- ICH GCP
- US-Register für klinische Studien
- Klinische Studie 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.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 3
Kontakte und Standorte
Studienkontakt
- Name: Zhimin Shao
- Telefonnummer: 86-021-64175590
- E-Mail: zhimingshao@fudan.edu.cn
Studienorte
-
-
-
Shanghai, China
- Rekrutierung
- breast cancer institute of Fudan University Cancer Hospital, shanghai, shanghai
-
Kontakt:
- Zhimin Shao, MD
- Telefonnummer: 86-021-641755901105
- E-Mail: zhimingshao@fudan.edu.cn
-
Hauptermittler:
- Zhimin Shao, MD
-
Unterermittler:
- Keda Yu, MD
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Aktiver Komparator: standard endocrine therapy
standard endocrine therapy |
standard endocrine therapy |
|
Experimental: 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. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Invasive Disease Free Survival
Zeitfenster: From enrollment to 3 years post-treatment
|
Invasive Disease Free Survival |
From enrollment to 3 years post-treatment
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
3-jähriges krankheitsfreies Überleben
Zeitfenster: Von der Einschreibung bis 3 Jahre nach der Behandlung
|
Von der Einschreibung bis 3 Jahre nach der Behandlung
|
|
|
Overall Survival
Zeitfenster: From enrollment to 3 years post-treatment
|
Overall Survival |
From enrollment to 3 years post-treatment
|
|
safety
Zeitfenster: 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
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- SCHBCC-N081
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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