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      소세포 폐암 환자에서 이리노테칸, 카보플라틴 주별 분할 항암요법의 효과 = Weekly irinotecan and carboplatin for patients with small cell lung cancer

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      https://www.riss.kr/link?id=A100246131

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      다국어 초록 (Multilingual Abstract)

      Background: Lung cancer is the most common cause of cancer-related death worldwide and in Korea, and small cell lung cancer (SCLC) is the most deadly tumor type in the different lung cancer histology. Chemotherapy is the main strategy of the treatment for SCLC, and etoposide and platinum regimen has been the only standard chemotherapy for about 30 years. To test feasibility of weekly divided dose irinotecan and carboplatin for Korean patients is the aim of this study.
      Methods: Patients with histologically or cytologically confirmed extensive stage SCLC were included. Patients with limited stage (LD), who could not tolerate concurrent chemoradiotherapy were also included. All the patients received irinotecan 60 mg/m2, carboplatin 2 area under the curve at day 1, 8, and 15 every 4 weeks. Study regimen was discontinued when the disease progressed or intolerable side effects occurred. No more than 6 cycles of chemotherapy were given.
      Results: Total 47 patients were enrolled, among them 9 patients were LD. Overall response rate was 74.5% (complete response, 14.9%; partial response, 59.6%). Side effects greater than grade 3 were neutropenia (25.5%), fatigue (12.8%), thrombocytopenia (8.5%), sepsis (4.3%), and pancytopenia (2.1%). There was no treatment related death.
      Conclusion: Weekly divided irinotecan and carboplatin regimen is effective, and safe as a first line therapy for both stage of SCLC. Large scaled, controlled study is feasible.
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      Background: Lung cancer is the most common cause of cancer-related death worldwide and in Korea, and small cell lung cancer (SCLC) is the most deadly tumor type in the different lung cancer histology. Chemotherapy is the main strategy of the treatment...

      Background: Lung cancer is the most common cause of cancer-related death worldwide and in Korea, and small cell lung cancer (SCLC) is the most deadly tumor type in the different lung cancer histology. Chemotherapy is the main strategy of the treatment for SCLC, and etoposide and platinum regimen has been the only standard chemotherapy for about 30 years. To test feasibility of weekly divided dose irinotecan and carboplatin for Korean patients is the aim of this study.
      Methods: Patients with histologically or cytologically confirmed extensive stage SCLC were included. Patients with limited stage (LD), who could not tolerate concurrent chemoradiotherapy were also included. All the patients received irinotecan 60 mg/m2, carboplatin 2 area under the curve at day 1, 8, and 15 every 4 weeks. Study regimen was discontinued when the disease progressed or intolerable side effects occurred. No more than 6 cycles of chemotherapy were given.
      Results: Total 47 patients were enrolled, among them 9 patients were LD. Overall response rate was 74.5% (complete response, 14.9%; partial response, 59.6%). Side effects greater than grade 3 were neutropenia (25.5%), fatigue (12.8%), thrombocytopenia (8.5%), sepsis (4.3%), and pancytopenia (2.1%). There was no treatment related death.
      Conclusion: Weekly divided irinotecan and carboplatin regimen is effective, and safe as a first line therapy for both stage of SCLC. Large scaled, controlled study is feasible.

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      참고문헌 (Reference)

      1 Evans WK, "VP-16 alone and in combination with cisplatin in previously treated patients with small cell lung cancer" 53 : 1461-1466, 1984

      2 Oken MM, "Toxicity and response criteria of the Eastern Cooperative Oncology Group" 5 : 649-655, 1982

      3 "Statistic of mortality of all ages in Republic of Korea for both sexes" Statistics Korea

      4 Ardizzoni A, "Standard versus intensified chemotherapy with granulocyte colony-stimulating factor support in small-cell lung cancer: a prospective European Organization for Research and Treatment of Cancer-Lung Cancer Group Phase III Trial-08923" 20 : 3947-3955, 2002

      5 Hanna N, "Randomized phase III trial comparing irinotecan/cisplatin with etoposide/cisplatin in patients with previously untreated extensive-stage disease small-cell lung cancer" 24 : 2038-2043, 2006

      6 Lara PN Jr, "Phase III trial of irinotecan/cisplatin compared with etoposide/cisplatin in extensive-stage small-cell lung cancer: clinical and pharmacogenomic results from SWOG S0124" 27 : 2530-2535, 2009

      7 Kim HS, "Phase II study of weekly carboplatin and irinotecan as first-line chemotherapy for patients with advanced non-small cell lung cancer" 71 : 1591-1597, 2013

      8 Eisenhauer EA, "New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)" 45 : 228-247, 2009

      9 Pao W, "New driver mutations in non-small-cell lung cancer" 12 : 175-180, 2011

      10 Kim YC, "National survey of lung cancer in Korea, 2005" 6 : 67-73, 2007

      1 Evans WK, "VP-16 alone and in combination with cisplatin in previously treated patients with small cell lung cancer" 53 : 1461-1466, 1984

      2 Oken MM, "Toxicity and response criteria of the Eastern Cooperative Oncology Group" 5 : 649-655, 1982

      3 "Statistic of mortality of all ages in Republic of Korea for both sexes" Statistics Korea

      4 Ardizzoni A, "Standard versus intensified chemotherapy with granulocyte colony-stimulating factor support in small-cell lung cancer: a prospective European Organization for Research and Treatment of Cancer-Lung Cancer Group Phase III Trial-08923" 20 : 3947-3955, 2002

      5 Hanna N, "Randomized phase III trial comparing irinotecan/cisplatin with etoposide/cisplatin in patients with previously untreated extensive-stage disease small-cell lung cancer" 24 : 2038-2043, 2006

      6 Lara PN Jr, "Phase III trial of irinotecan/cisplatin compared with etoposide/cisplatin in extensive-stage small-cell lung cancer: clinical and pharmacogenomic results from SWOG S0124" 27 : 2530-2535, 2009

      7 Kim HS, "Phase II study of weekly carboplatin and irinotecan as first-line chemotherapy for patients with advanced non-small cell lung cancer" 71 : 1591-1597, 2013

      8 Eisenhauer EA, "New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)" 45 : 228-247, 2009

      9 Pao W, "New driver mutations in non-small-cell lung cancer" 12 : 175-180, 2011

      10 Kim YC, "National survey of lung cancer in Korea, 2005" 6 : 67-73, 2007

      11 "National Institute of Health. Common terminology criteria for adverse events (CTCAE) version 4.0"

      12 "National Comprehnsive Cancer Network. Small cell lung cancer (version 2.2014); NCCN clinical practice guidelines in oncology (NCCN guidelines)" NCCN

      13 American Joint Commitee on Cancer, "Lung cancer staging" AJCC

      14 Ma MK, "Lessons learned from the irinotecan metabolic pathway" 10 : 41-49, 2003

      15 Noda K, "Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer" 346 : 85-91, 2002

      16 Mathijssen RH, "Irinotecan pathway genotype analysis to predict pharmacokinetics" 9 : 3246-3253, 2003

      17 Horn L, "Harrison’s principles of internal medicine" McGraw-Hill 737-753, 2012

      18 Ettinger DS, "Goldman’s cecil medicine" Elsevier/Saunders 1264-1272, 2012

      19 Hong WK, "Etoposide combined with cyclophosphamide plus vincristine compared with doxorubicin plus cyclophosphamide plus vincristine and with high-dose cyclophosphamide plus vincristine in the treatment of small-cell carcinoma of the lung: a randomized trial of the Bristol Lung Cancer Study Group" 7 : 450-456, 1989

      20 Ferlay J, "Estimates of worldwide burden of cancer in 2008:GLOBOCAN 2008" 127 : 2893-2917, 2010

      21 Pujol JL, "Dose-intensity of a four-drug chemotherapy regimen with or without recombinant human granulocytemacrophage colony-stimulating factor in extensive-stage small-cell lung cancer: a multicenter randomized phase III study" 15 : 2082-2089, 1997

      22 Han JY, "Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin" 24 : 2237-2244, 2006

      23 Mathijssen RH, "Clinical pharmacokinetics and metabolism of irinotecan (CPT-11)" 7 : 2182-2194, 2001

      24 Porter LL 3rd, "Cisplatin and etoposide combination chemotherapy for refractory small cell carcinoma of the lung" 69 : 479-481, 1985

      25 Pectasides D, "Bountouroglou N, Karvounis N, et al. Weekly chemotherapy with carboplatin, docetaxel and irinotecan in advanced non-small-celllung cancer: a phase II study" 38 : 1194-1200, 2002

      26 Schmittel A, "A German multicenter, randomized phase III trial comparing irinotecan-carboplatin with etoposide-carboplatin as first-line therapy for extensive-disease small-cell lung cancer" 22 : 1798-1804, 2011

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2022-01-01 학술지명변경 한글명 : Yeungnam University Journal of Medicine -> Journal of Yeungnam Medical Science
      외국어명 : 미등록 -> Journal of Yeungnam Medical Science
      KCI등재
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2016-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.03 0.03 0
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0 0 0 0
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