Evidence map›Paper›PMID 40562704›Full record

ArticleJournal for immunotherapy of cancer2025

SITC vision: Opportunities for deeper understanding of mechanisms of anti-tumor activity, toxicity, and resistance to optimize cancer immunotherapy.

Ryan J Sullivan, Anthony R Cillo, Robert L Ferris, Russell W Jenkins, Harriet M Kluger, Marleen Kok, Evan J Lipson, Luca Paruzzo, William L Redmond, Marco Ruella and 5 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. CD4Nature medicine · 2026
    Article
  7. Review
  8. Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Ryan J SullivanMass General Cancer Center, Krantz Family Center for Cancer Research, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA rsullivan7@mgh.harvard.edu charlie.garnett-benson@bms.com.ORCID http://orcid.org/0000-0001-5344-6645
Anthony R CilloUniversity of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID http://orcid.org/0000-0002-3213-3129
Robert L FerrisUNC Lineberger Comprehensive Cancer Center, UNC Health Care System, Chapel Hill, North Carolina, USA.ORCID http://orcid.org/0000-0001-6605-2071
Russell W JenkinsMass General Cancer Center, Krantz Family Center for Cancer Research, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Harriet M KlugerDepartment of Medicine (Medical Oncology), Yale University School of Medicine, New Haven, Connecticut, USA.ORCID http://orcid.org/0000-0002-4932-9873
Marleen KokDivision of Tumor Biology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Evan J LipsonMelanoma and Cancer Immunology Programs,The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID http://orcid.org/0000-0003-2976-0911
Luca ParuzzoDepartment of Medicine and Division of Hematology, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID http://orcid.org/0000-0002-6505-0194
William L RedmondEarle A Chiles Research Institute, Providence Cancer Institute, Portland, Oregon, USA.ORCID http://orcid.org/0000-0002-2572-1731
Marco RuellaDepartment of Medicine and Division of Hematology, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID http://orcid.org/0000-0003-4301-5811
Kurt A SchalperEarle A Chiles Research Institute, Providence Cancer Institute, Portland, Oregon, USA.ORCID http://orcid.org/0000-0001-5692-4833
Daniela S ThommenDivision of Molecular Oncology and Immunology, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-7431-2854
Keith TolleyPatient Advocate, District of Columbia, District of Columbia, USA.
Mark YarchoanDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopskins University School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Charlie Garnett-BensonBristol Myers Squibb, Princeton, New Jersey, USA rsullivan7@mgh.harvard.edu charlie.garnett-benson@bms.com.ORCID http://orcid.org/0000-0002-0238-3303

Funding

Project 3: Combinatorial and gene-editing approaches to enhance the efficacy of CAR T cell therapy of multiple myeloma.P01CA214278 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Joseph Anthony Fraietta · 2017 to 2026
$26.8M
MODULATION OF CD5 SIGNALING TO ENHANCE ADOPTIVE T-CELL THERAPIES FOR CANCERR37CA262362 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Marco Ruella · 2022 to 2026
$2.6M
Selective B Cell Depletion Using Engineered T Cells As A Curative Treatment For Acquired Thrombotic Thrombocytopenic PurpuraR01HL178849 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Vijay Bhoj, Marco Ruella · 2025 to 2026
$1.6M
FDA HHS R01 FD008168NCI NIH HHS P01 CA214278NCI NIH HHS R37 CA262362NHLBI NIH HHS R01 HL178849
6 · The paper itself

Abstract

Cancer immunotherapy has radically changed the management of several malignancies, and dozens of agents have been approved in the past 15 years. While these advances have changed the field, many challenges lie ahead and must be addressed if we are to optimize the management of cancer with these approaches. A more comprehensive understanding of the mechanisms of action, toxicity, and resistance is needed to guide the next decade of cancer immunotherapy development. To this end, members of the Society for Immunotherapy of Cancer met and identified challenges and opportunities to improve cancer immunotherapy by focusing on the mechanisms by which the specific agents work, the mechanisms of how they cause adverse effects, and the mechanisms of resistance that limit the effectiveness of these agents. The priorities of this effort were to (1) level set by describing the state of the field; (2) describe what is known about how these agents work, fail to work, and cause side effects as well as the key knowledge gaps in these areas and associated challenges for addressing them; (3) provide a patient perspective to highlight the importance of this work to the community most affected; (4) look ahead to the future by identifying and describing prioritized opportunities that the field may focus on to expand the knowledge base of the field and optimize the management of cancer with immunotherapy.

Indexed as

Drug Resistance, NeoplasmImmunotherapyNeoplasmsHumansAdoptive cell therapy - ACTBiomarkerEscape/evasionHematologic MalignanciesImmune Checkpoint Inhibitor

Identifiers

PMID40562704
PMCPMC12198810

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.