Abstract 1198P
Background
RYZ101 (225Ac-DOTATATE) is an alpha-emitting radiopharmaceutical in development for SSTR2+ solid tumors. Alpha-particles have a shorter path length/higher linear energy transfer than beta-particles, causing more frequent double-strand DNA breaks and potentially improved therapeutic index. ACTION-1 (NCT05477576) is a 2-part, global, randomized, controlled, open-label, phase 1b/3 trial of RYZ101 in advanced, well-differentiated SSTR+ GEP-NETs progressing after 177Lu-SSA therapy. Herein, we report results from the phase Ib portion of the trial.
Methods
The phase Ib portion had a dose de-escalation/Bayesian optimal interval design with boundaries based on a dose-limiting toxicity (DLT) rate of 25%. Patients (pts) received RYZ101 IV q8w x4 cycles. Planned dose levels (n=6/level): Level 0 (starting dose) 120kBq/kg; Level –1 90kBq/kg; Level –2 60kBq/kg. DLT was assessed for 56d after the first RYZ101 dose. Treatment-emergent adverse events (TEAEs) were graded by NCI-CTCAE v5.0. Dose de-escalation decisions/safety data were overseen by a Data Review Committee. Tumor response was assessed locally by RECIST v1.1.
Results
17 pts have received at least one dose of RYZ101 at 120kBq/kg (4 doses: 6 pts; 3 doses: 2 pts; 2 doses: 8 pts; 1 dose: 1 pt; median 8.9MBq). Baseline characteristics: median age 63y; male (n=11); ECOG PS 0/1 (n=10/7); primary tumor site GI/pancreas (n=12/5). No DLTs, no dose de-escalation and no treatment-related serious AEs (SAEs) occurred. TEAEs requiring dose reductions occurred in 2 pts (G2 thrombocytopenia, n=2). G3/4 TEAEs occurred in 6 pts, 3 related to RYZ101 (lymphopenia, n=2; weight decreased, n=1). SAEs occurred in 4 pts (all unrelated). Confirmed objective response was seen in 5 evaluable pts. Updated efficacy data will be provided at the congress.
Conclusions
RYZ101 was well tolerated and a fixed dose of 10.2MBq was declared the recommended phase 3 dose. Initial data suggest promising efficacy. Part 2 (phase 3) is enrolling and will compare RYZ101 at 10.2MBq q8w for 4 cycles with standard of care in pts with advanced SSTR2+ GEP-NETs progressing following prior 177Lu-labeled SSAs.
Clinical trial identification
ACTION-1 (NCT05477576).
Editorial acknowledgement
Editorial assistance for this abstract was provided by Lee Miller (Miller Medical Communications Ltd). This work was funded by the study sponsor (RayzeBio Inc).
Legal entity responsible for the study
RayzeBio Inc.
Funding
RayzeBio Inc.
Disclosure
J. Strosberg: Financial Interests, Personal, Speaker’s Bureau: Ipsen; Financial Interests, Personal, Advisory Board: Novartis, Tersera; Financial Interests, Institutional, Principal Investigator: Merck, Novartis, Alphamedix; Financial Interests, Personal, Advisory Role: Novartis. G. Ulaner: Financial Interests, Personal, Speaker’s Bureau: GE Healthcare, Lantheus; Financial Interests, Institutional, Research Grant: GE Healthcare, Lantheus, Nuclidium, Curium, RayzeBio, ImmaginAb, BriaCell, POINT; Financial Interests, Personal, Advisory Role: GE Healthcare, Lantheus, Nuclidium, POINT. H.P. Soares: Financial Interests, Personal, Advisory Board: TerSera, Ipsen, AstraZeneca, Novartis, ITM. L.B. Anthony: Financial Interests, Institutional, Principal Investigator: Rayzebio. H. Jacene: Financial Interests, Personal, Invited Speaker: Monrol, ITM; Financial Interests, Personal, Member of Board of Directors: SNMMI; Financial Interests, Personal, Royalties: Cambridge University Press; Financial Interests, Institutional, Funding: Blue Earth Diagnostics; Financial Interests, Personal, Speaker, Consultant, Advisor: Blue Earth Diagnostics, Spectrum Dynamics. D. Ferreira: Financial Interests, Personal, Full or part-time Employment: RayzeBio, Bayer; Financial Interests, Personal, Stocks or ownership: RayzeBio, Bayer, Medtronic. J. Li: Financial Interests, Personal, Full or part-time Employment: RayzeBio; Financial Interests, Personal, Stocks or ownership: RayzeBio. K. Ma: Financial Interests, Personal, Full or part-time Employment: RayzeBio; Financial Interests, Personal, Stocks or ownership: RayzeBio. J. Rearden: Financial Interests, Personal, Stocks or ownership: RayzeBio; Financial Interests, Personal, Full or part-time Employment: RayzeBio. S. Moran: Financial Interests, Personal, Full or part-time Employment: RayzeBio; Financial Interests, Personal, Stocks or ownership: RayzeBio. T. Hope: Financial Interests, Institutional, Research Funding: Clovis Oncology, Philips, GE Healthcare, Lantheus, Janssen, The Prostate Cancer Foundation, The National Cancer Institute; Financial Interests, Personal, Advisory Role: Ipsen, Bayer, BlueEarth Diagnostics, RayzeBio, Curium; Financial Interests, Personal, Stocks or ownership: RayzeBio, Curium. M. Morris: Financial Interests, Personal, Advisory Board: Gentem Health, Softhread; Financial Interests, Personal, Full or part-time Employment: AMIT; Financial Interests, Personal, Ownership Interest: AMIT, Gentem Health, Softhread; Financial Interests, Personal, Principal Investigator: AMIT; Financial Interests, Institutional, Proprietary Information: AMIT; Financial Interests, Institutional, Sponsor/Funding: AMIT. All other authors have declared no conflicts of interest.
Resources from the same session
1197P - Somatostatin analogs or active surveillance in sporadic non-functioning pancreatic neuroendocrine tumors
Presenter: Maria Grazia Maratta
Session: Poster session 13
1199P - MAVERIC: Phase II randomized study of everolimus as maintenance therapy for metastatic neuroendocrine neoplasms (mNEN) with pulmonary or gastroenteropancreatic (GEP) origin. Results on behalf of the GOIRC
Presenter: Lorenzo Antonuzzo
Session: Poster session 13
1200P - A phase II single-arm interventional trial evaluating the activity and safety of CABOzantinib (CBZ) plus TEMozolomide (TMZ) in lung and gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) progressed after SSA therapy, everolimus, sunitinib or PRRT: CABOTEM Trial
Presenter: oOttavia Clemente
Session: Poster session 13
1201P - Evaluation of efficacy TEMCAP regiment as first-line or further line therapy in patients with advanced, unresectable, progressive GEP-NET. Real-world data
Presenter: Agnieszka Kolasinska-Cwikla
Session: Poster session 13
1202P - Final analysis of TENEC trial: A phase II trial of temozolomide (TMZ) as second-line treatment for advanced neuroendocrine carcinomas (NEC) in patients (pts) with a poor performance status (PS)
Presenter: Claudia von Arx
Session: Poster session 13