Overview

Toripalimab and Anlotinib Combination Treatment in Patients With Recurrent or Metastatic Nasopharyngeal Carcinoma After Failure of at Least One Line of Platinum-Based Chemotherapy (TORAL)

Status:
Not yet recruiting
Trial end date:
2028-08-01
Target enrollment:
0
Participant gender:
All
Summary
This phase 2 trial studies toripalimab and anlotinib combination treatment in patients with recurrent or metastatic nasopharyngeal carcinoma after failure of at least one line of platinum-based chemotherapy
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sun Yat-sen University
Criteria
Inclusion Criteria:

- Histologically confirmed undifferentiated non-keratinizing carcinoma

- Patients suffered failure of at least one line of platinum-based chemotherapy. The
definition of treatment failure: progression during or after chemotherapy for
recurrence/metastasis; progression after concurrent chemoradiotherapy within 6 months.
Withdrawal of treatment due to drug intolerances is excluded ;

- Without other malignancy;

- Male or female, 18-70 years;

- Eastern Cooperative Oncology Group (ECOG) of 0-2;

- Life expectancy ≥ 3 months;

- Women of childbearing age must obtain the negative result of a pregnancy test (serum
or urine) , and they were willing to use reliable methods of contraception during the
trial;

- At least one evaluable lesion;

- Laboratory tests meet the following standards:

Blood routine: White blood cell count (WBC) ≥3.0×10 9 /L, neutrophil count (ANC) ≥1.5×10 9
/L, platelet count (PLT) ≥75×10 9 /L, hemoglobin (HGB) 90 g/L or higher; Liver function:
total bilirubin ≤1.5 times the upper limit of normal (ULN); glutamic-oxalacetic
transaminase (AST) and alanine transaminase (ALT) ≤2.5 times ULN, AST and ALT ≤2.5 times
ULN for the patients with liver metastases; Alkaline phosphatase ≤5 times ULN; Renal
function: Serum creatinine (Cr) ≤1.5 times ULN; Creatinine clearance ≥60mL/min; Urine
routine: urine protein <2+ ;baseline urine protein ≥2+ and 24 hours urine protein < 1g ;
Coagulation: International normalized ratio (INR) and activated partial thrombin time
(APTT) ≤1.5 times ULN; Albumin ≥28g/L Thyroid stimulating hormone (TSH)≤1 times ULN (free
triiodothyrosine [FT3] or free thyroxine [FT4] ≤1 times ULN can be included)

- No serious cardiopulmonary dysfunction;

- The informed consent has been signed.

- Ability to comply with test requirements

Exclusion Criteria:

- A known allergy to any of the drugs in the study;

- Pregnant or breastfeeding women;

- Participated in clinical trials of other drugs within 4 weeks prior to study
initiation;

- Previous treatment with bevacizumab or VEGFR-family small molecule tyrosine kinase
inhibitors (e.g., famitinib, sorafenib, Sunitinib, regofinib, Apatinib, Anlotinib,
fuquinitinib) ;

- Recurrent nasopharyngeal lesions after radiotherapy and who received secondary
radiotherapy;

- Palliative radiotherapy for symptom control within 28 days before enrollment;

- Immunosuppressive treatment with immunosuppressive agent, systemic or absorbable
topical hormone therapy ( prednisone or other therapeutic hormone at the dose greater
than 10mg/ day) within 2 weeks before enrollment;

- Active autoimmune diseases, with the necessity of systemic treatment (hormone
replacement therapy is not considered as a systemic treatment, such as type 1
diabetes) over the past two years; autoimmune diseases that did not require systemic
treatment in the past two years;

- A history of immunodeficiency, including acquired/congenital immunodeficiency
disorders, a history of organ transplantation;

- Vaccinated with live vaccine (inactivated virus vaccine for seasonal influenza is
allowed) within 4 weeks before enrollment;

- Invasion of important vessels (e.g. surrounding internal carotid artery/vein) on MRI;
tumor with a high risk of affecting vital blood vessels during treatment and causing
fatal hemorrhage, which is determined by investigators;

- A history of severe bleeding and any bleeding event with a severity rating of 3 or
higher in the NCI CTCAE within 4 weeks prior to screening;

- Abnormal coagulation (INR > 2.0, PT > 16s) and bleeding tendency (the INR must be
within the normal range without anticoagulants during14 days prior to signing the
informed consent); patients treated with anticoagulants or vitamin K antagonists such
as warfarin, heparin, or their analogests; low-dose warfarin (1 mg orally, once daily)
or low-dose aspirin (up to 100 mg daily) for preventive purposes, provided that the
international normalized ratio of prothrombin time (INR) is ≤ 1.5;

- Unstable angina and/or congestive heart failure or vascular disease with the need of
hospital treatment; other cardiac damage that may affect the drug safety;

- Patients with hypertension that is not well controlled with antihypertensive
medication (systolic > 140mmHg, diastolic > 90 mmHg); patients is taking a combination
of two or more antihypertensive drugs; Cardiovascular disease with clinical
significance, such as cerebrovascular accident (≤ 6 months before randomization),
myocardial infarction (≤ 6 months before randomization), unstable angina, congestive
heart failure of NYHA grade II or higher, or severe arrhythmias that cannot be
controlled with drugs or have a potential impact on experimental treatments;

- Patients with esophageal and gastric varices, active ulcers, intestinal perforation or
intestinal obstruction within 6 months before enrollment;

- A history of abdominal fistula, digestive tract perforation, intra-abdominal abscess
or acute gastrointestinal bleeding within 6 months before enrollment;

- Multiple factors affecting oral administration and absorption of drugs (e.g.,
inability to swallow, post-gastrointestinal resection, chronic diarrhea and intestinal
obstruction);

- Overoperation/venous thromboembolism events, NCI CTCAE grade 3 or higher venous
thromboembolism within 6 months before enrollment, such as cerebrovascular accident
(including temporary ischemic attack), deep venous thrombosis (except for those venous
thrombosis caused by venous catheterization due to previous chemotherapy and
determined to be cured by the researchers ), pulmonary embolism, etc.;

- Patients with past and present objective evidence of pulmonary fibrosis, interstitial
pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, or severe
impairment of lung function;

- Exacerbation of chronic obstructive pulmonary disease (COPD) or other respiratory
disease requiring hospitalization within 28 days before enrollment;

- Active pulmonary infection and/or acute bacterial or fungal infection requiring
intravenous antibiotic treatment within 28 days;

- Dominant jaundice due to abnormal liver function within 7 days;

- Renal insufficiency: routine urinalproteinuria > 2+ and confirmed 24 h urinary protein
quantification > 1.0g;

- Minor surgical operations (including catheterization, excluding central venous
catheterization via peripheral venipuncture) within 2 days before enrollment;

- Major surgery within 28 days before enrollment;

- A potent CYP3A4 inhibitor within one week prior to enrollment, or a potent CYP3A4
inducer within two weeks prior to study participation

- Long-term unhealed wounds or incomplete fractures;

- Symptomatic central nervous system metastases (e.g. brain edema, need for hormonal
intervention, or brain metastases)

- The presence of serious or uncontrolled infections;