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A Single Direct Intratumoral Injection of TTI-621 (SIRPαFc) Induces Antitumor Activity in Patients with Relapsed/Refractory Mycosis Fungoides and Sézary Syndrome: Preliminary Findings Employing an Immune Checkpoint Inhibitor Blocking the CD47 Do Not Eat Signal

2017· article· en· W2784746802 on OpenAlexaff
Christiane Querfeld, John A. Thompson, Matthew H. Taylor, Raju Pillai, Lisa D. Johnson, Tina Catalano, Penka S. Petrova, Robert A. Uger, Meghan Irwin, Eric L. Sievers, Oleg E. Akilov

Bibliographic record

VenueBlood · 2017
Typearticle
Languageen
FieldImmunology and Microbiology
TopicPhagocytosis and Immune Regulation
Canadian institutionsTrillium Therapeutics (Canada)
Fundersnot available
KeywordsMedicineMycosis fungoidesImmune checkpointTumor microenvironmentInternal medicineMelanomaImmune systemCancer researchCancerImmunologyOncologyLymphomaImmunotherapy

Abstract

fetched live from OpenAlex

Abstract Background CD47 is an immune checkpoint that binds to signal regulatory protein alpha (SIRPα) and delivers a “do not eat” signal to suppress macrophage phagocytosis. Tumor cells frequently overexpress CD47 to evade macrophage-mediated destruction. TTI-621 (SIRPαFc) is an immune checkpoint inhibitor consisting of the CD47 binding domain of human SIRPα linked to the Fc region of human IgG1 designed to both: 1) block the CD47 “do not eat” signal, and 2) engage macrophage Fcγ receptors with IgG1 Fc to enhance phagocytosis and antitumor activity. It is hypothesized that direct intratumoral injection of TTI-621 may enhance both local and systemic antitumor activity. Methods A Phase 1, multicenter, open-label study is ongoing to characterize the safety and tolerability of intratumoral injection of TTI-621 (NCT02890368). Eligible patients (pts) are adults with relapsed or refractory mycosis fungoides/Sezary syndrome or percutaneously-accessible solid tumors who have progressed on standard anticancer therapy or for whom no other approved therapy exists. Pts are enrolled in sequential cohorts to receive a single intratumoral injection of TTI-621 at increasing dose levels to characterize safety, pharmacokinetics, pharmacodynamics, and preliminary evidence of antitumor activity. Repeat TTI-621 intratumoral dosing has recently been initiated. Serial, post-injection biopsies are collected to assess the temporal impact of TTI-621 on the tumor microenvironment. Results Nine pts (6 M/3F, age 57-85 years) have been enrolled as of July 2017. Diagnoses include mycosis fungoides/Sezary syndrome (N=6), melanoma (N=1), leiomyosarcoma (N=1), and squamous cell carcinoma (N=1). A single intratumoral injection of 1 mg, 3 mg, or 10 mg TTI-621 has been well tolerated by all enrolled pts. The most frequently reported adverse events were fatigue in 5 pts, chills in 4 pts, and decreased appetite in 3 pts. All treatment-related AEs were Grade 1 or 2 in severity. No dose limiting toxicity has been observed to date. All 6 pts with mycosis fungoides/Sezary syndrome experienced decreases in tumor size and/or decreased circulating Sezary cells (3 of 3 pts) as determined by a decrease in a peripheral clonal T-cell populationor CD4:CD8 ratio after a single intratumoral injection of TTI-621. Responses ranged from loco-regional to systemic effects. One pt with localized refractory mycosis fungoides on the dorsum of the foot obtained a complete response of the injected lesion that is ongoing after 17+ weeks of follow up. NanoString analysis of peripheral blood and tumor tissue pre- and post-intratumoral injection of TTI-621 indicated alterations in genes associated with activation of the innate immune system and upregulation of IFN-associated genes. Conclusions These preliminary Phase 1 data suggest that mycosis fungoides and its leukemic variant, Sezary syndrome, are highly responsive to a single dose of TTI-621 delivered by intratumoral injection. One pt achieved a complete response of the injected lesion and 5 additional pts experienced decreases in tumor size and/or decreased circulating Sezary cells. Intratumoral injections were well tolerated by all pts. Evidence of innate immune activation was documented, consistent with the proposed function of TTI-621 as an innate immune checkpoint inhibitor. Disclosures Querfeld: Soligenix: Research Funding; Elorac: Research Funding; Celgene: Honoraria, Research Funding; MiRagen: Honoraria, Research Funding; Actelion: Honoraria, Research Funding; Medivir: Honoraria; Mallinckrodt: Honoraria; Mindera: Consultancy; Kyowa: Research Funding; Trillium Therapeutics: Research Funding; City of Hope: Employment. Thompson: Trillium Therapeutics: Research Funding. Taylor: Blue Print Medicines: Consultancy, Honoraria; Eisai Inc.: Consultancy, Honoraria, Speakers Bureau; Bristol Myers Squibb: Consultancy, Honoraria, Speakers Bureau; Trillium Therapeutics: Consultancy, Honoraria. Pillai: Trillium Therapeutics: Research Funding. Johnson: Trillium Therapeutics: Employment. Catalano: Trillium Therapeutics: Employment; Apotex Inc.: Employment. Petrova: Trillium Therapeutics: Employment, Equity Ownership. Uger: Trillium Therapeutics: Employment, Equity Ownership, Patents & Royalties. Irwin: Hoffmann La Roche: Employment, Equity Ownership; Trillium Therapeutics: Employment, Equity Ownership. Sievers: Trillium Therapeutics: Employment, Equity Ownership. Akilov: Seattle Genetics: Consultancy; Medivir: Consultancy; Actelion Pharmacuticals: Consultancy, Research Funding; Trillium Therapeutics: Research Funding.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.294
Threshold uncertainty score0.858

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0010.000
Scholarly communication0.0000.001
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.015
GPT teacher head0.220
Teacher spread0.206 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations17
Published2017
Admission routes1
Has abstractyes

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