Abstract 762P
Background
PROC is an area of high unmet medical need due to the generally poor outcomes and limited activity of standard systemic therapy. Clinical responses with TransCon IL-2 β/γ (TC-IL-2 β/γ, onvapegleukin alfa) +/- pembrolizumab in heavily pre-treated patients with anti-PD-(L)1 relapsed or refractory solid tumors have been reported (Starodub et al, ESMO23). Here, encouraging preliminary results from the PROC cohort are provided.
Methods
In this PROC cohort (progression within 6 months after completing prior platinum-based therapy), patients received the recommended phase 2 dose of 120 μg/kg TC-IL-2 β/γ IV Q3W plus physician’s choice of paclitaxel, docetaxel, or pemetrexed until disease progression or unacceptable toxicity. Disease response was assessed every 9 weeks per RECIST 1.1. Safety, efficacy, and biomarkers were evaluated.
Results
As of 16Apr24, 12 patients were treated with TC-IL-2 β/γ in combination with chemotherapy (pemetrexed, n=7; paclitaxel, n=4 and docetaxel, n=1). Median prior lines of therapy were 5 (range 2-7), including prior anti-PD-(L)1 in 25% of patients. The most common Treatment Related Adverse Events (TRAEs) were fatigue (66.7%), nausea (41.7%), and neutropenia (33.3%). TRAEs ≥ Grade 3 were neutropenia (n=3), fatigue (n=2), decreased appetite, chronic inflammatory demyelinating polyneuropathy and thrombocytopenia (n=1 each). Out of 6 efficacy-evaluable patients as of 06May24, ORR is 33% per RECIST 1.1 (2 confirmed PRs, progression after 3 and 7 lines of prior systemic treatments). Preliminary biomarker analysis shows selective expansion of cytotoxic lymphocytes (CLs), without meaningful expansion of eosinophils and Tregs for at least 3 weeks after dosing.
Conclusions
Initial data suggest that TC-IL-2 β/γ in combination with chemotherapy for PROC is generally well-tolerated with meaningful clinical responses in heavily pre-treated patients. Preliminary evaluation of biomarkers shows a sustained and specific expansion of CLs.
Clinical trial identification
NCT05081609.
Editorial acknowledgement
Legal entity responsible for the study
Ascendis Pharma.
Funding
Ascendis Pharma.
Disclosure
O. Yeku: Financial Interests, Personal, Other, Consultant: GIMV NV, TigaTx Inc; Financial Interests, Personal, Advisory Board: hC Bioscience; Financial Interests, Personal, Full or part-time Employment, Associate Editor: NEJM Evidence; Financial Interests, Personal, Full or part-time Employment: Massachusetts General Hospital; Financial Interests, Personal, Other, Patent Pending: MUC16 Directed Antibodies for therapeutic applications; Financial Interests, Personal, Other, Patent pending: Human Artificial Chromosomes for therapeutic applications; Financial Interests, Institutional, Local PI: Ascendis Pharma A/S, Duality Biologics, Immunocore Limited, Merck Sharp & Dohme Corporation, ProfoundBio. J-Y. Lee: Financial Interests, Personal, Invited Speaker: AstraZeneca, Takeda, MSD, Roche; Financial Interests, Personal, Advisory Board: Eisai, GI Innovation, Regeneron; Financial Interests, Institutional, Local PI: Alkermes, AstraZeneca, BergenBio, Cellid, Clovis Oncology, Eisai, GI Innovation, ImmunoGen, Janssen, Merck, Mersana, MSD, Novartis, OncoQuest, Roche, Seagen, Synthon, Regeneron, Ascendis Pharma, Advenchen, BMS, Kelun, Sutro; Financial Interests, Personal and Institutional, Local PI: BeiGene; Financial Interests, Personal, Steering Committee Member: AstraZeneca, OncoQuest, Seagen, ImmunoGen, MSD; Financial Interests, Institutional, Research Grant: Ono, Takeda, GSK; Financial Interests, Institutional, Other, Sub I: Corcept. B. Rimmel: Financial Interests, Personal, Advisory Board: GSK, AstraZeneca, Immunogen, Merck. S-B. Kim: Financial Interests, Personal, Advisory Board: Novartis, AstraZeneca, Lilly, DaeHwa Pharma, ISU Abx, Daiichi Sankyo, BeiGene, Samsung Bioepics, Obi Pharma; Financial Interests, Personal, Invited Speaker: Legochem Bioscience; Financial Interests, Personal, Ownership Interest: Genopeaks; Financial Interests, Institutional, Research Grant: Novartis, Sanofi-Genzyme, DongKook Pharm Co. T.F.A. Van Den Mooter: Financial Interests, Personal, Advisory Board: Seagen; Financial Interests, Personal, Expert Testimony: Astellas, Bayer; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Pfizer. G. Kichenadasse: Financial Interests, Personal, Full or part-time Employment: SOCRU; Financial Interests, Personal, Leadership Role: SOCRU. C. Krapp, S. Slavsky, S.M. Singel: Financial Interests, Personal, Full or part-time Employment: Ascendis Pharma. D. Torrejon Castro: Financial Interests, Personal, Full or part-time Employment: Ascendis Pharma Inc. V. Kwatra: Financial Interests, Personal, Advisory Board: Roche.
Resources from the same session
793TiP - A phase III, randomized, open-label, multicenter study of sacituzumab tirumotecan (sac-TMT) monotherapy vs treatment of physician’s choice chemotherapy in patients with endometrial cancer who have received prior chemotherapy and immunotherapy: ENGOT-en23/GOG-3095/MK-2870-005
Presenter: Domenica Lorusso
Session: Poster session 02
795TiP - A first-in-human phase I study of LY4170156, an antibody-drug conjugate targeting folate receptor α (FRα)-expressing advanced solid tumors
Presenter: Isabelle Ray-Coquard
Session: Poster session 02
796TiP - Rationale and study design of the KOV-HIPEC-04: A phase III randomized controlled trial in primary stage three and four ovarian cancer after interval cytoreductive surgery (FOCUS)
Presenter: Junhwan Kim
Session: Poster session 02
797TiP - Tislelizumab combined with chemotherapy as neoadjuvant treatment for advanced endometrial cancer: A prospective, single-arm, open-label clinical study
Presenter: Zheng Hu
Session: Poster session 02
798TiP - Stereotactic radiotherapy alone or followed by niraparib for oligometastases or oligoprogression in ovarian cancer following PARP inhibitor therapy: SOPRANO trial
Presenter: Susana Banerjee
Session: Poster session 02
856P - Safety of neoadjuvant PARP inhibitor and immunotherapy in locally advanced HPV-negative head and neck squamous cell carcinoma (PRIME H&N Study)
Presenter: Luigi Lorini
Session: Poster session 02
857P - Safety and efficacy of neoadjuvant immunochemotherapy in patients with locally advanced head and neck squamous cell carcinoma: A prospective single-arm clinical trial
Presenter: Jing Yan
Session: Poster session 02
Resources:
Abstract
858P - Preoperative neoadjuvant chemoimmunotherapy for locally advanced head and neck squamous cell carcinoma patients: A prospective, single-arm, phase II clinical study
Presenter: Ping Han
Session: Poster session 02