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Sintilimab Combined With Anlotinib Therapy for Initially Unresectable Non-small Cell Lung Cancer

23 maart 2022 bijgewerkt door: YueJuan Cheng, Peking Union Medical College Hospital

Sintilimab Combined With Anlotinib Therapy for Patients With Initially Unresectable Stage II-III Non-small Cell Lung Cancer: A Prospective, Single-arm Study

Concurrent or sequential chemoradiotherapy has been recommended as the standard treatment for locally advanced and unresectable non-small cell lung cancer (NSCLC). However, its efficacy remains to be improved. PD-1/PD-L1 inhibitors have been proven to be effective for late-stage NSCLC, and anti-angiogenesis agents have also been used for the first-line treatment of advanced or metastatic NSCLC. Therefore, we designed this single-arm clinical trial, which aims to investigate the safety and feasibility of sintilimab combined with anlotinib therapy for patients with initially unresectable stage II-III NSCLC.

Studie Overzicht

Toestand

Nog niet aan het werven

Gedetailleerde beschrijving

Concurrent or sequential chemoradiotherapy is the standard treatment for patients with locally advanced NSCLC, but patients receiving chemoradiotherapy have limited improvement in prognosis and are almost impossible to achieve a radical cure. Considering the excellent effect of immunotherapy and anti-angiogenesis therapy in NSCLC, we designed this single-arm clinical study, which aims to investigate the safety and feasibility of sintilimab combined with anlotinib therapy for patients with initially unresectable stage II-III NSCLC, in order to enable patients to achieve further surgical treatment and prolonged survival.

Studietype

Ingrijpend

Inschrijving (Verwacht)

93

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  1. According to the 8th edition of the AJCC/UICC TNM staging system for NSCLC, patients with locally advanced (stage II-III C) NSCLC confirmed by histology who are initially unable to undergo surgery and concomitant radiochemotherapy and are confirmed to have at least one measurable lesion according to RECIST 1.1.
  2. Age ≥18 years and ≤75 years.
  3. ECOG PS score: 0 to 1.
  4. The main organs function is normal, that is, the following criteria met:

    1. Good hematopoietic function, defined as absolute neutrophil count ≥1.5×109 /L, platelet count≥100 ×109 /L, hemoglobin ≥90g/L [no blood transfusion or no erythropoietin (EPO) dependence within 7 days before enrollment];
    2. Biochemical test results should meet the following criteria: BIL < 1.25 times the upper limit of normal value (ULN); ALT and AST < 2.5 × ULN; in case of liver metastases, ALT and AST < 5 × ULN; Cr ≤1.5×ULN or creatinine clearance (CCr) ≥60ml/min; Coagulation function is good, INR and PT ≤1.5 × ULN;
    3. The oxygen saturation of the finger tip ≥ 92% both at rest and during walking (without oxygen inhalation).
  5. The life expectancy ≥12 weeks.
  6. Signed and dated informed consent.

Exclusion Criteria:

  1. Subjects at risk of massive hemoptysis or with blood in sputum, including but not limited to tumor lesions no more than 5 mm away from large vessels, tumors invading large vessels, and obvious lung cavity/necrotizing tumors.
  2. Small cell lung cancer (including mixed small cell and non-small cell lung cancer) or central squamous cell carcinoma.
  3. With driver mutation (EGFR/ALK/ROS1).
  4. With uncontrollable hypertension (systolic pressure > 160 mmHg, diastolic pressure > 100 mmHg) even receiving antihypertensive drug therapy.
  5. Has an active autoimmune disease, history of allogeneic stem cell transplantation or organ transplantation that has required systemic treatment. Replacement therapy is not considered a form of systemic treatment and is allowed.
  6. Has an active infection requiring systemic therapy.
  7. Has other malignant tumors (except radical cervical carcinoma in situ, non-melanoma skin cancer, etc.) or concomitant diseases that seriously endanger the patients or affect the patients completing the study at the same time.
  8. With immunodeficiency status, including but not limited to HIV infection and primary immunodeficiency diseases.
  9. Previously treated with ICIs.
  10. Is pregnant, breastfeeding, or expecting to conceive or father a child within the projected duration of the study including 120 days following the last dose of study treatment.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Experimental arm

Sintilimab will be given intravenously at a dose of 200mg every 21 days. Anlotinib will be given at a dose of 12mg once daily on days 1-14 of a 21-day cycle.

Tumor evaluation will be conducted after treatment of the tested regimen every 2 cycles. Subsequent treatment will be determined based on the evaluation results: If the patients are not suitable for radical surgery, but the result of efficacy evaluation is CR, PR, or SD, they can continue to receive the tested regimen. If the patients are still not suitable for radical surgery after 6 cycles of the tested regimen, the standard first-line or immunotherapy after chemoradiotherapy or radiotherapy will be given. If patients are eligible for radical surgery, surgery will be performed within 4 weeks after completion of the last tested regimen.

Sintilimab will be given intravenously at a dose of 200mg every 21 days.
Andere namen:
  • IBI308
  • Tyvyt
Anlotinib will be given at a dose of 12mg once daily on days 1-14 of a 21-day cycle.
Andere namen:
  • AL3818
  • Anlotinib-hydrochloride

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Surgical conversion rate
Tijdsspanne: 18 weeks from the initiation of the tested regime therapy
The surgical conversion rate was defined as the proportion of subjects with the successful conversion over all subjects who received the tested regime.
18 weeks from the initiation of the tested regime therapy

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Objective response rate (ORR)
Tijdsspanne: 18 weeks from the initiation of the tested regime therapy
ORR is defined as the percentage of participants who have the best overall response (BOR) of complete response (CR) or partial response (PR) assessed based on RECIST 1.1.
18 weeks from the initiation of the tested regime therapy
R0 resection rate
Tijdsspanne: within 28 working days after operation
R0 resection rate is defined as the complete resection rate of all tumor under microscope.
within 28 working days after operation
Major pathological response rate
Tijdsspanne: within 28 working days after operation
Major pathological response rate is defined as the percentage of patients who achieved a major pathological response (residual tumor ≤10%).
within 28 working days after operation
Pathological complete response rate
Tijdsspanne: within 28 working days after operation
Pathological complete response rate is defined as the percentage of patients who achieved a pathological complete response (residual tumor = 0%).
within 28 working days after operation
Overall survival (OS)
Tijdsspanne: 2 years from the initiation of the tested regime therapy
OS is measured from the time from the treatment onset (date of first study dose) until the date of death from any cause.
2 years from the initiation of the tested regime therapy
Progression-free survival (PFS)
Tijdsspanne: 2 years from the initiation of the tested regime therapy
PFS is measured from the time from the treatment onset (date of first study dose) until the date of tumor progression or death from any cause.
2 years from the initiation of the tested regime therapy
Disease-free survival (DFS)
Tijdsspanne: 2 years from the initiation of the tested regime therapy
DFS is measured from the time from radical surgery until the date of tumor progression or death from any cause.
2 years from the initiation of the tested regime therapy
Treatment-related adverse events
Tijdsspanne: 3 months from the end of the tested regime therapy
Incidence and grade of treatment-related adverse events assessed based on CTCAE 5.0
3 months from the end of the tested regime therapy

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Chunmei Bai, Professor, Peking union medical colloge hospital

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Verwacht)

1 april 2022

Primaire voltooiing (Verwacht)

1 april 2024

Studie voltooiing (Verwacht)

1 april 2026

Studieregistratiedata

Eerst ingediend

21 maart 2022

Eerst ingediend dat voldeed aan de QC-criteria

23 maart 2022

Eerst geplaatst (Werkelijk)

1 april 2022

Updates van studierecords

Laatste update geplaatst (Werkelijk)

1 april 2022

Laatste update ingediend die voldeed aan QC-criteria

23 maart 2022

Laatst geverifieerd

1 maart 2022

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

De-identified individual participant data for all primary and secondary outcome measures will be made available.

IPD-tijdsbestek voor delen

Data will be available within 1 year of study completion

IPD-toegangscriteria voor delen

Data access requests will be reviewed by an external independent Review Panel. Requestors will be required to sign a Data Access Agreement

IPD delen Ondersteunend informatietype

  • LEERPROTOCOOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • MVO

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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