- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07616453
Efficacy and Safety of Culmerciclib Plus Aromatase Inhibitors in a Response-Adapted Neoadjuvant Strategy for Highly Proliferative ER-Positive/HER2-Negative Breast Cancer (TAYLOR-002)
Neoadjuvant Trastuzumab-rezetecan Plus Pertuzumab or Nab-Paclitaxel, Carboplatin, Trastuzumab, and Pyrotinib After Suboptimal Response to Neoadjuvant Dual HER2-Targeted Therapy Combined With Chemotherapy in HER2-Positive Early Breast Cancer: A Response-Guided Phase II Study (TAYLOR-002)
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
This is a prospective, response-adapted, phase II study designed to evaluate an individualized neoadjuvant treatment strategy based on culmerciclib in combination with aromatase inhibitors in patients with highly proliferative ER-positive/HER2-negative early breast cancer. The study incorporates an adaptive treatment algorithm guided by on-treatment assessment of tumor response, with the aim of optimizing therapeutic efficacy while minimizing unnecessary treatment exposure.
All eligible patients initially receive neoadjuvant treatment with culmerciclib plus endocrine therapy according to the study protocol. Following completion of a predefined initial treatment phase, tumor response is assessed using biological and clinical evaluation methods.
Patients who achieve an adequate response continue the same neoadjuvant regimen to complete the planned course of therapy. In contrast, patients demonstrating a suboptimal response are transitioned to alternative treatment strategies prior to surgery. Subsequent treatment selection and management are conducted according to protocol-defined principles and investigator assessment.
This response-adapted strategy is intended to address the clinical heterogeneity of endocrine sensitivity in ER-positive/HER2-negative breast cancer. By tailoring treatment intensity according to early response, the study seeks to maximize therapeutic benefit in responsive patients while facilitating timely treatment modification for those less likely to benefit from the initial regimen.
Primary and secondary objectives include evaluation of clinical efficacy, safety and tolerability of the response-adapted neoadjuvant strategy, and the feasibility of treatment modification based on early response assessment. Exploratory analyses will investigate potential biomarkers associated with treatment response and resistance, with the goal of informing future individualized treatment approaches.
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Yunxiang Zhou
- Numero di telefono: 15868131018
- Email: yxzhou@zju.edu.cn
Luoghi di studio
-
-
Zhejiang
-
Hangzhou, Zhejiang, Cina, 310009
- Reclutamento
- 2nd Affiliated Hospital, School of Medicine, Zhejiang University
-
Contatto:
- Yunxiang Zhou
- Numero di telefono: 15868131018
- Email: yxzhou@zju.edu.cn
-
Contatto:
- Email: yxzhou@zju.edu.cn
-
Sub-investigatore:
- Yunxiang Zhou
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria Female patients aged ≥18 and ≤75 years. Histologically confirmed estrogen receptor (ER)-positive (≥10%) and HER2-negative breast cancer, according to the 2018 ASCO/CAP guidelines. HER2-negative status is defined as immunohistochemistry (IHC) 0 or 1+, or IHC 2+ with negative in situ hybridization (ISH) (ISH ratio <2.0), as confirmed by a certified pathology laboratory.
Ki-67 ≥20% assessed on core needle biopsy samples. Newly diagnosed, treatment-naïve patients with stage I-IIIA disease according to the AJCC 8th edition.
Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
Adequate bone marrow function:
- Absolute neutrophil count ≥1.5 × 10⁹/L (without growth factor support within 14 days);
- Platelet count ≥100 × 10⁹/L (without transfusion or supportive therapy within 7 days);
- Hemoglobin ≥100 g/L (without transfusion within 7 days).
Adequate hepatic and renal function:
- Total bilirubin ≤1 × upper limit of normal (ULN);
- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3 × ULN (≤5 × ULN in patients with liver metastases);
- Blood urea nitrogen and serum creatinine ≤1.5 × ULN, and creatinine clearance ≥50 mL/min (calculated using the Cockcroft-Gault formula).
Left ventricular ejection fraction (LVEF) ≥50% as assessed by echocardiography. QT interval ≤480 ms on 12-lead electrocardiogram (ECG). Ability and willingness to undergo tumor biopsy. Provision of written informed consent. Exclusion Criteria Prior receipt of any anticancer therapy, including chemotherapy, radiotherapy, targeted therapy, or endocrine therapy.
Concurrent treatment with other anticancer agents. Bilateral breast cancer, inflammatory breast cancer, or occult breast cancer. Stage IV breast cancer. Breast cancer not confirmed by histopathology. History of other malignancies within the past 5 years, except for adequately treated carcinoma in situ of the cervix.
Severe dysfunction of major organs, including heart, liver, or kidneys. Conditions affecting oral drug administration or absorption, including inability to swallow, chronic diarrhea, or intestinal obstruction.
Participation in another interventional clinical trial within 4 weeks prior to enrollment.
Known hypersensitivity to any component of the study drugs; history of immunodeficiency, including HIV infection, active hepatitis B or C infection, other acquired or congenital immunodeficiency disorders, or history of organ transplantation.
History of significant cardiovascular disease, including but not limited to clinically significant arrhythmias requiring treatment, myocardial infarction, heart failure, or any other cardiac condition deemed unsuitable by the investigator.
Pregnant or breastfeeding women; women of childbearing potential with a positive pregnancy test at baseline, or unwilling to use effective contraception during the study period.
Any serious concomitant disease that, in the investigator's judgment, may compromise patient safety or compliance with the study, including but not limited to uncontrolled hypertension, severe diabetes, or active infection.
History of neurological or psychiatric disorders, including epilepsy or dementia.
Any other condition that, in the investigator's opinion, makes the patient unsuitable for participation in the study.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Culmerciclib plus AI
|
CDK2/4/6 inhibitor
Letrozole or anastrozole
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Complete cell cycle arrest (CCCA)
Lasso di tempo: 4 weeks
|
Ki67≤2.7%
|
4 weeks
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Tasso di risposta obiettiva (ORR)
Lasso di tempo: 24 settimane
|
24 settimane
|
|
|
Sopravvivenza libera da eventi (EFS)
Lasso di tempo: Circa cinque anni
|
L'EFS è definito come il tempo dalla randomizzazione a uno dei seguenti eventi: preclude l'intervento chirurgico, la recidiva locale o distante, la seconda neoplastica primaria o la morte dovuta a qualsiasi causa.
|
Circa cinque anni
|
|
Evento avverso (AE)
Lasso di tempo: Circa tre anni
|
Un AE è definito come qualsiasi occorrenza medica spiacevole in un partecipante allo studio ha somministrato un prodotto medicinale, temporalmente associato all'intervento dello studio, senza presunzione di causalità.
|
Circa tre anni
|
|
the proportion of patients with Residual Cancer Burden (RCB) class 0-1
Lasso di tempo: 24 weeks
|
24 weeks
|
|
|
Total Pathological Complete Response (tpCR) Rate
Lasso di tempo: 24 weeks
|
24 weeks
|
Collaboratori e investigatori
Investigatori
- Investigatore principale: Yiding Chen, Second Affiliated Hospital, School of Medicine, Zhejiang University
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Effetti fisiologici dei farmaci
- Meccanismi molecolari dell'azione farmacologica
- Ormoni, sostituti ormonali e antagonisti ormonali
- Inibitori enzimatici
- Inibitori della sintesi steroidea
- Antagonisti ormonali
- Antagonisti degli estrogeni
- Azioni farmacologiche
- Azioni e usi chimici
- Inibitori dell'aromatasi
Altri numeri di identificazione dello studio
- 2026-0417
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su HR+/HER2- Cancro al seno precoce
-
Novartis PharmaceuticalsReclutamentoCarcinoma mammario avanzato HR+/HER2-Stati Uniti, Singapore
-
Nanjing Sanhome Pharmaceutical, Co., Ltd.Attivo, non reclutanteHR+ / HER2- Carcinoma Mammario AvanzatoCina
-
BeOne MedicinesReclutamentoHR+/HER2- Cancro al senoStati Uniti, Giappone, Australia, Corea del Sud
-
Institut fuer FrauengesundheitLilly Deutschland GmbH GermanyNon ancora reclutamentoHR+/HER2- Cancro al seno precoceGermania
-
wanghaiboReclutamentoCarcinoma mammario avanzato HR positivo HER2 negativoCina
-
Institut fuer FrauengesundheitLilly Deutschland GmbH Germany; AGO-B Breast Study GroupReclutamentoHR+/HER2- Cancro al seno precoceGermania
-
Avenzo Therapeutics, Inc.ReclutamentoHR+/HER2- Cancro al seno | HR+, HER2-, carcinoma mammario avanzatoStati Uniti
-
Fondazione IRCCS Istituto Nazionale dei Tumori,...Fondazione Policlinico Universitario Agostino Gemelli IRCCS; Fondazione IRCCS... e altri collaboratoriReclutamentoCancro al seno | Neoplasie mammarie | Malattie del seno | Neoplasia mammaria | Tumori al seno | Carcinoma al seno | Neoplasie mammarie, maschio | Stadio del cancro al seno IV | Tumori maligni positivi al recettore ormonale della mammella | Cancro al seno HR-positivo | Carcinoma mammario positivo al recettore... e altre condizioniItalia
-
TYK Medicines, IncReclutamentoCarcinoma mammario avanzato HR-positivo, HER2-negativoCina
-
Cancer Institute and Hospital, Chinese Academy...Non ancora reclutamentoCancro al seno Cancro al seno in fase iniziale (fase 1-3) | Carcinoma mammario HR positivo/HER2 bassoCina