Overview
The clinical treatment of patients with resistant/relapsed/advanced gynecological malignancies is very difficult, and the difficulty lies in the selection of effective drugs. This study was a cohort study of recurrent/drug-resistant advanced ovarian high-grade serous carcinoma and advanced/recurrent endometrial adenocarcinoma treated in our hospital. A total of 20 cases were included in the proposed study group, including 12 cases of high-grade serous ovarian carcinoma and 8 cases of endometrial adenocarcinoma. Twenty patients who did not use PTC model to guide treatment at the same period were selected as controls. To compare the consistency of in vitro drug sensitivity detection results of PTC microtumor with clinical therapeutic effect, and to explore the feasibility of using PTC microtumor model to guide the treatment of patients with drug-resistant/recurrent advanced ovarian epithelial cancer or endometrial cancer. The clinical therapeutic effects of the study group and the control group were compared, and the rates of CR, PR, SD, PFS, OS and TTP were evaluated by RECIST1.1 standard. PTC models based on different clinical samples (tissue and ascites) were compared to analyze the consistency of in vitro drug sensitivity detection results and the relationship with clinical efficacy.
Eligibility
Inclusion Criteria:
- Age ≥18 years, ≤80 years
- Recurrent/drug-resistant gynecological tumors include: ① patients with advanced high-grade ovarian serous cancer whose tumor is uncontrolled or recurrent within 6 months after receiving platinum-based chemotherapy; ② Advanced ovarian high-grade serous cancer patients with platinum resistance at first treatment; ③ Patients with advanced or recurrent endometrial adenocarcinoma.
- Life expectancy > 6 months;
- Malignant tumors that are not being treated by other systems or are in an active phase;
- Have at least one measurable target lesion according to RECIST1.1 criteria;
- Specimen requirements: fresh specimens with sufficient cell culture, including tissue samples and abdominal effusion;
- Physical strength score: ECOG 0-2;
- Major organ functions must meet clinical treatment requirements:
- Blood routine: neutrophil (ANC) ≥1.5x109/L; Platelet count (PLT) ≥90x109/L; Hemoglobin (Hb) ≥90g/L; ② Blood biochemistry: total bilirubin (TBIL) ≤1.5x upper limit of normal value (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤1.5xULN; Urea nitrogen (BUN) and creatinine (Cr) ≤1.5 x ULN
(3) Heart color ultrasound: left ventricular ejection fraction (LVEF) ≥55%;
④ 12-lead ECG: Fridericia method corrected QT period (QTcF) < 470 msec. (9) Consent to
abstinence from sex or use of an effective contraceptive method during treatment and for at
least 7 months after the last dose in the study treatment for female patients who are not
menopausal or have not been surgically sterilized; (10) Patients participating in the study
(or their legal representatives) understand and voluntarily sign informed consent, have
good compliance, and are willing to cooperate with follow-up.
Exclusion Criteria:
1. Patients who are unable to provide sufficient fresh samples;
2. pregnant and lactating women, female patients with fertility and positive pregnancy
tests, or patients of childbearing age who are unwilling to take effective
contraceptive measures during the whole test period;
3. The patient has uncontrollable co-morbidity, including but not limited to: symptomatic
congestive heart failure, unstable angina pectoris and myocardial infarction,
uncontrolled grade III hypertension, liver insufficiency, renal insufficiency,
diabetes uncontrolled blood sugar, arrhythmia and mental illness;
4. Other circumstances in which the investigator determines that participation in the
study is not appropriate.