Abstract 741MO
Background
Luveltamab tazevibulin (luvelta) is a novel FolRα-targeting ADC with a stable cleavable linker and a 3-aminophenyl hemiasterlin warhead (DAR 4) that induces cytotoxic and immunogenic cell death. Using site-specific conjugation technology and proprietary cell-free protein synthesis platform, luvelta is designed to target a broad range of FolRα expressing cancers, including EEC.
Methods
Following completion of the STRO-002-GM1 phase 1 study, a dose expansion cohort was enrolled consisting of metastatic EEC with progression after ≥ 1 platinum or immunotherapy-based regimen (≤ 3 total lines) with ≥ 1% FolRα expression (any intensity using Ventana FolR1 IHC assay). Luvelta dose was 5.2 mg/kg q3w. In patients (pts) with prior pelvic irradiation, a dose of 4.3 mg/kg q3w was administered. The primary endpoint is objective response rate (RECIST v1.1) with secondary endpoints of safety and PK.
Results
17 pts were enrolled (8 pts at 5.2 mg/kg and 9 pts at 4.3 mg/kg). Prior therapy: median lines=2; prior platinum=17 pts; and prior PD-1=4 pts. Median exposure was 12 weeks (range 3-38). Initial efficacy data is presented in the table. Table: 741MO
Best response (RECIST v1.1)
Response evaluable patients (n=16) | Response evaluable patients with FolRα ≥ 25% (n=8) | |
Response (PR+PRu) | 6 (37.5%) | 4 (50%) |
PR | 4 (25%) | 2 (25%) |
PRu (unconfirmed PR) | 2 (12.5%) | 2 (25%) |
SD | 5 (31.3%) | 3 (37.5%) |
PD | 5 (31.3%) | 1 (12.5%) |
Disease control rate (PR+PRu+SD) | 11 (68.8%) | 7 (87.5%) |
The safety profile was consistent with prior reported data in ovarian cancer pts treated with luvelta. The most common Grade 3 or higher (G3+) adverse events (AEs) were neutropenia (53%), anemia (24%), and arthralgia(18%). There were no G3 eye disorder AEs, 1 G3+ pulmonary AE (G3 COVID pneumonia) and no G5 AEs. A single pt had an AE leading to discontinuation (G3 arthralgia).
Conclusions
Advanced EEC remains an area of high unmet need with a poor prognosis and limited treatment options. Preliminary data indicate that luvelta has a predictable and manageable safety profile with encouraging clinical activity in pts with recurrent/progressive FolRα expressing EEC. Luvelta warrants further development as a targeted agent for EEC.
Clinical trial identification
NCT03748186.
Editorial acknowledgement
Legal entity responsible for the study
Sutro Biopharma, Inc.
Funding
Sutro Biopharma, Inc.
Disclosure
B. Pothuri: Financial Interests, Personal, Advisory Board, Advisory Board: Eisai; Financial Interests, Personal, Advisory Board, Advisory board: AstraZeneca; Financial Interests, Personal, Advisory Board: Clovis Oncology, GSK, Merck, Tesaro, Sutro, Mersana, Lily, Seattle Genetics; Financial Interests, Personal, Other, consulting: Toray, Arquer Diagnostics, Atossa, Elevar, Deciphera, Imab; Financial Interests, Institutional, Local PI: Tesaro, Clovis Oncology, Roche Genentech, Takeda, Celsion, Celgene, AstraZeneca, Immunogen, Merck, GSK; Financial Interests, Institutional, Local PI, clinical trial: Incyte, Toray, Karyopharm, Sutro, Eisai, VBL Therapeutics, Mersana, Seattle Genetics; Non-Financial Interests, Other, Member of GOG Partners group: GOG Foundation; Non-Financial Interests, Member of Board of Directors: Society of Gynecologic Oncology. R.W. Naumann: Financial Interests, Personal, Advisory Role: Merck Sharp and Dohme, AstraZeneca, Clovis Oncology, OncoMed, Eisai, Bristol Myers Squibb, Seagen, Agenus, Sutro Biopharma, Inc., GOG Partners, GSK/Tesaro, Genelux, Laekna; Financial Interests, Personal, Invited Speaker: Seagen ; Financial Interests, Institutional, Research Funding: Bristol Myers Squibb, OncoMed, Sutro Biopharm, Inc., Gynecology Oncology Group, Mersana, GSK/Tesaro. L.P. Martin: Financial Interests, Personal, Advisory Role: Sutro Biopharma, Inc., Elucida Oncology, Immunogen, Myriad Genetics; Financial Interests, Personal, Research Funding: Agenus, AstraZeneca, Sutro Biopharma, Inc., Immunogen. D. O'Malley: Financial Interests, Institutional, Research Funding: AbbVie, Advaxis, Agenus, Alkemes, Aravive, Arcus Biosciences, AstraZeneca, BeiGene, Boston Biomedical, Bristol Squibb Myers, Clovis Oncology, Deciphera Pharma, Eisai, EMD Serono, Exelixis, Genentech, Inc., Genmab, GSK, GOG Foundation , F. Hoffmann-La Roche, Inc., Immunogen, Incyte Corporation, Iovance Biotherapeutics, Karyopharm, Leap Therapeutics, Inc., Ludwig Institute for Cancer, Merck and Co, Merck Sharp and Dohme, Mersana, NCI, Novartis, NovoCure, NRG Oncology, OncoC4, Inc., OncoQuest, Inc., Pfizer, Precision Therapeutics, Prelude Therapeutics, Regeneron Pharmaceuticals, Inc., RTOG, Rubius Therapeutics, Seattle Genetics, SWOG, Tesaro; Financial Interests, Personal, Advisory Role: AbbVie, Adaptimmune, Agenus, Arquer Diagnostics, Arcus Biosciences, AstraZeneca, Atossa Therapeutics, Boston Biomedical, Cardiff Oncology, Celcuity, Clovis Oncology, Corcept, Duality Bio, Eisai, Elevar, Exelixis, Genentech, Inc., Genelux, GSK, GOG Foundation, F. Hoffmann-La Roche, Inc., Immunogen, Inc., Imvax, InterVenn, INXMED, Iovance Therapeutics, Jannsen, Jazz Pharmaceuticals, Laekna, Leap Therapeutics, Luzsana Biotechnology, Merck and Co, Merck Sharpe and Dohme, Mersana, Myriad, Novartis, NovoCure, OncoC4, Inc., Onconova, Regeneron Pharmaceuticals, Repimmune, R Pharm, Roche Diagnostics, Seattle Genetics, Sorrento, Tarveda Therapeutics, Toray, Trillium, Umoja, Verastem, Inc., VBL Therapeutics, Vincerx Pharma, Xenocor, Zentalis; Financial Interests, Personal, Advisory Board: Sutro Biopharm, Inc. J.W. Moroney: Financial Interests, Institutional, Research Funding: Sutro Biopharma, Inc. J. Garcia-Donas: Financial Interests, Institutional, Research Funding: Sutro Biopharma. A. Redondo Sanchez: Financial Interests, Institutional, Research Funding: Sutro Biopharma, Inc. A. Gonzalez Martin: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, Clovis, GSK, Genmab, Alkermes, Sutro, Roche, SOTIO, PharmaMar, Oncoinvent, Novartis, Mersana, MSD, Macrogenics, Eisai, Inmunogen, Regeneron, HederaDx, Illumina; Financial Interests, Personal, Invited Speaker: GSK, AstraZeneca, Clovis, Roche, Novocure, MSD, Takeda, Zaylab; Financial Interests, Institutional, Coordinating PI, PI of ANITA trial: GSK, Roche; Financial Interests, Personal, Steering Committee Member, Member of ENGOT ov43-SC: MSD; Financial Interests, Institutional, Coordinating PI, ENGOT PI of EPIK-O trial: Novartis; Financial Interests, Institutional, Coordinating PI, ENGOT PI of AVB-500 phase III trial: ARAVIVE. D.G. Illescas: Financial Interests, Institutional, Research Funding: Sutro Biopharma, Inc. L. Liu: Financial Interests, Personal, Full or part-time Employment: Sutro Biopharma, Inc. C. Berman: Financial Interests, Personal, Full or part-time Employment, Employee: Sutro Biopharma. A. Oaknin: Financial Interests, Personal, Advisory Board: AstraZeneca, Clovis Oncology, Deciphera Pharmaceuticals, Genmab, GSK, Immunogen, Mersana Therapeutics, PharmaMar, Merck Sharps & Dohme de España, SA, Agenus, Sutro, Corcept Therapeutics, EMD Serono, Novocure, Sattucklabs, Itheos, Eisai, F. Hoffmann-La Roche, Seagen, OneXerna Therapeutics, Inc, Regeneron, Sutro Biopharma; Financial Interests, Personal, Other, Travel and accomodation: AstraZeneca, PharmaMar, Roche; Financial Interests, Institutional, Funding: Amgen, AbbVie Deutschland, Advaxis Inc., Aeterna Zentaris, Aprea Therapeutics AB, Regeneron Pharmaceuticals, Clovis Oncology Inc., EISAI limited Ltd., F. Hoffmann-La Roche Ltd., Immunogen Inc., Merck, Sharp & Dohme de España SA, Millennium Pharmaceuticals Inc., PharmaMar SA, Tesaro Inc., Bristol Myers Squibb; Non-Financial Interests, Leadership Role, on behalf of GEICO: GCIG; Non-Financial Interests, Officer, Chair of Gynaecological Track ESMO 2019. Scientific Track Member Gynaecological Cancers ESMO 2018, ESMO 2020, ESMO 2022. Member of Gynaecological Cancers Faculty and Subject Editor Gyn ESMO Guidelines: ESMO; Non-Financial Interests, Leadership Role, ESMO GYN Co-Chair 2023-2025: ESMO; Non-Financial Interests, Leadership Role, Chair de Cervix Committee. 2022-2024: GCIG; Non-Financial Interests, Member: ESMO, ASCO, GCIG, SEOM, GOG. All other authors have declared no conflicts of interest.
Resources from the same session
LBA43 - Updated response data and analysis of progression free survival by mechanism of mismatch repair loss in endometrial cancer (EC) patients (pts) treated with pembrolizumab plus carboplatin/paclitaxel (CP) as compared to CP plus placebo (PBO) in the NRG GY018 trial
Presenter: Ramez Eskander
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
740MO - Dostarlimab + chemotherapy for the treatment of primary advanced or recurrent endometrial cancer (pA/rEC): Analysis of progression free survival (PFS) and overall survival (OS) outcomes by molecular classification in the ENGOT-EN6-NSGO/GOG-3031/RUBY trial
Presenter: Mansoor Raza Mirza
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
742MO - Neoadjuvant immune checkpoint blockade in mismatch repair deficient endometrial cancer
Presenter: Marco de Bruyn
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
Invited Discussant LBA43, 740MO, 742MO and 741MO
Presenter: Christian Marth
Session: Mini oral session - Gynaecological cancers
Resources:
Slides
Webcast
743MO - Efficacy and safety of QL1706 plus paclitaxel and cisplatin/carboplatin +/- bevacizumab (Bev) as 1L treatment in recurrent or metastatic cervical cancer (r/mCC): A single-arm, multicenter phase II study
Presenter: Danbo Wang
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
744MO - AdvanTIG-202: Phase II randomized, multicenter, open-label study of tislelizumab (TIS) with or without ociperlimab (OCI) in patients (pts) with previously treated recurrent/metastatic (R/M) cervical cancer (CC)
Presenter: Jung-Yun Lee
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
LBA44 - Camrelizumab plus famitinib versus camrelizumab alone and investigator’s choice of chemotherapy in women with recurrent or metastatic cervical cancer
Presenter: Xiaohua Wu
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
Invited Discussant 743MO, 744MO and LBA44
Presenter: Alexandra Leary
Session: Mini oral session - Gynaecological cancers
Resources:
Slides
Webcast
LBA45 - Overall survival (OS) outcomes from NRG-GY004, a phase III study comparing single-agent olaparib or combination cediranib and olaparib to platinum (Plat) based chemotherapy in recurrent plat sensitive ovarian cancer (OvCa)
Presenter: Joyce Liu
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast
746MO - Randomized phase II trial of durvalumab in combination with olaparib and cediranib (DOC) compared to olaparib and cediranib (OC) or durvalumab and cediranib (DC) or standard of care chemotherapy (SOC) in platinum-resistant ovarian cancer with prior bevacizumab (NRG-GY023)
Presenter: Jung-Min Lee
Session: Mini oral session - Gynaecological cancers
Resources:
Abstract
Slides
Webcast