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1000 Titel
  • Adverse Events as Potential Predictive Factors of Activity in Patients with Advanced HCC Treated with Atezolizumab Plus Bevacizumab
1000 Autor/in
  1. Persano, Mara |
  2. Rimini, Margherita |
  3. Tada, Toshifumi |
  4. Suda, Goki |
  5. Shimose, Shigeo |
  6. Kudo, Masatoshi |
  7. Rossari, Federico |
  8. Yoo, Changhoon |
  9. Cheon, Jaekyung |
  10. Finkelmeier, Fabian |
  11. Lim, Ho Yeong |
  12. Presa, José |
  13. Masi, Gianluca |
  14. Bergamo, Francesca |
  15. Amadeo, Elisabeth |
  16. Vitiello, Francesco |
  17. Kumada, Takashi |
  18. Sakamoto, Naoya |
  19. Iwamoto, Hideki |
  20. Aoki, Tomoko |
  21. Chon, Hong Jae |
  22. Himmelsbach, Vera |
  23. Iavarone, Massimo Alberto |
  24. Cabibbo, Giuseppe |
  25. Montes, Margarida |
  26. Foschi, Francesco Giuseppe |
  27. Vivaldi, Caterina |
  28. Soldà, Caterina |
  29. Sho, Takuya |
  30. Niizeki, Takashi |
  31. Nishida, Naoshi |
  32. Steup, Christoph |
  33. Bruccoleri, Mariangela |
  34. Hirooka, Masashi |
  35. Kariyama, Kazuya |
  36. Tani, Joji |
  37. Atsukawa, Masanori |
  38. Takaguchi, Koichi |
  39. Itobayashi, Ei |
  40. Fukunishi, Shinya |
  41. Tsuji, Kunihiko |
  42. Ishikawa, Toru |
  43. Tajiri, Kazuto |
  44. Ochi, Hironori |
  45. Yasuda, Satoshi |
  46. Toyoda, Hidenori |
  47. Ogawa, Chikara |
  48. Nishimura, Takashi |
  49. Hatanaka, Takeshi |
  50. Kakizaki, Satoru |
  51. Shimada, Noritomo |
  52. Kawata, Kazuhito |
  53. Hiraoka, Atsushi |
  54. Tada, Fujimasa |
  55. Ohama, Hideko |
  56. Nouso, Kazuhiro |
  57. Morishita, Asahiro |
  58. Tsutsui, Akemi |
  59. Nagano, Takuya |
  60. Itokawa, Norio |
  61. Okubo, Tomomi |
  62. Imai, Michitaka |
  63. Kosaka, Hisashi |
  64. Naganuma, Atsushi |
  65. Koizumi, Yohei |
  66. Nakamura, Shinichiro |
  67. Kaibori, Masaki |
  68. Iijima, Hiroko |
  69. Hiasa, Yoichi |
  70. Foti, Silvia |
  71. Camera, Silvia |
  72. Piscaglia, Fabio |
  73. Scartozzi, Mario |
  74. Cascinu, Stefano |
  75. Casadei-Gardini, Andrea |
1000 Verlag Springer International Publishing
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-04-30
1000 Erschienen in
1000 Quellenangabe
  • 19(4):645-659
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s11523-024-01061-0 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11230956/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!In the context of patients with hepatocellular carcinoma (HCC) treated with systemic therapy, the correlation between the appearance of adverse events (AEs) and reported efficacy outcomes is well-known and widely investigated. From other pathological settings, we are aware of the prognostic and predictive value of the occurrence of immune-related AEs in patients treated with immune-checkpoint inhibitors.!##!Objective!#!This retrospective multicenter real-world study aims to investigate the potential prognostic value of AEs in patients with HCC treated with atezolizumab plus bevacizumab in the first-line setting.!##!Patients and methods!#!The study population consisted of 823 patients from five countries (Italy, Germany, Portugal, Japan, and the Republic of Korea).!##!Results!#!Of the patients, 73.3% presented at least one AE during the study period. The most common AEs were proteinuria (29.6%), arterial hypertension (27.2%), and fatigue (26.0%). In all, 17.3% of the AEs were grade (G) 3. One death due to bleeding was reported. The multivariate analysis confirmed the appearance of decreased appetite G < 2 [versus G ≥ 2; hazard ratio (HR) 0.60; 95% confidence interval (CI) 0.13-0.90; p < 0.01] and immunotoxicity G < 2 (versus G ≥ 2; HR: 0.70; 95% CI 0.24-0.99; p = 0.04) as independent prognostic factors for overall survival, and the appearance of decreased appetite G < 2 (versus G ≥ 2; HR: 0.73; 95% CI 0.43-0.95; p = 0.01), diarrhea (yes versus no; HR: 0.57, 95% CI 0.38-0.85; p = 0.01), fatigue (yes versus no; HR: 0.82, 95% CI 0.65-0.95; p < 0.01), arterial hypertension G < 2 (versus G ≥ 2; HR: 0.68, 95% CI 0.52-0.87; p < 0.01), and proteinuria (yes versus no; HR: 0.79, 95% CI 0.64-0.98; p = 0.03) as independent prognostic factors for progression-free survival.!##!Conclusions!#!As demonstrated for other therapies, there is also a correlation between the occurrence of AEs and outcomes for patients with HCC for the combination of atezolizumab plus bevacizumab.
1000 Sacherschließung
lokal Female [MeSH]
lokal Aged, 80 and over [MeSH]
lokal Aged [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Carcinoma, Hepatocellular/pathology [MeSH]
lokal Bevacizumab/therapeutic use [MeSH]
lokal Retrospective Studies [MeSH]
lokal Middle Aged [MeSH]
lokal Carcinoma, Hepatocellular/drug therapy [MeSH]
lokal Antineoplastic Combined Chemotherapy Protocols/therapeutic use [MeSH]
lokal Liver Neoplasms/pathology [MeSH]
lokal Male [MeSH]
lokal Antineoplastic Combined Chemotherapy Protocols/pharmacology [MeSH]
lokal Antibodies, Monoclonal, Humanized/therapeutic use [MeSH]
lokal Prognosis [MeSH]
lokal Bevacizumab/pharmacology [MeSH]
lokal Antibodies, Monoclonal, Humanized/pharmacology [MeSH]
lokal Original Research Article
lokal Antibodies, Monoclonal, Humanized/adverse effects [MeSH]
lokal Liver Neoplasms/drug therapy [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
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