{
  "abstract": "Background\n\nImmune checkpoint inhibitors have reshaped the treatment of several cancers, producing durable responses in a subset of patients. However, most individuals either fail to respond or eventually develop resistance. Tumor immune escape results from heterogeneous and often overlapping mechanisms, including impaired antigen presentation, limited T-cell infiltration, co-expression of multiple inhibitory receptors, and suppressive tumor microenvironmental signals. These limitations have driven the development of combination strategies aimed at restoring more effective and sustained antitumor immunity.Main body\n\nAmong combination approaches, dual immune checkpoint blockade represents the most established strategy. The combination of CTLA-4 and PD-1 inhibitors targets complementary phases of the immune response: early T-cell priming in lymphoid organs and effector function within the tumor microenvironment. Long-term clinical data across melanoma, lung cancer, renal cell carcinoma, mesothelioma, and hepatocellular carcinoma support the ability of this approach to induce durable survival in a meaningful proportion of patients, albeit with increased immune-related toxicity. Building on this foundation, next-generation checkpoint combinations aim to counteract adaptive resistance and T-cell exhaustion. In particular, LAG-3, TIM-3, and TIGIT are frequently co-expressed with programmed death-1 on dysfunctional T cells. Emerging checkpoints such as VISTA, B7-H3, and BTLA further expand the landscape, particularly by modulating myeloid-driven suppression and advanced T-cell dysfunction. In parallel, bispecific antibodies integrating dual checkpoint targeting within a single molecule may enhance coordinated pathway inhibition and tumor localization.Conclusion\n\nImmune checkpoint-based combinations represent an evolving strategy of immune restoration. Future advances will depend on biologically informed trial design, dynamic biomarkers, and rational optimization of dose and sequencing to maximize durable benefit while maintaining acceptable toxicity.",
  "abstract_shown": true,
  "affiliations": [
    "Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, via Alvaro del Portillo 200, 00128, Rome, Italy.",
    "Research Unit of Medical Oncology, Department of Medicine and Surgery, Università Campus Bio-Medico di Roma, via Alvaro del Portillo 21, 00128, Rome, Italy.",
    "Department of Medical Oncology, U.O. Oncologia Medica 2, IRCCS Ospedale Policlinico San Martino, Genova, Italy.",
    "Department of Melanoma, Cancer Immunotherapy and Development Therapeutics - Istituto Nazionale Tumori IRCCS Fondazione \"G. Pascale\", Napoli, Italy.",
    "Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, via Alvaro del Portillo 200, 00128, Rome, Italy. alessiocortellini@gmail.com.",
    "Research Unit of Medical Oncology, Department of Medicine and Surgery, Università Campus Bio-Medico di Roma, via Alvaro del Portillo 21, 00128, Rome, Italy. alessiocortellini@gmail.com.",
    "Department of Surgery and Cancer, Hammersmith Hospital Campus, Imperial College London, London, UK. alessiocortellini@gmail.com.",
    "Department of Neuroscience, Reproductive and Dental Sciences, Università degli Studi di Napoli \"Federico II\", Napoli, Italy."
  ],
  "article_type": "review article",
  "arxiv": null,
  "author_total": 12,
  "authors": [
    {
      "affs": [
        0,
        1
      ],
      "name": "Alessandro Mazzocca"
    },
    {
      "affs": [
        1
      ],
      "name": "Silvia Calagna"
    },
    {
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        1
      ],
      "name": "Emanuele Claudio Mingo"
    },
    {
      "affs": [
        1
      ],
      "name": "Silvia Cavaliere"
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    {
      "affs": [
        1
      ],
      "name": "Michele Iuliani"
    },
    {
      "affs": [
        2
      ],
      "name": "Agostina Lagodin D'Amato"
    },
    {
      "affs": [
        3
      ],
      "name": "Luigi Scarpato"
    },
    {
      "affs": [
        0,
        1
      ],
      "name": "Francesco Pantano"
    },
    {
      "affs": [
        0,
        1
      ],
      "name": "Giuseppe Tonini"
    },
    {
      "affs": [
        1
      ],
      "name": "Bruno Vincenzi"
    },
    {
      "affs": [
        4,
        5,
        6
      ],
      "name": "Alessio Cortellini"
    },
    {
      "affs": [
        3,
        7
      ],
      "name": "Paolo Antonio Ascierto"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/a8jjj3t20m5a4.bib",
  "cited_by": 0,
  "doi": "10.1186/s12967-026-08701-1",
  "fulltext_url": "https://europepmc.org/articles/PMC13726305",
  "id": "a8jjj3t20m5a4",
  "issns": [
    "1479-5876"
  ],
  "landing_url": "https://europepmc.org/article/MED/42968166",
  "language": "eng",
  "licence": "CC-BY-NC-ND",
  "licence_label": "CC BY-NC-ND",
  "licence_source": "article",
  "licence_url": "https://creativecommons.org/licenses/by-nc-nd/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "heading",
      "Review"
    ],
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      "openalex",
      "2730|Cancer Immunotherapy and Biomarkers"
    ]
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  "openalex": "W7172302322",
  "pdf_url": "https://europepmc.org/articles/PMC13726305?pdf=render",
  "pmcid": "PMC13726305",
  "pmid": "42968166",
  "published": "2026-08-03",
  "publisher": "BMC",
  "ris": "https://research.draconitic.com/paper/a8jjj3t20m5a4.ris",
  "sources": [
    {
      "first_seen": "2026-11-03T15:20:54Z",
      "native_id": "MED:42968166",
      "source": "europepmc",
      "url": "https://europepmc.org/article/MED/42968166"
    },
    {
      "first_seen": "2026-11-05T12:22:41Z",
      "native_id": "PMC13726305",
      "source": "pmc",
      "url": "https://doi.org/10.1186/s12967-026-08701-1"
    }
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  "subjects": [
    {
      "field": "medicine",
      "origin": "openalex:2730|Cancer Immunotherapy and Biomarkers",
      "subfield": "oncology"
    }
  ],
  "title": "Checkpoint-checkpoint combinations in cancer: from mechanistic rationale to translational impact.",
  "title_text": "Checkpoint-checkpoint combinations in cancer: from mechanistic rationale to translational impact.",
  "type": "peer-reviewed",
  "updated_at": "2026-11-05T12:22:41Z",
  "url": "https://research.draconitic.com/paper/a8jjj3t20m5a4",
  "venue": "Journal of translational medicine",
  "versions": []
}