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临床试验/ITMCTR1900002442
ITMCTR1900002442招募中4 期

Clinical study of Anlotinib as Third-Line or Further Treatment on Advanced Epithelial Ovarian Cancer

Oncology Department, Guangdong Provincial Hospital of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational study

入排标准

年龄范围
18 至 75(—)
性别
All

入选标准

  • (1) Aged 18-75 years;
  • (2) Epithelial ovarian cancer was diagnosed by pathology or cytology.
  • (3) The stage of diagnosis is stage IV or after the previous radical treatment, recurrence and metastasis are re-staged to stage IV;
  • (4) After the first-line and second-line treatmentthe tumor progresses again;
  • (5) Behavioral status PS (ECOG) 0-2;
  • (6) The estimated survival time is greater than 3 months;
  • (7) Normal function of bone marrow, liver and kidney:
  • Hb (hemoglobin) >= 80g / L;
  • NEUT (neutrophil count) >= 1.5*10^9 / L;
  • PLT (platelet) >= 90*10^9 / L;
  • Alanine aminotransferase (ALT)<= 2.5*upper limit of normal(ULN) (if combined with liver metastasis, ALT <= 5* ULN);
  • Total bilirubin (TB) <= 1.5 * ULN;
  • Protein (ALB) >= 30g / L;
  • Creatinine (Scr) <= 1.5 * ULN;
  • (8) Knowing to participate in the study, sign the informed consent, good compliance and can follow-up;
  • (9) Women in childbearing age were negative for pregnancy test (blood/urine hCG) within 7 days. And ensured effective contraception during the trial and within 6 months after the end of the trial.

排除标准

  • (1) Combined with hypertension and poor drug control, the blood pressure after standard antihypertensive treatment is higher than 140/90mmHg;
  • (2) Combined bleeding risk;
  • (3) Concomitant merger of other malignant tumors within five years;
  • (4) Those who combine active tuberculosis and other serious infectious diseases;
  • (5) Patients who have received radiotherapy;
  • (6) Has received other anti-angiogenic drugs;
  • (7) There are serious brain diseases or mental illnesses that affect the patient's ability to complain privately;
  • (8) With the history of organ transplantation;
  • (9) Participated in other clinical studies within 4 weeks;
  • (10) Pregnant or lactating women.

研究者

发起方
Oncology Department, Guangdong Provincial Hospital of Chinese Medicine

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