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Befotertinib Plus Chemotherapy With an MRD-guided Adaptive Strategy for Treatment Escalation and Response Optimization in EGFR-mutated NSCLC Patients (BE-MASTER)

2026년 7월 12일 업데이트: Zhu Yanjuan, Guangzhou University of Traditional Chinese Medicine
This is a multicenter, phase II exploratory clinical trial in untreated patients with EGFR-mutant non-small cell lung cancer (stages IIIB-IV) .All participants will receive oral befotertinib monotherapy for 3 weeks first, then serial minimal residual disease (MRD/MRD) testing is performed to adjust subsequent treatment. Patients with positive MRD will receive 4 cycles of pemetrexed plus platinum chemotherapy; patients with negative MRD will continue single-agent befotertinib. After induction, maintenance therapy will be given according to follow-up MRD results. The primary goal is to evaluate progression-free survival guided by dynamic MRD monitoring, and secondary endpoints include objective response rate, disease control rate, safety and MRD clearance rate.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

124

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

연구 장소

    • Guangdong
      • Guangzhou, Guangdong, 중국, 510120
        • Guangdong Provincial Hospital of Chinese Medicine
        • 연락하다:

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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설명

Inclusion Criteria:

  1. Histologically or cytologically confirmed stage IIIB-IV non-small cell lung cancer (NSCLC).
  2. Age ≥18 years, any gender.
  3. Confirmed EGFR exon 19 deletion or exon 21 (L858R) substitution mutation by central laboratory or site-validated testing assay.
  4. No prior systemic anti-tumor therapy.
  5. ECOG performance status 0-2.
  6. Expected survival ≥12 weeks.
  7. Able to swallow oral study medication.
  8. At least one measurable lesion per RECIST 1.1 criteria.
  9. Adequate organ function as defined below:

    1. Absolute neutrophil count ≥1.5 × 10^9/L;
    2. Platelet count ≥100 × 10^9/L;
    3. Hemoglobin ≥9 g/dL (transfusion allowed);
    4. Total bilirubin ≤1.5 × ULN;
    5. ALT/AST ≤2.5 × ULN (≤5 × ULN if liver metastasis);
    6. Serum creatinine ≤1.5 × ULN, or creatinine clearance ≥45 mL/min by Cockcroft-Gault formula if creatinine >1.5 × ULN.
  10. Fertile men and women agree to effective contraception during study treatment and for specified time after last dose.

Exclusion Criteria:

  1. Receiving other systemic anti-tumor therapy, or plan to combine other systemic anti-cancer agents during study.
  2. Participated in another investigational drug trial within 4 weeks prior to first study drug; major surgery within 4 weeks; unhealed wound, active ulcer or fracture; radiotherapy within 2 weeks without recovery.
  3. Severe cardiovascular disease: QTcF ≥450 ms or clinically significant ECG abnormality; uncontrolled hypertension (SBP>160 mmHg or DBP>100 mmHg); congestive heart failure, cardiomyopathy, arrhythmia requiring intervention, unstable angina, myocardial infarction, stroke or TIA within 6 months prior to treatment.
  4. Uncontrolled active infection including active HBV, HCV, HIV, active syphilis infection judged by investigator. Stable infection without safety risk is permitted.
  5. History of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis requiring steroids, or active interstitial lung disease.
  6. Active hemorrhage, clinically significant hemoptysis, high thromboembolic risk or prior severe thromboembolic events unsuitable for study treatment.
  7. Renal dysfunction with creatinine clearance <45 mL/min; prior intolerable toxicity to pemetrexed; severe hypersensitivity to pemetrexed or its excipients.
  8. Positive serum pregnancy test within 7 days before treatment, pregnant or breastfeeding women; fertile subjects refusing contraception during study and 3 months after last dose.
  9. Known severe hypersensitivity to befotertinib, cisplatin, carboplatin or their excipients.
  10. Any other medical, metabolic, physical or lab abnormality that may compromise subject safety or interfere with study results per investigator judgment.

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: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Befotertinib with chemotherapy guided by dynamic MRD monitoring

All participants receive oral befotertinib 75 mg once daily for 3 weeks as induction therapy, followed by MRD detection. Treatment is adjusted dynamically based on serial MRD results: MRD-positive patients get 4 cycles of befotertinib plus pemetrexed-platinum chemotherapy; MRD-negative patients continue single-agent befotertinib. Subsequent MRD tests every 12 weeks guide treatment adjustment: patients who have not previously received pemetrexed

-platinum chemotherapy and convert to MRD-positive will receive 4 cycles of befotertinib plus pemetrexed-platinum chemotherapy; patients who have previously received pemetrexed-platinum chemotherapy will receive single agent befotertinib if MRD-negative or befotertinib plus pemetrexed maintenance if MRD-positive.Treatment cycles are 21 days, continued until disease progression, intolerable toxicity, withdrawal of consent or death.

Oral administration, initial dose 75 mg once daily; dose adjusted to 100 mg once daily based on safety and clinical benefit. Used as induction, single-agent maintenance, or combined with chemotherapy.
This is induction combination chemotherapy for MRD-positive patients after initial befotinib monotherapy. Pemetrexed at 500 mg/m² is given intravenously on Day 1 of each 21-day cycle, combined with either Cisplatin (75 mg/m² IV Day 1) or Carboplatin (AUC 5 IV Day 1) at investigator's discretion based on patient renal function and tolerability, for up to 4 cycles. Standard premedication with folic acid, vitamin B12 and dexamethasone is administered per pemetrexed prescribing guidelines.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Progression-Free Survival (PFS)
기간: Up to 48 months after the last participant enrollment,including at least 24 months of follow-up after the last participant is enrolled.
Time from first dose of study treatment to first radiographically confirmed isease progression according to RECIST version 1.1 or death from any cause, whichever occurs first.
Up to 48 months after the last participant enrollment,including at least 24 months of follow-up after the last participant is enrolled.

2차 결과 측정

결과 측정
측정값 설명
기간
Median Overall Survival (OS)
기간: Including at least 24 months of follow-up after the last participant is enrolled.Participants lost to follow-up will be censored at the last date they were known to be alive.
Defined as the time from first dose of study treatment to death from any cause.
Including at least 24 months of follow-up after the last participant is enrolled.Participants lost to follow-up will be censored at the last date they were known to be alive.
Objective response rate (ORR)
기간: including at least 24 months of follow-up after the last participant is enrolled.
Defined as the proportion of participants achieving confirmed complete response (CR) or partial response (PR) per RECIST version 1.1.
including at least 24 months of follow-up after the last participant is enrolled.
Disease control rate (DCR)
기간: including at least 24 months of follow-up after the last participant is enrolled.
defined as the proportion of participants achieving confirmed complete response (CR), partial response (PR) or stable disease (SD) per RECIST version 1.1.
including at least 24 months of follow-up after the last participant is enrolled.
Time to intolerable toxicity
기간: Including at least 24 months of follow-up after the last participant is enrolled.
Defined as the time from the first dose of study treatment to the first occurrence of treatment-related intolerable adverse event leading to permanent discontinuation of study therapy.
Including at least 24 months of follow-up after the last participant is enrolled.

공동 작업자 및 조사자

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스폰서

협력자

수사관

  • 수석 연구원: Xiaoshu Chai, MD, Guangdong Provincial Hospital of Traditional Chinese Medicine

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 7월 5일

기본 완료 (추정된)

2030년 7월 31일

연구 완료 (추정된)

2030년 7월 31일

연구 등록 날짜

최초 제출

2026년 7월 12일

QC 기준을 충족하는 최초 제출

2026년 7월 12일

처음 게시됨 (실제)

2026년 7월 16일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 16일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 12일

마지막으로 확인됨

2026년 7월 1일

추가 정보

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