Abstract 2855
Background
The RELAY (NCT02411448) phase III study demonstrated a statistically significant and clinically meaningful improvement in progression-free survival (PFS) for ERL plus RAM (RAM+ERL) versus ERL plus PL (PL+ERL) in patients with previously untreated EGFR mutation (mut)-positive (EGFR exon 19 deletion or exon 21 mut (L858R)) mNSCLC (median PFS 19.4 vs 12.4mo, HR 0.591 (95% CI 0.461–0.760), p < 0.0001). EGFR sensitizing and T790M mut status was monitored in circulating tumor DNA (ctDNA) from patients who participated in the Japan liquid biopsy exploratory substudy.
Methods
Plasma samples were collected before and during treatment (Baseline, Cycle 4, 13 and every 6 cycles up to Cycle 53) as well as post-discontinuation (the 30-day follow-up). Isolated ctDNA of plasma were subjected to droplet digital PCR (ddPCR) to determine EGFR mut status. Statistical analyses for T790M were performed for the population of patients with disease progression who had valid results from baseline and 30 day follow-up.
Results
The ddPCR population included 42 patients and had a similar PFS HR (0.61, 95% CI 0.33-1.15) to the full ITT population. The rates of EGFR T790M mut positivity at the 30-day follow-up were not different between treatment groups: 26% (5 of 19) (95% CI 12-49%) in RAM+ERL and 30% (7 of 23) (95% CI, 16-51%) in PL+ERL (p = 1.0). When evaluating the cumulative post-progression T790M rates according to the number of cycles received prior to disease progression, the rates for patients who had progressed by Cycle 4, Cycle 12, or Cycle 53 were 0%, 17% and 26% for RAM+ERL, and 0%, 33%, and 30% for PL+ERL, suggesting that RAM+ERL potentially may delay the occurrence of resistance by the T790M mutation.
Conclusions
Treatment with RAM+ERL resulted in superior PFS, with similar T790M rates at progression as compared to PL+ERL, suggesting the potential for effective EGFR-directed therapy after progression on RAM+ERL.
Clinical trial identification
NCT02411448.
Editorial acknowledgement
Legal entity responsible for the study
Eli Lilly and Company.
Funding
Eli Lilly and Company.
Disclosure
K. Nishio: Speaker Bureau / Expert testimony, Research grant / Funding (institution): Nippon Boehringer Ingelheim Co., Ltd.; Speaker Bureau / Expert testimony, Research grant / Funding (institution): Eli Lilly Japan K.K.; Research grant / Funding (institution): Ignyta,Inc.; Speaker Bureau / Expert testimony: Chugai Pharmaceutical Co.,Ltd.; Speaker Bureau / Expert testimony: Eisai Co., Ltd.; Speaker Bureau / Expert testimony: Pfizer Inc.; Speaker Bureau / Expert testimony: Novartis Pharma K.K.; Speaker Bureau / Expert testimony: MSD K.K.; Speaker Bureau / Expert testimony: Ono Pharmaceutical Co., Ltd.; Speaker Bureau / Expert testimony: Bristol-Myers Squibb Company; Speaker Bureau / Expert testimony: SymBio Pharmaceuticals Limited. ; Speaker Bureau / Expert testimony: Life Technologies Japan Ltd.; Speaker Bureau / Expert testimony: Solasia Pharma K.K. ; Speaker Bureau / Expert testimony: Yakult Honsha Co., Ltd.; Speaker Bureau / Expert testimony: Roche Diagnostics K.K. K. Sakai: Speaker Bureau / Expert testimony: AstraZeneca K.K.; Speaker Bureau / Expert testimony: Chugai Pharmaceutical Co.; Speaker Bureau / Expert testimony: Roche Diagnostics K.K.; Speaker Bureau / Expert testimony: SRL. T. Seto: Honoraria (self): AstraZeneca; Honoraria (self): Bristol-Myers Squibb; Honoraria (self), Research grant / Funding (institution): Chugai Pharmaceutical; Honoraria (self), Research grant / Funding (institution): Eli Lilly Japan; Honoraria (self), Research grant / Funding (institution): MSD; Honoraria (self): Nippon Boehringer Ingelheim; Honoraria (self), Research grant / Funding (institution): Novartis Pharma; Honoraria (self), Research grant / Funding (institution): Pfizer Japan; Honoraria (self): Taiho Pharmaceutical; Honoraria (self), Research grant / Funding (institution): Takeda Pharmaceutical; Honoraria (self): Thermo Fisher Scientific; Research grant / Funding (institution): Daiichi Sankyo; Research grant / Funding (institution): LOXO Oncology; Research grant / Funding (institution): Kissei Pharmaceutical. M. Nishio: Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Ono Pharmaceutical; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Bristol-Myers Squibb; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Pfizer; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Chugai Pharmaceutical; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Eli Lilly; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Taiho Pharmaceutical; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): AstraZeneca; Honoraria (self), Advisory / Consultancy: Boehringer-ingelheim; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): MSD; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Novartis; Advisory / Consultancy: Daiichi Sankyo Healthcare; Advisory / Consultancy: Merck Serono. M. Reck: Honoraria (self), Advisory / Consultancy: AbbVie; Honoraria (self), Advisory / Consultancy: Amgen; Honoraria (self), Advisory / Consultancy: AstraZeneca; Honoraria (self), Advisory / Consultancy: BMS; Honoraria (self), Advisory / Consultancy: Boehringer Ingelheim; Honoraria (self), Advisory / Consultancy: Celgene; Honoraria (self), Advisory / Consultancy: Lilly; Honoraria (self), Advisory / Consultancy: Merck; Honoraria (self), Advisory / Consultancy: MSD; Honoraria (self), Advisory / Consultancy: Novartis; Honoraria (self), Advisory / Consultancy: Pfizer; Honoraria (self), Advisory / Consultancy: Roche. E.B. Garon: Research grant / Funding (institution): Eli Lilly; Research grant / Funding (institution): AstraZeneca; Research grant / Funding (institution): BMS; Research grant / Funding (institution): Genentech; Research grant / Funding (institution): Merck; Research grant / Funding (institution): Novartis; Research grant / Funding (institution): Iovance; Research grant / Funding (institution): Neon; Research grant / Funding (institution): Dynavax; Research grant / Funding (institution): Mirati; Advisory / Consultancy: Dracen; Honoraria (self), Personal Fee for Steering Committee: EMD Serono. C.M. Visseren-Grul: Shareholder / Stockholder / Stock options, Full / Part-time employment: Eli Lilly & Co. R.R. Hozak: Shareholder / Stockholder / Stock options, Full / Part-time employment: Eli Lilly & Co. S.R. Wijayawardana: Shareholder / Stockholder / Stock options, Full / Part-time employment: Eli Lilly & Co. S. Enatsu: Shareholder / Stockholder / Stock options, Full / Part-time employment: Eli Lilly & Co. K. Nakagawa: Research grant / Funding (institution): MSD K.K., Icon Japan K.K., Takeda Pharmaceutical Co.,Ltd., Eli Lilly Japan K.K., Bristol-Myers Squibb Company, Taiho Pharmaceutical Co.,Ltd., Parexel International Corp., Ono Pharmaceutical Co.,Ltd., IQVIA., A2 Healthcare Corp., AbbVie Inc., ; Research grant / Funding (institution): Chugai Pharmaceutical Co.,Ltd., SymBio Pharmaceuticals Limited., Merck Serono Co., Ltd., AstraZeneca K.K., Astellas Pharma Inc., Novartis Pharma K.K., Quintiles Inc., CMIC Shift Zero K.K., Eisai Co., Ltd., Nippon Boehringer Ingelheim Co.,Ltd., ; Research grant / Funding (institution): Kissei Pharmaceutical Co.,Ltd., Pfizer Japan Inc., Kyowa Hakko Kirin Co.,Ltd., EPS Corporation., Daiichi Sankyo Co., Ltd., Bayer Yakuhin, Ltd. ; Honoraria (institution): Astellas Pharma Inc., AstraZeneca K.K. MSD K.K., Ono Pharmaceutical Co.,Ltd., Daiichi Sankyo Co., Ltd., Taiho Pharmaceutical Co.,Ltd., Bristol-Myers Squibb Company, Kyorin Pharmaceutical Co.,Ltd., CareNet,Inc, Nichi-Iko Pharmaceutical Co., Ltd., ; Honoraria (institution): Hisamitsu Pharmaceutical Co.,Inc., Yodosha Co., LTD., Takeda Pharmaceutical Co.,Ltd., Chugai Pharmaceutical Co.,Ltd., Eli Lilly Japan K.K., Nippon Boehringer Ingelheim Co.,Ltd., Novartis Pharma K.K., Pfizer Japan Inc., Nikkei Business Publications, Inc., ; Honoraria (institution): Medicus Shuppan, Publishers Co., Ltd., Thermo Fisher Scientific K.K., Nanzando Co.,Ltd, Medical Review Co., Ltd., Yomiuri Telecasting Corporation; Advisory / Consultancy: Astellas Pharma Inc., Takeda Pharmaceutical Co.,Ltd. Linguistic correction
Resources from the same session
3409 - Effect and safety of immune checkpoint inhibitors for brain metastases from non-small cell lung cancer
Presenter: Toshihiko Iuchi
Session: Poster Display session 1
Resources:
Abstract
3683 - Impact of Radiotherapy on efficacy of anti-programmed death 1 (PD-1) antibodies in metastatic NSCLC
Presenter: Evangeline Samuel
Session: Poster Display session 1
Resources:
Abstract
3924 - Pembrolizumab frontline monotherapy in patients with NSCLC and high PD-L1 expression: Real World Data from a European Cohort with focus on subgroups of interest
Presenter: Giannis Mountzios
Session: Poster Display session 1
Resources:
Abstract
3970 - Patients with metastatic non-small cell lung cancer and PD-L1 expression in Germany. Treatment and first outcome from the prospective German Registry Platform CRISP (AIO-TRK-0315)
Presenter: Martin Sebastian
Session: Poster Display session 1
Resources:
Abstract
5350 - The efficacy and safety of pembrolizumab as a first-line therapy in PD-L1 50% positive advanced NSCLC (HOPE-001)
Presenter: Motohiro Tamiya
Session: Poster Display session 1
Resources:
Abstract
3832 - Osimertinib in epidermal growth factor receptor (EGFR) T790M advanced non-small cell lung cancer (NSCLC): analysis of patients with central nervous system (CNS) metastases in a real-world study (ASTRIS)
Presenter: Giulio Metro
Session: Poster Display session 1
Resources:
Abstract
4082 - Real-world (RW) treatment patterns and outcomes for second-line (2L) therapy and beyond in patients (pts) with epidermal growth factor receptor-mutated (EGFRm) advanced NSCLC receiving a first-line (1L) first- or second-generation (1G/2G) EGFR tyrosine kinase inhibitor (TKI)
Presenter: Riyaz Shah
Session: Poster Display session 1
Resources:
Abstract
2911 - Apatinib combined with EGFR - TKI in treating advanced non-small cell lung cancer with EGFR - TKI resistance
Presenter: Ruifen Tian
Session: Poster Display session 1
Resources:
Abstract
2100 - Updated analysis of a phase I trial of afatinib (Afa) and bevacizumab (Bev) in chemo-naïve patients (pts) with advanced non-small-cell lung cancer (NSCLC) harboring EGFR-mutations: OLCSG1404
Presenter: Takashi Ninomiya
Session: Poster Display session 1
Resources:
Abstract
4325 - Multiple synchronous mechanisms may contribute to osimertinib resistance in non-small cell lung cancer (NSCLC) patients: insights of the MATCH-R study
Presenter: Diego Enrico
Session: Poster Display session 1
Resources:
Abstract