| Eligibility |
Inclusion Criteria:
1. Have fully understood the study and voluntarily signed the informed consent
2. Age =18 years old, male or female
3. Advanced metastatic colorectal adenocarcinoma confirmed by histopathology
4. The best efficacy evaluation of first-line chemotherapy (mFOLFOX6, XELOX, or FOLFIRI)
in previous patients must be partial response (PR) or above or progression-free
survival (PFS) =1 year, with a first-line drug withdrawal interval of more than 1
year. Pre-adjuvant/neoadjuvant therapy is allowed. If recurrence or metastasis occurs
during or within 6 months after completion of adjuvant/neoadjuvant therapy,
adjuvant/neoadjuvant therapy is considered a failure of first-line chemotherapy for
advanced disease
5. The patient has failed at least previous second-line treatment,The use of Cetuximab
(KRAS and Braf wild type) and bevacizumab in previous anti-tumor regiments is
required,Prior treatment with regorafenib or TAS-102 is permitted
6. ECOG status 0-2 points
7. Expected survival =12 weeks
8. Have at least one measurable lesion (RECIST version 1.1)
9. Inadequate bone marrow reserve or organ function, as demonstrated by any of the
following laboratory values: Absolute neutrophil count (ANC) =1.5×109/L Platelet count
=80×109 / L Hemoglobin=80 g/L(<8 g/dL) Serum albumin =3g/dL Alanine aminotransferase
<2.5 × upper limit of normal (ULN) if no demonstrable liver metastases or <5 × ULN in
the presence of liver metastases. Aspartate aminotransferase (AST) <2.5 × ULN if no
demonstrable liver metastases or < 5 × ULN in the presence of liver metastases. Total
bilirubin (TBL)<1.5 × ULN Creatinine= 1.5 × ULN concurrent with creatinine clearance
=50 mL/min (measured or calculated by the Cockcroft-Gault equation) confirmation of
creatinine clearance is only required when creatinine is =1.5 × ULN.
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).
11. Good compliance, cooperate with follow-up.
Exclusion Criteria:
- 1: Patients with known dMMR or MSI-H colorectal cancer who have not previously used
anti-PD-1 or PD-L1 inhibitors
2: Previously received small molecule targeted drug therapy with fuquinitinib
3: Symptomatic brain or meningeal metastases (except those with brain metastases that
have undergone local radiotherapy or surgery for more than 6 months and whose disease
control is stable)
4: Severe infection (such as intravenous infusion of antibiotics, antifungals, or
antiviral drugs) within 4 weeks prior to treatment, or unexplained fever > 38.5 ° C
during screening/first administration
5: Have high blood pressure that is not well controlled by antihypertensive
medications (systolic blood pressure =150 mmHg or diastolic blood pressure =100 mmHg)
6: Obvious clinical bleeding symptoms or obvious bleeding tendency within 3 months
prior to treatment (bleeding > 30 mL within 3 months, hematemesis, black stool, blood
in the stool), hemoptysis (> 5 mL of fresh blood within 4 weeks), etc. Or treatment of
arterial venous thrombosis events within the preceding 6 months, such as
cerebrovascular accidents (including transient ischemic attack, cerebral hemorrhage,
cerebral infarction), deep vein thrombosis, and pulmonary embolism
7: Long-term anticoagulant therapy with warfarin or heparin, or long-term antiplatelet
therapy (aspirin =300 mg/day or clopidogrel =75 mg/day) is required
8: During screening, it was found that the tumor invaded large vascular structures,
such as pulmonary artery, superior vena cava or inferior vena cava, etc., and the
researchers judged that there was a risk of major bleeding
9: 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 .Active heart disease, including myocardial infarction, severe/unstable
angina, occurs 6 months before treatment. Left ventricular ejection fraction <50% by
echocardiography showed poor arrhythmia control.
10: Patients with other malignant tumors (except cured basal cell carcinoma of the
skin and carcinoma in situ of the cervix) in the past 5 years or at the same time
11: Known allergy to the investigational drug or any of its excipients
12: Active or uncontrolled severe infection
1. Known human immunodeficiency virus (HIV) infection
2. Known history of clinically significant liver disease, including viral hepatitis
[active HBV infection, i.e., positive HBV DNA (>1×104 copies /mL or >2000 IU/ml)
must be excluded for known hepatitis B virus (HBV) carriers
3. Known hepatitis C virus infection (HCV) and HCV RNA positive (>1×103 copies /mL),
or other hepatitis, cirrhosis]
13. Any other medical condition, clinically significant metabolic abnormality,
physical abnormality or laboratory abnormality, in which, in the investigator's
judgment, there is reason to suspect that the patient has a medical condition or
condition that is not suitable for the use of the investigational drug (such as having
seizures and requiring treatment), or which would affect the interpretation of the
study results or place the patient at high risk
14. Urine routine indicated urinary protein =2+, and 24-hour urinary protein quantity
>1.0g.
15. Incomplete healing of skin wounds, surgical sites, trauma sites, severe mucosal
ulcers or fractures
16. Stroke events and/or transient cerebral ischemia occurred within 12 months prior
to enrollment
17. The patient has any current disease or condition that affects drug absorption, or
the patient is unable to take fuquintinib orally
18. Women who are pregnant (positive pregnancy test before medication) or
breastfeeding
19. The patients considered by the investigators to be unsuitable for inclusion in
this study.
|
