A Phase I Study to Evaluate the Safety and Preliminary Efficacy of [225Ac]Ac-DOTATATE Injection Combined With Tislelizumab in the Maintenance Treatment Period for Patients of Extensive-stage Small Cell Lung Cancer (ES-SCLC) With Somatostatin Receptors (SSTR)+ as First-line Treatment

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-80
SponsorPeking University Cancer Hospital & Institute

About this trial

This is a phase I study to evaluate the safety and preliminary efficacy of \[225Ac\]Ac-DOTATATE injection combined with tislelizumab in the maintenance treatment period for patients of extensive-stage small cell lung cancer (ES-SCLC) with somatostatin receptors (SSTR)+ as first-line treatment.Patients with ES-SCLC who have completed the induction therapy of first-line standard treatment and are yet to enter the maintenance treatment period are planned to be enrolled.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients must have the ability to understand and sign an approved informed consent form (ICF).

Patients must be >= 18 and <=80 years of age.

Extensive-stage small cell lung cancer that requires histopathological or cytological confirmation.

Presence of at least 1 measurable site of disease (based on RECIST 1.1).

Disqualifiers

Pregnant or lactating females.

Received systemic antitumor therapy such as targeted therapy, immunotherapy, antitumor herbal therapy, chemotherapy within 4 weeks prior to initiation of study treatment.

Uncontrolled congestive heart failure.

uncontrolled diabetes mellitus, including baseline fasting glucose > 2 x ULN.

Trial design

Design model

Sequential

Treatments tested in this trial

  • [225Ac]Ac-DOTATATE

    Drug

    During the dose escalation phase, the "3+3" dose escalation method was adopted. There were two dose groups: the single-dose administration dose of the first dose group was 90 kBq/kg, and that of the second dose group was 120 kBq/kg.During the dose expansion phase, the subjects received the RP2D dose of the \[225Ac\]Ac-DOTATATE injection. The administration method, combination therapy, etc. were all the same as those in the dose escalation phase.

Treatment groups

24 Participants
are divided into 1 treatment group
Group A: [225Ac]Ac-DOTATATEExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

During the dose escalation phase, the efficacy of [225Ac]Ac-DOTATATE injection at the RP2D dose for maintenance treatment in first-line therapy for SSTR-positive ES-SCLC patients when used in combination with tislelizumab was evaluated.

Incidence and severity of adverse events (AEs) DLT MTD RP2D

Time frame
6 months after last dose administration
2

During the dose expansion phase, the efficacy of [225Ac]Ac-DOTATATE injection at the RP2D dose for maintenance treatment in first-line therapy for SSTR-positive ES-SCLC patients when used in combination with tislelizumab was evaluated.

PFS

Time frame
12 months after last dose administration

Secondary outcomes

1

During the dose escalation phase, the efficacy of [225Ac]Ac-DOTATATE injection for use as a maintenance treatment in the first-line therapy of SSTR-positive ES-SCLC patients when combined with tislelizumab was evaluated.

PFS

Time frame
12 months after last dose administration
2

During the dose escalation phase, the efficacy of [225Ac]Ac-DOTATATE injection for use as a maintenance treatment in the first-line therapy of SSTR-positive ES-SCLC patients when combined with tislelizumab was evaluated.

ORR

Time frame
12 months after last dose administration
3

During the dose escalation phase, the efficacy of [225Ac]Ac-DOTATATE injection for use as a maintenance treatment in the first-line therapy of SSTR-positive ES-SCLC patients when combined with tislelizumab was evaluated.

DCR

Time frame
12 months after last dose administration
4

During the dose escalation phase, the efficacy of [225Ac]Ac-DOTATATE injection for use as a maintenance treatment in the first-line therapy of SSTR-positive ES-SCLC patients when combined with tislelizumab was evaluated.

OS

Time frame
12 months after last dose administration

Other outcomes

Sponsors and contacts

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