RSS-Feed abonnieren

DOI: 10.1055/s-0044-1787537
Early Hyperprogression of Rhabdomyosarcoma Detected by 18F-FDG PET/CT Three Weeks after CAR-T Treatment
Autoren
Abstract
Chimeric antigen receptor T-cell (CAR-T) treatment has been widely used in the treatment of hematological malignancies, and its application has been gradually expanded to the research and treatment of solid tumors. However, unconventional types of response may occur after CAR-T treatment, such as hyperprogression, resulting in terrible outcomes. Here, we report the case of a 13-year-old adolescent boy with relapsed and refractory rhabdomyosarcoma who developed early hyperprogression 3 weeks after CAR-T treatment (target: B7H3 and CD171), which was detected by fluorine-18 fluorodeoxyglucose (18F-FDG) positron emission tomography (PET)/computed tomography (CT). The patient eventually underwent amputation. Attention should be paid to the possibility of early hyperprogression after CAR-T treatment, and 18F-FDG PET/CT has an absolute advantage in early evaluating treatment response to immunotherapy.
Authors' Contributions
S.G. participated in data analysis and interpretation, and wrote the original draft of the manuscript text. Z.T. provided the clinical data, and revised the manuscript. W.G. provided the pathological images and related figure legend. Y.Y. contributed to conceptualization, participated in the interpretation, and revised the manuscript. S.G. and Z.T. contributed equally to this work and should be considered co-first authors.
* These authors contributed equally to this work.
Publikationsverlauf
Artikel online veröffentlicht:
20. Juni 2024
© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
-
Reference
- 1 McEvoy MT, Siegel DA, Dai S. et al. Pediatric rhabdomyosarcoma incidence and survival in the United States: an assessment of 5656 cases, 2001-2017. Cancer Med 2023; 12 (03) 3644-3656
- 2 Hegde M, Joseph SK, Pashankar F. et al. Tumor response and endogenous immune reactivity after administration of HER2 CAR T cells in a child with metastatic rhabdomyosarcoma. Nat Commun 2020; 11 (01) 3549
- 3 Wang Q, Gao J, Wu X. Pseudoprogression and hyperprogression after checkpoint blockade. Int Immunopharmacol 2018; 58: 125-135
- 4 Sterner RC, Sterner RM. CAR-T cell therapy: current limitations and potential strategies. Blood Cancer J 2021; 11 (04) 69
- 5 Miao L, Zhang J, Zhang Z. et al. A bibliometric and knowledge-map analysis of CAR-T cells from 2009 to 2021. Front Immunol 2022; 13: 840956
- 6 Han XJ, Alu A, Xiao YN, Wei YQ, Wei XW. Hyperprogression: a novel response pattern under immunotherapy. Clin Transl Med 2020; 10 (05) e167
- 7 Fuentes-Antrás J, Provencio M, Díaz-Rubio E. Hyperprogression as a distinct outcome after immunotherapy. Cancer Treat Rev 2018; 70: 16-21
- 8 Frelaut M, du Rusquec P, de Moura A, Le Tourneau C, Borcoman E. Pseudoprogression and hyperprogression as new forms of response to immunotherapy. BioDrugs 2020; 34 (04) 463-476
- 9 Gao Y, Hu S, Li R. et al. Hyperprogression of cutaneous T cell lymphoma after anti-PD-1 treatment. JCI Insight 2023; 8 (04) e164793
- 10 Li LX, Cappuzzo F, Matos I, Socinski MA, Hopkins AM, Sorich MJ. Low risk of hyperprogression with first-line chemoimmunotherapy for advanced non-small cell lung cancer: pooled analysis of 7 clinical trials. Oncologist 2023; 28 (04) e205-e211
- 11 Wang J, Wang X, Yang X, Zhao H, Huo L. FDG PET findings of hyperprogression during immunotherapy in a patient with hepatocellular carcinoma. Clin Nucl Med 2020; 45 (01) 92-93
- 12 Singh B, Kaur P, Maroules M. Hyperprogression in a patient with hepatocellular cancer treated with atezolizumab and bevacizumab: a case report and review of literature. J Investig Med High Impact Case Rep 2021; 9: 2324709621992207
- 13 Caner B, Ertas H, Ocak B, Cubukcu E. Hyperprogression and hypercalcemia after nivolumab treatment in three cases with renal cell carcinoma. J Oncol Pharm Pract 2022; 28 (07) 1645-1649
- 14 Yilmaz M, Akovali B. Hyperprogression after nivolumab for melanoma: a case report. J Oncol Pharm Pract 2020; 26 (01) 244-251
- 15 Feng D, Guan Y, Liu M. et al. Excellent response to atezolizumab after clinically defined hyperprogression upon previous treatment with pembrolizumab in metastatic triple-negative breast cancer: a case report and review of the literature. Front Immunol 2021; 12: 608292
- 16 Izreig S, Alzahrani F, Earles J. et al. Hyperprogression of a sinonasal squamous cell carcinoma following programmed cell death protein-1 checkpoint blockade. JAMA Otolaryngol Head Neck Surg 2020; 146 (12) 1176-1178
- 17 Xiang JJ, Uy NF, Minja FJ, Verter EE, Burtness BA. Hyperprogression after one dose of nivolumab in sinonasal cancer: a case report. Laryngoscope 2020; 130 (04) 907-910
- 18 Yang HY, Du YX, Hou YJ, Lu DR, Xue P. Hyperprogression after anti-programmed death-1 therapy in a patient with urothelial bladder carcinoma: a case report. World J Clin Cases 2023; 11 (28) 6841-6849
- 19 Zhou W, Zhou Y, Yi C. et al. Case report: immune and genomic characteristics associated with hyperprogression in a patient with metastatic deficient mismatch repair gastrointestinal cancer treated with anti-PD-1 antibody. Front Immunol 2021; 12: 749204
- 20 Ferrari C, Maggialetti N, Masi T. et al. Early evaluation of immunotherapy response in lymphoma patients by 18F-FDG PET/CT: a literature overview. J Pers Med 2021; 11 (03) 217
- 21 Costa LB, Queiroz MA, Barbosa FG. et al. Reassessing patterns of response to immunotherapy with PET: from morphology to metabolism. Radiographics 2021; 41 (01) 120-143
- 22 Aide N, Hicks RJ, Le Tourneau C, Lheureux S, Fanti S, Lopci E. FDG PET/CT for assessing tumour response to immunotherapy: report on the EANM symposium on immune modulation and recent review of the literature. Eur J Nucl Med Mol Imaging 2019; 46 (01) 238-250
- 23 He L, Deng Y, Deng Y, Xie H, Zhang W. Early hyperprogression of lymphoma detected by 18 F-FDG PET/CT after chimeric antigen receptor T-cell therapy. Clin Nucl Med 2023; 48 (03) 256-258

