← Back to all signals
RESEARCH PAPER ANALYSIS

Targeting the intracellular immune checkpoint CISH with CRISPR-Cas9-edited T cells in patients with metastatic colorectal cancer: a first-in-human, single-centre, phase 1 trial.

AI interpretation is pending for this paper.

Open original publication →
PMID40315882
JournalThe Lancet. Oncology
Publication Date2025-04-29
Ingested2026-08-02 12:04 AM
EXECUTIVE SUMMARY

What the AI sees

Not AI summarized yet.

WHY IT MATTERS

Research significance

Pending deeper interpretation.

ABSTRACT

Source abstract

BACKGROUND: Over the past decade, immunotherapeutic strategies-mainly targeting the PD-1-PD-L1 immune checkpoint axis-have altered cancer treatment for many solid tumours, but few patients with gastrointestinal forms of cancer have benefited to date. There remains an urgent need to extend immunotherapy efficacy to more patients while addressing resistance to current immune checkpoint inhibitors. The aim of this study was to determine the safety and anti-tumour activity of knockout of CISH, which encodes cytokine-inducible SH2-containing protein, a novel intracellular immune checkpoint target and a founding member of the SOCS family of E3-ligases, using tumour infiltrating lymphocyte (TILs) genetically edited with CRISPR-Cas9 in patients with metastatic gastrointestinal epithelial cancers. METHODS: For this first-in-human, single-centre, phase 1 trial, patients aged 18-70 years with a diagnosis of metastatic gastrointestinal epithelial cancer with progressive disease following at least one first line standard therapy, measurable disease with at least one lesion identified as resectable for TIL generation and at least one other lesion meeting RECIST criteria as measurable to serve as an indicator of disease response, and an ECOG performance status of 0 or 1 were screened and enrolled if meeting these and all other eligibility criteria. TILs procured from tumour biopsies were expanded on the basis of neoantigen reactivity, subjected to CRISPR-Cas9-mediated CISH knockout, and infused intravenously into 12 patients after non-myeloablative lymphocyte depleting chemotherapy (cyclophosphamide 60 mg/kg per dose on study days -6 and -5, and fludarabine 25 mg/m2 per dose on days -7 to -3) followed by high-dose IL-2 (aldesleukin; 720 000 IU/kg per dose). The primary endpoint was safety of administration of neoantigen-reactive TILs with knockout of the CISH gene, and a key secondary endpoint was anti-tumour activity measured as objective radiographic response and progression-free and overall survival. This study is registered with ClinicalTrials.gov, NCT04426669, and is complete. FINDINGS: Between May 12, 2020, and Sept 16, 2022, 22 participants were enrolled in the trial (one patient was enrolled twice owing to lack of TIL outgrowth on the first attempt); ten patients were female, and 11 were male (self-defined). One patient was Asian, the remainder were White (self-defined). We successfully manufactured CISH knockout TIL products for 19 (86%) of the patients, of whom 12 (63%) received autologous CISH knockout TIL infusion. The median follow-up time for the study was 129 days (IQR 15-283). All 12 (100%) patients had treatment-related severe adverse events. The most common grade 3-4 adverse events included haematological events (12 patients [100%]) attributable to the preparative lymphodepleting chemotherapy regimen or expected effects of IL-2, fatigue (four patients [33%]), and anorexia (three patients [25%]). Deaths of any cause for patients on study were attributed to the underlying disease under study (metastatic gastrointestinal cancer) and related complications (10 patients) or infection (grade 5 septicaemia in one patient). There were no severe (≥grade 3) cytokine release or neurotoxicity events. Six (50%) of 12 patients had stable disease by day 28, and four (33%) had stable disease ongoing at 56 days. One young adult patient with microsatellite-instability-high colorectal cancer refractory to anti-PD1/CTLA-4 therapies had a complete and ongoing response (>21 months). INTERPRETATION: These results support the safety and potential antitumour activity of inhibiting the immune checkpoint CISH through the administration of neoantigen-reactive CISH-knockout TILs, with implications for patients with advanced metastatic cancers refractory to checkpoint inhibitor immunotherapies, and provide the first evidence that a novel intracellular checkpoint can be targeted with therapeutic effect. FUNDING: Intima Bioscience.

SUPPORTING PAPER SET

32 more papers to review

Ranked by current scoring engine
1 Maternal smoking and risk of childhood cancer: a report from the Childhood Cancer and Leukemia International Consortium. International journal of epidemiology 64.0 2 Profile of Invasive Fungal Infections in a Paediatric Haemato-Oncology Unit: A Five-Year Retrospective Cohort Study From a Tertiary Care Centre in South India. Cureus 70.8 3 Prevalence and risk factors of persistent and neuropathic pain following resection of pediatric extremity soft tissue sarcomas: A nationwide cohort study. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology 69.4 4 Neonatal airway emergency: congenital laryngeal myxoma. Journal of surgical case reports 47.9 5 Burkitt Lymphoma Presenting as Renal Failure: Learning From Diagnostic Pitfalls in Pediatrics. Clinical case reports 51.5 6 Reference frame for Adult Brainstem gliomas. The oncologist 68.2 7 Pharmacogenomics of cancer therapy-related cardiomyopathy in childhood cancer survivors. Pharmacogenomics 68.44 8 HPV Vaccination Uptake Among Children Attending Polish Primary Schools and Parental Factors Influencing Vaccination: A Cross-sectional Study. Journal of community health 59.0 9 Social Media and HPV Vaccine Hesitancy: How Misinformation Affects Latino Parents. Journal of community health 63.2 10 Overcoming Primary Graft Failure in Pediatric Allogeneic HSCT: Insights from Ten Centers of the Spanish Group for Hematopoietic Transplantation and Cellular Therapy (GETH-TC). Transplantation and cellular therapy 61.94 11 Beyond the Favorable-Risk Label: Sequential Measurable Residual Disease and KIT Variant Status in Pediatric Core-Binding Factor Acute Myeloid Leukemia. Annals of laboratory medicine 47.5 12 Incidence rates of non-Hodgkin lymphoma subtypes among Black Africans with and without HIV in South Africa: a national registry-based study. The Lancet regional health. Africa 67.9 13 Primary extranodal marginal zone lymphoma of gastric mucosa-associated lymphoid tissue in children: a case report and review of the literature. Journal of medical case reports 57.4 14 Neurofibromatosis Type 1: An Imaging Review of Multisystem Manifestations in Children. Journal of neuroimaging : official journal of the American Society of Neuroimaging 58.4 15 Reconstructive Strategies for Abdominal Wall Defects in Patients With Stomas: A Systematic Review of Mesh and Flap Techniques. Cureus 74.5 16 Landscape of cancer genomics and precision oncology in Japan, South Korea, China, and Australia. The Lancet regional health. Western Pacific 57.0 17 Deep learning segmentation of the cerebral ventricular system and brainstem for pediatric radiotherapy planning. Physics and imaging in radiation oncology 71.94 18 Real-world clinical outcomes and safety of anlotinib-containing regimens in pediatric solid tumors: a retrospective cohort study at a Chinese center. Frontiers in oncology 72.2 19 Regression of severe sclerotic chronic graft-versus-host disease after a second haploidentical hematopoietic stem cell transplantation: a case report. Frontiers in medicine 62.2 20 Editorial: Advances in the diagnosis and treatment of pediatric hematological disorders. Frontiers in pediatrics 50.74 21 Disability pension receipt five years after cancer diagnosis: a matched registry study of working-age cancer survivors in Norway. Frontiers in health services 64.0 22 Early discontinuation vs. continuation of empirical antibiotics in patients with cancer and febrile neutropenia: a systematic review and meta-analysis of randomized controlled trials. Frontiers in microbiology 82.0 23 Novel juxtamembrane FLT3 in-frame insertion in a child with refractory AML: a case report of durable remission following allogeneic HSCT and FLT3 inhibitor therapy. Frontiers in oncology 64.48 24 Case Report: Pallister-Hall syndrome diagnosed in adulthood during evaluation of recurrent hypoglycemia. Frontiers in endocrinology 49.0 25 Efficacy and safety of immunotherapy in pediatric malignant brain tumors: a systematic review and exploratory meta-analysis. Frontiers in oncology 84.42 26 Case Report: DICER1 mutation-associated anaplastic sarcoma of the kidney in a child. Frontiers in oncology 49.9 27 Epstein-Barr virus and hepatic failure: pathogenesis, clinical manifestations, and management. Frontiers in immunology 62.0 28 Fibrous hamartoma of infancy: a case report. Frontiers in pediatrics 49.9 29 ST6Gal2 promotes α2,6-sialylation and aggressive phenotypes in neuroblastoma cells. bioRxiv : the preprint server for biology 66.8 30 Prevalence and genotype distribution of human papillomavirus (HPV) among adolescent girls and young women in a high HIV burden rural area of South Africa: a cross-sectional survey. Research square 61.0 31 Language of Hope in Conversations between Pediatric Oncologists, Children with Advanced Cancer, and their Families. Research square 57.6 32 Fifteen-year surveillance of non-typhoidal Salmonella bloodstream infections in a tertiary care hospital in southern Türkiye. Journal of infection in developing countries 67.0
PATIENT-FRIENDLY SUMMARY

Targeting the intracellular immune checkpoint CISH with CRISPR-Cas9-edited T cells in patients with metastatic colorectal cancer: a first-in-human, single-centre, phase 1 trial.

For education only—not personal medical advice.

Before you continue

AI-assisted research information

Neurocompute uses AI to summarize scientific papers, interpret research signals, and suggest relevant reference links. AI-generated content can be incomplete, misleading, or wrong, and generated links may be irrelevant or unavailable.

Our reviewed outputs have performed strongly to date, but past accuracy is not a guarantee. Verify summaries, scores, claims, and links against the original publication before relying on them.

This platform is for research and education only. It does not provide medical advice, diagnosis, treatment recommendations, or clinical guidance.

Pediatric cancer research intelligence graphic
PEDIATRIC CANCER VISUAL SYSTEM

Open the Research Intelligence Map

Explore the active pediatric oncology analysis view.

Expand Intelligence View →
Full Pediatric cancer research intelligence graphic