecan and carboplatin is active and tolerable in patients with ED-SCLC. This regimen could be considered as a treatment option for patients of advanced age.[PUBLICATION ABSTRACT]
Author Park, Jeong Woong
Jung, Sung Hwan
Shin, Dong Bok
Cho, Eun Kyung
Kim, Young Saing
Sym, Sun Jin
Park, Jinny
Kyung, Sun Young
Park, Se Hoon
Lee, Jae Hoon
Lee, Sang Pyo
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CitedBy_id crossref_primary_10_1002_jbm_b_31858
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Keywords Carboplatin
Irinotecan
Chemotherapy
Small-cell lung cancer
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Snippet This study was designed to evaluate the efficacy and safety of irinotecan in combination with carboplatin in previously untreated, extensive-disease small-cell...
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SubjectTerms Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Bone Neoplasms - drug therapy
Bone Neoplasms - secondary
Brain Neoplasms - drug therapy
Brain Neoplasms - secondary
Camptothecin - administration & dosage
Camptothecin - analogs & derivatives
Carboplatin - administration & dosage
Disease Progression
Female
Hematology
Humans
Internal Medicine
Liver Neoplasms - drug therapy
Liver Neoplasms - secondary
Lung cancer
Lung Neoplasms - drug therapy
Lung Neoplasms - pathology
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Staging
Oncology
Original Paper
Pathology
Small Cell Lung Carcinoma - drug therapy
Small Cell Lung Carcinoma - pathology
Treatment Outcome
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Title Irinotecan plus carboplatin in patients with extensive-disease small-cell lung cancer
URI https://link.springer.com/article/10.1007/s12032-010-9453-z
https://www.ncbi.nlm.nih.gov/pubmed/20198458
https://www.proquest.com/docview/853689596/abstract/
https://search.proquest.com/docview/853996800
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