| Eligibility |
Inclusion Criteria:
- Have fully understood and voluntarily sign the ICF for this study (the icf must be
signed before any trial-specific procedures are performed);
- Age of 18-75 years (inclusive); BMI =18.5 kg/m2;
- Tumor types:
- Fruquintinib plus sintilimab treatment arm
- Dose escalation phase: patients with histologically or cytologically confirmed
inoperable or metastatic advanced solid tumors (including but not limited to HCC,
ovarian cancer, endometrial cancer, thymic cancer, NSCLC, renal cell carcinoma);
- Dose expansion phase: histologically or cytologically confirmed inoperable metastatic
advanced HCC (Barcelona Clinic Liver Cancer [BCLC] stage B or C), advanced renal cell
carcinoma with clear cell component, advanced endometrial cancer, advanced gastric
adenocarcinoma or gastroesophageal junction adenocarcinoma, advanced colorectal
adenocarcinoma, advanced NSCLC, advanced cervical cancer, etc.;
- Fruquintinib monotherapy treatment arm: histologically or cytologically confirmed
metastatic advanced endometrial cancer that cannot be surgically resected or treated
with radical radiotherapy;
- In the expansion phase, patients should agree to provide tissue specimens for
detection of PD-L1 expression levels and/or MSI or dMMR status;
- Requirement for prior systemic antitumor therapy:
- Fruquintinib plus sintilimab treatment arm:
- Dose escalation phase: patients who have failed standard treatment (PD or intolerable
toxicity after treatment), have no available standard treatment or cannot receive
standard treatment (such as economic limitations);
- Dose expansion phase:
- Part 1
- Patients (HCC, renal cell carcinoma, endometrial cancer, gastric adenocarcinoma or
gastroesophageal junction adenocarcinoma, colorectal adenocarcinoma, cervical cancer,
NSCLC) should have PD or intolerable toxicity after 1 standard treatment, or cannot
receive standard treatment (such as economic limitations or patient's wishes, etc.).
Among them, requirements of standard treatment are defined as follows:
- Patients with HCC who have received 1 molecular targeted therapy (sorafenib or
lenvatinib) or/and systemic chemotherapy (arsenious acid monotherapy or
oxaliplatin-based combination therapy);
- Patients with renal cell carcinoma who have received 1 standard systemic antitumor
therapy (sunitinib, sorafenib, pazopanib, axitinib, cabozantinib, bevacizumab plus
IFN-a, temsirolimus);
- Patients with endometrial cancer who have received =2 line of platinum-based double
drug systemic antitumor therapy (excluding hormonal therapy) and had PD or Grade =3
SAE, or had recurrence or PD after completion of at least 4 cycles of platinum-based
double drug chemotherapy. Patients with recurrence or metastasis during or within 12
months after completion of neoadjuvant/adjuvant chemotherapy with platinum-based
regimen are considered to have received first-line treatment (4 cycles are required
for neoadjuvant/adjuvant chemotherapy, and if less than 4 cycles, it is also eligible
to have PD or Grade =3 SAE during the treatment);
- Patients with cervical cancers who have recurrent or metastasized squamous cell
carcinoma, adenocarcinoma, or adeno-squamous carcinoma after at least one line of
platinum-based chemotherapy (patients are considered to have received first-line
treatment if they have recurrent or metastasized during or within 6 months after
platinum-based neoadjuvant or adjuvant chemotherapy);
- Patients with gastric adenocarcinoma and gastroesophageal junction adenocarcinoma who
have failed prior standard chemotherapy and can provide tumor tissues for PD-L1
expression detection with CPS =1;
- Patients with colorectal adenocarcinoma previously treated with
fluoropyrimidine+leucovorin calcium+platinum or irinotecan+cetuximab/bevacizumab.
- Advanced NSCLC (stage IV NSCLC diagnosed per AJCC 8th version):
- Patients with negative driver gene (EGFR/ALK/ROS-1 negative) who have failed prior
standard treatment or have intolerable toxicity, or cannot receive or are unwilling to
receive current standard treatment, and with PD-L1 expression level TPS (tumor
proportion score) =1% tested by central laboratory arranged by the sponsor.
- Patients with NSCLC diagnosed with squamous cell carcinoma do not require test of EGFR
mutation, ALK and ROS1 fusion per current diagnosis and treatment guidelines. Other
non-squamous NSCLC patients can be included if they have a prior test report
demonstrating no driver gene mutation/rearrangement (EGFR, ALK, ROS1); if there is no
prior corresponding gene report, archived or fresh tissue needs to be collected for
testing at the study site, or at the central laboratory arranged by sponsor.
- Patients who have recurrence or metastasis during or within 6 months after prior
neoadjuvant/adjuvant therapy are considered as having received first-line therapy.
- Part 2
- To enroll patients with renal cell carcinoma who have not received systemic therapy,
the specific requirements are as follows:
- Patients with renal cell carcinoma have not received any prior systemic antitumor
therapy for renal cell carcinoma (patients with recurrence or PD >6 months after
postoperative adjuvant chemotherapy can be enrolled), and patients with prior cytokine
therapy are allowed.
- Fruquintinib monotherapy arm: patients with histologically or cytologically confirmed
advanced recurrent or metastatic endometrial cancer who cannot be surgically resected
or treated with radical radiotherapy and have failed at least 1 standard treatment
(including PD and intolerable toxicity).
- ECOG performance status (ECOG PS) of 0 or 1;
- Child-Pugh Class A (<7 points) for liver function, only applicable to patients with
HCC;
- Measurable tumor lesions per RECIST 1.1, where patients with gastric tumor are
required to have measurable lesions outside of the stomach (in the dose escalation
phase, patients with only the evaluable lesions are acceptable); if the lesion priorly
treated with local therapy (radiotherapy, ablation, interventional therapy, etc.) is
the only lesion, there must be definite imaging evidence of PD for that lesion;
- Laboratory test results of bone marrow, liver and kidney function, and coagulation
function within 7 days before the first dose should meet the following criteria (no
blood transfusion, blood products, granulocyte colony-stimulating factor or other
hematopoietic stimulating factor correction within 7 days before the laboratory test)
- Absolute neutrophil count (ANC) =1.5×109/L and platelets =100×109/L (platelets
=80×109/L in patients with HCC) and hemoglobin =90 g/L;
- Serum total bilirubin (TBIL) =1.5 times upper limit of normal (×ULN);
- Alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) =1.5×ULN
without liver metastases; ALT and/or AST =3×ULN with liver metastases and HCC;
- Serum albumin =28 g/L;
- Serum creatinine =1.5×ULN or creatinine clearance =50 mL/min (calculated per
Cockcroft-Gault formula);
- Protein urine < 2+; if protein urine = 2+, 24-hour protein urine quantification
should be <1 g;
- International normalized ratio (INR) =1.5 and activated partial thromboplastin
time (APTT) =1.5×ULN (except for prophylactic use of anticoagulant drugs);
- Life expectancy of =12 weeks;
- Female of childbearing potential must have a negative blood pregnancy test within 7
days before the first dose. Male or female patients of childbearing potential should
voluntarily use an effective contraceptive method during the study and within 6 months
after the last dose of study drug, such as double-barrier contraceptive method,
condom, oral or injectable contraceptives, intrauterine device, abstinence, etc. All
female patients are considered to be of childbearing potential unless they are
postmenopausal, have undergone artificial menopause, or are sterilized (hysterectomy,
excision of both adnexa).
Exclusion Criteria:
- The AEs related to prior antitumor therapy which do not recover to = CTCAE Grade 1
before the first dose, except alopecia and peripheral neurotoxicity of CTCAE Grade =2
caused by platinum chemotherapy;
- Patients with other malignant tumors (except cured cutaneous basal cell carcinoma or
squamous cell carcinoma, cervical carcinoma in situ) within 5 years before screening,
only applicable to patients in expansion phase;
- Histological diagnosed fibrolamellar HCC, sarcomatoid HCC or mixed components of the
above pathological types; or gastric squamous cell carcinoma or gastric adenosquamous
carcinoma; or carcinosarcoma or sarcoma (endometrial cancer); or pathological
diagnosis MSI-H or dMMR (endometrial cancer)
- Patients with previous or screening stage central nervous system (CNS) metastasis
during screen period (for lung cancer patients with brain metastasis who have prior
treatment, if there is no evidence of radiographic progression within =4 weeks before
the first dose of study drug, and are clinically stable for =2 weeks after treatment,
and have discontinued corticosteroids within 3 days before the first dose, the patient
could be enrolled; for patients with untreated, asymptomatic lung cancer with brain
metastasis [i.e., no neurological symptoms, no need for corticosteroid or
antiepileptic treatment, no brain metastasis >1.5 cm in long diameter, no significant
edema around brain metastasis], they could be enrolled);
- Systemic antitumor therapy approved or under study within 4 weeks before the first
dose, including but not limited to: chemotherapy (oral fluoropyrimidines washout
period of 2 weeks), endocrine therapy, biological immunotherapy, targeted therapy
(small molecule targeted therapy washout period of 2 weeks or 5 half-lives, whichever
shorter), Traditional Chinese Medicine treatment (Traditional Chinese Medicine
treatment with definite antitumor indications in the instructions, a 1-week washout
period before the first dose is acceptable);
- Radical radiotherapy (including more than 25% bone marrow radiotherapy) within 4 weeks
before the first dose;
- Brachytherapy (such as implantation of radioactive particles) within 60 days before
the first dose;
- Patients previously treated with any anti-programmed cell death receptor 1 (PD-1)
antibody, anti-PD-L1 antibody, anti-PD-L2 antibody or anti-cytotoxic T
lymphocyte-associated antigen-4 (CTLA-4) antibody (or any other antibody acting on T
cell costimulation or checkpoint pathway) (only for the fruquintinib plus sintilimab
treatment arm), or fruquintinib;
- Corticosteroids (dose >10 mg/day prednisone or equivalent of other corticosteroids) or
other immunosuppressive drugs for systemic treatment within 4 weeks before the first
dose; nasal spray, inhalation or other topical use of corticosteroids (i.e., no more
than 10 mg/day prednisone or equivalent of other glucocorticoids) are allowed;
- Patients with any active autoimmune disease requiring systemic treatment (i.e., use of
disease remission drugs, glucocorticoids or immunosuppressive drugs) within the past 2
years; patients who only need replacement therapy (thyroid, adrenal or pituitary
dysfunction with thyroid, insulin or physiological glucocorticoid replacement therapy)
can be enrolled;
- Any live or attenuated live vaccines within 4 weeks before the first dose or planned
administration during the study;
- Major surgical operation within 60 days before the first dose;
- Any surgery or invasive treatment within 4 weeks before the first dose (stable fistula
formation required for fistulization for 4 weeks, except needle biopsy, venous
fistula); or unhealed wounds, ulcers, fractures;
- Uncontrolled malignant pleural effusion, ascites or pericardial effusion (defined as
not effectively controlled by diuretics or paracentesis, as judged by the
investigator);
- Patients with hypertension uncontrolled by drugs, defined as: systolic blood pressure
=140 mmHg and/or diastolic blood pressure =90 mmHg;
- Patients with any disease or condition that affects drug absorption, or the patient
could not take the drug orally;
- Strong cytochrome P450 (CYP) 3A4 inducer/inhibitor, p-glycoprotein (P-gp) substrate
and breast cancer resistance protein (BCRP) substrate within 2 weeks or less than 5
half-lives (whichever is longer) before the first dose;
- Patients with active gastric and duodenal ulcer, ulcerative colitis and other
gastrointestinal diseases or unresected tumor with active bleeding, or other
conditions that may cause gastrointestinal bleeding and perforation as judged by the
investigator; or patients with prior gastrointestinal perforation or gastrointestinal
fistula who had not recovered after surgical treatment;
- Patients with evidence or history of bleeding tendency (such as melena, hematemesis,
hemoptysis, bloody feces, etc.) within 2 months before the first dose, regardless of
severity;
- Tumor invading major vascular structures, such as pulmonary artery, superior/inferior
vena cava, etc. found during screening, with greater risk of bleeding judged by the
investigator;
- Patients with a history of arterial thrombosis or deep venous thrombosis within 6
months before the first dose; or patients with stroke events and/or transient ischemic
attack within 12 months; except that patients with thrombosis caused by implantable
venous infusion pump or catheter, or patients with stable superficial venous
thrombosis after conventional anticoagulant therapy;
- Patients with clinically significant cardiovascular disease, including but not limited
to acute myocardial infarction, severe/unstable angina or coronary artery bypass
grafting within 6 months before the first dose; congestive heart failure of New York
Heart Association (NYHA) class = 2; left ventricular ejection fraction (LVEF) of <
50%;
- Patients with an active infection or unexplained fever (body temperature >38.5oC)
during the screening period or before the first dose;
- Patients with active pulmonary tuberculosis who are receiving anti-tuberculosis
treatment or received anti-tuberculosis treatment within 1 year before the first dose;
- Patients with prior and current pulmonary fibrosis, interstitial pneumonia,
pneumoconiosis, radiation pneumonitis, drug-related pneumonia, severely impaired
pulmonary function and other conditions that may interfere with the detection and
treatment of suspected drug-related pulmonary toxicity;
- Known human immunodeficiency virus (HIV) infection;
- Known history of clinically significant liver disease, including active viral
hepatitis, (hepatitis B virus surface antigen [HBsAg] and/or hepatitis B virus core
antibody [HbcAb] positive, hepatitis B virus [HBV] DNA >10000 copies/mL or > 2000
IU/mL; hepatitis C virus [HCV] antibody positive and HCV RNA positive), or other
active hepatitis, clinically significant moderate to severe cirrhosis;
- Other clinical drug treatment that has not been approved or marketed in China within 4
weeks before the first dose;
- Women who are pregnant (positive pregnancy test before dose) or breastfeeding;
- Known hypersensitivity to any component of the sintilimab, fruquintinib formulation,
or prior history of severe allergy to any other monoclonal antibody;
- Patient with any other condition or laboratory abnormalities that, in the opinion of
the investigator, will increase the risk of study participation or interfere with the
interpretation of study results, and is not suitable for the clinical study.
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