The PARP1 selective inhibitor saruparib (AZD5305) elicits potent and durable antitumor activity in patient-derived BRCA1/2-associated cancer models

Collectively, these results show that the novel PARP1 selective inhibitor AZD5305 yields a potent antitumor response in PDX models with HRD and delays PARPi resistance alone or in combination with carboplatin or ceralasertib, which supports its use in the clinic as a new therapeutic option.

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Publication Details

Journal
Genome Medicine
Published
2024-08-26
DOI
https://doi.org/10.1186/s13073-024-01370-z
Citations
53
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
14.97

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article

The PARP1 selective inhibitor saruparib (AZD5305) elicits potent and durable antitumor activity in patient-derived BRCA1/2-associated cancer models

Orland Dı́ez, Joanna Domènech-Vivó, Elisabetta Leo, Anna D. Staniszewska et al.
53 citations
Genome Medicine
PARP inhibition in cancer therapy
14.97
article

The PARP1 selective inhibitor saruparib (AZD5305) elicits potent and durable antitumor activity in patient-derived BRCA1/2-associated cancer models

Orland Dı́ez, Joanna Domènech-Vivó, Elisabetta Leo, Anna D. Staniszewska, Enrique J. Arenas, Flaminia Pedretti, Eduardo García‐Galea, Olga Rodríguez, Helena Verdaguer, Alan Lau, Mark J. O’Connor, Alejandro Moles‐Fernández, Sara Gutiérrez‐Enríquez, Alba Llop‐Guevara, Luis Tobalina, Violeta Serra, Fernando J. Calero‐Nieto, Joaquı́n Arribas, Sara Talbot, Paolo Giovanni Nuciforo, Teresa Macarulla, Andrea Herencia-Ropero, Josep V. Forment, Marta Guzmán, Mark R. Albertella, Rodrigo Dienstmann, Heura Domènech, Judith Balmaña
article en
53 citations

Abstract

Collectively, these results show that the novel PARP1 selective inhibitor AZD5305 yields a potent antitumor response in PDX models with HRD and delays PARPi resistance alone or in combination with carboplatin or ceralasertib, which supports its use in the clinic as a new therapeutic option.

Genome MedicineVol. 16(1)
AstraZeneca (United Kingdom) (GB), Institució Catalana de Recerca i Estudis Avançats (ES), Hebron University (PS), Universitat Autònoma de Barcelona (ES), Universitat Pompeu Fabra (ES), Josep Carreras Leukaemia Research Institute (ES), Vall d'Hebron Institut de Recerca (ES), Centro de Investigación Biomédica en Red (ES), Vall d'Hebron Hospital Universitari (ES), Hospital Del Mar (ES), Centro de Investigación Biomédica en Red de Cáncer (ES), Vall d'Hebron Institute of Oncology (ES), Universitat de Barcelona (ES)
Fundación Cellex, Ministerio de Ciencia, Innovación y Universidades, Centres de Recerca de Catalunya, Fundación Científica Asociación Española Contra el Cáncer, Generalitat de Catalunya, Fundación Fero, Agència de Gestió d'Ajuts Universitaris i de Recerca, Instituto de Salud Carlos III, Departament de Salut, Generalitat de Catalunya, Agencia Estatal de Investigación, Departament d'Empresa i Coneixement, Generalitat de Catalunya
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Openalex Percentile: Top 1%
PARP inhibition in cancer therapy
14.97
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