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オシメルチニブ + 化学療法 vs オシメルチニブ 1L 投与後の 3 週目 ctDNA EGFRm 持続性 EGFRm NSCLC (FLAME)

The Efficacy and Safety of Osimertinib Plus Carboplatin and Pemetrexed Versus Osimertinib Monotherapy in Locally Advanced or Metastatic EGFRm NSCLC Patients With EGFRm Persistence in ctDNA at 3 Weeks After 1L Osimertinib: A Multicenter, Randomized Controlled Study

This is a prospective, randomised, open-label, positive-controlled study to investigate the efficacy and safety of Osimertinib plus Carboplatin/Pemetrexed versus Osimertinib monotherapy in locally advanced or metastatic EGFRm NSCLC patients with EGFRm persistence in ctDNA at 3 weeks after first-line therapy with Osimertinib.

調査の概要

研究の種類

介入

入学 (実際)

80

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Beijing、中国
        • Cancer Hospital Chinese Academy of Medical Sciences

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Provision and signed of informed consent prior to any study specific procedures;
  • Male or female, aged at least 18 years;
  • Eastern Cooperative Oncology Group (ECOG) performance-status score of 0 or 1;
  • Newly diagnosed, and histologically documented locally advanced or metastatic non-squamous NSCLC with sensitizing EGFR mutations positive (either Exon 19 deletion or 21 L858R, confirmed by histology or cytology ), and classified as stage IIIB, IIIC, IV or recurrent NSCLC which are not amenable to curative surgery or radiotherapy;
  • Life expectancy of at least 3 months at recruitment;
  • Only the patients receiving osimertinib as 1L treatment and meeting the following criteria will be considered:

A. Prior to 1L osimertinib:

  1. History of EGFRm (exon 19 deletion or exon 21 L858R) in the plasma ctDNA by the local testing methods.
  2. No previous systemic treatment. Adjuvant therapies, or definitive radiation/chemoradiation are permitted as long as treatment was completed at least 6 months prior to receiving 1L treatment.
  3. Patients with asymptomatic and stable CNS metastases for at least 2 weeks will be allowed, including leptomeningeal metastases.

B. Prior to randomization: Patients after 3 weeks of 1L osimertinib treatment who have persistence ctDNA EGFRm by SuperARMS at 3 weeks will be considered to be enrolled. They will need to further meet the criteria below before randomization:

  1. Patients without disease progression by RECIST 1.1 evaluation;
  2. At least 1 measurable extracranial lesion according to RECIST 1.1 .
  3. Female subjects should be using highly effective contraceptive measures, and must have a negative pregnancy test and not be breast-feeding prior to start of dosing if of child-bearing potential, or must have evidence of non-child-bearing potential.
  4. Male subjects should be willing to agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures and agreement to refrain from donating sperm.

Exclusion Criteria:

  • Involvement in the planning and/or conduct of the study;
  • History of hypersensitivity to active or inactive excipients of Osimertinib and/or Pemetrexed and/or Carboplatin or drugs with a similar chemical structure or class to Osimertinib and/or Pemetrexed and/or Carboplatin;
  • For patients, inability to collect plasma samples at baseline and disease progression;
  • QT prolongation or any clinically important abnormalities in rhythm;
  • Any evidence of severe or uncontrolled systemic diseases;
  • Currently receiving medications or herbal supplements known to be strong inducers of CYP3A4;
  • Any unresolved toxicities from prior therapy greater than CTCAE 5.0 grade 1 at the time of starting study treatment.
  • Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of osimertinib.
  • Inadequate bone marrow reserve or organ function;
  • Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease.
  • Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements.
  • Contraindication for osimertinib, pemetrexed and carboplatin according to China approved label.
  • Women who are pregnant or breast-feeding.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Osimertinib 80 mg QD and platinum-based chemotherapy

Osimertinib 80 mg in combination with pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.

Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.

他の名前:
  • AZD9291
  • タグリッソ

Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.

アクティブコンパレータ:Osimertinib 80mg QD

All patients randomized into this will only receive Osimertinib 80mg.

Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.

他の名前:
  • AZD9291
  • タグリッソ

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Progression free survival
時間枠:The analysis of PFS based on Investigator assessment (according to RECIST 1.1) will occur when approximately 54 progression events have been observed in the 80 randomized patients (approximately 67.5% PFS maturity).

Progression-free survival (PFS) using Investigator assessment as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1).

The analysis of PFS based on Investigator assessment (according to RECIST 1.1) will occur when approximately 54 progression events have been observed in the 80 randomized patients (approximately 67.5% PFS maturity).

二次結果の測定

結果測定
メジャーの説明
時間枠
OS rate at 18 months
時間枠:The OS rate at 18 months will be defined as the Kaplan-Meier estimate of OS at 18 months.

Proportion of patients alive at 18 months

The OS rate at 18 months will be defined as the Kaplan-Meier estimate of OS at 18 months.
Objective Response Rate (ORR)
時間枠:Objective Response Rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

ORR (per RECIST 1.1 using Investigator assessments) is defined as the number (percent) of patients with at least 1 visit response of CR or PR.

Objective Response Rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
Disease Control Rate (DCR)
時間枠:Disease control rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

Disease control rate (DCR) is defined as the percentage of subjects who have a best overall response of CR or PR or SD by RECIST 1.1 as assessed by the Investigator.

Disease control rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
Duration of Response (DoR)
時間枠:Duration of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

DoR is defined as the time from the date of first documented response until the date of documented progression or death in the absence of disease progression.

Duration of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
Depth of Response
時間枠:Depth of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

Depth of response by Investigator is defined as the relative change in the sum of the longest diameters of RECIST target lesions at the nadir in the absence of NLs or progression of NTLs when compared to baseline.

Depth of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
Safety and tolerability: Adverse event
時間枠:Safety and tolerability analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

All Adverse events/≥grade 3 AE/SAE incidence rate (AE/SAE graded by CTCAE v5); All ADR incidence rate; AESI: ILD/pneumonitis-like event, Cardiac failure

Safety and tolerability analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
Molecular resistance mechanism
時間枠:Molecular resistance mechanism analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

To evaluate potential molecular resistance mechanism by biomarker analysis of plasma at baseline and disease progression and tissue samples (if applicable) by next-generation sequencing (NGS).

Molecular resistance mechanism analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2022年2月7日

一次修了 (実際)

2026年1月26日

研究の完了 (実際)

2026年1月26日

試験登録日

最初に提出

2021年2月19日

QC基準を満たした最初の提出物

2021年2月22日

最初の投稿 (実際)

2021年2月24日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月6日

QC基準を満たした最後の更新が送信されました

2026年11月4日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制機器製品の研究

いいえ

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