Literature DB >> 30796151

Clinical Outcomes of Patients with Advanced Cancer and Pre-Existing Autoimmune Diseases Treated with Anti-Programmed Death-1 Immunotherapy: A Real-World Transverse Study.

Alessio Cortellini1,2, Sebastiano Buti3, Daniele Santini4, Fabiana Perrone3, Raffaele Giusti5, Marcello Tiseo3, Melissa Bersanelli3, Maria Michiara3, Antonino Grassadonia6, Davide Brocco7, Nicola Tinari6, Michele De Tursi6, Federica Zoratto8, Enzo Veltri8, Riccardo Marconcini9, Francesco Malorgio10, Carlo Garufi10, Marco Russano4, Cecilia Anesi4, Tea Zeppola4, Marco Filetti5, Paolo Marchetti5,11, Andrea Botticelli5, Gian Carlo Antonini Cappellini11, Federica De Galitiis11, Maria Giuseppa Vitale12, Roberto Sabbatini12, Sergio Bracarda13, Rossana Berardi14, Silvia Rinaldi14, Marianna Tudini15, Rosa Rita Silva15, Annagrazia Pireddu16, Francesco Atzori16, Rita Chiari17, Biagio Ricciuti17, Daniela Iacono18, Maria Rita Migliorino18, Antonio Rossi19, Giampiero Porzio20,2, Katia Cannita2, Valeria Ciciarelli21,2, Maria Concetta Fargnoli21,2, Paolo Antonio Ascierto22, Corrado Ficorella20,2.   

Abstract

BACKGROUND: Patients with a history of autoimmune diseases (AIDs) have not usually been included in clinical trials with immune checkpoint inhibitors.
MATERIALS AND METHODS: Consecutive patients with advanced cancer, treated with anti-programmed death-1 (PD-1) agents, were evaluated according to the presence of pre-existing AIDs. The incidence of immune-related adverse events (irAEs) and clinical outcomes were compared among subgroups.
RESULTS: A total of 751 patients were enrolled; median age was 69 years. Primary tumors were as follows: non-small cell lung cancer, 492 (65.5%); melanoma, 159 (21.2%); kidney cancer, 94 (12.5%); and others, 6 (0.8%). Male/female ratio was 499/252. Eighty-five patients (11.3%) had pre-existing AIDs, further differentiated in clinically active (17.6%) and inactive (82.4%). Among patients with pre-existing AIDs, incidence of irAEs of any grade was significantly higher when compared with patients without AIDs (65.9% vs. 39.9%). At multivariate analysis, both inactive (p = .0005) and active pre-existing AIDs (p = .0162), female sex (p = .0004), and Eastern Cooperative Oncology Group Performance Status <2 (p = .0030) were significantly related to a higher incidence of irAEs of any grade. No significant differences were observed regarding grade 3/4 irAEs and objective response rate among subgroups. Pre-existing AIDs were not significantly related with progression-free survival and overall survival.
CONCLUSION: This study quantifies the increased risk of developing irAEs in patients with pre-existing AIDs who had to be treated with anti-PD-1 immunotherapy. Nevertheless, the incidence of grade 3/4 irAEs is not significantly higher when compared with control population. The finding of a greater incidence of irAEs among female patients ranks among the "hot topics" in gender-related differences in immuno-oncology. IMPLICATIONS FOR PRACTICE: Patients with a history of autoimmune diseases (AIDs) have not usually been included in clinical trials with immune checkpoint inhibitors but are frequent in clinical practice. This study quantifies the increased risk of developing immune-related adverse events (irAEs) in patients with pre-existing AIDs who had to be treated with anti-programmed death-1 immunotherapy. Nevertheless, their toxicities are mild and the incidence of grade 3/4 irAEs is not significantly higher compared with those of controls. These results will help clinicians in everyday practice, improving their ability to offer a proper counselling to patients, in order to offer an immunotherapy treatment even to patients with pre-existing autoimmune disease. © AlphaMed Press 2019.

Entities:  

Keywords:  Anti‐programmed death‐1; Autoimmune disease; Immune checkpoint inhibitors; Immunotherapy; Performance status; Sex

Year:  2019        PMID: 30796151      PMCID: PMC6656514          DOI: 10.1634/theoncologist.2018-0618

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  26 in total

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Authors:  E A Eisenhauer; P Therasse; J Bogaerts; L H Schwartz; D Sargent; R Ford; J Dancey; S Arbuck; S Gwyther; M Mooney; L Rubinstein; L Shankar; L Dodd; R Kaplan; D Lacombe; J Verweij
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10.  Safety of Programmed Death-1 Pathway Inhibitors Among Patients With Non-Small-Cell Lung Cancer and Preexisting Autoimmune Disorders.

Authors:  Giulia C Leonardi; Justin F Gainor; Mehmet Altan; Sasha Kravets; Suzanne E Dahlberg; Lydia Gedmintas; Roxana Azimi; Hira Rizvi; Jonathan W Riess; Matthew D Hellmann; Mark M Awad
Journal:  J Clin Oncol       Date:  2018-05-10       Impact factor: 44.544

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  45 in total

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Review 8.  Evolving insights into the mechanisms of toxicity associated with immune checkpoint inhibitor therapy.

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