Elsevier eBooks, Год журнала: 2025, Номер unknown, С. 131 - 152
Опубликована: Янв. 1, 2025
Elsevier eBooks, Год журнала: 2025, Номер unknown, С. 131 - 152
Опубликована: Янв. 1, 2025
Annals of Oncology, Год журнала: 2023, Номер 34(4), С. 358 - 376
Опубликована: Янв. 17, 2023
Язык: Английский
Процитировано
342New England Journal of Medicine, Год журнала: 2023, Номер 389(21), С. 1935 - 1948
Опубликована: Ноя. 8, 2023
Osimertinib is a third-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) that selective for EGFR-TKI-sensitizing and
Язык: Английский
Процитировано
267Annals of Oncology, Год журнала: 2023, Номер 35(1), С. 77 - 90
Опубликована: Окт. 23, 2023
Amivantamab plus carboplatin-pemetrexed (chemotherapy) with and without lazertinib demonstrated antitumor activity in patients refractory epidermal growth factor receptor (EGFR)-mutated advanced non-small-cell lung cancer (NSCLC) phase I studies. These combinations were evaluated a global III trial.
Язык: Английский
Процитировано
190Journal of Clinical Oncology, Год журнала: 2023, Номер 41(35), С. 5363 - 5375
Опубликована: Сен. 10, 2023
Patritumab deruxtecan, or HER3-DXd, is an antibody-drug conjugate consisting of a fully human monoclonal antibody to epidermal growth factor receptor 3 (HER3) attached topoisomerase I inhibitor payload via stable tetrapeptide-based cleavable linker. We assessed the efficacy and safety HER3-DXd in patients with (
Язык: Английский
Процитировано
118Annals of Oncology, Год журнала: 2024, Номер 35(7), С. 588 - 606
Опубликована: Май 27, 2024
Advancements in the field of precision medicine have prompted European Society for Medical Oncology (ESMO) Precision Medicine Working Group to update recommendations use tumour next-generation sequencing (NGS) patients with advanced cancers routine practice.
Язык: Английский
Процитировано
114New England Journal of Medicine, Год журнала: 2024, Номер 391(16), С. 1486 - 1498
Опубликована: Июнь 26, 2024
BackgroundAmivantamab plus lazertinib (amivantamab–lazertinib) has shown clinically meaningful and durable antitumor activity in patients with previously untreated or osimertinib-pretreated EGFR (epidermal growth factor receptor)–mutated advanced non–small-cell lung cancer (NSCLC).MethodsIn a phase 3, international, randomized trial, we assigned, 2:2:1 ratio, EGFR-mutated (exon 19 deletion L858R), locally metastatic NSCLC to receive amivantamab–lazertinib (in an open-label fashion), osimertinib blinded fashion, assess the contribution of treatment components). The primary end point was progression-free survival group as compared group, assessed by independent central review.ResultsOverall, 1074 underwent randomization (429 amivantamab–lazertinib, 429 osimertinib, 216 lazertinib). median significantly longer than (23.7 vs. 16.6 months; hazard ratio for disease progression death, 0.70; 95% confidence interval [CI], 0.58 0.85; P<0.001). An objective response observed 86% (95% CI, 83 89) 85% those 81 88) group; among confirmed (336 314 group), duration 25.8 months 20.1 could not be estimated) 16.8 14.8 18.5), respectively. In planned interim overall analysis death 0.80 0.61 1.05). Predominant adverse events were EGFR-related toxic effects. incidence discontinuation all agents due treatment-related 10% 3% osimertinib.ConclusionsAmivantamab–lazertinib showed superior efficacy first-line NSCLC. (Funded Janssen Research Development; MARIPOSA ClinicalTrials.gov number, NCT04487080.)
Язык: Английский
Процитировано
112New England Journal of Medicine, Год журнала: 2024, Номер 391(7), С. 585 - 597
Опубликована: Июнь 2, 2024
Osimertinib is a recommended treatment for advanced non-small-cell lung cancer (NSCLC) with an epidermal growth factor receptor (
Язык: Английский
Процитировано
101Journal of Clinical Oncology, Год журнала: 2024, Номер 42(11), С. 1252 - 1264
Опубликована: Янв. 22, 2024
PURPOSE The phase III CheckMate 722 trial (ClinicalTrials.gov identifier: NCT02864251 ) evaluated nivolumab plus chemotherapy versus in patients with epidermal growth factor receptor ( EGFR)–mutated metastatic non–small-cell lung cancer (NSCLC) after disease progression on EGFR tyrosine kinase inhibitors (TKIs). METHODS Patients first- or second-generation TKI therapy (without T790M mutation) osimertinib (with/without were randomly assigned 1:1 to (360 mg once every 3 weeks) platinum-doublet (once alone for four cycles. Primary end point was progression-free survival (PFS). Secondary points included 9- and 12-month PFS rates, overall (OS), objective response rate (ORR), duration of (DOR). RESULTS Overall, 294 assigned. At final analysis (median follow-up, 38.1 months), not significantly improved (median, 5.6 v 5.4 months; hazard ratio [HR], 0.75 [95% CI, 0.56 1.00]; P = .0528), rates 25.9% 19.8%, 21.2% 15.9%, respectively. Post hoc subgroup analyses showed a trend favoring tumors harboring sensitizing mutations (HR, 0.72 0.54 0.97]), one line previous (0.72 both (0.64 0.47 0.88]). Median OS 19.4 months 15.9 chemotherapy, while ORR 31.3% 26.7%, median DOR 6.7 months, Grade 3/4 treatment-related adverse events occurred 44.7% 29.4% treated alone, CONCLUSION Nivolumab did improve EGFR-mutated NSCLC previously TKIs. No new safety signals identified.
Язык: Английский
Процитировано
73Nature Reviews Disease Primers, Год журнала: 2024, Номер 10(1)
Опубликована: Сен. 26, 2024
Язык: Английский
Процитировано
63Journal of Clinical Oncology, Год журнала: 2023, Номер 42(7), С. 808 - 820
Опубликована: Дек. 3, 2023
We report CNS efficacy of first-line osimertinib plus chemotherapy versus monotherapy in patients with epidermal growth factor receptor (
Язык: Английский
Процитировано
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