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Iparomlimab and Tuvonralimab (QL1706) Plus Lenvatinib and Chemotherapy for Extrapulmonary Neuroendocrine Carcinoma

2026년 7월 28일 업데이트: Dan Cao, West China Hospital

A Prospective, Randomized, Controlled Clinical Trial of Iparomlimab and Tuvonralimab Injection (QL1706) Plus Lenvatinib and Chemotherapy as First-Line Treatment for Extrapulmonary Neuroendocrine Carcinoma

The aim of this prospective, randomized, controlled clinical trial is to evaluate the efficacy and safety of iparomlimab and tuvonralimab injection (QL1706) plus lenvatinib and etoposide-based platinum chemotherapy, consisting of etoposide plus cisplatin or carboplatin, compared with etoposide-based platinum chemotherapy alone as first-line treatment for patients with extrapulmonary neuroendocrine carcinoma. Potential predictive biomarkers will also be explored through analyses of tumor tissue, peripheral blood, and relevant clinical and pathological data.

연구 개요

상세 설명

This is a prospective, randomized, controlled clinical trial evaluating iparomlimab and tuvonralimab (QL1706) plus lenvatinib and platinum-etoposide chemotherapy as first-line treatment for patients with unresectable or metastatic extrapulmonary neuroendocrine carcinoma.

The study includes a safety lead-in phase and a randomized phase. During the safety lead-in phase, six participants will receive QL1706 plus lenvatinib and platinum-etoposide chemotherapy. Dose-limiting toxicities will be evaluated. If two or more participants experience a dose-limiting toxicity, the starting dose of lenvatinib in the randomized phase will be reduced from 8 mg to 4 mg once daily.

In the randomized phase, eligible participants will be assigned to receive either QL1706 plus lenvatinib and platinum-etoposide chemotherapy or platinum-etoposide chemotherapy alone. After six cycles of combination treatment, participants in the experimental group will receive maintenance treatment with QL1706 plus lenvatinib until disease progression, unacceptable toxicity, or another protocol-defined reason for discontinuation. Participants in the control group will enter follow-up observation after completing six cycles of chemotherapy.

The study will evaluate treatment efficacy and safety, including the 6-month PFS rate, PFS, OS, tumor response, duration of response, and treatment-related adverse events. Potential predictive biomarkers will also be explored using tumor tissue, peripheral blood, and relevant clinical and pathological data.

연구 유형

중재적

등록 (추정된)

92

단계

  • 2 단계

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

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아니

설명

Inclusion Criteria:

  1. Histologically and/or cytologically confirmed locally advanced unresectable or metastatic extrapulmonary neuroendocrine carcinoma. Eligible primary sites include the gastrointestinal tract, pancreas, biliary tract, and other extrapulmonary organs. Neuroendocrine carcinoma of the digestive system must be diagnosed according to the 2019 World Health Organization Classification of Tumours of the Digestive System.
  2. Age ≥18 years, with no restriction on sex.
  3. Life expectancy of at least 12 weeks.
  4. Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1.
  5. Patients must not have received prior first-line systemic anticancer therapy for advanced or metastatic disease. Patients who previously received adjuvant therapy following curative surgery are eligible, provided that disease recurrence occurred more than 6 months after completion of adjuvant therapy.
  6. At least one measurable lesion according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1).
  7. No severe complications related to the primary tumor, including perforation, obstruction, or major bleeding that cannot be adequately controlled with medical treatment.
  8. Adequate organ function, as demonstrated by the following laboratory results obtained within 7 days before enrollment. Patients must not have received blood transfusion, granulocyte colony-stimulating factor (G-CSF), or other supportive treatment affecting the relevant laboratory parameters within 14 days before the first dose of study treatment: Hemoglobin ≥90 g/L; Platelet count ≥75 × 10⁹/L; White blood cell count ≥3.0 × 10⁹/L; Absolute neutrophil count ≥1.5 × 10⁹/L; Total bilirubin ≤1.5 × the upper limit of normal (ULN); Serum creatinine ≤1.5 × ULN; Alanine aminotransferase and aspartate aminotransferase ≤2.5 × ULN, or ≤5 × ULN in participants with liver metastases.
  9. Participants with active hepatitis B virus or hepatitis C virus infection must have received antiviral therapy for at least 14 days before the first dose of study treatment. Hepatitis B virus DNA must be ≤500 IU/mL or ≤2,500 copies/mL, and hepatitis C virus RNA must be below the lower limit of detection of the applicable assay. Such participants must be willing to continue effective antiviral treatment throughout the study.
  10. Voluntary participation in the study and provision of written informed consent.

Exclusion Criteria:

  1. Histologically confirmed neuroendocrine tumor, mixed adenoneuroendocrine carcinoma, or other non-neuroendocrine carcinoma pathological types.
  2. History of another malignancy with a disease-free interval of less than 5 years, except for adequately treated basal cell carcinoma of the skin, carcinoma in situ of the cervix, or a gastrointestinal tumor confirmed to have been cured by endoscopic mucosal resection.
  3. Uncontrolled hypertension despite medical treatment, defined as systolic blood pressure >150 mmHg or diastolic blood pressure >90 mmHg.
  4. Urine protein ≥2+ on routine urinalysis or 24-hour urinary protein ≥1 g.
  5. Major surgery within 4 weeks before enrollment, excluding diagnostic biopsy, or an incompletely healed surgical wound.
  6. Severe gastrointestinal disorders that may affect drug absorption, including but not limited to peptic ulcer, ulcerative colitis, active gastrointestinal bleeding, gastrointestinal obstruction, or severe diarrhea.
  7. A history of severe bleeding within the previous 3 months, defined as a single bleeding episode of >30 mL; hemoptysis within the previous 1 month, defined as a single episode of >5 mL; or a thromboembolic event within the previous 12 months, including pulmonary embolism or cerebral infarction.
  8. Severe cardiovascular disease, including but not limited to acute myocardial infarction, unstable angina, heart failure, ventricular arrhythmia requiring medical treatment, left ventricular ejection fraction <50%, or New York Heart Association cardiac functional class II or higher.
  9. Corrected QT interval (QTc) >480 ms on electrocardiography.
  10. Active autoimmune disease, a history of autoimmune disease with a risk of recurrence, or another condition requiring immunosuppressive treatment, such as prior organ transplantation. Participants with type 1 diabetes mellitus, hypothyroidism requiring only hormone replacement therapy, or skin disorders not requiring systemic treatment, such as vitiligo, psoriasis, or alopecia, may be enrolled.
  11. A history of interstitial lung disease or noninfectious pneumonitis that is symptomatic, or a previous pulmonary condition that may interfere with the evaluation or management of study treatment-related pulmonary toxicity.
  12. Active pulmonary tuberculosis within 1 year before the first dose of study treatment. Patients with a history of active pulmonary tuberculosis more than 1 year before the first dose must undergo careful evaluation, including sputum smear examination, T-SPOT.TB testing, erythrocyte sedimentation rate testing, and chest computed tomography. Such participants may be enrolled only if there is no evidence of active pulmonary tuberculosis.
  13. A history of chronic persistent diarrhea or the presence of complete intestinal obstruction.
  14. Requirement for systemic treatment with corticosteroids at a prednisone-equivalent dose of >10 mg/day or other immunosuppressive agents within 14 days before the first dose of study treatment. Inhaled or topical corticosteroids and adrenal replacement therapy at a prednisone-equivalent dose of ≤10 mg/day are permitted in the absence of active autoimmune disease. Short-term corticosteroid use for ≤7 days is permitted for prophylaxis, such as prevention of contrast-media allergy, or for the treatment of non-autoimmune conditions, such as delayed hypersensitivity caused by contact allergens.
  15. Prior treatment with any antibody or drug targeting a T-cell co-regulatory protein or immune checkpoint, including but not limited to anti-PD-1, anti-PD-L1, anti-CTLA-4, anti-OX-40, anti-CD137, anti-TIM-3, or anti-LAG-3 therapies.
  16. Immunodeficiency disorder or human immunodeficiency virus infection.
  17. Severe medical or surgical comorbidities that impair organ function, or an acute infection associated with a body temperature >38°C, which, in the investigator's judgment, would make the patient unsuitable for the study.
  18. Leptomeningeal metastases or symptomatic brain metastases.
  19. Pregnant or breastfeeding women, or patients of reproductive potential, including male patients and women who have been postmenopausal for less than 1 year, who are unwilling to use effective contraception.
  20. A history of allergy or hypersensitivity to any component of the study treatments.
  21. Any other condition that, in the investigator's judgment, makes the patient unsuitable for participation in the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Iparomlimab and tuvonralimab injection (QL1706) + Lenvatinib + EP/EC
This arm includes a safety run-in cohort followed by a randomized experimental cohort. In the safety run-in, six participants will receive iparomlimab and tuvonralimab (QL1706), lenvatinib 8 mg once daily, and etoposide plus cisplatin or carboplatin. If DLTs occur in at least 2 of the 6 participants, the starting lenvatinib dose in the randomized experimental cohort will be reduced to 4 mg once daily; otherwise, 8 mg once daily will be used. Participants in the randomized experimental cohort will receive six cycles of combination treatment, followed by maintenance QL1706 plus lenvatinib until disease progression, unacceptable toxicity, or treatment discontinuation.
Participants will receive iparomlimab and tuvonralimab injection (QL1706) at 5 mg/kg intravenously on Day 1, etoposide at 100 mg/m² intravenously on Days 1-3, and either cisplatin at 75 mg/m² intravenously per cycle or carboplatin at AUC 5 intravenously on Day 1 of each 21-day cycle. Lenvatinib will be administered orally once daily at 8 mg or 4 mg, as determined by the safety findings from the safety run-in phase. After six cycles of combination treatment, participants without disease progression or unacceptable toxicity will continue maintenance treatment with QL1706 plus lenvatinib until disease progression, unacceptable toxicity, or another protocol-defined reason for discontinuation.
활성 비교기: EP/EC
Participants in the randomized control arm will receive etoposide plus cisplatin or carboplatin as first-line treatment for six cycles, followed by observation and follow-up.
Patients will receive etoposide 100 mg/m² intravenously on Days 1-3, together with either cisplatin 75 mg/m² intravenously per cycle or carboplatin AUC 5 intravenously on Day 1 of each 21-day cycle.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
6-month PFS rate
기간: Up to 24 months
The 6-month PFS rate is defined as the proportion of patients who are alive and free from radiographic disease progression at 6 months after enrollment, as assessed by blinded independent radiologic review. Disease progression or death from any cause, whichever occurs first, will be considered a progression-free survival event.
Up to 24 months

2차 결과 측정

결과 측정
측정값 설명
기간
PFS
기간: 2 years
PFS is defined as the time from enrollment to the first documented radiographic disease progression, as assessed by blinded independent radiologic review, or death from any cause, whichever occurs first.
2 years
OS
기간: 2 years
OS is defined as the time from enrollment to death from any cause.
2 years
ORR
기간: 2 years
ORR is defined as the proportion of patients whose best overall response is complete response or partial response, as assessed according to Response Evaluation Criteria in Solid Tumors version 1.1 by blinded independent radiologic review.
2 years
DCR
기간: 2 years
DCR is defined as the proportion of participants whose best overall response is complete response, partial response, or stable disease, as assessed according to Response Evaluation Criteria in Solid Tumors version 1.1 by blinded independent radiologic review.
2 years
DoR
기간: 2 years
DoR is defined as the time from the first documented complete response or partial response to the first documented radiographic disease progression, as assessed by blinded independent radiologic review according to Response Evaluation Criteria in Solid Tumors version 1.1 or death from any cause, whichever occurs first.
2 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 8월 1일

기본 완료 (추정된)

2030년 8월 1일

연구 완료 (추정된)

2030년 9월 1일

연구 등록 날짜

최초 제출

2026년 7월 25일

QC 기준을 충족하는 최초 제출

2026년 7월 28일

처음 게시됨 (실제)

2026년 7월 31일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 31일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 28일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • 2026(1754)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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