Abstract
Recent studies have not only shown better prognosis of lymphoma with the advancement of therapeutic drug development, but also suggested more attention should be paid to drug-induced lung injury. Early diagnosis is critical for treatment of drug-induced lung injury. 18F-FDG-PET/CT, the standard imaging method for prognosis evaluation of Hodgkin’s lymphoma and some non-Hodgkin’s lymphoma, has also shown the potential for early detection of drug-induced lung injury in our study. A total of 579 lymphoma patients evaluated by 18F-FDG-PET/CT between June 2016 and March 2018 are studied retrospectively. Clinical and imaging characteristics are described in 32 patients (average age of 55), who were diagnosed with drug-induced lung injury. The incidence of drug-induced lung injury was 5.53% (32/579); most of the chemotherapy regimens include rituximab (90.63%, 29/32). Twelve patients demonstrated fever, cough, and dyspnea, and the other 20 had no significant symptoms. 18F-FDG-PET/CT showed multiple or diffused distribution of ground glass and patchy shadows, with increased FDG uptake in both lungs (SUVmax 2.28 ± 1.13, standardized uptake ratio-blood pool, SUR-BP = 0.59–4.07, median SUR-BP 1.32). SUVmax and SUR-BP in patients with symptoms (SUVmax 3.03 ± 1.33 and SUR-BP 2.12 ± 1.06) were significantly higher than in those without symptoms (SUVmax 1.84 ± 0.70 and SUR-BP 1.18 ± 0.48) (P = 0.002 for both SUVmax and SUR-BP). After temporary drug withdrawal, changing chemotherapy regimens, and corticosteroid usage, the pulmonary lesions in all patients were relieved, confirmed with chest CT. Drug-induced lung injury can be a co-finding during 18F-FDG-PET/CT assessment of lymphoma. With positive correlation between FDG uptake and symptoms, 18F-FDG-PET/CT provided value in early detection of lung injury in asymptomatic patients.
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References
Zhou T, Shen Q, Peng H, Chao T, Zhang L, Huang L, Yang K, Thapa S, Yu S, Jiang Y (2018) Incidence of interstitial pneumonitis in non-Hodgkin’s lymphoma patients receiving immunochemotherapy with pegylated liposomal doxorubicin and rituximab. Ann Hematol 97:141–147. https://doi.org/10.1007/s00277-017-3160-1
Madabhavi I, Modi G, Patel A, Anand A, Panchal H, Parikh S (2017) Pulmonary toxicity following bleomycin use: a single-center experience. J Cancer Res Ther 13:466–470. https://doi.org/10.4103/0973-1482.204887
Salmasi G, Li M, Sivabalasundaram V, Panzarella T, Tsang R, Kukreti V, Crump M, Kuruvilla J (2015) Incidence of pneumonitis in patients with non-Hodgkin lymphoma receiving chemoimmunotherapy with rituximab. Leuk Lymphoma 56:1659–1664. https://doi.org/10.3109/10428194.2014.963075
Cella L, Liuzzi R, D'Avino V, Conson M, Di BA, Picardi M, Pugliese N, Solla R, Salvatore M, Pacelli R (2014) Pulmonary damage in Hodgkin’s lymphoma patients treated with sequential chemo-radiotherapy: predictors of radiation-induced lung injury. Acta Oncol 53:613–619. https://doi.org/10.3109/0284186X.2013.850739
Ghesquieres H (2005) Severe interstitial pneumonitis following rituximab and bleomycin-containing combination chemotherapy. Ann Oncol 16:1399. https://doi.org/10.1093/annonc/mdi232
Buchler T, Bomanji J, Lee SM (2007) FDG-PET in bleomycin-induced pneumonitis following ABVD chemotherapy for Hodgkin’s disease--a useful tool for monitoring pulmonary toxicity and disease activity. Haematologica 92:e120–e121. https://doi.org/10.3324/haematol.11856
Dimopoulou I, Bamias A, Lyberopoulos P, Dimopoulos MA (2006) Pulmonary toxicity from novel antineoplastic agents. Ann Oncol 17:372–379. https://doi.org/10.1093/annonc/mdj057
Matsuno O (2012) Drug-induced interstitial lung disease: mechanisms and best diagnostic approaches. Respir Res 13:39. https://doi.org/10.1186/1465-9921-13-39
Burton C, Kaczmarski R, Jan-Mohamed R (2003) Interstitial pneumonitis related to rituximab therapy. N Engl J Med 348:2690–2691; discussion 2690-2691. https://doi.org/10.1056/NEJM200306263482619
Sakai F, Johkoh T, Kusumoto M, Arakawa H, Takahashi M (2012) Drug-induced interstitial lung disease in molecular targeted therapies: high-resolution CT findings. Int J Clin Oncol 17:542–550. https://doi.org/10.1007/s10147-012-0489-2
Mei-xin Z, Wei-fang Z (2017) 18F-FDG-PET/CT in diagnosis of chemotherapy-induced lung injury in patients with lymphoma. Chin J Med Imaging Technol 33:40–43
Adams HJ, Kwee TC (2016) Interim PET-CT scan in advanced Hodgkin’s lymphoma. N Engl J Med 375:999–1000. https://doi.org/10.1056/NEJMc1609333
Kazama T, Faria SC, Uchida Y, Ito H, Macapinlac HA (2008) Pulmonary drug toxicity: FDG-PET findings in patients with lymphoma. Ann Nucl Med 22:111–114. https://doi.org/10.1007/s12149-007-0089-9
Falay O, Öztürk E, Bölükbaşı Y, Gümüş T, Örnek S, Özbalak M, Çetiner M, Demirkol O, Ferhanoğlu B (2017) Use of fluorodeoxyglucose positron emission tomography for diagnosis of bleomycin-induced pneumonitis in Hodgkin lymphoma. Leuk Lymphoma 58:1114–1122. https://doi.org/10.1080/10428194.2016.1236379
Liu X, Hong XN, Gu YJ, Wang BY, Luo ZG, Cao J (2008) Interstitial pneumonitis during rituximab-containing chemotherapy for non-Hodgkin lymphoma. Leuk Lymphoma 49:1778–1783. https://doi.org/10.1080/10428190802270886
Barber NA, Ganti AK (2011) Pulmonary toxicities from targeted therapies: a review. Target Oncol 6:235–243. https://doi.org/10.1007/s11523-011-0199-0
Bonanni A, Calatroni M, D'Alessandro M, Signa S, Bertelli E, Cioni M, Di ME, Biassoni R, Caridi G, Ingrasciotta G, Bertelli R, Di DA, Bruschi M, Canepa A, Piaggio G, Ravani P, Ghiggeri GM (2018) Adverse events linked with the use of chimeric and humanized anti-CD20 antibodies in children with idiopathic nephrotic syndrome. Br J Clin Pharmacol 84:1238–1249. https://doi.org/10.1111/bcp.13548
Franzen D, Ciurea A, Bratton DJ, Clarenbach CF, Latshang TD, Russi EW, Kyburz D, Kohler M (2016) Effect of rituximab on pulmonary function in patients with rheumatoid arthritis. Pulm Pharmacol Ther 37:24–29. https://doi.org/10.1016/j.pupt.2016.02.002
Kim KM, Kim HC, Jeon KN, Kim HG, Kang JH, Hahm JR, Lee GW (2008) Rituximab-CHOP induced interstitial pneumonitis in patients with disseminated extranodal marginal zone B cell lymphoma. Yonsei Med J 49:155–158. https://doi.org/10.3349/ymj.2008.49.1.155
Zhang X, Guo X, Pan J (2015) Increased levels of tumor necrosis factor-α involved in rituximab-related acute pulmonary fibrosis in diffuse large B-cell lymphoma. Am J Clin Pathol 143:725–727
Akira M, Suganuma N (2014) Acute and subacute chemical-induced lung injuries: HRCT findings. Eur J Radiol 83:1461–1469. https://doi.org/10.1016/j.ejrad.2014.04.024
Yamane T, Daimaru O, Ito S, Nagata T, Yoshiya K, Fukaya N, Ito S, Imai T, Uchida H (2008) Drug-induced pneumonitis detected earlier by 18F-FDG-PET than by high-resolution CT: a case report with non-Hodgkin’s lymphoma. Ann Nucl Med 22:719–722. https://doi.org/10.1007/s12149-008-0183-7
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Zhao, M., Zhang, W. Early detection value of 18F-FDG-PET/CT for drug-induced lung injury in lymphoma. Ann Hematol 98, 909–914 (2019). https://doi.org/10.1007/s00277-018-3558-4
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DOI: https://doi.org/10.1007/s00277-018-3558-4