NCT07060807RECRUITING

Estudio clínico de Fase 3 de Patritumab Deruxtecan para el tratamiento del cáncer de mama HR+/HER2- avanzado o metastásico

Patrocinado por: Merck Sharp & Dohme LLC
Verificado por CT.lat

Resumen del Estudio

Este estudio clínico de Fase 3 busca evaluar una nueva opción terapéutica para pacientes con cáncer de mama del subtipo HR+/HER2- (receptor hormonal positivo y HER2 negativo) que se encuentra en una etapa localmente avanzada no operable o metastásica. La investigación está diseñada para pacientes cuyo cáncer ha progresado o recurrido después de recibir tratamientos estándar previos, específicamente terapia endocrina combinada con inhibidores de CDK4/6. El objetivo principal es determinar si el fármaco en investigación, Patritumab Deruxtecan (un conjugado anticuerpo-fármaco dirigido a HER3), logra controlar el crecimiento del tumor y prolongar la supervivencia de las pacientes de manera más efectiva que la quimioterapia estándar o el Trastuzumab Deruxtecan. Los participantes serán asignados aleatoriamente para recibir el fármaco experimental o el tratamiento de elección del médico.

Criterios de Elegibilidad

Resumen de Elegibilidad:Pueden participar pacientes con diagnóstico confirmado de cáncer de mama HR+/HER2- irresecable o metastásico que hayan progresado tras una terapia previa con inhibidores de CDK4/6. No son elegibles pacientes con mutaciones BRCA tratables con inhibidores PARP, historial de neumonitis/enfermedad pulmonar intersticial, o que ya hayan recibido quimioterapia para la fase metastásica.

Nota: La lista detallada se muestra en el idioma original por falta de traducción estructurada.
Criterios de Inclusión
  • Has a diagnosis of hormone receptor positive (HR+)/human epidermal growth factor receptor 2 (HER2)- invasive breast carcinoma that is either locally advanced disease not amenable to resection with curative intent (herein called unresectable) or metastatic disease not treatable with curative intent
  • Has centrally-confirmed HR+ and HER2- results and human epidermal growth factor receptor 3 (HER3) evaluable results from a biopsy obtained from a distant metastatic site or a locally advanced lesion on or after the most recent line of therapy (with certain exceptions)
  • Must have had progression or recurrence on prior cyclin-dependent kinase (CDK)4/6 inhibitor + endocrine therapy (ET) with one of the following:
  • Radiographic disease progression, as assessed by the investigator, on CDK4/6 inhibitor + ET as 1L for treatment of unresectable locally advanced or metastatic HR+/HER2- breast cancer. CDK4/6 inhibitor + ET must be the only line of therapy received in the advanced setting, or
  • Disease recurrence, either radiographic and/or confirmed histologically via biopsy as assessed by the investigator, while on adjuvant ET in combination with a CDK4/6 inhibitor OR within 24 months from the date of last dose of adjuvant CDK4/6 inhibitor
  • Has measurable disease per RECIST 1.1 as assessed by the local site investigator/radiology
  • Human immunodeficiency virus (HIV)-infected participants must have well controlled HIV on antiretroviral therapy
  • Has an Eastern Cooperative Oncology Group performance status of 0 or 1 assessed within 7 days before randomization
Criterios de Exclusión
  • Has breast cancer amenable to treatment with curative intent
  • Is eligible to receive additional endocrine-based treatment in the advanced setting as determined by the investigator
  • Has a known germline breast cancer gene (BRCA) mutation (deleterious or suspected deleterious) where poly (ADP-ribose) polymerase (PARP) inhibitor(s) is a potential treatment option
  • Has current visceral crisis or is at risk for impending visceral crisis that has or may cause imminent organ compromise and/or other life-threatening complications
  • Has any of the following: a pulse oximeter reading \<92% at rest, or requires intermittent supplemental oxygen, or requires chronic supplemental oxygen
  • Has uncontrolled, significant cardiovascular disease or cerebrovascular disease
  • Has ≥Grade 2 peripheral neuropathy.
  • Has clinically significant corneal disease
  • Has received prior chemotherapy for unresectable locally advanced or metastatic breast cancer
  • Has received prior treatment with an anti-HER3 antibody and/or antibody-drug conjugate that consists of a topoisomerase I inhibitor (eg, T-DXd) or any other topoisomerase I inhibitor therapy
  • Has received prior systemic anticancer therapy within 4 weeks (or 5 half-lives, whichever is shorter) before randomization; participants previously treated with ET plus a CDK4/6 inhibitor may participate as long as at least 2 weeks have elapsed since the last dose of therapy was administered
  • Has received prior radiotherapy for non-central nervous system disease, or required corticosteroids for radiation-related toxicities, within 14 days of the first dose of study intervention
  • Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy
  • Has known additional malignancy that is progressing or has required active treatment within the past 3 years
  • Has history of (noninfectious) pneumonitis/interstitial lung disease (ILD) that required steroids, has current pneumonitis/interstitial lung disease, or has suspected ILD/pneumonitis that cannot be ruled out by imaging at Screening
  • Has severe hypersensitivity (≥Grade 3) to HER3-DXd and/or any of its excipients
  • Has severe hypersensitivity (≥Grade 3) to all the available TPC and/or any of their excipients