- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT06637150
Dalpicilib-Enhanced vs. Standard Endocrine Therapy in ER+ HER2- Early Breast Cancer
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.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Zhimin Shao
- Telefonnummer: 86-021-64175590
- E-post: zhimingshao@fudan.edu.cn
Studiesteder
-
-
-
Shanghai, Kina
- Rekruttering
- breast cancer institute of Fudan University Cancer Hospital, shanghai, shanghai
-
Ta kontakt med:
- Zhimin Shao, MD
- Telefonnummer: 86-021-641755901105
- E-post: zhimingshao@fudan.edu.cn
-
Hovedetterforsker:
- Zhimin Shao, MD
-
Underetterforsker:
- Keda Yu, MD
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Women aged 18-70 years
- ECOG score of 0-1
- Histologically confirmed unilateral invasive cancer (regardless of pathology type)
- No macroscopic or microscopic tumor residue after surgical resection
- 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)
- 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
- No prior neoadjuvant treatment
- Time from surgery or completion of chemotherapy or radiotherapy (whichever occurs later) to randomization does not exceed 8 weeks
- Good postoperative recovery, at least 1 week after surgery
- 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
- Women of childbearing age must use contraception during treatment
- Subjects voluntarily join this study, sign informed consent, demonstrate good compliance, and cooperate with follow-up
Exclusion Criteria:
- Bilateral breast cancer or ductal/lobular carcinoma in situ (DCIS/LCIS)
- Received treatment for advanced disease
- Metastasis at any site
- Any tumor > T4a (with skin involvement, fixation, inflammatory breast cancer)
- Clinically or radiologically suspected malignancy in the contralateral breast not confirmed and requiring biopsy
- Received neoadjuvant therapy, including chemotherapy, radiotherapy, and endocrine therapy
- 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
- Patient has been enrolled in other clinical trials
- Patient has severe systemic diseases and/or uncontrolled infections that prevent participation in the study
- 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)
- Known allergy to relevant medications
- Women of childbearing age who refuse contraception during treatment and for 8 weeks after treatment completion
- Pregnant or breastfeeding women
- Positive pregnancy test before drug administration after joining the trial
- 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)
- Individuals without personal freedom and independent civil capacity
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Aktiv komparator: standard endocrine therapy
standard endocrine therapy |
standard endocrine therapy |
|
Eksperimentell: 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. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
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 |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
3-års sykdomsfri overlevelse
Tidsramme: Fra innskriving til 3 år etter behandling
|
Fra innskriving til 3 år etter 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
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- SCHBCC-N081
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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. .