Late immune-related adverse events in long-term responders to PD-1/PD-L1 checkpoint inhibitors: A multicentre study

被引:53
|
作者
Nigro, Olga [1 ]
Pinotti, Graziella [1 ]
De Galitiis, Federica [2 ]
Di Pietro, Francesca Romana [2 ,3 ]
Giusti, Raffaele [3 ]
Filetti, Marco [3 ]
Bersanelli, Melissa [4 ]
Lazzarin, Alessandro [4 ]
Bordi, Paola [4 ]
Catino, Annamaria [5 ]
Pizzutilo, Pamela [5 ]
Galetta, Domenico [5 ]
Marchetti, Paolo [2 ,6 ]
Botticelli, Andrea [6 ]
Scagnoli, Simone [6 ]
Russano, Marco [7 ]
Santini, Daniele [7 ]
Torniai, Mariangela [8 ]
Berardi, Rossana [8 ]
Ricciuti, Biagio [9 ]
De Giglio, Andrea [9 ]
Chiari, Rita [10 ]
Russo, Alessandro [11 ]
Adamo, Vincenzo [11 ]
Tudini, Marianna [12 ]
Silva, Rosa Rita [12 ]
Bolzacchini, Elena [13 ]
Giordano, Monica [13 ]
Di Marino, Pietro [14 ]
De Tursi, Michele [15 ]
Rijavec, Erika [16 ]
Ghidini, Michele [16 ]
Vallini, Ilaria [1 ]
Stucci, Luigia Stefania [17 ]
Tucci, Marco [17 ,25 ]
Pala, Laura [18 ]
Conforti, Fabio [18 ]
Queirolo, Paola [18 ]
Tanda, Enrica [19 ]
Spagnolo, Francesco [19 ]
Cecchi, Federica [19 ]
Bracarda, Sergio [20 ]
Macrini, Serena [20 ]
Santoni, Matteo [21 ]
Battelli, Nicola [21 ]
Fargnoli, Maria Concetta [22 ,23 ]
Porzio, Giampiero [22 ,24 ]
Tuzi, Alessandro [1 ]
Suter, Matteo Basilio [1 ]
Ficorella, Corrado [22 ,24 ]
机构
[1] Osped Circolo & Fdn Macchi, ASST Sette Laghi, Med Oncol, Varese, Italy
[2] IDI IRCCS, Oncol & Oncol Dermatol, Rome, Italy
[3] Azienda Osped Univ St Andrea, Med Oncol, Rome, Italy
[4] Azienda Osped Univ Parma, Med Oncol, Parma, Italy
[5] IRCCS Ist Tumori Giovanni Paolo II, Thorac Oncol Unit, Bari, Italy
[6] Univ Roma La Sapienza, Dipartimento Sci Med Chirurg & Med Traslaz, Rome, Italy
[7] Med Oncol, Campus Biomed, Rome, Italy
[8] Univ Politecn Marche, Clin Oncol, Azienda Osped Univ Osped Riuniti Umberto 1, GM Lancisi, Ancona, Italy
[9] Univ Perugia, Dept Surg & Biomed Sci, Perugia, Italy
[10] Osped Riuniti Padova Sud Madre Teresa Di Calcutta, Med Oncol, Monselice, Italy
[11] Univ Messina, AO Papardo & Dept Human Pathol, Med Oncol, Messina, Italy
[12] ASUR Marche, Area Vasta 2, Med Oncol, Fabriano, Italy
[13] Osped St Anna, ASST Lariana, Med Oncol, Como, Italy
[14] SS Annunziata Hosp, Clin Oncol Unit, Chieti, Italy
[15] Univ G DAnnunzio, Dept Med Oral & Biotechnol Sci, Chieti, Italy
[16] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Med Oncol Unit, Milan, Italy
[17] Univ Bari, Med Oncol Unit, Dept Biomed Sci & Human Oncol, Bari, Italy
[18] IRCCS, European Inst Oncol, Div Med Oncol Melanoma Sarcoma & Rare Tumors, IEO, Milan, Italy
[19] Osped Policlin San Martino, IRCCS, Genoa, Italy
[20] Santa Maria Hosp, Dept Med Oncol, Terni, Italy
[21] Macerata Hosp, Dept Oncol, Macerata, Italy
[22] St Salvatore Hosp, Dept Dermatol, Laquila, Italy
[23] Univ Aquila, Dept Biotechnol & Appl Clin Sci, Laquila, Italy
[24] St Salvatore Hosp, Med Oncol, Laquila, Italy
[25] Tumori Inst Giovanni Paolo II, Natl Canc Res Ctr, Bari, Italy
关键词
Immunotherapy; Immune checkpoint; Nivolumab; Pembrolizumab; Atezolizumab; Immune-related adverse events; ELDERLY-PATIENTS; CANCER;
D O I
10.1016/j.ejca.2020.04.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Data on spectrum and grade of immune-related adverse events (irAEs) in long-term responders to immune checkpoint inhibitors (ICIs) are lacking. Methods: We performed a retrospective multicenter study to characterized irAEs occurring after a 12-months minimum treatment period with PD-(L)1 ICIs in patients with advanced cancer. IrAEs were categorized into 'early' (<= 12 months) and 'late' (>12 months). Results: From September 2013 to October 2019, 436 consecutive patients were evaluated. Two hundred twenty-three experienced any grade early-irAEs (51.1%), whereas 132 experienced any grade late-irAEs (30.3%) (p < 0.0001). Among the latter, 29 (22%) experienced a recurrence of an early-irAEs, whereas 103 (78%) experienced de novo late-irAEs involving different system/organ. Among patients with late-irAEs, 21 experienced GIII/GIV irAEs (4.8%). Median time to onset of early-irAEs was 3.4 months (95% confidence interval [CI]: 2.8-4.2), whereas the median time to onset of late-irAEs was 16.6 months (95% CI: 15.8-17.6). Cumulative time-adjusted risk of disease progression according to both the early-irAEs (hazard ratio [HR] = 0.63 [95% CI: 0.30-1.29], p = 0.204) and late-irAEs occurrence revealed no statistically significant differences (HR = 0.75 [95% CI: 0.37-1.56], p = 0.452). In addition, the time-adjusted cumulative risk of death in accordance with both early-irAEs (HR = 0.79 [95% CI: 0.34-1.86], p = 0.598) and late-irAEs (HR = 0.92 [95% CI: 0.49-1.74], p = 0.811) did not show statistically significant differences. Conclusion: Although less frequent than early-irAEs, late-irAEs are quite common in long responders to PD-(L)1 ICIs and are different in terms of spectrum and grade. Time-adjusted analysis revealed that the cumulative risk of disease progression and death were not significantly reduced in patients who experienced late-irAEs. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 28
页数:10
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