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Dalpicilib-Enhanced vs. Standard Endocrine Therapy in ER+ HER2- Early Breast Cancer

27. september 2026 opdateret af: Zhimin Shao, Fudan University

A Phase III Randomized Controlled Trial Comparing Dalpicilib-Enhanced Adjuvant Endocrine Therapy With Standard Adjuvant Endocrine Therapy in ER+ HER2- Lymph Node-Negative Early Breast Cancer With Risk Factors

This study aims to conduct a randomized controlled clinical trial to compare the efficacy and safety of dalpicilib combined with endocrine therapy versus standard endocrine therapy in ER-positive, HER2-negative, lymph node-negative patients with risk factors, in order to further optimize the regimen for adjuvant endocrine therapy in breast cancer.

Studieoversigt

Status

Rekruttering

Betingelser

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

1388

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

      • Shanghai, Kina
        • Rekruttering
        • breast cancer institute of Fudan University Cancer Hospital, shanghai, shanghai
        • Kontakt:
        • Ledende efterforsker:
          • Zhimin Shao, MD
        • Underforsker:
          • Keda Yu, MD

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 70 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Beskrivelse

Inclusion Criteria:

  1. Women aged 18-70 years
  2. ECOG score of 0-1
  3. Histologically confirmed unilateral invasive cancer (regardless of pathology type)
  4. No macroscopic or microscopic tumor residue after surgical resection
  5. Early-stage breast cancer, pathologically confirmed as ER-positive and HER2-negative (ER-positive defined as immunohistochemical detection of ER >10% of tumor cells positive; HER2 0-1+ or HER2 2+ but FISH negative, with no amplification, defined as HER2-negative)
  6. Postoperative pathological staging of pT1c or above, N0M0, and meeting one of the following criteria: (1) G3; (2) G2 and meeting one of the following: i. Ki-67 ≥20%; ii. 21-gene recurrence score ≥26 or high genomic risk profile; iii. Age ≤40 years and vascular invasion positive
  7. No prior neoadjuvant treatment
  8. Time from surgery or completion of chemotherapy or radiotherapy (whichever occurs later) to randomization does not exceed 8 weeks
  9. Good postoperative recovery, at least 1 week after surgery
  10. Normal function of major organs, meeting the following criteria: (1) Hematological criteria: HB ≥90 g/L (no blood transfusion in the last 14 days); ANC ≥1.5 × 10^9 /L; PLT ≥100 × 10^9 /L; (2) Biochemical criteria: TBIL ≤1.5 × ULN (upper limit of normal); ALT and AST ≤3 × ULN; serum Cr ≤1.5 × ULN
  11. Women of childbearing age must use contraception during treatment
  12. Subjects voluntarily join this study, sign informed consent, demonstrate good compliance, and cooperate with follow-up

Exclusion Criteria:

  1. Bilateral breast cancer or ductal/lobular carcinoma in situ (DCIS/LCIS)
  2. Received treatment for advanced disease
  3. Metastasis at any site
  4. Any tumor > T4a (with skin involvement, fixation, inflammatory breast cancer)
  5. Clinically or radiologically suspected malignancy in the contralateral breast not confirmed and requiring biopsy
  6. Received neoadjuvant therapy, including chemotherapy, radiotherapy, and endocrine therapy
  7. History of malignant tumors within the past 5 years (excluding basal cell carcinoma of the skin and cervical carcinoma in situ), including contralateral breast cancer
  8. Patient has been enrolled in other clinical trials
  9. Patient has severe systemic diseases and/or uncontrolled infections that prevent participation in the study
  10. Severe cardiovascular or cerebrovascular diseases within 6 months prior to randomization (e.g., unstable angina, chronic heart failure, uncontrolled hypertension >150/90 mmHg, myocardial infarction, or stroke)
  11. Known allergy to relevant medications
  12. Women of childbearing age who refuse contraception during treatment and for 8 weeks after treatment completion
  13. Pregnant or breastfeeding women
  14. Positive pregnancy test before drug administration after joining the trial
  15. Individuals with mental illness or cognitive impairment who cannot understand the trial protocol and its side effects, unable to comply with the protocol and follow-up (systematic assessment required prior to enrollment)
  16. Individuals without personal freedom and independent civil capacity

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: standard endocrine therapy

standard endocrine therapy

standard endocrine therapy

Eksperimentel: standard endocrine therapy plus dalpicilib

standard endocrine therapy plus dalpicilib

standard endocrine therapy

Dalpicilib 100 mg once daily from day 1 to day 21, every 4 weeks, for a total of 3 years, in combination with endocrine therapy for 5 years.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Invasive Disease Free Survival
Tidsramme: From enrollment to 3 years post-treatment

Invasive Disease Free Survival

From enrollment to 3 years post-treatment

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
3-års sygdomsfri overlevelse
Tidsramme: Fra indskrivning til 3 år efter behandling
Fra indskrivning til 3 år efter behandling
Overall Survival
Tidsramme: From enrollment to 3 years post-treatment

Overall Survival

From enrollment to 3 years post-treatment
safety
Tidsramme: From enrollment to 3 years post-treatment

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

From enrollment to 3 years post-treatment
Patient reported outcomes
Tidsramme: From enrollment to 3 years post-treatment

Patient-Reported Outcomes (PROs) Assessed by the EORTC QLQ-C30 Questionnaire. Provide a brief description of what aspects of the patient's health or experience the tool will measure (e.g., quality of life, symptom burden, treatment side effects).

From enrollment to 3 years post-treatment

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

9. januar 2025

Primær færdiggørelse (Anslået)

30. september 2030

Studieafslutning (Anslået)

30. september 2030

Datoer for studieregistrering

Først indsendt

28. september 2024

Først indsendt, der opfyldte QC-kriterier

9. oktober 2024

Først opslået (Faktiske)

15. oktober 2024

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

29. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

27. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • SCHBCC-N081

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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