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

被引:2
作者
Canino, Fabio [1 ]
Barbolini, Monica [2 ]
De Giorgi, Ugo [3 ]
Fontana, Tommaso [4 ]
Gaspari, Valeria [5 ]
Gianni, Caterina [3 ]
Gianni, Lorenzo [5 ]
Maestri, Antonio [6 ]
Minichillo, Santino [6 ]
Moscetti, Luca [2 ]
Mura, Antonella [6 ]
Nicoletti, Stefania Vittoria Luisa [5 ]
Omarini, Claudia [2 ]
Pagani, Rachele [4 ]
Sarti, Samanta [3 ]
Toss, Angela [1 ,2 ]
Zamagni, Claudio [4 ]
Costantini, Riccardo Cuoghi [7 ]
Caggia, Federica [1 ]
Antonelli, Giuseppina [1 ]
Baglio, Federica [1 ]
Belluzzi, Lorenzo [1 ]
Martinelli, Giulio [1 ]
Natalizio, Salvatore [1 ]
Ponzoni, Ornella [1 ]
Dominici, Massimo [1 ,2 ]
Piacentini, Federico [1 ,2 ]
机构
[1] Univ Hosp Modena, Dept Med & Surg Sci Children & Adults, Div Med Oncol, Largo Pozzo 71, I-41124 Modena, Italy
[2] Univ Hosp Modena, Dept Oncol & Hematol, Div Med Oncol, Modena, Italy
[3] IRCCS Ist Romagnolo Tumori Studio IRST Dino Amador, Dept Med Oncol, Meldola, Italy
[4] Azienda Osped Univ Bologna, Ist Ricovero & Cura Carattere Sci IRCCS, Bologna, Italy
[5] AUSL Romagna, Infermi Hosp, Dept Med Oncol, Rimini, Italy
[6] AUSL Bologna, Dept Med Oncol, Bologna, Italy
[7] Univ Hosp Modena, Unit Clin Stat, Modena, Italy
关键词
Neoadjuvant treatment; HER2+; Early breast cancer; Pertuzumab; HER2 dual blockade; Real world data; CARDIAC SAFETY; OPEN-LABEL; MULTICENTER; NEOSPHERE; REGIMENS;
D O I
10.1186/s12885-024-12506-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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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