Skip to Main Content (Press Enter)

Logo UNIMORE
  • ×
  • Home
  • Corsi
  • Insegnamenti
  • Professioni
  • Persone
  • Pubblicazioni
  • Strutture
  • Terza Missione
  • Attività
  • Competenze

UNI-FIND
Logo UNIMORE

|

UNI-FIND

unimore.it
  • ×
  • Home
  • Corsi
  • Insegnamenti
  • Professioni
  • Persone
  • Pubblicazioni
  • Strutture
  • Terza Missione
  • Attività
  • Competenze
  1. Pubblicazioni

Safety and efficacy analysis of neoadjuvant pertuzumab, trastuzumab and standard chemotherapy for HER2–positive early breast cancer: real–world data from NeoPowER study

Articolo
Data di Pubblicazione:
2024
Citazione:
Safety and efficacy analysis of neoadjuvant pertuzumab, trastuzumab and standard chemotherapy for HER2–positive early breast cancer: real–world data from NeoPowER study / Canino, F.; Barbolini, M.; De Giorgi, U.; Fontana, T.; Gaspari, V.; Gianni, C.; Gianni, L.; Maestri, A.; Minichillo, S.; Moscetti, L.; Mura, A.; Nicoletti, S. V. L.; Omarini, C.; Pagani, R.; Sarti, S.; Toss, A.; Zamagni, C.; Cuoghi Costantini, R.; Caggia, F.; Antonelli, G.; Baglio, F.; Belluzzi, L.; Martinelli, G.; Natalizio, S.; Ponzoni, O.; Dominici, M.; Piacentini, F.. - In: BMC CANCER. - ISSN 1471-2407. - 24:1(2024), pp. 735-753. [10.1186/s12885-024-12506-0]
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.
Tipologia CRIS:
Articolo su rivista
Keywords:
Early breast cancer; HER2 dual blockade; HER2+; Neoadjuvant treatment; Pertuzumab; Real world data
Elenco autori:
Canino, F.; Barbolini, M.; De Giorgi, U.; Fontana, T.; Gaspari, V.; Gianni, C.; Gianni, L.; Maestri, A.; Minichillo, S.; Moscetti, L.; Mura, A.; Nicoletti, S. V. L.; Omarini, C.; Pagani, R.; Sarti, S.; Toss, A.; Zamagni, C.; Cuoghi Costantini, R.; Caggia, F.; Antonelli, G.; Baglio, F.; Belluzzi, L.; Martinelli, G.; Natalizio, S.; Ponzoni, O.; Dominici, M.; Piacentini, F.
Autori di Ateneo:
CAGGIA Federica
CUOGHI COSTANTINI RICCARDO
Canino Fabio
DOMINICI Massimo
NATALIZIO SALVATORE
OMARINI Claudia
PIACENTINI Federico
TOSS ANGELA
Link alla scheda completa:
https://iris.unimore.it/handle/11380/1366008
Link al Full Text:
https://iris.unimore.it//retrieve/handle/11380/1366008/721109/12885_2024_Article_12506.pdf
Pubblicato in:
BMC CANCER
Journal
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.5.0.0