PRIMARY OBJECTIVE:
I. To evaluate the efficacy of sintilimab in subjects with undifferentiated pleomorphic
sarcoma (UPS) (overall response rate [ORR] at 12 weeks [12W] by Response Evaluation Criteria
in Solid Tumors [RECIST] 1.1).
SECONDARY OBJECTIVE:
I. To evaluate the ORR (RECIST 1.1) and disease control rate (DCR), PFS, overall survival
(OS), safety and duration of response (DOR) of sintilimab in subjects with UPS.
EXPLORATORY OBJECTIVES:
I. To evaluate the correlation between biomarkers in tumor tissue and efficacy, including but
not restricted to PD-L1 expression level, tertiary lymphoid structures (TLS) transcriptome
sequencing, single-cell sequencing, and multicolor immunohistochemistry (IHC) analyses.
II. To evaluate the correlation between biomarkers in peripheral blood and efficacy,
including but not restricted to soluble PD-L1, circulating tumor deoxyribonucleic acid (DNA)
(ctDNA), identification/quantification of immunologic changes, and cytokine analyses.
OUTLINE:
Patients receive sintilimab intravenously (IV) over 30-60 minutes on day 1. Cycles repeat
every 3 weeks for up to 24 months in the absence of disease progression or unacceptable
toxicity.
After completion of study treatment, patients are followed up at 30 days and then every 60
days for 3 years.
Inclusion Criteria:
- Histopathologically confirmed unresectable, locally advanced, recurrent or metastatic
UPS
- Refractory or intolerant to at least one line of systemic chemotherapy. Patient
ineligible for cytotoxic chemotherapy are eligible
- Aged >= 18
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1
- Subject must be unsuitable for definitive treatment, such as definitive
chemoradiotherapy and/or surgery
- Could provide archival or fresh tissues for correlative analysis
- Have at least one measurable lesion as per RECIST version (v)1.1
- Absolute neutrophil count (ANC) >= 1.0 x 10^9/L
- Note: Subjects cannot receive blood transfusion, erythropoietin (EPO), or
granulocyte-colony stimulating factor (GSF) within 7 days prior to the blood
collection
- Platelet (PLT) count >= 75 x 10^9/L
- Note: Subjects cannot receive blood transfusion, erythropoietin (EPO), or
granulocyte-colony stimulating factor (GSF) within 7 days prior to the blood
collection
- Hemoglobin (HGB) >= 8.0 g/dL
- Note: Subjects cannot receive blood transfusion, erythropoietin (EPO), or
granulocyte-colony stimulating factor (GSF) within 7 days prior to the blood
collection
- Total bilirubin (TBIL) =< 1.5 x upper limit of normal (ULN) and alanine
aminotransferase (ALT) and aspartate aminotransferase (AST) =< 2.5 x upper limit of
normal (ULN) in subjects without hepatic metastasis
- TBIL =< 1.5 x ULN and ALT and AST =< 5 x ULN in subjects with hepatic metastasis.
Exception: Patients with known Gilbert disease: serum bilirubin level =< 3 x ULN
- Urine protein < 2+ from random sample or < 1 g from 24-hour urine collection, and
creatinine clearance rate (Ccr) >= 60 mL/min by Cockcroft-Gault formula
- Adequate coagulation function, defined as international normalized ratio (INR) =< 1.5
or prothrombin time (PT) =< 1.5 x ULN; if the subject is receiving anticoagulant
therapy, the results of coagulation tests need to be within the acceptable range for
anticoagulants
- Expected survival >= 12 weeks
- Subject (female subjects of childbearing age or male subjects whose partners are of
childbearing age) must take effective contraceptive measures during the entire course
of the trial and until 180 days after the last dose
- Signed the informed consent form (ICF) and be able to comply with the scheduled
follow-up visits and related procedures required in the protocol
Exclusion Criteria:
- Received treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or
anti-CTLA-4 antibody, or any other antibody or drug that specifically targets T-cell
co-stimulation or immune checkpoint pathways
- Enrolled in another interventional clinical study, unless only involved in an
observational study (non-interventional) or in the follow-up phase of an
interventional study
- Received palliative therapy for local lesion within 2 weeks prior to the first dose
- Received systemic treatment with anti-cancer indications or immunomodulators
(including thymosins, interferons, and interleukins) within 2 weeks prior to the first
dose of study treatment
- Received systemic immunosuppressants within 2 weeks prior to first dose, excluding
local use of glucocorticoids administered by nasal, inhaled, or other routes, and
systemic glucocorticoids at physiological doses (no more than 10 mg/day of prednisone
or equivalents), or glucocorticoids to prevent allergies to contrast media
- Received a live attenuated vaccine within 4 weeks prior to the first dose of study
treatment or be scheduled to receive live attenuated vaccine during the study period.
- Note: Seasonal inactivated influenza virus vaccines within 4 weeks prior to the
first dose of study treatment are permitted, but attenuated influenza vaccines
are not
- Received major surgery (craniotomy, thoracotomy, or laparotomy) within 4 weeks prior
to the first dose of study treatment or is scheduled to receive major surgery during
the course of the trial
- Any toxicity (excluding alopecia, events that are not clinically significant, or
asymptomatic laboratory abnormalities) due to prior anti-tumor therapy that has not
yet resolved to National Cancer Institute Common Terminology Criteria for Adverse
Events (NCI CTCAE) v5.0 grade 0 or 1 prior to the first dose of study treatment
- Known symptomatic central nervous system (CNS) metastasis or carcinomatous meningitis.
Subjects with brain metastases who have received prior treatment can be enrolled if
the disease is stable (no imaging evidence of progressive disease (PD) for at least 4
weeks prior to the first dose of study treatment), there is no evidence of new brain
metastases or progression of the existing metastatic lesion(s) upon repeated imaging,
and corticosteroids have not been required for at least 14 days prior to the first
dose of study treatment. Patients with carcinomatous meningitis are ineligible,
regardless of whether the disease is clinically stable or not
- Subjects with bone metastases at risk of paraplegia
- Known active autoimmune disease requiring treatment or previous disease history within
2 years (subjects with vitiligo, psoriasis, alopecia, or Graves' disease not requiring
systemic treatment, hypothyroidism only requiring thyroid replacement, or type I
diabetes only requiring insulin can be enrolled)
- Known history of primary immunodeficiency diseases
- Known active pulmonary tuberculosis
- Known history of allogeneic organ transplantation or allogeneic hematopoietic stem
cell transplantation
- Human immunodeficiency virus (HIV)-infected subjects (positive anti-HIV antibody)
- Active or poorly controlled serious infections
- Symptomatic congestive heart failure (New York Heart Association [NYHA] class II-IV)
or symptomatic or poorly controlled arrhythmia
- Uncontrolled hypertension (systolic blood pressure >= 160 mmHg or diastolic blood
pressure >= 100 mmHg) despite of standard treatment
- Any arterial thromboembolic event within 6 months prior to enrollment, including
myocardial infarction, unstable angina, cerebrovascular accident, or transient
cerebral ischemic attack
- Significant malnutrition, such as those requiring continuous parenteral nutrition >= 7
days; excluding those having received intravenous treatment for malnutrition for more
than 4 weeks before the first dose of study treatment
- History of clinically significant deep venous thrombosis, pulmonary embolism, or other
serious thromboembolic events within 3 months prior to enrollment (implantable port or
catheter-related thrombosis or incidental PE detected on scan without symptoms or
superficial venous thrombosis are not considered as "serious" thromboembolisms)
- Uncontrolled metabolic disorders, non-malignant organ or systemic diseases, or
cancer-related secondary diseases that may lead to higher medical risks and/or
survival evaluation uncertainties
- Hepatic encephalopathy, hepatorenal syndrome, or cirrhosis with Child-Pugh class B or
C
- Bowel obstruction or history of the following diseases: inflammatory bowel disease,
extensive bowel resection (partial colectomy or extensive small intestine resection
accompanied with chronic diarrhea), Crohn's disease, or ulcerative colitis
- Known acute or chronic active hepatitis B (positive hepatitis B surface antigen
[HBsAg] and hepatitis B virus [HBV] DNA viral load >= 104 copies/mL or > 2000 IU/mL),
or acute or chronic active hepatitis C (hepatitis C virus [HCV] ribonucleic acid [RNA]
> 103 copies/mL), or simultaneously positive for HBsAg and HCV antibody
- History of gastrointestinal (GI) perforation and/or fistula within 6 months prior to
the enrollment, excluding gastrostomy or enterostomy
- Interstitial lung disease requiring corticosteroids
- History of other primary malignant tumors, excluding:
- Malignant tumors that achieved a complete response (CR) at least 2 years prior to
enrollment and expected to require no treatment during the trial
- Adequately treated nonmelanoma skin cancer or lentigo maligna with no sign of
disease recurrence
- Adequately treated carcinoma in situ with no sign of disease recurrence
- Prostate, chronic lymphocytic leukemia (CLL) or other cancers where the indolent
nature of tumor allows for and patient is cancer under active surveillance
- Pregnant or breastfeeding female subjects
- Acute or chronic diseases, psychiatric disorders, or laboratory abnormalities that may
lead to the following consequences: increased investigational drug-related risks,
interference with interpretation of trial results or considered ineligible for
participating in the trial by the investigators
