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Spots Global Cancer Trial Database for Combination of Talimogene Laherparepvec With Atezolizumab in Early Breast Cancer

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Trial Identification

Brief Title: Combination of Talimogene Laherparepvec With Atezolizumab in Early Breast Cancer

Official Title: Combination of Talimogene Laherparepvec With Atezolizumab in Patients With Residual Breast Cancer After Standard Neoadjuvant Multi-agent Chemotherapy (PROMETEO TRIAL)

Study ID: NCT03802604

Conditions

Breast Cancer

Study Description

Brief Summary: PROMETEO is a window opportunity, single arm, exploratory study to evaluate the effect of T- VEC combined with Atezolizumab in women with operable early breast cancer who present residual disease after Neoadjuvant Chemotherapy (NAC). Other eligibility criteria include TNBC or LumB like primary tumor sized at least 1.5 cm, ECOG PS 0-1 and evaluable diagnostic tumor sample.

Detailed Description: Primary objective: • To evaluate the efficacy (as measured by residual cancer burden \[RCB\] class 0/1 rate) of Talimogene Laherparepvec with Atezolizumab given to subjects with operable early breast cancer who present residual disease after neoadjuvant chemotherapy (NAC). Secondary objectives include: * To assess the rate of pathological complete response (pCR) in the breast (pCRB) and breast and axilla (pCRBL) at definitive surgery after neoadjuvant treatment with T-VEC and atezolizumab. * To determine the clinical and radiological ORR of breast tumors to TVEC- atezolizumab given in the neoadjuvant setting. * To assess RCB index in continuous variable and by the 4 RCB class (RCB0, RCB1, RCB2 and RCB 3) after treatment with T-VEC and atezolizumab. * Comparing the expression of a gene signature tracking activated CD8 T-cells at surgery after treatment with T-VEC and atezolizumab with residual disease after NAC. * To evaluate the safety of T-VEC in combination with atezolizumab as assessed by incidence of treatment-emergent and treatment-related adverse events. * Translational and exploratory objectives are included.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Hospital Universitari Vall d'Hebrón, Barcelona, , Spain

Hospital Clínic de Barcelona, Barcelona, , Spain

Centro Integral Oncológico Clara Campal, Madrid, , Spain

Hospital Clínico universitario de Valencia, Valencia, , Spain

Contact Details

Name: Aleix Prat

Affiliation: Hospital Clinic of Barcelona

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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