146P Updated survival analysis in NEOPERSUR trial: Neoadjuvant pertuzumab in a real-world population in the south of Spain

A. Falcon Gonzalez(Hospital Universitario Virgen del Rocío), Josefina Cruz Jurado(Hospital Universitario de Canarias), E. Llabrés Valentí(Hospital Universitario Insular de Gran Canaria), Rocío Urbano Cubero(Complejo Hospitalario de Jaén), María del Carmen Álamo de la Gala(Hospital Universitario Virgen Macarena), Alexander A. Martínez(Complejo Hospitalario Torrecárdenas), Rocío Álvarez Ambite(Hospital Universitario de Canarias), Carlos José Rodríguez González(Instituto de Investigación Biosanitaria de Granada), Marta Amérigo Góngora(Hospital Juan Ramón Jiménez), L. Rodriguez Perez(Hospital Universitario Puerta del Mar), Martina Álvarez(Hospital Universitario de Valme), Pedro Sánchez‐Rovira(Complejo Hospitalario de Jaén), Encarnación González‐Flores(Hospital Universitario Virgen de las Nieves), Fernando Henao(Hospital Universitario Virgen Macarena), Juan Lucas Bayo Calero(Hospital Juan Ramón Jiménez), M. Valero Arbizu(Hospital Quirónsalud Sagrado Corazón), Alicia Quílez Cutillas(Hospital Universitario Puerto Real), F.J. Salvador Bofill(Hospital Universitario Virgen del Rocío), Manuel Ruíz Borrego(Hospital Universitario Virgen del Rocío)
ESMO Open
May 1, 2023
Cited by 0Open Access
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Abstract

Pertuzumab (P) has been approved in neoadjuvant setting for HER2-positive early breast cancer patients (pts) in association with Trastuzumab (T) and chemotherapy. Diverse studies support this treatment. The pathologic complete response (pCR) showed achieve percentages from 45.8 % to 66.6% depending on chemotherapy combination. This is a retrospective and multicentric study. We have collected all HER2-positive early breast cancer pts treated with P in neoadjuvant setting in our hospitals between 2015 and 2018. The effect of adding P on pCR was analyzed, as well as other predictive factors of response using logistic regression analyses. Kaplan Meier analysis has been used for survival analysis. A total of 310 pts met the selection criteria. The median age was 51 years (22-88 years), 54,5% were premenopausal. 4 pts were stage I, 204 pts stage II, 101 pts were stage III. The majority of the patient received anthracyclines and taxanes with P and T regimen (77,1%), 16,5% received carboplatin-docetaxel-P-T combination and 6,5% received taxane-P-T. 307 pts were analysed for response. pCR was seen in 62,2 % of the pts, dividing by hormonal receptor (HR) status, pCR was 53,8% in HR-positive and 71,1% in HR-negative. Treatment was well tolerated with only 14.8 % G3-4 adverse events related to chemotherapy and 1.9% related to antiHER2 therapy. Different adjuvant treatments patterns were seen between hospitals. After a follow-up of 7,5 years, 43 pts (13,9%) had a distant relapse, 16 of them (37,2%) had achieved a previous pCR. 38,5% had CNS recurrence and 61,5% non-CNS recurrence. In multivariate analysis non-pCR pts have 3.9 relative risk of experience disease relapse event (p 0.0001; 1.84-8.88), and patients with stage III at diagnosis have 4.3 relative risk (p 0.00004; 2.15-8.75). Disease free-survival (DFS) rates at 7.5 years is 86.4 %. After separating between pCR outcomes, results were statistical significative (p < 0.0001) with DFS rates of 89.4% in pCR pts and 70.6% in non-pCR pts. In our knowledge, this is the first real-world study that shows survival results for adding Pertuzumab in the neoadjuvant setting of HER2-positive breast cancer patients. Our results are consistent with those previously published.


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