Pseudoprogression in patients treated with immune checkpoint inhibitors for microsatellite instability-high/mismatch repair-deficient metastatic colorectal cancer

被引:40
作者
Colle, Raphael [1 ,4 ]
Radzik, Anna [2 ]
Cohen, Romain [1 ,3 ]
Pellat, Anna [1 ]
Lopez-Tabada, Daniel [1 ]
Cachanado, Marine [4 ]
Duval, Alex [3 ]
Svrcek, Magali [3 ,5 ]
Menu, Yves [2 ]
Andre, Thierry [1 ,2 ,3 ]
机构
[1] Sorbonne Univ, Dept Med Oncol, St Antoine Hosp, AP HP, 184 Rue Faubourg St Antoine, F-75012 Paris, France
[2] Sorbonne Univ, Dept Radiol, St Antoine Hosp, AP HP, 184 Rue Faubourg St Antoine, F-75012 Paris, France
[3] Sorbonne Univ, INSERM, UMRS 938, Microsatellite Instabil & Canc,St Antoine Res Ctr, 184 Rue Faubourg St Antoine, F-75012 Paris, France
[4] Sorbonne Univ, Clin Res Unit, St Antoine Hosp, AP HP, 184 Rue Faubourg St Antoine, F-75012 Paris, France
[5] Sorbonne Univ, Dept Pathol, St Antoine Hosp, AP HP, 184 Rue Faubourg St Antoine, F-75012 Paris, France
关键词
Pseudoprogression; Microsatellite instability; Mismatch repair; Immunotherapy; PD1; CTLA-4; RESPONSE CRITERIA; GUIDELINES; NIVOLUMAB;
D O I
10.1016/j.ejca.2020.11.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The efficacy of immune checkpoint inhibitors (ICIs) in microsatellite instability-high/DNA mismatch repair (MSI/dMMR) metastatic colorectal cancer (mCRC) is well established. ICIs are responsible for pseudoprogression (PSPD) that complicates clinical decisions. We evaluated the PSPD frequency in patients with MSI/dMMR mCRC treated with ICIs. Patients and methods: Consecutive patients with MSI/dMMR mCRC treated with ICIs from February 2015 to December 2019 at Saint-Antoine Hospital were included. Imaging was retrospectively and centrally reviewed according to Response Evaluation Criteria in Solid Tumours, version 1.1 (RECIST 1.1) and immune RECIST (iRECIST). PSPD was defined as an unconfirmed disease progression by iRECIST. Results: One hundred twenty-three patients with MSI/dMMR mCRC were included. Thirty-six patients (29%) had radiological PD according to RECIST 1.1 during the median follow-up of 22.3 months (95% confidence interval [CI], 1.5-62.2), including 22 in the first 3 months (the primary radiological PD). Twenty-nine patients continued ICIs beyond PD. Twelve patients experienced PSPD, representing 10% of the population and 52% of the primary radiological PD. The median time to PSPD was 5.7 weeks (95% CI, 4.1-11.4). No PSPD was observed after 3 months. The PSPD incidence was 14.8% in patients treated with anti-PD1 alone (n = 9/61) and 4.8% in case of anti-PD1 plus anti-CTLA-4 (n = 3/62). Eight patients with PSPD experienced an objective response. The 2-year progression-free survival and overall survival rates for patients with PSPD were 70.0% (95% CI, 32.9-89.2) and 75.0% (95% CI, 29.8-93.4), respectively. Conclusion: Patients with MSI/dMMR mCRC treated with ICIs experienced PSPDs. PSPD occurred within the first 3 months and represented most of the primary radiological PDs. The use of iRECIST criteria should be questioned after 3 months. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9 / 16
页数:8
相关论文
共 29 条
[1]   Radiomics, Tumor Volume, and Blood Biomarkers for Early Prediction of Pseudoprogression in Patients with Metastatic Melanoma Treated with Immune Checkpoint Inhibition [J].
Basler, Lucas ;
Gabrys, Hubert S. ;
Hogan, Sabrina A. ;
Pavic, Matea ;
Bogowicz, Marta ;
Vuong, Diem ;
Tanadini-Lang, Stephanie ;
Forster, Robert ;
Kudura, Ken ;
Huellner, Martin W. ;
Dummer, Reinhard ;
Guckenberger, Matthias ;
Levesque, Mitchell P. .
CLINICAL CANCER RESEARCH, 2020, 26 (16) :4414-4425
[2]   Novel patterns of response under immunotherapy [J].
Borcoman, E. ;
Kanjanapan, Y. ;
Champiat, S. ;
Kato, S. ;
Servois, V. ;
Kurzrock, R. ;
Goel, S. ;
Bedard, P. ;
Le Tourneau, C. .
ANNALS OF ONCOLOGY, 2019, 30 (03) :385-396
[3]   Pseudoprogression in microsatellite instability-high colorectal cancer during treatment with combination T cell mediated immunotherapy: a case report and literature review [J].
Chae, Young Kwang ;
Wang, Si ;
Nimeiri, Halla ;
Kalyan, Aparna ;
Giles, Francis J. .
ONCOTARGET, 2017, 8 (34) :57889-57897
[4]   Site-specific response patterns, pseudoprogression, and acquired resistance in patients with melanoma treated with ipilimumab combined with anti-PD-1 therapy [J].
da Silva, Ines Pires ;
Lo, Serigne ;
Quek, Camelia ;
Gonzalez, Maria ;
Carlino, Matteo S. ;
Long, Georgina, V ;
Menzies, Alexander M. .
CANCER, 2020, 126 (01) :86-97
[5]   Multicenter study demonstrates radiomic features derived from magnetic resonance perfusion images identify pseudoprogression in glioblastoma [J].
Elshafeey, Nabil ;
Kotrotsou, Aikaterini ;
Hassan, Ahmed ;
Elshafei, Nancy ;
Hassan, Islam ;
Ahmed, Sara ;
Abrol, Srishti ;
Agarwal, Anand ;
El Salek, Kamel ;
Bergamaschi, Samuel ;
Acharya, Jay ;
Moron, Fanny E. ;
Law, Meng ;
Fuller, Gregory N. ;
Huse, Jason T. ;
Zinn, Pascal O. ;
Colen, Rivka R. .
NATURE COMMUNICATIONS, 2019, 10 (1)
[6]   Biomarkers of hyperprogression and pseudoprogression with immune checkpoint inhibitor therapy [J].
Failing, Jarrett J. ;
Dudek, Olivia A. ;
Acevedo, Julian A. Marin ;
Chirila, Razvan M. ;
Dong, Haidong ;
Markovic, Svetomir N. ;
Dronca, Roxana S. .
FUTURE ONCOLOGY, 2019, 15 (22) :2645-2656
[7]   Pseudoprogression in Non-Small Cell Lung Cancer upon Immunotherapy: Few Drops in the Ocean? [J].
Ferrara, Roberto ;
Caramella, Caroline ;
Besse, Benjamin ;
Champiat, Stephane .
JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (03) :328-331
[8]   Pseudoprogression and Hyperprogression as New Forms of Response to Immunotherapy [J].
Frelaut, Maxime ;
du Rusquec, Pauline ;
de Moura, Alexandre ;
Le Tourneau, Christophe ;
Borcoman, Edith .
BIODRUGS, 2020, 34 (04) :463-476
[9]   Pseudoprogression in Previously Treated Patients with Non-Small Cell Lung Cancer Who Received Nivolumab Monotherapy [J].
Fujimoto, Daichi ;
Yoshioka, Hiroshige ;
Kataoka, Yuki ;
Morimoto, Takeshi ;
Hata, Tae ;
Kim, Young Hak ;
Tomii, Keisuke ;
Ishida, Tadashi ;
Hirabayashi, Masataka ;
Hara, Satoshi ;
Ishitoko, Manabu ;
Fukuda, Yasushi ;
Hwang, Moon Hee ;
Sakai, Naoki ;
Fukui, Motonari ;
Nakaji, Hitoshi ;
Morita, Mitsunori ;
Mio, Tadashi ;
Yasuda, Takehiro ;
Sugita, Takakazu ;
Hirai, Toyohiro .
JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (03) :468-474
[10]   Long-Term Survival in Patients Responding to Anti-PD-1/PD-L1 Therapy and Disease Outcome upon Treatment Discontinuation [J].
Gauci, Marie-Lea ;
Lanoy, Emilie ;
Champiat, Stephane ;
Caramella, Caroline ;
Ammari, Samy ;
Aspeslagh, Sandrine ;
Varga, Andrea ;
Baldini, Capucine ;
Bahleda, Rastilav ;
Gazzah, Anas ;
Michot, Jean-Marie ;
Postel-Vinay, Sophie ;
Angevin, Eric ;
Ribrag, Vincent ;
Hollebecque, Antoine ;
Soria, Jean-Charles ;
Robert, Caroline ;
Massard, Christophe ;
Marabelle, Aurelien .
CLINICAL CANCER RESEARCH, 2019, 25 (03) :946-956