A Phase II Clinical Study of Cadonilimab in Treatment-naïve or Relapsed Extensive Small Cell Lung Cancer

NCT06406673 | Unknown Phase 2

• 1 other identifier: AK104-SCLC-01
• Study Type: interventional
• Target: 70
• Locations: 1 country
• Sites: 1

Brief Summary

Small cell lung cancer (SCLC) accounts for 15% of lung cancer cases and is an aggressive cancer characterized by rapid growth, early metastasis, and a poor prognosis. Approximately 75% of SCLC patients present with extensive-stage disease at the time of diagnosis, which is classically defined as a disease that cannot be encompassed by a single radiation field. Before the era of immunotherapy, the standard first-line therapy for ES-SCLC was platinum-based chemotherapy with etoposide; Once complete remission (CR) or partial remission (PR) was achieved after chemotherapy, consolidative thoracic radiation was recommended. Despite this standard treatment, the median overall survival (OS) of ES-SCLC is about 8-11 months, which has not changed for about 40 years. Combining concurrent radiotherapy of the thorax and immunochemotherapy may have a synergistic effect. Besides, for patients with recurrent SCLC, topotecan remains the only approved second-line treatment, and the outcomes are poor. With the most recent approval of EP plus a programmed death ligand 1(PD-L1) inhibitor, there are now more therapeutic options for managing ES-SCLC.The best second-line therapy after combination of chemo-immunotherapy is not well defined, as many second-line therapies were studied only after use of EP. However, second-line treatment options for patients with relapsed ES-SCLC are limited and include reintroduction of EP (with or without an immunotherapy), lurbinectedin, and topotecan. Therefore, we designed this trial to explore the efficacy and safety of cadonilimab as second-line therapy for ES-SCLC. We present a safety profile and a final analysis of ORR. In this single-center phase 2 trial, Cohort\_1 patients with no history of previous systemic treatment for ES-SCLC received cadonilimab with EC/EP for two cycles (induction phase), then, those who did not progress received concurrent palliative RT and two cycles of cadonilimab with EC/EP (combination phase). Afterward they received cadonilimab every 3 weeks for a maximum of 2 years after study enrolment (maintenance phase). Cohort\_2 patients with recurrent SCLC and after at most one systemic treatment received cadonilimab plus vorolanib, until disease progression or unacceptable toxicity. The primary endpoints was objective response rate (ORR); the second endpoints were progression-free survival (PFS), disease control rate (DCR), overall survival (OS) and treatment-emergent adverse event (TEAE) .

Conditions

Extensive Small Cell Lung Cancer

Outcome Measures

Primary Outcomes (1)

• Objective response rate (ORR)

  ORR is defined as the percentage of participants, who has a CR (disappearance of all target lesions) or PR (at least a 30% decrease in the sum of diameters of target lesions). The percentage of participants who experiences a confirmed CR or PR is according to RECIST 1.1.

  24 months

Secondary Outcomes (4)

• Progression-free survival (PFS)

  24 months

• Disease control rate (DCR)

  24 months

• Overall survival (OS)

  24 months

• Treatment-Emergent Adverse Event (TEAE)

  24 months

Study Arms (2)

Cohort_1

EXPERIMENTAL

Cohort\_1 patients with no history of previous systemic treatment for ES-SCLC received cadonilimab with EC/EP and received concurrent palliative RT.

Drug: Cadonilimab+EC/ET+RT

Cohort_2

EXPERIMENTAL

Cohort\_2 patients with recurrent SCLC and after at most one systemic treatment received cadonilimab plus vorolanib.

Drug: Cadonilimab+vorolanib

Interventions

Cadonilimab+EC/ET+RT DRUG

Cohort\_1 patients with no history of previous systemic treatment for ES-SCLC received cadonilimab with EC/EP for two cycles (induction phase), then, those who did not progress received concurrent palliative RT and two cycles of cadonilimab with EC/EP (combination phase). Afterward they received cadonilimab every 3 weeks for a maximum of 2 years after study enrolment (maintenance phase).

Cohort_1

Cadonilimab+vorolanib DRUG

Cohort\_2 patients with recurrent SCLC and after at most one systemic treatment received cadonilimab plus vorolanib, until disease progression or unacceptable toxicity.

Cohort_2

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• All subjects voluntarily participated in the study and signed informed consent;
• Male or female aged ≥18 years ;
• Expected survival time ≥3 months;
• ECOG 0-1;
• Patients with extensive-stage small-cell Lung cancer confirmed by histopathology and/or cytology (according to Veterans Administration Lung Study Group (VALG) staging); 5-1）Cohort\_1 patients who have not received any previous systemic anti-tumor therapy for extensive-stage small cell lung cancer, and included all patients with ≤5 extrapulmonary metastases.
• ）Cohort\_2 patients with previous failure or intolerance to standard therapy for extensive-stage small cell lung cancer and received at most one systemic treatment:
• a) Those who have previously failed first-line platinum-based chemotherapy combined with immune checkpoint inhibitors, and have received at most one systemic treatment, as follows:
• Receiving less than 2 lines of systemic therapy in the advanced stage of the disease;
• ②Immune checkpoint inhibitors include atezolizumab, durvalumab, slulimumab, adebelimab, etc.;
• ③Disease progression confirmed by imaging during or after the latest treatment b) Those who have only received first-line platinum-containing drug treatment in the past and failed, and have not received immune checkpoint inhibitor treatment, as follows:
• Receiving less than 2 lines of systemic therapy in the advanced stage of the disease; ② The first-line treatment must be platinum-containing chemotherapy; ③ Disease progression confirmed by imaging during or after the latest treatment

You may not qualify if:

• Must have at least one measurable lesion according to RECIST v1.1 definition; Lesions that had been previously treated with radiation could be included in a measurable lesion only if there was definite disease progression after radiation therapy.
• Organ function level must meet the following criteria： 8-1) Blood routine: hemoglobin (HGB) ≥ 90g/L; Absolute neutrophil count (NEUT) ≥ 1.5×10 9 /L; Platelet count (PLT) ≥ 100×10 9 /L; 8-2) Renal function: creatinine (Cr) ≤1.5 ULN, or creatinine clearance (Ccr) ≥50 mL/min (according to Cockcroft and Gault formula).
• ) Liver function: total bilirubin (TBIL≤1.5 ULN), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were all ≤2.5 ULN, and AST and ALT were both ≤5.0 ULN when liver metastasis was present; 8-4) coagulation function: international normalized ratio (INR) ≤1.5 and activated partial thromboplastin time (APTT) ≤1.5ULN; 8-5) no severe cardiac dysfunction with left ventricular ejection fraction ≥50%; 8-6) proteinuria ≤2+ or ≤1000mg/24h; 8-7) Toxicity of previous antineoplastic therapy has returned to ≤ grade 1 as defined by NCI-CTCAE v5.0 (except for asymptomatic laboratory abnormalities such as ALP elevation, hyperuricemia, and hyperglycemia, as judged by the investigator, and toxicity without safety risk, such as alopecia, grade 2 peripheral neurotoxicity, or decreased hemoglobin ≥90g/L, as judged by the investigator); 8-8) For premenopausal women with childbearing potential, a pregnancy test must be performed within 7 days before the start of treatment, the serum or urine pregnancy test must be negative, and the patient must not be lactating; All enrolled patients should take adequate barrier contraception during the whole treatment cycle and for 6 months after the end of treatment.
• Women of reproductive age should agree to use effective contraception during the study period and for six months after the study ends; Have a negative serum or urine pregnancy test within 7 days prior to study enrollment and must be non-lactating; Men should agree to use contraception during the study period and for six months after the study period ends;
• Patients will be able to communicate well with the investigator, understand and comply with the requirements of the study.
• Histologically or cytologically confirmed NSCLC;
• Previous medications:For Cohort\_1: Exclude those who have received systemic anti-tumor therapy or with \>5 extrapulmonary metastases; For Cohort\_2: Those who have received more than one systemic treatment regimen
• Participated in other domestic unapproved or unmarketed drug clinical trials and accepted the corresponding experimental drug treatment within 4 weeks before enrollment;
• Imaging during the screening period shows that the tumor surrounds important blood vessels or has obvious necrosis or cavities, and the researcher determines that entering the study will cause a risk of bleeding(Only for Cohort\_2).
• Received any surgery or invasive treatment or operation within 4 weeks before enrollment (excluding intravenous catheterization, puncture drainage, puncture biopsy, etc.)
• The patient currently has central nervous system (CNS) metastases or active brain or meningeal metastases. Treated subjects with BMS were required to meet the following criteria: asymptomatic; No radiographically demonstrated progression ≥4 weeks after completion of treatment; Completion of treatment ≥14 days before the first dose of the study drug; Systemic corticosteroid therapy (\> 10mg/ day prednisone or equivalent) is not required for ≤14 days prior to the first dose of the study drug
• Known allogeneic organ transplantation (except corneal transplantation) or allogeneic hematopoietic stem cell transplantation;
• Any other medical condition, clinically significant metabolic abnormality, physical abnormality, or laboratory abnormality that, in the investigator's judgment, reasonably suspects the patient to have a medical condition or condition that is not suitable for the use of the study drug (such as having seizures that require treatment), or that would affect the interpretation of the study results, or put the patient at high risk;
• Have received or plan to receive live attenuated vaccine within 4 weeks prior to initial administration;
• Currently receiving anti-HBV treatment;

Sponsors & Collaborators

• Henan Cancer Hospital: lead

Study Sites (1)

Henan Cancer Hospital

Zhengzhou, Henan, 450000, China

RECRUITING

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER GOV
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 6, 2024
• First Posted: May 9, 2024
• Study Start: October 16, 2023
• Primary Completion: August 30, 2024
• Study Completion: December 31, 2024
• Last Updated: May 9, 2024

Record last verified: 2023-09

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)