PURPOSE
Preclinical data suggest that the anti-cancer efficacy of ATR inhibitors can be synergistically enhanced by low-dose gemcitabine. To test the clinical feasibility of this regimen, we conducted a phase 1 trial of low-dose gemcitabine combined with the ATR inhibitor elimusertib (BAY1895344).
PATIENTS AND METHOD...
T. Jayakrishnan, Rebecca L. Porter, Alice P. Chen et al.· Cancer Research Communicatio...· 0 citations
The combination of azenosertib and gemcitabine was associated with substantial myelosuppression in patients with metastatic PDAC previously treated with FOLFIRINOX, limiting further clinical evaluation of this dosing strategy.
B. Huffman, Haeseong Park, N. Jackson et al.· Cancer Research· 0 citations
Cell-cycle dysregulation is a central driver of breast cancer progression and a major therapeutic vulnerability, particularly in hormone receptor–positive/human epidermal growth factor receptor 2–negative (HR+/HER2–) disease. The clinical success of cyclin-dependent kinase (CDK) 4/6 inhibitors combined with endocrine t...
D. Seriak, J. Kim, G. Shapiro et al.· Journal of Clinical Investig...· 0 citations
The combination of the ATR inhibitor berzosertib with carboplatin demonstrated a lower ORR and more frequent ≥ grade 3 TrAEs compared with docetaxel + carboplatin in this heavily pretreated, biomarker-unselected mCRPC population.
A. Choudhury, C. Zhong, Wan-Ling Xie et al.· Cancer Research Communicatio...· 0 citations
Findings identify MYC-driven transcription as a therapeutic vulnerability in CIC -rearranged sarcoma and support combined CDK2 and CDK9 inhibition as a promising treatment strategy.
Quentin Odom-Lewis, S. Davis, Stephan Pieper et al.· Communications Medicine· 0 citations
Homologous recombination repair deficiency (HRD) occurs in approximately 10% of breast tumors and represents a major targetable vulnerability across multiple cancer types. Impairment of the homologous recombination DNA repair pathway — arising through somatic and germline mutations in homologous recombination repair ge...
Charlotte S. Walmsley, Adela Rodríguez, P. Konstantinopoulos et al.· Journal of Clinical Investig...· 0 citations
Abstract Background Poly (ADP-ribose) polymerase inhibitors (PARPis) have improved outcomes of BRCA-associated breast cancer; however, treatment-related toxicity remains a major clinical challenge. Currently approved PARPis broadly inhibit multiple members of the PARP protein family. However, preclinical studies sugges...
Adam Nelson, Kelly F. Zheng, C. Wanderley et al.· Journal for ImmunoTherapy of...· 0 citations
Only limited benefit of PD-1/PD-L1 blockade in augmenting PARPi activity is suggested and the need for alternative strategies to sustain PARPi-induced immunity is highlighted.
F. Lynce, Kenichi Shimada, Claudine Isaacs et al.· bioRxiv· 0 citations
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