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临床试验/JPRN-jRCTs061180082
JPRN-jRCTs061180082已完成2 期

A randomized phase II study of daily administrations versus alternate-day administrations of S-1 with completely resected pathological stage I (T>2cm) of non-small cell lung cancer (Setouchi Lung Cancer Group SLCG1301) - SLCG1301

Toyooka Shinichi0 个研究点目标入组 93 人开始时间: 2019年3月20日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
93

研究概览

简要总结

Alternate-day oral administration of S-1 for 1 year as adjuvant chemotherapy was demonstrated to be feasible with low toxicity in completely resected stage I (tumor diameter > 2 cm) NSCLC

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 < 75age old(—)
性别
All

入选标准

  • 1) Pathologically proven non-small cell lung cancer
  • 2) Neither previous chemotherapy nor radiotherapy before operation
  • 3) Complete resection
  • 4) Pathological stage I (T>2cm)
  • 5) LN dissection (ND2a)
  • 6) Aged 20-75 years old enrollment
  • 7) ECOG PS 0-1
  • 8) Adequate organ function:
  • 1. WBC >=3000/mm3
  • 2. Neutrophil count >= 1,500 /mm3
  • 3. Platelet count >= 100,000 /mm3
  • 4. Hemoglobin >= 9.0 g/dL
  • 5. total bilirubin <= 1.5 mg/dL
  • 6. AST and ALT x 2.5 of upper limit of normal (ULN)
  • 7. Creatinine clearance >=40mL/min
  • 8. PaO2 >= 60mmHg or SpO2 >= 90%
  • 9) At least lobectomy, within 8 weeks after surgery
  • 10) Signed informed consent

排除标准

  • 1. Allergy against S-1
  • 2. Severe myelosuppression, renal dysfunction or liver dysfunction
  • 3. Usage of other fluorinated pyrimidine drugs
  • 4. Usage of flucytosine
  • 5. Severe drug allergy
  • 6. Unstable angina or Myocardial Infarction within 6 months
  • 7. Apparent interstitial pneumonitis or pulmonary fibrosis at chest rentogenogram
  • 8. Concomitant therapy Warfarin Potassium or Dabigatran
  • 9. Abnormality of EGG or UCG
  • 10. Severe heart disease, serious psychiatric illness, severe infection, severe other complications
  • 11. Uncontrolled Diabetes Mellitus
  • 13. Diarrhea
  • 14. Uncontrolled cancer
  • 15. HBs antigen positive
  • 16. Other patients who are unfit for the study as determined by the attending physician.

研究者

发起方
Toyooka Shinichi

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