Immune-checkpoint inhibitor use in patients with cancer and pre-existing autoimmune diseases.


Journal

Nature reviews. Rheumatology
ISSN: 1759-4804
Titre abrégé: Nat Rev Rheumatol
Pays: United States
ID NLM: 101500080

Informations de publication

Date de publication:
11 2022
Historique:
accepted: 06 09 2022
pubmed: 6 10 2022
medline: 28 10 2022
entrez: 5 10 2022
Statut: ppublish

Résumé

Immune-checkpoint inhibitors (ICIs) have dramatically changed the management of advanced cancers. Designed to enhance the antitumour immune response, they can also cause off-target immune-related adverse events (irAEs), which are sometimes severe. Although the efficacy of ICIs suggests that they could have wide-ranging benefits, clinical trials of the drugs have so far excluded patients with pre-existing autoimmune disease. However, evidence is accumulating with regard to the use of ICIs in this 'at-risk' population, with retrospective data suggesting that they have an acceptable safety profile, but that there is a risk of disease flare or other irAE occurrence. The management of immunosuppressive drugs at ICI initiation in patients with autoimmune disease (or later in instances of disease flare or irAE) remains a question of particular interest in clinical practice, in which there is always a search for the balance between protecting against autoimmunity and ensuring a good tumour response. Although temporary use of immunosuppressants seems safe, prolonged use or use at ICI initiation might hamper the antitumour immune response, prompting clinicians to use the minimal efficient immunosuppressive regimen. However, a new paradigm is emerging, in which inhibitors of TNF or IL-6 could have synergistic effects with ICIs on tumour response, while also preventing severe irAEs. If confirmed, this 'decoupling' effect on toxicity and efficacy could change therapeutic practice in this field. Knowledge of the current use of ICIs in patients with pre-existing autoimmune disease, particularly with regard to the use of immunosuppressive drugs and/or biologic DMARDs, can help to guide clinical practice.

Identifiants

pubmed: 36198831
doi: 10.1038/s41584-022-00841-0
pii: 10.1038/s41584-022-00841-0
doi:

Substances chimiques

Antirheumatic Agents 0
Biological Products 0
Immune Checkpoint Inhibitors 0
Immunosuppressive Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

641-656

Informations de copyright

© 2022. Springer Nature Limited.

Références

Postow, M. A., Sidlow, R. & Hellmann, M. D. Immune-related adverse events associated with immune checkpoint blockade. N. Engl. J. Med. 378, 158–168 (2018).
pubmed: 29320654 doi: 10.1056/NEJMra1703481
Manson, G. et al. Worsening and newly diagnosed paraneoplastic syndromes following anti-PD-1 or anti-PD-L1 immunotherapies, a descriptive study. J. Immunother. Cancer 7, 337 (2019).
pubmed: 31796119 pmcid: 6892018 doi: 10.1186/s40425-019-0821-8
Abdel-Wahab, N., Shah, M., Lopez-Olivo, M. A. & Suarez-Almazor, M. E. Use of immune checkpoint inhibitors in the treatment of patients with cancer and preexisting autoimmune disease: a systematic review. Ann. Intern. Med. 168, 121–130 (2018).
pubmed: 29297009 doi: 10.7326/M17-2073
Ridker, P. M. et al. Effect of interleukin-1β inhibition with canakinumab on incident lung cancer in patients with atherosclerosis: exploratory results from a randomised, double-blind, placebo-controlled trial. Lancet 390, 1833–1842 (2017).
pubmed: 28855077 doi: 10.1016/S0140-6736(17)32247-X
Nocturne, G. & Mariette, X. B cells in the pathogenesis of primary Sjögren syndrome. Nat. Rev. Rheumatol. 14, 133–145 (2018).
pubmed: 29416129 doi: 10.1038/nrrheum.2018.1
Franks, A. L. & Slansky, J. E. Multiple associations between a broad spectrum of autoimmune diseases, chronic inflammatory diseases and cancer. Anticancer. Res. 32, 1119–1136 (2012).
pubmed: 22493341 pmcid: 3349285
Askling, J. et al. Haematopoietic malignancies in rheumatoid arthritis: lymphoma risk and characteristics after exposure to tumour necrosis factor antagonists. Ann. Rheum. Dis. 64, 1414–1420 (2005).
pubmed: 15843454 pmcid: 1755232 doi: 10.1136/ard.2004.033241
Dreyer, L. et al. Incidences of overall and site specific cancers in TNFα inhibitor treated patients with rheumatoid arthritis and other arthritides — a follow-up study from the DANBIO Registry. Ann. Rheum. Dis. 72, 79–82 (2013).
pubmed: 22945500 doi: 10.1136/annrheumdis-2012-201969
Mercer, L. K. et al. Risk of lymphoma in patients exposed to antitumour necrosis factor therapy: results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Ann. Rheum. Dis. 76, 497–503 (2017).
pubmed: 27502891 doi: 10.1136/annrheumdis-2016-209389
Mercer, L. K. et al. Risk of solid cancer in patients exposed to anti-tumour necrosis factor therapy: results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Ann. Rheum. Dis. 74, 1087–1093 (2015).
pubmed: 24685910 doi: 10.1136/annrheumdis-2013-204851
Seror, R. & Mariette, X. Malignancy and the risks of biologic therapies: current status. Rheum. Dis. Clin. North. Am. 43, 43–64 (2017).
pubmed: 27890173 doi: 10.1016/j.rdc.2016.09.006
Mariette, X. et al. Malignancies associated with tumour necrosis factor inhibitors in registries and prospective observational studies: a systematic review and meta-analysis. Ann. Rheum. Dis. 70, 1895–1904 (2011).
pubmed: 21885875 doi: 10.1136/ard.2010.149419
De Cock, D. & Hyrich, K. Malignancy and rheumatoid arthritis: epidemiology, risk factors and management. Best. Pract. Res. Clin. Rheumatol. 32, 869–886 (2018).
pubmed: 31427060 doi: 10.1016/j.berh.2019.03.011
Lopez-Olivo, M. A. et al. Risk of malignancies in patients with rheumatoid arthritis treated with biologic therapy: a meta-analysis. JAMA 308, 898–908 (2012).
pubmed: 22948700 doi: 10.1001/2012.jama.10857
Ytterberg, S. R. et al. Cardiovascular and cancer risk with tofacitinib in rheumatoid arthritis. N. Engl. J. Med. 386, 316–326 (2022).
pubmed: 35081280 doi: 10.1056/NEJMoa2109927
Manger, B. & Schett, G. Rheumatic paraneoplastic syndromes — a clinical link between malignancy and autoimmunity. Clin. Immunol. 186, 67–70 (2018).
pubmed: 28736272 doi: 10.1016/j.clim.2017.07.021
Moinzadeh, P. et al. Association of anti-RNA polymerase III autoantibodies and cancer in scleroderma. Arthritis Res. Ther. 16, R53 (2014).
pubmed: 24524733 pmcid: 3978927 doi: 10.1186/ar4486
Joseph, C. G. et al. Association of the autoimmune disease scleroderma with an immunologic response to cancer. Science 343, 152–157 (2014).
pubmed: 24310608 doi: 10.1126/science.1246886
Yadav, S. et al. Autoantibodies as diagnostic and prognostic cancer biomarker: detection techniques and approaches. Biosens. Bioelectron. 139, 111315 (2019).
pubmed: 31132724 doi: 10.1016/j.bios.2019.111315
Gajewski, T. F., Fuertes, M., Spaapen, R., Zheng, Y. & Kline, J. Molecular profiling to identify relevant immune resistance mechanisms in the tumor microenvironment. Curr. Opin. Immunol. 23, 286–292 (2011).
pubmed: 21185705 doi: 10.1016/j.coi.2010.11.013
Tivol, E. A. et al. Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity 3, 541–547 (1995).
pubmed: 7584144 doi: 10.1016/1074-7613(95)90125-6
Matsumura, N., Ohtsuka, M., Kikuchi, N. & Yamamoto, T. Exacerbation of psoriasis during nivolumab therapy for metastatic melanoma. Acta Derm. Venereol. 96, 259–260 (2016).
pubmed: 26270860 doi: 10.2340/00015555-2212
Huang, C. et al. Immune checkpoint molecules. Possible future therapeutic implications in autoimmune diseases. J. Autoimmun. 104, 102333 (2019).
pubmed: 31564474 doi: 10.1016/j.jaut.2019.102333
Doroshow, D. B. et al. PD-L1 as a biomarker of response to immune-checkpoint inhibitors. Nat. Rev. Clin. Oncol. 18, 345–362 (2021).
pubmed: 33580222 doi: 10.1038/s41571-021-00473-5
Tawbi, H. A. et al. Relatlimab and nivolumab versus nivolumab in untreated advanced melanoma. N. Engl. J. Med. 386, 24–34 (2022).
pubmed: 34986285 doi: 10.1056/NEJMoa2109970
Hodi, F. S. et al. Improved survival with ipilimumab in patients with metastatic melanoma. N. Engl. J. Med. 363, 711–723 (2010).
pubmed: 20525992 pmcid: 3549297 doi: 10.1056/NEJMoa1003466
Pardoll, D. M. The blockade of immune checkpoints in cancer immunotherapy. Nat. Rev. Cancer 12, 252–264 (2012).
pubmed: 22437870 pmcid: 4856023 doi: 10.1038/nrc3239
Hirsch, L., Zitvogel, L., Eggermont, A. & Marabelle, A. PD-Loma: a cancer entity with a shared sensitivity to the PD-1/PD-L1 pathway blockade. Br. J. Cancer 120, 3–5 (2019).
pubmed: 30413824 doi: 10.1038/s41416-018-0294-4
Wolchok, J. D. et al. Long-term outcomes with nivolumab plus ipilimumab or nivolumab alone versus ipilimumab in patients with advanced melanoma. J. Clin. Oncol. 40, 127–137 (2022).
pubmed: 34818112 doi: 10.1200/JCO.21.02229
Weber, J. S. et al. Safety profile of nivolumab monotherapy: a pooled analysis of patients with advanced melanoma. J. Clin. Oncol. 35, 785–792 (2017).
pubmed: 28068177 doi: 10.1200/JCO.2015.66.1389
Yoest, J. M. Clinical features, predictive correlates, and pathophysiology of immune-related adverse events in immune checkpoint inhibitor treatments in cancer: a short review. Immunotargets Ther. 6, 73–82 (2017).
pubmed: 29067284 pmcid: 5644546 doi: 10.2147/ITT.S126227
Hu, W., Wang, G., Wang, Y., Riese, M. J. & You, M. Uncoupling therapeutic efficacy from immune-related adverse events in immune checkpoint blockade. iScience 23, 101580 (2020).
pubmed: 33083746 pmcid: 7554032 doi: 10.1016/j.isci.2020.101580
Abdel-Wahab, N., Shah, M. & Suarez-Almazor, M. E. Adverse events associated with immune checkpoint blockade in patients with cancer: a systematic review of case reports. PLoS One 11, e0160221 (2016).
pubmed: 27472273 pmcid: 4966895 doi: 10.1371/journal.pone.0160221
Belkhir, R. et al. Rheumatoid arthritis and polymyalgia rheumatica occurring after immune checkpoint inhibitor treatment. Ann. Rheum. Dis. 76, 1747–1750 (2017).
pubmed: 28600350 doi: 10.1136/annrheumdis-2017-211216
Michot, J. M. et al. Immune-related adverse events with immune checkpoint blockade: a comprehensive review. Eur. J. Cancer 54, 139–148 (2016).
pubmed: 26765102 doi: 10.1016/j.ejca.2015.11.016
Horvat, T. Z. et al. Immune-related adverse events, need for systemic immunosuppression, and effects on survival and time to treatment failure in patients with melanoma treated with ipilimumab at Memorial Sloan Kettering Cancer Center. J. Clin. Oncol. 33, 3193–3198 (2015).
pubmed: 26282644 pmcid: 5087335 doi: 10.1200/JCO.2015.60.8448
Warner, B. M. et al. Sicca syndrome associated with immune checkpoint inhibitor therapy. Oncologist 24, 1259–1269 (2019).
pubmed: 30996010 pmcid: 6738284 doi: 10.1634/theoncologist.2018-0823
Carbonnel, F. et al. Inflammatory bowel disease and cancer response due to anti-CTLA-4: is it in the flora? Semin. Immunopathol. 39, 327–331 (2017).
pubmed: 28093620 doi: 10.1007/s00281-016-0613-x
Calabrese, L. H., Calabrese, C. & Cappelli, L. C. Rheumatic immune-related adverse events from cancer immunotherapy. Nat. Rev. Rheumatol. 14, 569–579 (2018).
pubmed: 30171203 doi: 10.1038/s41584-018-0074-9
Brahmer, J. R. et al. Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immune checkpoint inhibitor-related adverse events. J. Immunother. Cancer 9, e002435 (2021).
pubmed: 34172516 pmcid: 8237720 doi: 10.1136/jitc-2021-002435
Jing, Y. et al. Multi-omics prediction of immune-related adverse events during checkpoint immunotherapy. Nat. Commun. 11, 4946 (2020).
pubmed: 33009409 pmcid: 7532211 doi: 10.1038/s41467-020-18742-9
Robert, C. et al. Nivolumab in previously untreated melanoma without BRAF mutation. N. Engl. J. Med. 372, 320–330 (2015).
pubmed: 25399552 doi: 10.1056/NEJMoa1412082
Ribas, A. et al. Pembrolizumab versus investigator-choice chemotherapy for ipilimumab-refractory melanoma (KEYNOTE-002): a randomised, controlled, phase 2 trial. Lancet Oncol. 16, 908–918 (2015).
pubmed: 26115796 pmcid: 9004487 doi: 10.1016/S1470-2045(15)00083-2
Reck, M. et al. Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer. N. Engl. J. Med. 375, 1823–1833 (2016).
pubmed: 27718847 doi: 10.1056/NEJMoa1606774
Brahmer, J. et al. Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer. N. Engl. J. Med. 373, 123–135 (2015).
pubmed: 26028407 pmcid: 4681400 doi: 10.1056/NEJMoa1504627
Borghaei, H. et al. Nivolumab versus docetaxel in advanced nonsquamous non-small-cell lung cancer. N. Engl. J. Med. 373, 1627–1639 (2015).
pubmed: 26412456 pmcid: 5705936 doi: 10.1056/NEJMoa1507643
Subudhi, S. K. et al. Clonal expansion of CD8 T cells in the systemic circulation precedes development of ipilimumab-induced toxicities. Proc. Natl Acad. Sci. USA 113, 11919–11924 (2016).
pubmed: 27698113 pmcid: 5081579 doi: 10.1073/pnas.1611421113
Oh, D. Y. et al. Immune toxicities elicited by CTLA-4 blockade in cancer patients are associated with early diversification of the T-cell repertoire. Cancer Res. 77, 1322–1330 (2017).
pubmed: 28031229 doi: 10.1158/0008-5472.CAN-16-2324
Lozano, A. X. et al. T cell characteristics associated with toxicity to immune checkpoint blockade in patients with melanoma. Nat. Med. https://doi.org/10.1038/s41591-021-01623-z (2022).
doi: 10.1038/s41591-021-01623-z pubmed: 35840727 pmcid: 8866214
Johnson, D. B. et al. Fulminant myocarditis with combination immune checkpoint blockade. N. Engl. J. Med. 375, 1749–1755 (2016).
pubmed: 27806233 pmcid: 5247797 doi: 10.1056/NEJMoa1609214
Berner, F. et al. Association of checkpoint inhibitor-induced toxic effects with shared cancer and tissue antigens in non-small cell lung cancer. JAMA Oncol. 5, 1043–1047 (2019).
pubmed: 31021392 doi: 10.1001/jamaoncol.2019.0402
Läubli, H. et al. The T cell repertoire in tumors overlaps with pulmonary inflammatory lesions in patients treated with checkpoint inhibitors. Oncoimmunology 7, e1386362 (2018).
pubmed: 29308309 doi: 10.1080/2162402X.2017.1386362
Kim, K. H. et al. Immune-related adverse events are clustered into distinct subtypes by T-cell profiling before and early after anti-PD-1 treatment. Oncoimmunology 9, 1722023 (2020).
pubmed: 32076579 pmcid: 6999841 doi: 10.1080/2162402X.2020.1722023
Grigoriou, M. et al. Regulatory T-cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors. Cancer Immunol. Res. 9, 726–734 (2021).
pubmed: 33820810 pmcid: 7611354 doi: 10.1158/2326-6066.CIR-20-0969
Gonugunta, A. S. et al. Humoral and cellular correlates of a novel immune-related adverse event and its treatment. J. Immunother. Cancer 9, e003585 (2021).
pubmed: 34880115 pmcid: 8655605 doi: 10.1136/jitc-2021-003585
Reschke, R. et al. Distinct immune signatures indicative of treatment response and immune-related adverse events in melanoma patients under immune checkpoint inhibitor therapy. Int. J. Mol. Sci. 22, 8017 (2021).
pubmed: 34360781 pmcid: 8348898 doi: 10.3390/ijms22158017
Kim, S. T. et al. Distinct molecular and immune hallmarks of inflammatory arthritis induced by immune checkpoint inhibitors for cancer therapy. Nat. Commun. 13, 1970 (2022).
pubmed: 35413951 pmcid: 9005525 doi: 10.1038/s41467-022-29539-3
Luoma, A. M. et al. Molecular pathways of colon inflammation induced by cancer immunotherapy. Cell 182, 655–671.e22 (2020).
pubmed: 32603654 pmcid: 7415717 doi: 10.1016/j.cell.2020.06.001
Wang, R. et al. High-dimensional analyses of checkpoint-inhibitor related arthritis synovial fluid cells reveal a unique, proliferating CD38hi cytotoxic CD8 T cell population induced by type I IFN [abstract]. Arthritis Rheumatol. 72 (Suppl. 10): abstract 1443 (2020).
Murray-Brown, W. et al. Nivolumab-induced synovitis is characterized by florid T cell infiltration and rapid resolution with synovial biopsy-guided therapy. J. Immunother. Cancer 8, e000281 (2020).
pubmed: 32571993 pmcid: 7311067 doi: 10.1136/jitc-2019-000281
Das, R. et al. Early B cell changes predict autoimmunity following combination immune checkpoint blockade. J. Clin. Invest. 128, 715–720 (2018).
pubmed: 29309048 pmcid: 5785243 doi: 10.1172/JCI96798
Patel, A. J. et al. Regulatory B cell repertoire defects predispose lung cancer patients to immune-related toxicity following checkpoint blockade. Nat. Commun. 13, 3148 (2022).
pubmed: 35672305 pmcid: 9174492 doi: 10.1038/s41467-022-30863-x
de Moel, E. C. et al. Autoantibody development under treatment with immune-checkpoint inhibitors. Cancer Immunol. Res. 7, 6–11 (2019).
pubmed: 30425107 doi: 10.1158/2326-6066.CIR-18-0245
Huang, Y.-T., Chen, Y.-P., Lin, W.-C., Su, W.-C. & Sun, Y.-T. Immune checkpoint inhibitor-induced myasthenia gravis. Front. Neurol. 11, 634 (2020).
pubmed: 32765397 pmcid: 7378376 doi: 10.3389/fneur.2020.00634
Kobayashi, T. et al. Patients with antithyroid antibodies are prone to develop destructive thyroiditis by nivolumab: a prospective study. J. Endocr. Soc. 2, 241–251 (2018).
pubmed: 29600292 pmcid: 5836529 doi: 10.1210/js.2017-00432
Mammen, A. L. et al. Pre-existing antiacetylcholine receptor autoantibodies and B cell lymphopaenia are associated with the development of myositis in patients with thymoma treated with avelumab, an immune checkpoint inhibitor targeting programmed death-ligand 1. Ann. Rheum. Dis. 78, 150–152 (2019).
pubmed: 30185415 doi: 10.1136/annrheumdis-2018-213777
Tarhini, A. A. et al. Baseline circulating IL-17 predicts toxicity while TGF-β1 and IL-10 are prognostic of relapse in ipilimumab neoadjuvant therapy of melanoma. J. Immunother. Cancer 3, 39 (2015).
pubmed: 26380086 pmcid: 4570556 doi: 10.1186/s40425-015-0081-1
Lim, S. Y. et al. Circulating cytokines predict immune-related toxicity in melanoma patients receiving anti-PD-1-based immunotherapy. Clin. Cancer Res. 25, 1557–1563 (2019).
pubmed: 30409824 doi: 10.1158/1078-0432.CCR-18-2795
Husain, B. et al. Inflammatory markers in autoimmunity induced by checkpoint inhibitors. J. Cancer Res. Clin. Oncol. 147, 1623–1630 (2021).
pubmed: 33837821 pmcid: 8076116 doi: 10.1007/s00432-021-03550-5
Wang, Y. N. et al. Elevated levels of IL-17A and IL-35 in plasma and bronchoalveolar lavage fluid are associated with checkpoint inhibitor pneumonitis in patients with non-small cell lung cancer. Oncol. Lett. 20, 611–622 (2020).
pubmed: 32565986 pmcid: 7285943 doi: 10.3892/ol.2020.11618
Khan, S. et al. Immune dysregulation in cancer patients developing immune-related adverse events. Br. J. Cancer 120, 63–68 (2019).
pubmed: 30377338 doi: 10.1038/s41416-018-0155-1
Iwama, S. et al. Pituitary expression of CTLA-4 mediates hypophysitis secondary to administration of CTLA-4 blocking antibody. Sci. Transl. Med. 6, 230ra45 (2014).
pubmed: 24695685 doi: 10.1126/scitranslmed.3008002
Cappelli, L. C., Dorak, M. T., Bettinotti, M. P., Bingham, C. O. & Shah, A. A. Association of HLA-DRB1 shared epitope alleles and immune checkpoint inhibitor-induced inflammatory arthritis. Rheumatology 58, 476–480 (2019).
pubmed: 30508191 doi: 10.1093/rheumatology/key358
Hasan Ali, O. et al. Human leukocyte antigen variation is associated with adverse events of checkpoint inhibitors. Eur. J. Cancer 107, 8–14 (2019).
pubmed: 30529903 doi: 10.1016/j.ejca.2018.11.009
Wölffer, M. et al. Biomarkers associated with immune-related adverse events under checkpoint inhibitors in metastatic melanoma. Cancers 14, 302 (2022).
pubmed: 35053465 pmcid: 8773840 doi: 10.3390/cancers14020302
Dubin, K. et al. Intestinal microbiome analyses identify melanoma patients at risk for checkpoint-blockade-induced colitis. Nat. Commun. 7, 10391 (2016).
pubmed: 26837003 pmcid: 4740747 doi: 10.1038/ncomms10391
Andrews, M. C. et al. Gut microbiota signatures are associated with toxicity to combined CTLA-4 and PD-1 blockade. Nat. Med. 27, 1432–1441 (2021).
pubmed: 34239137 doi: 10.1038/s41591-021-01406-6
Johnson, D. B. et al. Ipilimumab therapy in patients with advanced melanoma and preexisting autoimmune disorders. JAMA Oncol. 2, 234–240 (2016).
pubmed: 26633184 doi: 10.1001/jamaoncol.2015.4368
Lee, B. et al. The use of ipilimumab in patients with rheumatoid arthritis and metastatic melanoma. Ann. Oncol. 27, 1174–1177 (2016).
pubmed: 26861600 doi: 10.1093/annonc/mdw056
Menzies, A. M. et al. Anti-PD-1 therapy in patients with advanced melanoma and preexisting autoimmune disorders or major toxicity with ipilimumab. Ann. Oncol. 28, 368–376 (2017).
pubmed: 27687304 doi: 10.1093/annonc/mdw443
Gutzmer, R. et al. Programmed cell death protein-1 (PD-1) inhibitor therapy in patients with advanced melanoma and preexisting autoimmunity or ipilimumab-triggered autoimmunity. Eur. J. Cancer 75, 24–32 (2017).
pubmed: 28214654 doi: 10.1016/j.ejca.2016.12.038
Danlos, F.-X. et al. Safety and efficacy of anti-programmed death 1 antibodies in patients with cancer and pre-existing autoimmune or inflammatory disease. Eur. J. Cancer 91, 21–29 (2018).
pubmed: 29331748 doi: 10.1016/j.ejca.2017.12.008
Mitchell, E. L. et al. Rheumatic immune-related adverse events secondary to anti-programmed death-1 antibodies and preliminary analysis on the impact of corticosteroids on anti-tumour response: a case series. Eur. J. Cancer 105, 88–102 (2018).
pubmed: 30439628 doi: 10.1016/j.ejca.2018.09.027
Richter, M. D. et al. Brief report: cancer immunotherapy in patients with preexisting rheumatic disease: the Mayo Clinic experience. Arthritis Rheumatol. 70, 356–360 (2018).
pubmed: 29363290 doi: 10.1002/art.40397
Leonardi, G. C. et al. Safety of programmed death-1 pathway inhibitors among patients with non-small-cell lung cancer and preexisting autoimmune disorders. J. Clin. Oncol. 36, 1905–1912 (2018).
pubmed: 29746230 pmcid: 6553840 doi: 10.1200/JCO.2017.77.0305
Kähler, K. C. et al. Ipilimumab in metastatic melanoma patients with pre-existing autoimmune disorders. Cancer Immunol. Immunother. 67, 825–834 (2018).
pubmed: 29487980 doi: 10.1007/s00262-018-2134-z
Cortellini, A. et al. Clinical outcomes of patients with advanced cancer and pre-existing autoimmune diseases treated with anti-programmed death-1 immunotherapy: a real-world transverse study. Oncologist 24, e327–e337 (2019).
pubmed: 30796151 pmcid: 6656514 doi: 10.1634/theoncologist.2018-0618
Tison, A. et al. Safety and efficacy of immune checkpoint inhibitors in patients with cancer and preexisting autoimmune disease: a nationwide, multicenter cohort study. Arthritis Rheumatol. 71, 2100–2111 (2019).
pubmed: 31379105 doi: 10.1002/art.41068
Martinez Chanza, N. et al. Safety and efficacy of immune checkpoint inhibitors in advanced urological cancers with pre-existing autoimmune disorders: a retrospective international multicenter study. J. Immunother. Cancer 8, e000538 (2020).
pubmed: 32217762 pmcid: 7174076 doi: 10.1136/jitc-2020-000538
Abu-Sbeih, H. et al. Immune checkpoint inhibitor therapy in patients with preexisting inflammatory bowel disease. J. Clin. Oncol. 38, 576–583 (2020).
pubmed: 31800340 doi: 10.1200/JCO.19.01674
Loriot, Y. et al. Safety and efficacy of atezolizumab in patients with autoimmune disease: subgroup analysis of the SAUL study in locally advanced/metastatic urinary tract carcinoma. Eur. J. Cancer 138, 202–211 (2020).
pubmed: 32905959 doi: 10.1016/j.ejca.2020.07.023
Efuni, E. et al. Risk of toxicity after initiating immune checkpoint inhibitor treatment in patients with rheumatoid arthritis. J. Clin. Rheumatol. 27, 267–271 (2021).
pubmed: 31977647 pmcid: 7374048 doi: 10.1097/RHU.0000000000001314
Hoa, S. et al. Preexisting autoimmune disease and immune-related adverse events associated with anti-PD-1 cancer immunotherapy: a national case series from the Canadian Research Group of Rheumatology in Immuno-Oncology. Cancer Immunol. Immunother. 70, 2197–2207 (2021).
pubmed: 33471137 doi: 10.1007/s00262-021-02851-5
Tully, K. H. et al. Risk of immune-related adverse events in melanoma patients with preexisting autoimmune disease treated with immune checkpoint inhibitors: a population-based study using SEER-medicare data. Am. J. Clin. Oncol. 44, 413–418 (2021).
pubmed: 34081033 doi: 10.1097/COC.0000000000000840
van der Kooij, M. K. et al. Safety and efficacy of checkpoint inhibition in patients with melanoma and preexisting autoimmune disease: a cohort study. Ann. Intern. Med. 174, 641–648 (2021).
pubmed: 33587686 doi: 10.7326/M20-3419
Bhatlapenumarthi, V., Patwari, A. & Harb, A. J. Immune-related adverse events and immune checkpoint inhibitor tolerance on rechallenge in patients with irAEs: a single-center experience. J. Cancer Res. Clin. Oncol. 147, 2789–2800 (2021).
pubmed: 33774736 doi: 10.1007/s00432-021-03610-w
Yeung, C. et al. Safety and clinical outcomes of immune checkpoint inhibitors in patients with cancer and preexisting autoimmune diseases. J. Immunother. 44, 362–370 (2021).
pubmed: 34121061 doi: 10.1097/CJI.0000000000000377
Panhaleux, M. et al. Anti-programmed death ligand 1 immunotherapies in cancer patients with pre-existing systemic sclerosis: a postmarketed phase IV safety assessment study. Eur. J. Cancer 160, 134–139 (2022).
pubmed: 34810048 doi: 10.1016/j.ejca.2021.10.018
Ansel, S., Rulach, R., Trotter, N. & Steele, N. Pembrolizumab for advanced non-small cell lung cancer (NSCLC): impact of autoimmune comorbidity and outcomes following treatment completion. J. Oncol. Pharm. Pract. https://doi.org/10.1177/10781552221079356 (2022).
doi: 10.1177/10781552221079356 pubmed: 35167399
Gulati, N. et al. Preexisting immune-mediated inflammatory disease is associated with improved survival and increased toxicity in melanoma patients who receive immune checkpoint inhibitors. Cancer Med. 10, 7457–7465 (2021).
pubmed: 34647433 pmcid: 8559502 doi: 10.1002/cam4.4239
Brown, L. J. et al. Combination anti-PD1 and ipilimumab therapy in patients with advanced melanoma and pre-existing autoimmune disorders. J. Immunother. Cancer 9, e002121 (2021).
pubmed: 33963010 pmcid: 8108669 doi: 10.1136/jitc-2020-002121
Wu, C., Zhong, L., Wu, Q., Lin, S. & Xie, X. The safety and efficacy of immune-checkpoint inhibitors in patients with cancer and pre-existing autoimmune diseases. Immunotherapy 13, 527–539 (2021).
pubmed: 33715386 doi: 10.2217/imt-2020-0230
Kostine, M. et al. EULAR points to consider for the diagnosis and management of rheumatic immune-related adverse events due to cancer immunotherapy with checkpoint inhibitors. Ann. Rheum. Dis. 80, 36–48 (2021).
pubmed: 32327425 doi: 10.1136/annrheumdis-2020-217139
Klavdianou, K., Melissaropoulos, K., Filippopoulou, A. & Daoussis, D. Should we be afraid of immune check point inhibitors in cancer patients with pre-existing rheumatic diseases? Immunotherapy in pre-existing rheumatic diseases. Mediterr. J. Rheumatol. 32, 218–226 (2021).
pubmed: 34964025 pmcid: 8693295 doi: 10.31138/mjr.32.3.218
Nishino, M., Giobbie-Hurder, A., Hatabu, H., Ramaiya, N. H. & Hodi, F. S. Incidence of programmed cell death 1 inhibitor-related pneumonitis in patients with advanced cancer: a systematic review and meta-analysis. JAMA Oncol. 2, 1607–1616 (2016).
pubmed: 27540850 doi: 10.1001/jamaoncol.2016.2453
Jaberg-Bentele, N. F., Kunz, M., Abuhammad, S. & Dummer, R. Flare-up of rheumatoid arthritis by anti-CTLA-4 antibody but not by anti-PD1 therapy in a patient with metastatic melanoma. Case Rep. Dermatol. 9, 65–68 (2017).
pubmed: 28611624 pmcid: 5465736 doi: 10.1159/000454875
Benson, Z., Gordon, S., Nicolato, P. & Poklepovic, A. Immunotherapy for metastatic melanoma with right atrial involvement in a patient with rheumatoid arthritis. Case Rep. Oncol. Med. 2017, 8095601 (2017).
pubmed: 29445556 pmcid: 5763099
Thomas, R., Patel, H. & Scott, J. Dermatomyositis flare with immune checkpoint inhibitor therapy for melanoma. Cureus 13, e14387 (2021).
pubmed: 33981507 pmcid: 8106943
Montfort, A. et al. Combining nivolumab and ipilimumab with infliximab or certolizumab in patients with advanced melanoma: first results of a phase Ib clinical trial. Clin. Cancer Res. 27, 1037–1047 (2021).
pubmed: 33272982 doi: 10.1158/1078-0432.CCR-20-3449
Ghosh, N. et al. Lower baseline autoantibody levels are associated with immune-related adverse events from immune checkpoint inhibition. J. Immunother. Cancer 10, e004008 (2022).
pubmed: 35091456 pmcid: 8804686 doi: 10.1136/jitc-2021-004008
Sakakida, T. et al. Safety and efficacy of PD-1/PD-L1 blockade in patients with preexisting antinuclear antibodies. Clin. Transl. Oncol. 22, 919–927 (2020).
pubmed: 31576495 doi: 10.1007/s12094-019-02214-8
Toi, Y. et al. Profiling preexisting antibodies in patients treated with anti-PD-1 therapy for advanced non-small cell lung cancer. JAMA Oncol. 5, 376–383 (2019).
pubmed: 30589930 doi: 10.1001/jamaoncol.2018.5860
Wang, D. et al. Immune-related adverse events predict the efficacy of immune checkpoint inhibitors in lung cancer patients: a meta-analysis. Front. Oncol. 11, 631949 (2021).
pubmed: 33732650 pmcid: 7958877 doi: 10.3389/fonc.2021.631949
Hussaini, S. et al. Association between immune-related side effects and efficacy and benefit of immune checkpoint inhibitors — a systematic review and meta-analysis. Cancer Treat. Rev. 92, 102134 (2021).
pubmed: 33302134 doi: 10.1016/j.ctrv.2020.102134
Teulings, H.-E. et al. Vitiligo-like depigmentation in patients with stage III–IV melanoma receiving immunotherapy and its association with survival: a systematic review and meta-analysis. J. Clin. Oncol. 33, 773–781 (2015).
pubmed: 25605840 doi: 10.1200/JCO.2014.57.4756
Yee, C. et al. Melanocyte destruction after antigen-specific immunotherapy of melanoma: direct evidence of T cell-mediated vitiligo. J. Exp. Med. 192, 1637–1644 (2000).
pubmed: 11104805 pmcid: 2193107 doi: 10.1084/jem.192.11.1637
Chapman, N. M. & Chi, H. Metabolic adaptation of lymphocytes in immunity and disease. Immunity 55, 14–30 (2022).
pubmed: 35021054 pmcid: 8842882 doi: 10.1016/j.immuni.2021.12.012
Arbour, K. C. et al. Impact of baseline steroids on efficacy of programmed cell death-1 and programmed death-ligand 1 blockade in patients with non-small-cell lung cancer. J. Clin. Oncol. 36, 2872–2878 (2018).
pubmed: 30125216 doi: 10.1200/JCO.2018.79.0006
Strehl, C. & Buttgereit, F. Optimized glucocorticoid therapy: teaching old drugs new tricks. Mol. Cell. Endocrinol. 380, 32–40 (2013).
pubmed: 23403055 doi: 10.1016/j.mce.2013.01.026
Fucà, G. et al. Modulation of peripheral blood immune cells by early use of steroids and its association with clinical outcomes in patients with metastatic non-small cell lung cancer treated with immune checkpoint inhibitors. ESMO Open 4, e000457 (2019).
pubmed: 30964126 pmcid: 6435242 doi: 10.1136/esmoopen-2018-000457
Draghi, A. et al. Differential effects of corticosteroids and anti-TNF on tumor-specific immune responses: implications for the management of irAEs. Int. J. Cancer 145, 1408–1413 (2019).
pubmed: 30575963 doi: 10.1002/ijc.32080
Brown, P. M., Pratt, A. G. & Isaacs, J. D. Mechanism of action of methotrexate in rheumatoid arthritis, and the search for biomarkers. Nat. Rev. Rheumatol. 12, 731–742 (2016).
pubmed: 27784891 doi: 10.1038/nrrheum.2016.175
Downey, S. G. et al. Prognostic factors related to clinical response in patients with metastatic melanoma treated by CTL-associated antigen-4 blockade. Clin. Cancer Res. 13, 6681–6688 (2007).
pubmed: 17982122 pmcid: 2147083 doi: 10.1158/1078-0432.CCR-07-0187
Schadendorf, D. et al. Efficacy and safety outcomes in patients with advanced melanoma who discontinued treatment with nivolumab and ipilimumab because of adverse events: a pooled analysis of randomized phase II and III trials. J. Clin. Oncol. 35, 3807–3814 (2017).
pubmed: 28841387 pmcid: 5791828 doi: 10.1200/JCO.2017.73.2289
Paz-Ares, L. G. et al. First-line nivolumab plus ipilimumab in advanced NSCLC: 4-year outcomes from the randomized, open-label, phase 3 CheckMate 227 Part 1 Trial. J. Thorac. Oncol. 17, 289–308 (2022).
pubmed: 34648948 doi: 10.1016/j.jtho.2021.09.010
Reck, M. et al. First-line nivolumab plus ipilimumab with two cycles of chemotherapy versus chemotherapy alone (four cycles) in advanced non-small-cell lung cancer: CheckMate 9LA 2-year update. ESMO Open 6, 100273 (2021).
pubmed: 34607285 pmcid: 8493593 doi: 10.1016/j.esmoop.2021.100273
Waterhouse, D. M. et al. Continuous versus 1-year fixed-duration nivolumab in previously treated advanced non-small-cell lung cancer: CheckMate 153. J. Clin. Oncol. 38, 3863–3873 (2020).
pubmed: 32910710 pmcid: 7676888 doi: 10.1200/JCO.20.00131
Bilger, G. et al. Discontinuation of immune checkpoint inhibitor (ICI) above 18 months of treatment in real-life patients with advanced non-small cell lung cancer (NSCLC): INTEPI, a multicentric retrospective study. Cancer Immunol. Immunother. https://doi.org/10.1007/s00262-021-03114-z (2021).
doi: 10.1007/s00262-021-03114-z pubmed: 34821950
Chatzidionysiou, K., Liapi, M., Tsakonas, G., Gunnarsson, I. & Catrina, A. Treatment of rheumatic immune-related adverse events due to cancer immunotherapy with immune checkpoint inhibitors — is it time for a paradigm shift? Clin. Rheumatol. 40, 1687–1695 (2021).
pubmed: 32989505 doi: 10.1007/s10067-020-05420-w
Chen, A. Y., Wolchok, J. D. & Bass, A. R. TNF in the era of immune checkpoint inhibitors: friend or foe? Nat. Rev. Rheumatol. 17, 213–223 (2021).
pubmed: 33686279 pmcid: 8366509 doi: 10.1038/s41584-021-00584-4
Bertrand, F. et al. TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma. Nat. Commun. 8, 2256 (2017).
pubmed: 29273790 pmcid: 5741628 doi: 10.1038/s41467-017-02358-7
Hailemichael, Y. et al. Interleukin-6 blockade abrogates immunotherapy toxicity and promotes tumor immunity. Cancer Cell 40, 509–523.e6 (2022).
pubmed: 35537412 doi: 10.1016/j.ccell.2022.04.004
Perez-Ruiz, E. et al. Prophylactic TNF blockade uncouples efficacy and toxicity in dual CTLA-4 and PD-1 immunotherapy. Nature 569, 428–432 (2019).
pubmed: 31043740 doi: 10.1038/s41586-019-1162-y
Lesage, C. et al. Incidence and clinical impact of anti-TNFα treatment of severe immune checkpoint inhibitor-induced colitis in advanced melanoma: the Mecolit Survey. J. Immunother. 42, 175–179 (2019).
pubmed: 31090656 doi: 10.1097/CJI.0000000000000268
Wang, Y. et al. Immune-checkpoint inhibitor-induced diarrhea and colitis in patients with advanced malignancies: retrospective review at MD Anderson. J. Immunother. Cancer 6, 37 (2018).
pubmed: 29747688 pmcid: 5946546 doi: 10.1186/s40425-018-0346-6
Verheijden, R. J. et al. Association of anti-TNF with decreased survival in steroid refractory ipilimumab and anti-PD1-treated patients in the Dutch Melanoma Treatment Registry. Clin. Cancer Res. 26, 2268–2274 (2020).
pubmed: 31988197 doi: 10.1158/1078-0432.CCR-19-3322
Zou, F. et al. Efficacy and safety of vedolizumab and infliximab treatment for immune-mediated diarrhea and colitis in patients with cancer: a two-center observational study. J. Immunother. Cancer 9, e003277 (2021).
pubmed: 34789551 pmcid: 8601082 doi: 10.1136/jitc-2021-003277
Laino, A. S. et al. Serum interleukin-6 and C-reactive protein are associated with survival in melanoma patients receiving immune checkpoint inhibition. J. Immunother. Cancer 8, e000842 (2020).
pubmed: 32581042 pmcid: 7312339 doi: 10.1136/jitc-2020-000842
Campochiaro, C. et al. Tocilizumab for the treatment of immune-related adverse events: a systematic literature review and a multicentre case series. Eur. J. Intern. Med. 93, 87–94 (2021).
pubmed: 34391591 doi: 10.1016/j.ejim.2021.07.016
Weber, J. S. et al. 1040 O Phase II trial of ipilimumab, nivolumab and tocilizumab for unresectable metastatic melanoma. Ann. Oncol. 32, S869 (2021).
doi: 10.1016/j.annonc.2021.08.1425
Lebbé, C. et al. Evaluation of two dosing regimens for nivolumab in combination with ipilimumab in patients with advanced melanoma: results from the phase IIIb/IV CheckMate 511 Trial. J. Clin. Oncol. 37, 867–875 (2019).
pubmed: 30811280 pmcid: 6455714 doi: 10.1200/JCO.18.01998
Delyon, J. & Lebbe, C. IL-6 blockade in cancer patients treated with immune checkpoint blockade: a win-win strategy. Cancer Cell 40, 450–451 (2022).
pubmed: 35537409 doi: 10.1016/j.ccell.2022.04.010
Haanen, J. B. A. G. et al. Management of toxicities from immunotherapy: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 29, iv264–iv266 (2018).
pubmed: 29917046 doi: 10.1093/annonc/mdy162
Thompson, J. A. et al. Management of immunotherapy-related toxicities, version 1.2019. J. Natl Compr. Canc. Netw. 17, 255–289 (2019).
pubmed: 30865922 doi: 10.6004/jnccn.2019.0013
Kennedy, L. C., Bhatia, S., Thompson, J. A. & Grivas, P. Preexisting autoimmune disease: implications for immune checkpoint inhibitor therapy in solid tumors. J. Natl Compr. Canc. Netw. 17, 750–757 (2019).
pubmed: 31200356 doi: 10.6004/jnccn.2019.7310
Schneider, B. J. et al. Management of immune-related adverse events in patients treated with immune checkpoint inhibitor therapy: ASCO guideline update. J. Clin. Oncol. 39, 4073–4126 (2021).
pubmed: 34724392 doi: 10.1200/JCO.21.01440
Haanen, J. et al. Autoimmune diseases and immune-checkpoint inhibitors for cancer therapy: review of the literature and personalized risk-based prevention strategy. Ann. Oncol. 31, 724–744 (2020).
pubmed: 32194150 doi: 10.1016/j.annonc.2020.03.285
Michot, J.-M. et al. The 2016–2019 ImmunoTOX assessment board report of collaborative management of immune-related adverse events, an observational clinical study. Eur. J. Cancer 130, 39–50 (2020).
pubmed: 32172197 doi: 10.1016/j.ejca.2020.02.010
Naidoo, J. et al. A multidisciplinary toxicity team for cancer immunotherapy-related adverse events. J. Natl Compr. Canc. Netw. 17, 712–720 (2019).
pubmed: 31200355 doi: 10.6004/jnccn.2018.7268
Calabrese, L. & Mariette, X. The evolving role of the rheumatologist in the management of immune-related adverse events (irAEs) caused by cancer immunotherapy. Ann. Rheum. Dis. 77, 162–164 (2018).
pubmed: 28928270 doi: 10.1136/annrheumdis-2017-212061
Nabel, C. S. et al. Anti-PD-1 immunotherapy-induced flare of a known underlying relapsing vasculitis mimicking recurrent cancer. Oncologist 24, 1013–1021 (2019).
pubmed: 31088979 pmcid: 6693726 doi: 10.1634/theoncologist.2018-0633
Yamada, T. et al. Non-small cell lung cancer treated by an anti-programmed cell death-1 antibody without a flare-up of preexisting granulomatosis with polyangiitis. Intern. Med. 58, 3129–3132 (2019).
pubmed: 31292396 pmcid: 6875450 doi: 10.2169/internalmedicine.3018-19
Maul, L. V., Weichenthal, M., Kähler, K. C. & Hauschild, A. Successful anti-PD-1 antibody treatment in a metastatic melanoma patient with known severe autoimmune disease. J. Immunother. 39, 188–190 (2016).
pubmed: 27023060 doi: 10.1097/CJI.0000000000000118

Auteurs

Alice Tison (A)

Department of Rheumatology, Brest University Hospital, Brest, France.
B Lymphocytes, Autoimmunity and Immunotherapies, UMR 1227, Brest, France.

Soizic Garaud (S)

B Lymphocytes, Autoimmunity and Immunotherapies, UMR 1227, Brest, France.

Laurent Chiche (L)

Department of Internal Medicine, Hôpital Européen, Marseille, France.

Divi Cornec (D)

Department of Rheumatology, Brest University Hospital, Brest, France.
B Lymphocytes, Autoimmunity and Immunotherapies, UMR 1227, Brest, France.

Marie Kostine (M)

Department of Rheumatology, Bordeaux University Hospital, Bordeaux, France. marie.kostine@chu-bordeaux.fr.
ImmunoConcEpt, CNRS, UMR 5164, University of Bordeaux, Bordeaux, France. marie.kostine@chu-bordeaux.fr.

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