Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer.
Antibodies, Monoclonal, Humanized
/ adverse effects
Antineoplastic Agents, Immunological
/ adverse effects
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Breast Neoplasms
/ drug therapy
Camptothecin
/ analogs & derivatives
Disease Progression
Female
Humans
Immunoconjugates
/ adverse effects
Immunohistochemistry
Receptor, ErbB-2
/ analysis
Trastuzumab
/ adverse effects
Journal
The New England journal of medicine
ISSN: 1533-4406
Titre abrégé: N Engl J Med
Pays: United States
ID NLM: 0255562
Informations de publication
Date de publication:
07 07 2022
07 07 2022
Historique:
pubmed:
7
6
2022
medline:
9
7
2022
entrez:
6
6
2022
Statut:
ppublish
Résumé
Among breast cancers without human epidermal growth factor receptor 2 (HER2) amplification, overexpression, or both, a large proportion express low levels of HER2 that may be targetable. Currently available HER2-directed therapies have been ineffective in patients with these "HER2-low" cancers. We conducted a phase 3 trial involving patients with HER2-low metastatic breast cancer who had received one or two previous lines of chemotherapy. (Low expression of HER2 was defined as a score of 1+ on immunohistochemical [IHC] analysis or as an IHC score of 2+ and negative results on in situ hybridization.) Patients were randomly assigned in a 2:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival in the hormone receptor-positive cohort. The key secondary end points were progression-free survival among all patients and overall survival in the hormone receptor-positive cohort and among all patients. Of 557 patients who underwent randomization, 494 (88.7%) had hormone receptor-positive disease and 63 (11.3%) had hormone receptor-negative disease. In the hormone receptor-positive cohort, the median progression-free survival was 10.1 months in the trastuzumab deruxtecan group and 5.4 months in the physician's choice group (hazard ratio for disease progression or death, 0.51; P<0.001), and overall survival was 23.9 months and 17.5 months, respectively (hazard ratio for death, 0.64; P = 0.003). Among all patients, the median progression-free survival was 9.9 months in the trastuzumab deruxtecan group and 5.1 months in the physician's choice group (hazard ratio for disease progression or death, 0.50; P<0.001), and overall survival was 23.4 months and 16.8 months, respectively (hazard ratio for death, 0.64; P = 0.001). Adverse events of grade 3 or higher occurred in 52.6% of the patients who received trastuzumab deruxtecan and 67.4% of those who received the physician's choice of chemotherapy. Adjudicated, drug-related interstitial lung disease or pneumonitis occurred in 12.1% of the patients who received trastuzumab deruxtecan; 0.8% had grade 5 events. In this trial involving patients with HER2-low metastatic breast cancer, trastuzumab deruxtecan resulted in significantly longer progression-free and overall survival than the physician's choice of chemotherapy. (Funded by Daiichi Sankyo and AstraZeneca; DESTINY-Breast04 ClinicalTrials.gov number, NCT03734029.).
Sections du résumé
BACKGROUND
Among breast cancers without human epidermal growth factor receptor 2 (HER2) amplification, overexpression, or both, a large proportion express low levels of HER2 that may be targetable. Currently available HER2-directed therapies have been ineffective in patients with these "HER2-low" cancers.
METHODS
We conducted a phase 3 trial involving patients with HER2-low metastatic breast cancer who had received one or two previous lines of chemotherapy. (Low expression of HER2 was defined as a score of 1+ on immunohistochemical [IHC] analysis or as an IHC score of 2+ and negative results on in situ hybridization.) Patients were randomly assigned in a 2:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival in the hormone receptor-positive cohort. The key secondary end points were progression-free survival among all patients and overall survival in the hormone receptor-positive cohort and among all patients.
RESULTS
Of 557 patients who underwent randomization, 494 (88.7%) had hormone receptor-positive disease and 63 (11.3%) had hormone receptor-negative disease. In the hormone receptor-positive cohort, the median progression-free survival was 10.1 months in the trastuzumab deruxtecan group and 5.4 months in the physician's choice group (hazard ratio for disease progression or death, 0.51; P<0.001), and overall survival was 23.9 months and 17.5 months, respectively (hazard ratio for death, 0.64; P = 0.003). Among all patients, the median progression-free survival was 9.9 months in the trastuzumab deruxtecan group and 5.1 months in the physician's choice group (hazard ratio for disease progression or death, 0.50; P<0.001), and overall survival was 23.4 months and 16.8 months, respectively (hazard ratio for death, 0.64; P = 0.001). Adverse events of grade 3 or higher occurred in 52.6% of the patients who received trastuzumab deruxtecan and 67.4% of those who received the physician's choice of chemotherapy. Adjudicated, drug-related interstitial lung disease or pneumonitis occurred in 12.1% of the patients who received trastuzumab deruxtecan; 0.8% had grade 5 events.
CONCLUSIONS
In this trial involving patients with HER2-low metastatic breast cancer, trastuzumab deruxtecan resulted in significantly longer progression-free and overall survival than the physician's choice of chemotherapy. (Funded by Daiichi Sankyo and AstraZeneca; DESTINY-Breast04 ClinicalTrials.gov number, NCT03734029.).
Identifiants
pubmed: 35665782
doi: 10.1056/NEJMoa2203690
pmc: PMC10561652
mid: NIHMS1931098
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Antineoplastic Agents, Immunological
0
Immunoconjugates
0
trastuzumab deruxtecan
5384HK7574
Receptor, ErbB-2
EC 2.7.10.1
Trastuzumab
P188ANX8CK
Camptothecin
XT3Z54Z28A
Banques de données
ClinicalTrials.gov
['NCT03734029']
Types de publication
Clinical Trial, Phase III
Comparative Study
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
9-20Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Investigateurs
Thomas Kühr
(T)
Clemens Schmitt
(C)
Richard Greil
(R)
Daniel Egle
(D)
Hans Wildiers
(H)
Andrea Gombos
(A)
Jean-Luc Canon
(JL)
François Duhoux
(F)
Jan-Willem Henning
(JW)
Jamil Asselah
(J)
Binghe Xu
(B)
Xichun Hu
(X)
Qingyuan Zhang
(Q)
Tao Sun
(T)
Qiang Liu
(Q)
Wei Li
(W)
Xiaojia Wang
(X)
Yueyin Pan
(Y)
Xian Wang
(X)
Xinhong Wu
(X)
Xi Chen
(X)
Ting Luo
(T)
Wenjing Hu
(W)
Jingfen Wang
(J)
Xiaoyan Lin
(X)
William Jacot
(W)
Hugues Bourgeois
(H)
Claudia Lefeuvre-Plesse
(C)
Anne-Claire Hardy Bessard
(AC)
Jean-Sebastien Frenel
(JS)
Joseph Gligorov
(J)
Jean-Yves Pierga
(JY)
Christelle Levy
(C)
Julien Grenier
(J)
Carole Helissey-Danis
(C)
Fabrice André
(F)
Paule Augereau
(P)
Javed Sahir
(J)
Frederic Viret
(F)
Helene Simon
(H)
Cristian Villanueva
(C)
Marinos Tsiatas
(M)
Konstantinos Papazisis
(K)
Dimitrios Mavroudis
(D)
Flora Zagouri
(F)
Christos Papandreou
(C)
Ioannis Boukovinas
(I)
Sofia Baka
(S)
Athanasios Kotsakis
(A)
Gabor Rubovszky
(G)
Klara Mezei
(K)
Amir Sonnenblick
(A)
Rinat Bernstein Molho
(R)
Rinat Yerushalmi
(R)
Ruth Perets
(R)
Ella Evron
(E)
Beatrice Uziely
(B)
Lorenzo Gianni
(L)
Claudio Zamagni
(C)
Pier Francesco Tassone
(PF)
Hector Soto Parra
(H)
Marina Elena Cazzaniga
(ME)
Ilaria Portarena
(I)
Marco Colleoni
(M)
Giovanna Masci
(G)
Emiliano Tamburini
(E)
Michelino De Laurentiis
(M)
Rebecca Pedersini
(R)
Emilio Bria
(E)
Stefania Gori
(S)
Yoichi Naito
(Y)
Kan Yonemori
(K)
Takayuki Kobayashi
(T)
Hiroji Iwata
(H)
Tsutomu Iwasa
(T)
Yasuaki Sagara
(Y)
Yuko Tanabe
(Y)
Toshinari Yamashita
(T)
Kenjiro Aogi
(K)
Eriko Tokunaga
(E)
Tomomi Hayashi
(T)
Nobumoto Tomioka
(N)
Hiroyuki Yasojima
(H)
Kenichi Inoue
(K)
Yasuo Miyoshi
(Y)
Mitsuya Ito
(M)
Junji Tsurutani
(J)
Naoki Niikura
(N)
Seock-Ah Im
(SA)
Yeon Hee Park
(YH)
Jee Hyun Kim
(JH)
Sung-Bae Kim
(SB)
Joo Hyuk Sohn
(JH)
Keun Seok Lee
(KS)
Yee Soo Chae
(YS)
Moon-Hee Lee
(MH)
Ana Rita Sousa
(AR)
Matilde Salgado
(M)
Ana Luisa Faria
(AL)
António Moreira Pinto
(A)
Antonio Teira
(A)
Ana Rodrigues
(A)
Catarina Portela
(C)
Inna Ganshina
(I)
Daniil Stroyakovskiy
(D)
Nikolay Kislov
(N)
Javier Cortes Castan
(J)
Miguel Gil-Gil
(M)
Maria Vidal
(M)
Silvia Antolin Novoa
(S)
Maria Fernandez Abad
(M)
Jose Angel Garcia Saenz
(JA)
Cristina Saura Manich
(C)
Sonia Servitja Tormo
(S)
Esteban Nogales Fernandez
(E)
Maria Jose Bermejo Perez
(MJ)
Josefina Cruz Jurado
(J)
Manuel Ruiz Borrego
(M)
Henrik Lindman
(H)
Anna-Karin Wennstig
(AK)
Kristina Weibring
(K)
Andreas Müller
(A)
Marcus Vetter
(M)
Jens Huober
(J)
Konstantin Dedes
(K)
Khalil Zaman
(K)
Michael Schwitter
(M)
Wei-Pang Chung
(WP)
Yen-Shen Lu
(YS)
Ming-Feng Hou
(MF)
Peter Schmid
(P)
Duncan Wheatley
(D)
Srinivasan Madhusudan
(S)
Shanu Modi
(S)
Nicholas McAndrew
(N)
Mikhail Shtivelband
(M)
Naoto Ueno
(N)
Zahi Mitri
(Z)
Stephen Dyar
(S)
Anna Litvak
(A)
Jane Raymond
(J)
John McKnight
(J)
Eugene Ahn
(E)
Cynthia Lynch
(C)
Hope Rugo
(H)
Ian Krop
(I)
David Chan
(D)
Halle Moore
(H)
Reshma Mahtani
(R)
Polly Niravath
(P)
Shakeela Bahadur
(S)
Shaker Dakhil
(S)
Adriana Milillo-Naraine
(A)
Fauzia Riaz
(F)
David Schumaker
(D)
Philip Lammers
(P)
Timothy Pluard
(T)
Sylvia Adams
(S)
Hyo Han
(H)
Fadi Kayali
(F)
Erika Hamilton
(E)
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2022 Massachusetts Medical Society.
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