Evolution and recurrence of gastrointestinal immune-related adverse events induced by immune checkpoint inhibitors

被引:42
作者
de Malet, Alice [1 ]
Antoni, Guillemette [2 ]
Collins, Michael [1 ,3 ]
Soularue, Emilie [1 ,3 ]
Marthey, Lysiane [1 ]
Vaysse, Thibaut [1 ]
Coutzac, Clelia [4 ,5 ]
Chaput, Nathalie [4 ,5 ,6 ]
Mateus, Christine [7 ]
Robert, Caroline [7 ]
Carbonnel, Franck [1 ,3 ]
机构
[1] Bicetre Hosp, AP HP, Dept Gastroenterol, F-94270 Le Kremlin Bicetre, France
[2] INSERM, SC10 US19, Villejuif, France
[3] Univ Paris Saclay, Fac Med, F-94276 Le Kremlin Bicetre, France
[4] CNRS, UMS 3655, Lab Immunomonitoring Oncol, Gustave Roussy Canc Campus,114 Rue Edouard Vailla, F-94805 Villejuif, France
[5] INSERM, US23, Gustave Roussy Canc Campus,114 Rue Edouard Vailla, F-94805 Villejuif, France
[6] Univ Paris Saclay, Fac Pharm, F-92296 Chatenay Malabry, France
[7] Dept Med, Dermatol Unit, Gustave Roussy Canc Campus,114 Rue Edouard Vailla, F-94805 Villejuif, France
关键词
Immunotherapy; Drug toxicity; Gastrointestinal toxicity; OPEN-LABEL; ADVANCED MELANOMA; CELL-CARCINOMA; T-CELLS; IPILIMUMAB; NIVOLUMAB; CANCER; ANTI-CTLA-4; CTLA-4; PEMBROLIZUMAB;
D O I
10.1016/j.ejca.2018.10.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Immune checkpoint inhibitors (ICIs), such as anti-CTLA-4 and anti-PD-1 antibodies, are effective against several malignancies. They are associated with gastrointestinal immune-related adverse events (GI-IrAEs), which may be severe and lead to ICI discontinuation. We assessed the risk of evolution of GI-IrAEs to chronic GI inflammation and the risk of recurrence after a second line of ICI. Patients and methods: This was a single-centre study. Included patients had a GI-IrAE due to ICIs between September 2010 and July 2017. We assessed the persistence of symptoms, endoscopic and/or histological inflammation, and the risk of recurrent GI-IrAEs after the second line of ICIs. Results: Eighty patients were included. The median follow-up was 8.4 months (0.36-72.3). The median duration of GI symptoms was 1.5 months (5 days-10.3 months): 1.4 months (7 days-4.9 months) with antieCTLA-4, 2.0 months (5 days-10.3 months) with anti-PD-1 and 1.0 month (8 days-3.4 months) with combination therapy (log-rank test: p = 0.02). Three and 6 months after the beginning of GI-IrAEs, 22% (95% confidence interval: 14%-33%) and 5.4% (2.0%-14.7%) of patients had persistent symptoms, respectively. After a median of 6 months, 20/27 patients had endoscopic and/or histological inflammation, of whom, seven were symptom free. After the first episode, 6/26 patients relapsed after receiving another course of ICIs. Among these 26, 89% (77%-100%) had no recurrence after 3 months, 71% or 95% if the second line was anti-CTLA-4 or anti-PD-1, respectively. Conclusion: GI-IrAEs seem to be acute or subacute, not chronic. Reintroduction of ICIs is possible in patients who had GI-IrAE. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:106 / 114
页数:9
相关论文
共 38 条
[1]
Akel R, 2017, CASE REP ONCOL, V10, P456, DOI 10.1159/000475709
[2]
Infliximab for IPILIMUMAB-Related Colitis-Letter [J].
Arriola, Edurne ;
Wheater, Matthew ;
Karydis, Ioannis ;
Thomas, Gareth ;
Ottensmeier, Christian .
CLINICAL CANCER RESEARCH, 2015, 21 (24) :5642-5643
[3]
CTLA-4 promotes Foxp3 induction and regulatory T cell accumulation in the intestinal lamina propria [J].
Barnes, M. J. ;
Griseri, T. ;
Johnson, A. M. F. ;
Young, W. ;
Powrie, F. ;
Izcue, A. .
MUCOSAL IMMUNOLOGY, 2013, 6 (02) :324-334
[4]
Refining Immunotherapy Approvals [J].
Bates, Susan E. .
CLINICAL CANCER RESEARCH, 2017, 23 (17) :4948-4949
[5]
Enterocolitis in patients with cancer after antibody blockade of cytotoxic T-lymphocyte-associated antigen 4 [J].
Beck, Kimberly E. ;
Blansfield, Joseph A. ;
Tran, Khoi Q. ;
Feldman, Andrew L. ;
Hughes, Marybeth S. ;
Royal, Richard E. ;
Kammula, Udai S. ;
Topalian, Suzanne L. ;
Sherry, Richard M. ;
Kleiner, David ;
Quezado, Martha ;
Lowy, Israel ;
Yellin, Michael ;
Rosenberg, Steven A. ;
Yang, James C. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (15) :2283-2289
[6]
Safety profiles of anti-CTLA-4 and anti-PD-1 antibodies alone and in combination [J].
Boutros, Celine ;
Tarhini, Ahmad ;
Routier, Emilie ;
Lambotte, Olivier ;
Ladurie, Francois Leroy ;
Carbonnel, Franck ;
Izzeddine, Hassane ;
Marabelle, Aurelien ;
Champiat, Stephane ;
Berdelou, Armandine ;
Lanoy, Emilie ;
Texier, Matthieu ;
Libenciuc, Cristina ;
Eggermont, Alexander M. M. ;
Soria, Jean-Charles ;
Mateus, Christine ;
Robert, Caroline .
NATURE REVIEWS CLINICAL ONCOLOGY, 2016, 13 (08) :473-486
[7]
Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: American Society of Clinical Oncology Clinical Practice Guideline [J].
Brahmer, Julie R. ;
Lacchetti, Christina ;
Schneider, Bryan J. ;
Atkins, Michael B. ;
Brassil, Kelly J. ;
Caterino, Jeffrey M. ;
Chau, Ian ;
Ernstoff, Marc S. ;
Gardner, Jennifer M. ;
Ginex, Pamela ;
Hallmeyer, Sigrun ;
Chakrabarty, Jennifer Holter ;
Leighl, Natasha B. ;
Mammen, Jennifer S. ;
McDermott, David F. ;
Naing, Aung ;
Nastoupil, Loretta J. ;
Phillips, Tanyanika ;
Porter, Laura D. ;
Puzanov, Igor ;
Reichner, Cristina A. ;
Santomasso, Bianca D. ;
Seigel, Carole ;
Spira, Alexander ;
Suarez-Almazor, Maria E. ;
Wang, Yinghong ;
Weber, Jeffrey S. ;
Wolchok, Jedd D. ;
Thompson, John A. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (17) :1714-+
[8]
Inflammatory gastrointestinal diseases associated with PD-1 blockade antibodies [J].
Collins, M. ;
Michot, J. M. ;
Danlos, F. X. ;
Mussini, C. ;
Soularue, E. ;
Mateus, C. ;
Loirat, D. ;
Buisson, A. ;
Rosa, I. ;
Lambotte, O. ;
Laghouati, S. ;
Chaput, N. ;
Coutzac, C. ;
Voisin, A. L. ;
Soria, J. C. ;
Marabelle, A. ;
Champiat, S. ;
Robert, C. ;
Carbonnel, F. .
ANNALS OF ONCOLOGY, 2017, 28 (11) :2860-2865
[9]
Nivolumab with or without ipilimumab treatment for metastatic sarcoma (Alliance A091401): two open-label, non-comparative, randomised, phase 2 trials [J].
D'Angelo, Sandra P. ;
Mahoney, Michelle R. ;
Van Tine, Brian A. ;
Atkins, James ;
Milhem, Mohammed M. ;
Jahagirdar, Balkrishna N. ;
Antonescu, Cristina R. ;
Horvath, Elise ;
Tap, William D. ;
Schwartz, Gary K. ;
Streicher, Howard .
LANCET ONCOLOGY, 2018, 19 (03) :416-426
[10]
Pembrolizumab therapy for microsatellite instability high (MSI-H) colorectal cancer (CRC) and non-CRC. [J].
Diaz, Luis A. ;
Marabelle, Aurelien ;
Delord, Jean-Pierre ;
Shapira-Frommer, Ronnie ;
Geva, Ravit ;
Peled, Nir ;
Kim, Tae Won ;
Andre, Thierry ;
Van Cutsenn, Eric ;
Guimbaud, Rosine ;
Jaeger, Dirk ;
Elez, Elena ;
Yoshino, Takayuki ;
Joe, Andrew K. ;
Lam, Baohoang ;
Gause, Christine K. ;
Pruitt, Scott Knowles ;
Kang, S. Peter ;
Le, Dung T. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35