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Induction Trastuzumab Rezetecan Followed by Maintenance Dalpiciclib and Endocrine Therapy as First-line Treatment of HR+/HER2 Low mBC

9. november 2026 oppdatert av: Tong Liu, Harbin Medical University

A Phase II Exploratory Study of Induction Trastuzumab Rezetecan Followed by Maintenance Dalpiciclib Combined With Endocrine Therapy as First-Line Treatment for HR+/HER2-Low Advanced Breast Cancer

This study is a prospective, open-label, randomized phase II clinical trial designed to evaluate the efficacy and safety of two treatment modalities in the first-line treatment of HR+/HER2-low advanced breast cancer: induction therapy with trastuzumab rezetecan for 6 cycles followed by maintenance dalpiciclib, versus the standard care of dalpiciclib combined with endocrine therapy.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Antatt)

100

Fase

  • Fase 2

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  • Female patients aged ≥18 years and ≤75 years (premenopausal or perimenopausal female patients must be willing to receive LHRH agonist therapy during the study period).
  • Female breast cancer patients with pathologically confirmed HR-positive, HER2-low expression, with evidence of locoregional recurrence or metastasis, not suitable for curative-intent surgical resection or radiotherapy, and without clinical indication for chemotherapy:

HR-positive defined as: ER-positive and/or PR-positive, with positive staining tumor cells accounting for ≥1% of all tumor cells; HER2-low expression defined as: standard immunohistochemistry (IHC) 1+/2+ and ISH/CISH negative.

  • No prior systemic anticancer therapy for locoregional recurrence or metastatic disease, or relapse >12 months after completion of (neo)adjuvant CDK4/6 inhibitor therapy (if the patient progressed during adjuvant AI therapy, the first-line treatment for advanced disease must use the dalpiciclib plus fulvestrant regimen).
  • ECOG performance status score of 0-1.
  • Adequate organ function meeting the following criteria (no blood components or cell growth factors used for corrective treatment within 14 days before the first dose):
  • Female subjects of childbearing potential must have a negative pregnancy test result at screening and must agree to use highly effective contraceptive methods from the time of signing informed consent until 7 months after the last dose of investigational drug.
  • Voluntary participation in the clinical study with signed informed consent, good compliance, and willingness to cooperate with visits and study-related procedures.

Exclusion Criteria:

  • Uncontrolled active central nervous system metastases (defined as symptomatic or requiring glucocorticoids or mannitol to control symptoms). Patients with stable brain metastases are permitted to enroll.
  • Disease progression or relapse during or within ≤12 months of completing neoadjuvant or adjuvant endocrine therapy.
  • Patients judged by the investigator to be unsuitable for endocrine therapy, including those with symptomatic visceral dissemination or at risk of life-threatening complications in the short term (e.g., third-space fluid accumulation that cannot be controlled by drainage [massive ascites, pleural effusion, pericardial effusion], pulmonary lymphangitis, or liver involvement >50%).
  • Prior treatment with dalpiciclib or any antibody-drug conjugate containing an exatecan derivative topoisomerase I inhibitor.
  • Prior surgery (major surgery for cancer treatment), radiotherapy, chemotherapy, immunotherapy, molecular targeted therapy, biologic therapy, or other clinical investigational therapy within 4 weeks before the first dose.

Other malignancies within the past 5 years, excluding cured basal cell carcinoma of the skin and cervical carcinoma in situ.

  • Human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS); active hepatitis B (HBV DNA ≥1000 IU/mL); hepatitis C (positive hepatitis C antibody and HCV-RNA above the lower limit of detection of the assay); or co-infection with hepatitis B and hepatitis C. Liver cirrhosis, or severe infection requiring antibiotics, antivirals, or antifungals.
  • History of any of the following cardiac diseases: (1) angina pectoris; (2) arrhythmia requiring medication or clinically significant arrhythmia; (3) myocardial infarction; (4) heart failure; (5) any other cardiac disease judged by the investigator to be unsuitable for participation in this trial.

History of clinically significant pulmonary disease, including but not limited to interstitial pneumonia, pneumonitis, pulmonary fibrosis, and radiation pneumonitis (except for radiation changes not requiring corrective treatment), or suspected presence of such conditions identified during screening.

  • Severe infection within 4 weeks before the first dose (e.g., requiring intravenous antibiotics, antifungals, or antivirals per clinical practice guidelines), or unexplained fever >38.5°C during screening or before the first dose.
  • Inability to swallow, intestinal obstruction, or other factors affecting drug administration and absorption.
  • Known allergy to any investigational drug or any of its excipients.
  • Toxicity from prior anticancer therapy that has not recovered to ≤ Grade 1 per NCI-CTCAE v6.0.
  • Presence of any other serious physical or mental illness or laboratory abnormality that may increase the risk of participating in the study, interfere with study results, or render the patient unsuitable for participation in the investigator's judgment.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Arm 1: SHR-A1811 → Dalpiciclib+ET

Induction SHR-A1811 4.8mg/kg IV Q3W for 6 cycles followed by maintenance Dalpiciclib plus endocrine therapy

Aktiv komparator: Arm 2: Dalpiciclib + ET

Dalpiciclib 125mg po D1-21 Q4W + endocrine therapy(AI or Fulvestrant)

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
PFS
Tidsramme: up to 3 years

from randomization to disease progression, unacceptable toxicity or death, whichever occurs first

up to 3 years

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
ORR
Tidsramme: up to 3 years

objective response rate, assessed every 12 weeks

up to 3 years
DoR
Tidsramme: up to 3 years

Duration of response

up to 3 years
PFS2
Tidsramme: up to 5 years

from randomization to disease progression on the first subsequent anticancer therapy or death from any cause, whichever occurs first.

up to 5 years

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

15. desember 2026

Primær fullføring (Antatt)

15. desember 2031

Studiet fullført (Antatt)

30. juni 2032

Datoer for studieregistrering

Først innsendt

9. november 2026

Først innsendt som oppfylte QC-kriteriene

9. november 2026

Først lagt ut (Faktiske)

13. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • MA-BC-II-147

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .