Eligibility |
Inclusion Criteria:
1. Have fully understood the study and voluntarily signed the informed consent;
2. Age =18 years old;
3. Histologically or cytologically confirmed patients with unresectable or metastatic
soft tissue sarcoma;
4. The patient must have at least one measurable lesion (RECIST1.1);
5. Previous failure of anthracycline-containing chemotherapy was defined as disease
progression during treatment or within 3 months after the last treatment, or disease
progression during adjuvant treatment with anthracycline-containing chemotherapy or
within 6 months after adjuvant treatment, and toxic side effects of
anthracycline-containing chemotherapy were not tolerated. (Neoadjuvant or adjuvant
chemotherapy is allowed in the early stage. If disease progression/recurrence occurs
during neoadjuvant/adjuvant therapy or within 6 months after the end of treatment,
neoadjuvant/adjuvant therapy is considered a failure of first-line systemic
chemotherapy for progressive disease);
6. Patients with previous anti-angiogenic efficacy and failure were defined as: tumor
progression occurred in SD or above patients after withdrawal of SD (CR/PR) during the
course of anti-angiogenic therapy (including anti-angiogenic small molecule inhibitors
or monoclonal antibodies), or tumor progression occurred in SD patients over 12 weeks;
Or the toxic side effects of treatment are intolerable.
7. ECOG physical status 0 or 1 points (PS0-2 points for amputees);
8. Expected survival =12 weeks;
9. Blood test (without blood transfusion within 14 days)
1) Neutrophil absolute value =1.5×10^9/L, platelets =100×10^9/L, hemoglobin concentration
=9g/dL);
2) Liver function test (aspartate aminotransferase and glutamic aminotransferase =2.5×ULN,
total bilirubin =1.5×ULN; In case of liver metastasis, AST and ALT=5×ULN);
3) Renal function (serum creatinine =1.5×ULN, creatinine clearance (CCr)=60ml/min)
10. Fertile male or female patients voluntarily used effective contraceptive methods, such
as double barrier methods, condoms, oral or injectable contraceptives, intrauterine
devices, etc., during the study period and within 6 months of the last study dose. All
female patients will be considered fertile unless they have undergone natural menopause,
artificial menopause, or sterilization (such as hysterectomy, bilateral adnexectomy, or
irradiation of radioactive ovaries).
Exclusion Criteria:
1. Patients who have received previous treatment with Surufatinib;
2. Consider toxic reactions associated with anti-vascular targeting drugs if they have
previously been intolerable
3. Participated in other domestic unapproved or unmarketed drug clinical trials and
accepted the corresponding experimental drug treatment within 4 weeks before
enrollment;
4. Received any surgery or invasive treatment or operation (except intravenous
catheterization, puncture drainage, etc.) within 4 weeks before enrollment;
5. International Standardized Ratio (INR)>1.5 or partially activated prohemase time
(APTT)>1.5×ULN;
6. The investigator identified clinically significant electrolyte abnormalities;
7. The patient currently has high blood pressure that cannot be controlled by drugs,
which is defined as: systolic blood pressure =140mmHg and/or diastolic blood pressure
=90mmHg;
8. Unsatisfactory blood glucose control (FBG > 10mmol/L);
9. The patient has any current disease or condition that affects the absorption of the
drug, or the patient cannot take sofantinib orally;
10. The patient currently has gastrointestinal diseases such as active gastric and
duodenal ulcers, ulcerative colitis, or active bleeding from unresectosed tumors, or
other conditions determined by researchers that may cause gastrointestinal bleeding or
perforation;
11. Patients with evidence or history of significant bleeding tendency within 3 months
prior to enrollment (bleeding within 3 months >30mL, hematemesis, stool, stool blood),
hemoptysis (within 4 weeks >5mL of fresh blood) or had a thromboembolic event
(including stroke events and/or transient ischemic attacks) within 12 months;
12. Clinically significant cardiovascular disease, including but not limited to the
following: acute myocardial infarction, severe/unstable angina pectoris, or coronary
artery bypass grafting within 6 months prior to enrollment; Congestive Heart Failure
New York Heart Association (NYHA) Grades > Lv.2; Ventricular arrhythmias requiring
medical treatment; LVEF(Left ventricular Ejection Fraction)<50%;
13. Have had other malignancies within the past 5 years, except basal cell or squamous
cell carcinoma of the skin after radical surgery, or carcinoma in situ of the cervix;
14. Active or uncontrolled severe infection;
1) Known human immunodeficiency virus (HIV) infection;
2) A known history of clinically significant liver disease, including viral hepatitis A
known hepatitis B virus (HBV) carrier must rule out active HBV infection, i.e., positive
HBVDNA (>1×10^4 copies /mL or >2000IU/ml);
3) Known hepatitis C virus infection (HCV) and HCVRNA positive (>1×10^3 copies /mL), or
other hepatitis, cirrhosis;
15. The patient has current central nervous system (CNS) metastases or previous brain
metastases;
16. Patients with persistent toxicity due to any previous antitumor therapy that has not
returned to = grade 2, but with alopecia or lymphocytopenia of any grade are admitted to
this study;
17. Women who are pregnant (positive pregnancy test before medication) or breastfeeding;
18. Any other medical condition, a clinically significant metabolic abnormality, abnormal
physical examination, or abnormal laboratory examination, which, in the investigator's
judgment, reasonably suspects the patient to have a medical condition or condition that is
not suitable for the use of the investigational drug (such as the presence of epileptic
seizures requiring treatment), or which would affect the interpretation of the study
results, or place the patient at a high risk;
19. Urine routine indicated urinary protein =2+, and 24-hour urinary protein quantification
> 1.0g.
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