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临床试验/JPRN-jRCTs031190152
JPRN-jRCTs031190152进行中(未招募)2 期

JCOG1802: A randomized phase II trial of 2nd line treatment for advanced soft tissue sarcoma comparing trabectedin, eribulin and pazopanib - 2ND-STEP

TANAKA Kazuhiro0 个研究点目标入组 120 人开始时间: 2019年12月5日最近更新:
适应症

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 16age old 至 ot applicable(—)
性别
All

入选标准

  • (1) Histologically proven soft tissue sarcoma
  • (2) H&E slides used for diagnosis of (1) are available
  • (3) Soft tissue sarcoma with metastatic disease (Stage IV in AJCC- TNM 8th edition), unresectable primary sarcoma, or unresectable recurrent sarcoma
  • (4) Disease progression confirmed within 6 months
  • (5) Disease to fulfill either following (i)-(iv), chemotherapy including perioperative chemotherapy
  • (i) Disease progression (local progression or metaetatsis) after chemotherapy including doxorubicin
  • (ii) Disease progression after termination of chemotherapy including doxorubicin because of other than disease progression
  • (iii) Reccurence of disease which is disappeared by chemotherapy including doxorubicin (local and distant recurrence)
  • (iv) Disease progression of residual disease after chemotherapy including doxorubicin
  • (6) History of chemotherapy for sarcoma is only regimen including doxorubicin
  • (7) No treatment history for sarcoma and other cancers with trabectedin, eribulin or pazopanib
  • (8) Age 16 years or older
  • (9)ECOG status (PS): 0-2
  • (10) Measurable or non-measurable disease
  • (11) Adequate oral intake
  • (12)Latest adequate organ function as proved by the following laboratory studies within 14 days prior to registration
  • [1] Nutrophil count>=1,500 /mm3
  • [2] Hemoglobin>=8.0 g/dL
  • [3] Platelet count>=100,000 /mm3
  • [4] Total bilirubin<=1.5 mg/dL
  • [5] AST<=100 U/L
  • [6] ALT<=100 U/L
  • [7] Renal function to fulfill either following (a) or (b),
  • (a) Creatinine<=1.5 mg/dL
  • (b) Creatinine clearance>=50 mL/min
  • [8] ALP<=900 U/L (JSCC method), ALP<=315 U/L (IFCC method)
  • [9] CPK,=600 U/L for men, <=400 U/L for woman
  • [10] PT-INR<=1.38
  • [11] APTT<=44.4 sec
  • [12] TSH: 0.5-4.5 micro U/mL
  • [13] FT4: 0.9-1.8 ng/dL
  • (13) Normal findings or no need of treatment in case of abnormal findings on electrocardiogram (ECG) within 28 days prior to registration
  • (14) Ejection fraction of cardiac ultrasound examination: more than 50% within 28 days prior to registration
  • (15) Written informed consent (If the patient's age is under 20 years old, the additional consent must be obtained from the patient's parent or legal guardian.)

排除标准

  • (1) Synchronous or metachronous (within 2 years) malignancy except cancer with 2-year relative survival rate of 95% or more
  • (2) Diagnosed with active infectious disease requiring systemic treatment
  • (3) Febrile more than 38 degrees Celsius at the registation
  • (4) Pregnancy, possible pregnancy, within 28 days after delivery or breast-feeding. Male subjects who want pregnancy of their partner
  • (5) Psychological disorder difficult to participate in this clinical study
  • (6) Receiving continuous systemic corticosteroid or immunesuppressant treatment (systemically or intravenously)
  • (7)Systolic blood pressure>140 mmHg and diastolic blood pressure>90 mmHg two consecutive times measured in a hospital on the day of registration (irrespective of antihypertensive agents use)
  • (8) Interstitial pneumonia , pulmonary fibrosis or severe emphysema based on chest CT
  • (9) HBs antigen positive
  • (10) History of cardiovascular disease
  • [1] Myocardial infarction within the last 6 months, unstable angina pectoris within the last 3 weeks
  • [2] Angioplasty surgery or stent implantation, or coronary artery bypass graft within 6 months
  • [3] Heart failure class III or IV accorging to NYHA
  • [4] Uncontrolled valve disease, dilative cardiomyopathy, or hypertrophic myocardiopathy
  • (11) Active bleeding
  • (12) Symptomatic brain metastasis or brain metastasis requiring treatment (screening of brain metastasis is not required for clinically unnecessary patients)
  • (13) Pleural effusion, ascitic fluid, pericardial effusion requiring drainage

研究者

发起方
TANAKA Kazuhiro

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