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Poster session 04

883TiP - A phase I/II open-label study (IOV-GM1-201) of TALEN-mediated PD-1 inactivated autologous tumor-infiltrating lymphocytes (TIL; IOV-4001) in patients with advanced melanoma and NSCLC

Date

10 Sep 2022

Session

Poster session 04

Topics

Targeted Therapy;  Cell-Based Therapy

Tumour Site

Melanoma;  Non-Small Cell Lung Cancer

Presenters

Jason Chesney

Citation

Annals of Oncology (2022) 33 (suppl_7): S356-S409. 10.1016/annonc/annonc1059

Authors

J. Chesney1, T. Wise-draper2, A.A. Sarnaik3, F. Graf Finckenstein4, P. Hari4, M. Jagasia5, A. Desai4, A. Suzuki4, X. Wu6, A. Betof Warner7

Author affiliations

  • 1 Department Of Medicine, Brown Cancer Center University of Louisville, 40202 - Louisville/US
  • 2 Hematology Oncology Dept, Vontz Center for Molecular Studies, 45267-0521 - Cincinnati/US
  • 3 Cutaneous Oncology, H. Lee Moffitt Cancer Center & Research Institute - Magnolia Campus, 33612 - Tampa/US
  • 4 Clinical Science, Iovance Biotherapeutics, 94070 - San Carlos/US
  • 5 Medical Affairs, Iovance Biotherapeutics, 94070 - San Carlos/US
  • 6 Biostatistics, Iovance Biotherapeutics, 94070 - San Carlos/US
  • 7 Medicine Department, Memorial Sloan Kettering Cancer Center, 10065 - New York/US

Resources

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Abstract 883TiP

Background

Adoptive cell therapy with TIL has demonstrated efficacy in patients (pts) with advanced solid tumors, including melanoma (Sarnaik JCO 2021) and NSCLC (Schoenfeld SITC 2021). IOV-4001 is a TALEN®-mediated PDCD-1 knockout autologous TIL cell therapy product. Preclinical studies suggest that PD-1 inactivation by PDCD-1 gene knockout may enhance TIL cell therapy efficacy, with similar quality attributes and phenotypes to those of non-edited TIL (Natarajan AACR 2022).

Trial design

This first-in-human phase 1/2, open-label, nonrandomized, multicenter study (NCT05361174; open to enrollment) will enroll ∼53 adult pts. During the phase 1 portion, enrollment and dose level decisions will be based on emerging safety and tolerability data in a 28-day dose-limiting toxicity (DLT) observation period. Cohort 1 will include pts with unresectable/metastatic melanoma that has progressed during/within 12 wks of last anti–PD-1/PD-L1 dose (pts must have also received a BRAF ± MEK inhibitor if BRAF V600 mutation-positive). Cohort 2 will include pts with advanced NSCLC who have received ≤3 prior therapies and whose disease progressed either: (1) during/within 12 wks after last anti–PD-1/PD-L1 dose (pts without oncogene-driven mutations) or (2) during/after ≥1 targeted therapy and either platinum doublet chemotherapy or during/within 12 wks after last anti–PD-1/PD-L1 dose (pts with oncogene-driven tumors). Pts must have ECOG PS ≤1, ≥1 resectable lesion(s) (≥1.5 cm), ≥1 remaining RECIST-measurable lesion(s) and recovered from prior surgery/anticancer treatment-related AEs (grade ≤1). IOV-4001 is generated from resected tumor in a centralized GMP process. The regimen includes nonmyeloablative lymphodepletion, IOV-4001 infusion, and a short course of high-dose IL-2. The primary endpoints of phases 1 and 2 are safety (DLTs and AEs) and objective response rate per RECIST v1.1, respectively. Secondary endpoints include complete response rate, duration of response, disease control rate, progression-free survival, overall survival, feasibility, and additional safety.

Clinical trial identification

NCT05361174.

Editorial acknowledgement

Medical writing support was provided by Second City Science (Vaniam Group, LLC) and funded by Iovance Biotheraputics, Inc.

Legal entity responsible for the study

Iovance Biotherapeutics, Inc.

Funding

Iovance Biotherapeutics, Inc.

Disclosure

J. Chesney: Financial Interests, Personal, Other, Consultant: Amgen; Financial Interests, Personal, Funding, Research Funding: Amgen, Iovance Biotherapeutic, Bristol Myers Squibb, InstillBio, Replimune. T. Wise-draper: Financial Interests, Personal, Research Grant, Clinical Research Grants (IITs): Merck , Bristol Myers Squibb, AstraZeneca, Tesaro/GSK, Janssen, IsoRay; Financial Interests, Personal, Advisory Board: Merck ; Financial Interests, Personal, Other, Consulting: Rakuten, Shattuck Labs, Caris Life Sciences ; Financial Interests, Personal, Other, Steering Committee: Exicure; Financial Interests, Personal, Other, HNC POA Chair: Caris Life Sciences. A.A. Sarnaik: Financial Interests, Personal, Other, Honoraria: Physicans' Education Resource; Financial Interests, Personal, Funding, Research Funding: Provectus, Genentech, Iovance Biotherapeutics; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Iovance Biotherapeutics; Financial Interests, Personal, Advisory Role: Iovance Biotherapeutics, B4CC, Guidepoint Global, Defined Health, Gerson Lehrman Group. F. Graf Finckenstein: Financial Interests, Personal, Full or part-time Employment: Iovance Biotherapeutics, Inc; Financial Interests, Personal, Stocks/Shares: Iovance Biotherapeutics, Inc. P. Hari: Financial Interests, Personal, Full or part-time Employment: Iovance Biotherapeutics, Inc; Financial Interests, Personal, Stocks/Shares: Iovance Biotherapeutics, Inc. M. Jagasia: Financial Interests, Personal, Full or part-time Employment: Iovance Biotherapeutics, Inc; Financial Interests, Personal, Stocks/Shares: Iovance Biotherapeutics, Inc. A. Desai: Financial Interests, Personal, Full or part-time Employment: Iovance Biotherapeutics, Inc; Financial Interests, Personal, Stocks/Shares: Iovance Biotherapeutics, Inc. A. Suzuki: Financial Interests, Personal, Full or part-time Employment: Iovance Biotherapeutics, Inc; Financial Interests, Personal, Stocks/Shares: Iovance Biotherapeutics, Inc. X. Wu: Financial Interests, Personal, Full or part-time Employment: Iovance Biotherapeutics, Inc; Financial Interests, Personal, Stocks/Shares: Iovance Biotherapeutics, Inc. A. Betof Warner: Financial Interests, Personal, Other, Honoraria: LG Chem; Financial Interests, Personal, Advisory Role: Nanbiotix, Iovance Biotherapeutics, Novartis, Shanghai Jo’Ann Medical Technology, BluePath Solutions, Pfizer; Financial Interests, Personal, Funding, Research Funding: Leap Therapeutics.

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