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Safety and efficacy analysis of neoadjuvant pertuzumab, trastuzumab and standard chemotherapy for HER2-positive early breast cancer: real-world data from NeoPowER study.
Canino, Fabio; Barbolini, Monica; De Giorgi, Ugo; Fontana, Tommaso; Gaspari, Valeria; Gianni, Caterina; Gianni, Lorenzo; Maestri, Antonio; Minichillo, Santino; Moscetti, Luca; Mura, Antonella; Nicoletti, Stefania Vittoria Luisa; Omarini, Claudia; Pagani, Rachele; Sarti, Samanta; Toss, Angela; Zamagni, Claudio; Cuoghi Costantini, Riccardo; Caggia, Federica; Antonelli, Giuseppina; Baglio, Federica; Belluzzi, Lorenzo; Martinelli, Giulio; Natalizio, Salvatore; Ponzoni, Ornella; Dominici, Massimo; Piacentini, Federico.
Afiliação
  • Canino F; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy. fabio.canino@unimore.it.
  • Barbolini M; Division of Medical Oncology, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.
  • De Giorgi U; Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
  • Fontana T; Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Gaspari V; Department of Medical Oncology, Infermi Hospital, AUSL della Romagna, Rimini, Italy.
  • Gianni C; Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
  • Gianni L; Department of Medical Oncology, Infermi Hospital, AUSL della Romagna, Rimini, Italy.
  • Maestri A; Department of Medical Oncology, AUSL di Bologna, Bologna, Italy.
  • Minichillo S; Department of Medical Oncology, AUSL di Bologna, Bologna, Italy.
  • Moscetti L; Division of Medical Oncology, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.
  • Mura A; Department of Medical Oncology, AUSL di Bologna, Bologna, Italy.
  • Nicoletti SVL; Department of Medical Oncology, Infermi Hospital, AUSL della Romagna, Rimini, Italy.
  • Omarini C; Division of Medical Oncology, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.
  • Pagani R; Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Sarti S; Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
  • Toss A; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Zamagni C; Division of Medical Oncology, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.
  • Cuoghi Costantini R; Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Caggia F; Unit of Clinical Statistics, University Hospital of Modena, Modena, Italy.
  • Antonelli G; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Baglio F; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Belluzzi L; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Martinelli G; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Natalizio S; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Ponzoni O; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Dominici M; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
  • Piacentini F; Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Largo del Pozzo 71, Modena, 41124, Italy.
BMC Cancer ; 24(1): 735, 2024 Jun 15.
Article em En | MEDLINE | ID: mdl-38879498
ABSTRACT

BACKGROUND:

The addition of pertuzumab (P) to trastuzumab (H) and standard chemotherapy (CT) as neoadjuvant treatment (NaT) for patients with HER2 + breast cancer (BC), has shown to increase the pathological complete response (pCR) rate, without main safety concerns. The aim of NeoPowER trial is to evaluate safety and efficacy of P + H + CT in a real-world population.

METHODS:

We retrospectively reviewed the medical records of stage II-III, HER2 + BC patients treated with NaT who received P + H + CT (neopower group) in 5 Emilia Romagna institutions were compared with an historical group who received H + CT (control group). The primary endpoint was the safety, secondary endpoints were pCR rate, DRFS and OS and their correlation to NaT and other potential variables.

RESULTS:

260 patients were included, 48% received P + H + CT, of whom 44% was given anthraciclynes as part of CT, compared to 83% in the control group. The toxicity profile was similar, excluding diarrhea more frequent in the neopower group (20% vs. 9%). Three patients experienced significant reductions in left ventricular ejection fraction (LVEF), all receiving anthracyclines. The pCR rate was 46% (P + H + CT) and 40% (H + CT) (p = 0.39). The addition of P had statistically correlation with pCR only in the patients receiving anthra-free regimens (OR = 3.05,p = 0.047). Preoperative use of anthracyclines (OR = 1.81,p = 0.03) and duration of NaT (OR = 1.18,p = 0.02) were statistically related to pCR. 12/21 distant-relapse events and 14/17 deaths occurred in the control group. Patients who achieve pCR had a significant increase in DRFS (HR = 0.23,p = 0.009).

CONCLUSIONS:

Adding neoadjuvant P to H and CT is safe. With the exception of diarrhea, rate of adverse events of grade > 2 did not differ between the two groups. P did not increase the cardiotoxicity when added to H + CT, nevertheless in our population all cardiac events occurred in patients who received anthracycline-containing regimens. Not statistically significant, higher pCR rate is achievable in patients receiving neoadjuvant P + H + CT. The study did not show a statistically significant correlation between the addition of P and long-term outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Receptor ErbB-2 / Terapia Neoadjuvante / Anticorpos Monoclonais Humanizados / Trastuzumab Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: BMC Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Receptor ErbB-2 / Terapia Neoadjuvante / Anticorpos Monoclonais Humanizados / Trastuzumab Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: BMC Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália