The Spectrum of Anaplastic Large-cell Lymphoma
Jianping Kong
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA
Search for more papers by this authorAndrew L. Feldman
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA
Search for more papers by this authorJianping Kong
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA
Search for more papers by this authorAndrew L. Feldman
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA
Search for more papers by this authorOwen A. O'Connor M.D., Ph.D.
American Cancer Society Research Professor Professor of Medicine
Department of Medicine, Division of Hematology and Oncology, Program for T-Cell Lymphoma Research, Department of Microbiology, Immunology, and Cancer Research, University of Virginia Cancer Center, Charlottesville, VA, USA
Search for more papers by this authorWon Seog Kim
Sungkyunkwan University School of Medicine, Seoul, Korea
Search for more papers by this authorPier Luigi Zinzani M.D., Ph.D.
Professor of Hematology
Department of Medicine, Program for Lymphomas and Chronic Lymphocytic Leukemia, University of Bologna, Bologna, Italy
Search for more papers by this authorSummary
Anaplastic large-cell lymphoma (ALCL) is defined as a group of T-cell non-Hodgkin lymphomas (NHLs) which show unifying pathological characteristics, but heterogeneous clinical and genetic features. The World Health Organization includes four distinct ALCL entities: anaplastic lymphoma kinase-positive (ALK+) ALCL, ALK-negative (ALK–) ALCL, primary cutaneous (pc) ALCL, and breast implant-associated ALCL (BIA-ALCL, a newly included provisional entity). Patients diagnosed with ALCL require pretreatment evaluation. CD30 and ALK are required for accurate diagnosis and subclassification, and also serve as therapeutic targets in ALCL. Strategies to improve outcomes in ALCL include the design of next generation drugs and the use of combined therapies that simultaneously target multiple nodes essential for cell survival. Immune checkpoint inhibitors work by blocking checkpoint proteins from binding with their partner proteins and have been approved by the FDA for a variety of cancer types.
References
- Parrilla Castellar, E.R., Jaffe, E.S., Said, J.W. et al. (2014). ALK-negative anaplastic large cell lymphoma is a genetically heterogeneous disease with widely disparate clinical outcomes. Blood 124 (9): 1473–1480.
- Swerdlow, S., Campo, E., Harris, N. et al. (2017). WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, ( rev. 4ed). Lyon: International Agency for Research on Cancer.
- Al-Hamadani, M., Habermann, T.M., Cerhan, J.R. et al. (2015). Non-Hodgkin lymphoma subtype distribution, geodemographic patterns, and survival in the US: a longitudinal analysis of the National Cancer Data Base from 1998 to 2011. Am J Hematol 90 (9): 790–795.
-
Mora, J., Filippa, D.A., Thaler, H.T. et al. (2000). Large cell non-Hodgkin lymphoma of childhood: analysis of 78 consecutive patients enrolled in 2 consecutive protocols at the Memorial Sloan-Kettering Cancer Center. Cancer
88 (1): 186–197.
10.1002/(SICI)1097-0142(20000101)88:1<186::AID-CNCR26>3.0.CO;2-5 CAS PubMed Web of Science® Google Scholar
- Siaghani, P.J., Wong, J.T., Chan, J. et al. (2019). Epidemiology and pathology of T- and NK-cell lymphomas. Cancer Treat Res 176: 1–29.
- Vose, J., Armitage, J., Weisenburger, D., and International TCLP (2008). International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol 26 (25): 4124–4130.
- Adams, S.V., Newcomb, P.A., and Shustov, A.R. (2016). Racial patterns of peripheral T-cell lymphoma incidence and survival in the United States. J Clin Oncol 34 (9): 963–971.
- Guru Murthy, G.S., Hamadani, M., Bhatt, V.R. et al. (2017). Systemic anaplastic lymphoma kinase-positive anaplastic large cell lymphoma: a population-based analysis of incidence and survival. Clin Lymphoma Myeloma Leuk 17 (4): 201–206.
- Booken, N., Goerdt, S., and Klemke, C.D. (2012). Clinical spectrum of primary cutaneous CD30-positive anaplastic large cell lymphoma: an analysis of the Mannheim Cutaneous Lymphoma Registry. J Dtsch Dermatol Ges 10 (5): 331–339.
- McCarthy, C.M., Loyo-Berrios, N., Qureshi, A.A. et al. (2019). Patient registry and outcomes for breast implants and anaplastic large cell lymphoma etiology and epidemiology (PROFILE): initial report of findings, 2012–2018. Plast Reconstr Surg 143 (3 Suppl): 65S–73S.
- Savage, K.J., Harris, N.L., Vose, J.M. et al. (2008). ALK- anaplastic large-cell lymphoma is clinically and immunophenotypically different from both ALK+ ALCL and peripheral T-cell lymphoma, not otherwise specified: report from the International Peripheral T-Cell Lymphoma Project. Blood 111 (12): 5496–5504.
- DePaola, N.E.K. and Coggins, H. (2019). Breast implant-associated anaplastic large cell lymphoma: what we know. J Adv Pract Oncol 10 (1): 54–61.
- Ali, A.S., Al-Shraim, M., Al-Hakami, A.M., and Jones, I.M. (2015). Epstein- Barr virus: clinical and epidemiological revisits and genetic basis of Oncogenesis. Open Virol J 9: 7–28.
- Kim, Y.C., Yang, W.I., Lee, M.G. et al. (2006). Epstein-Barr virus in CD30 anaplastic large cell lymphoma involving the skin and lymphomatoid papulosis in South Korea. Int J Dermatol 45 (11): 1312–1316.
- Pitman, S.D., Rowsell, E.H., Cao, J.D. et al. (2004). Anaplastic large cell lymphoma associated with Epstein-Barr virus following cardiac transplant. Am J Surg Pathol 28 (3): 410–415.
- Taniai, H., Furusyo, N., Murata, M. et al. (2013). A case report of human immunodeficiency virus-associated anaplastic lymphoma kinase protein-negative anaplastic large cell lymphoma. Springerplus 2: 400.
- Narwal, A., Yadav, A.B., Prakash, S., and Gupta, S. (2016). Anaplastic lymphoma kinase negative anaplastic large cell lymphoma of hard palate as first clinical manifestation of acquired immune deficiency syndrome. Contemp Clin Dent 7 (1): 114–117.
- Castillo, J.J., Beltran, B.E., Bibas, M. et al. (2011). Prognostic factors in patients with HIV-associated peripheral T-cell lymphoma: a multicenter study. Am J Hematol 86 (3): 256–261.
- Lamant, L., Pileri, S., Sabattini, E. et al. (2010). Cutaneous presentation of ALK-positive anaplastic large cell lymphoma following insect bites: evidence for an association in five cases. Haematologica 95 (3): 449–455.
- Fallah, M., Liu, X., Ji, J. et al. (2014). Autoimmune diseases associated with non-Hodgkin lymphoma: a nationwide cohort study. Ann Oncol 25 (10): 2025–2030.
- Ekstrom Smedby, K., Vajdic, C.M., Falster, M. et al. (2008). Autoimmune disorders and risk of non-Hodgkin lymphoma subtypes: a pooled analysis within the InterLymph Consortium. Blood 111 (8): 4029–4038.
- Menotti, M., Ambrogio, C., Cheong, T.C. et al. (2019). Wiskott-Aldrich syndrome protein (WASP) is a tumor suppressor in T cell lymphoma. Nat Med 25 (1): 130–140.
- Clarke, C.A., Morton, L.M., Lynch, C. et al. (2013). Risk of lymphoma subtypes after solid organ transplantation in the United States. Br J Cancer 109 (1): 280–288.
- Kadin, M.E., Morgan, J., Xu, H. et al. (2018). IL-13 is produced by tumor cells in breast implant-associated anaplastic large cell lymphoma: implications for pathogenesis. Hum Pathol 78: 54–62.
- Querfeld, C., Khan, I., Mahon, B. et al. (2010). Primary cutaneous and systemic anaplastic large cell lymphoma: clinicopathologic aspects and therapeutic options. Oncology (Williston Park) 24 (7): 574–587.
- Ferreri, A.J., Govi, S., Pileri, S.A., and Savage, K.J. (2013). Anaplastic large cell lymphoma, ALK-negative. Crit Rev Oncol Hematol 85 (2): 206–215.
- Keech, J.A. Jr. and Creech, B.J. (1997). Anaplastic T-cell lymphoma in proximity to a saline-filled breast implant. Plast Reconstr Surg 100 (2): 554–555.
- de Boer, M., van Leeuwen, F.E., Hauptmann, M. et al. (2018). Breast implants and the risk of anaplastic large-cell lymphoma in the breast. JAMA Oncol 4 (3): 335–341.
- Brody, G.S., Deapen, D., Taylor, C.R. et al. (2015). Anaplastic large cell lymphoma occurring in women with breast implants: analysis of 173 cases. Plast Reconstr Surg 135 (3): 695–705.
- Campanale, A., Boldrini, R., and Marletta, M. (2018). 22 cases of breast implant-associated ALCL: awareness and outcome tracking from the Italian Ministry of Health. Plast Reconstr Surg 141 (1): 11e–19e.
- Malcolm, T.I., Hodson, D.J., Macintyre, E.A., and Turner, S.D. (2016). Challenging perspectives on the cellular origins of lymphoma. Open Biol 6 (9): 160232.
- Eckerle, S., Brune, V., Doring, C. et al. (2009). Gene expression profiling of isolated tumour cells from anaplastic large cell lymphomas: insights into its cellular origin, pathogenesis and relation to Hodgkin lymphoma. Leukemia 23 (11): 2129–2138.
- Malcolm, T.I., Villarese, P., Fairbairn, C.J. et al. (2016). Anaplastic large cell lymphoma arises in thymocytes and requires transient TCR expression for thymic egress. Nat Commun 7: 10087.
- Hassler, M.R., Pulverer, W., Lakshminarasimhan, R. et al. (2016). Insights into the pathogenesis of anaplastic large-cell lymphoma through genome-wide DNA methylation profiling. Cell Rep 17 (2): 596–608.
- Sokolowska-Wojdylo, M., Olek-Hrab, K., and Ruckemann-Dziurdzinska, K. (2015). Primary cutaneous lymphomas: diagnosis and treatment. Postepy Dermatol Alergol 32 (5): 368–383.
- Xerri, L., Adelaide, J., Avenin, M. et al. (2019). Common origin of sequential cutaneous CD30+ lymphoproliferations with nodal involvement evidenced by genome-wide clonal evolution. Histopathology 74 (4): 654–662.
- Turner, S.D., Inghirami, G., Miranda, R.N., and Kadin, M.E. (2019). Cell of origin and immunologic events in the pathogenesis of breast implant-associated anaplastic large-cell lymphoma. Am J Pathol 190 (1): 2–10.
- Tsuyama, N., Sakamoto, K., Sakata, S. et al. (2017). Anaplastic large cell lymphoma: pathology, genetics, and clinical aspects. J Clin Exp Hematop 57 (3): 120–142.
- Swerdlow, S.H., Campo, E., Pileri, S.A. et al. (2016). The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood 127 (20): 2375–2390.
- Chiarle, R., Podda, A., Prolla, G. et al. (1999). CD30 in normal and neoplastic cells. Clin Immunol 90 (2): 157–164.
- Wendtner, C.M., Schmitt, B., Gruss, H.J. et al. (1995). CD30 ligand signal transduction involves activation of a tyrosine kinase and of mitogen-activated protein kinase in a Hodgkin's lymphoma cell line. Cancer Res 55 (18): 4157–4161.
- Watanabe, M., Sasaki, M., Itoh, K. et al. (2005). JunB induced by constitutive CD30-extracellular signal-regulated kinase 1/2 mitogen-activated protein kinase signaling activates the CD30 promoter in anaplastic large cell lymphoma and reed-sternberg cells of Hodgkin lymphoma. Cancer Res 65 (17): 7628–7634.
- Watanabe, M., Itoh, K., Togano, T. et al. (2012). Ets-1 activates overexpression of JunB and CD30 in Hodgkin's lymphoma and anaplastic large-cell lymphoma. Am J Pathol 180 (2): 831–838.
- Hirsch, B., Hummel, M., Bentink, S. et al. (2008). CD30-induced signaling is absent in Hodgkin's cells but present in anaplastic large cell lymphoma cells. Am J Pathol 172 (2): 510–520.
- Boddicker, R.L., Kip, N.S., Xing, X. et al. (2015). The oncogenic transcription factor IRF4 is regulated by a novel CD30/NF-kappaB positive feedback loop in peripheral T-cell lymphoma. Blood 125 (20): 3118–3127.
- Horie, R., Watanabe, M., Ishida, T. et al. (2004). The NPM-ALK oncoprotein abrogates CD30 signaling and constitutive NF-kappaB activation in anaplastic large cell lymphoma. Cancer Cell 5 (4): 353–364.
- Bai, R.Y., Dieter, P., Peschel, C. et al. (1998). Nucleophosmin-anaplastic lymphoma kinase of large-cell anaplastic lymphoma is a constitutively active tyrosine kinase that utilizes phospholipase C-gamma to mediate its mitogenicity. Mol Cell Biol 18 (12): 6951–6961.
- Thakral, C., Hutchison, R.E., Shrimpton, A. et al. (2012). ALK+ anaplastic large cell lymphoma exhibits phosphatidylinositol-3 kinase/Akt activity with retained but inactivated PTEN--a report from the Children's Oncology Group. Pediatr Blood Cancer 59 (3): 440–447.
- Amin, H.M., Lin, Q., and Lai, R. (2006). Jak3 contributes to the activation of ALK and Stat3 in ALK(+) anaplastic large cell lymphoma. Lab Invest 86 (4): 417–419; author reply 420–411.
- Marzec, M., Kasprzycka, M., Ptasznik, A. et al. (2005). Inhibition of ALK enzymatic activity in T-cell lymphoma cells induces apoptosis and suppresses proliferation and STAT3 phosphorylation independently of Jak3. Lab Invest 85 (12): 1544–1554.
- Singh, R.R., Cho-Vega, J.H., Davuluri, Y. et al. (2009). Sonic hedgehog signaling pathway is activated in ALK-positive anaplastic large cell lymphoma. Cancer Res 69 (6): 2550–2558.
- Bergalet, J., Fawal, M., Morello, D., and Espinos, E. (2015). ALK-mediated post-transcriptional regulation: focus on RNA-binding proteins. Front Biosci (Landmark Ed) 20: 1250–1258.
- Ducray, S.P., Natarajan, K., Garland, G.D. et al. (2019). The transcriptional roles of ALK fusion proteins in tumorigenesis. Cancers (Basel) 11 (8): 1074.
- Han, J.J., O'Byrne, M., Stenson, M.J. et al. (2018). Prognostic and therapeutic significance of phosphorylated STAT3 and protein tyrosine phosphatase-6 in peripheral-T cell lymphoma. Blood Cancer J 8 (11): 110.
- Blombery, P., Thompson, E., Ryland, G.L. et al. (2018). Frequent activating STAT3 mutations and novel recurrent genomic abnormalities detected in breast implant-associated anaplastic large cell lymphoma. Oncotarget 9 (90): 36126–36136.
- Zamo, A., Chiarle, R., Piva, R. et al. (2002). Anaplastic lymphoma kinase (ALK) activates Stat3 and protects hematopoietic cells from cell death. Oncogene 21 (7): 1038–1047.
- Bandini, C., Pupuleku, A., Spaccarotella, E. et al. (2018). IRF4 mediates the oncogenic effects of STAT3 in anaplastic large cell lymphomas. Cancers (Basel) 10 (1): 21.
- Crescenzo, R., Abate, F., Lasorsa, E. et al. (2015). Convergent mutations and kinase fusions lead to oncogenic STAT3 activation in anaplastic large cell lymphoma. Cancer Cell 27 (4): 516–532.
- Xing, X. and Feldman, A.L. (2015). Anaplastic large cell lymphomas: ALK positive, ALK negative, and primary cutaneous. Adv Anat Pathol 22 (1): 29–49.
- Boddicker, R.L. and Feldman, A.L. (2015). Progress in the identification of subgroups in ALK-negative anaplastic large-cell lymphoma. Biomark Med 9 (8): 719–722.
- Oishi, N., Brody, G.S., Ketterling, R.P. et al. (2018). Genetic subtyping of breast implant-associated anaplastic large cell lymphoma. Blood 132 (5): 544–547.
- Bennani-Baiti, N., Ansell, S., and Feldman, A.L. (2016). Adult systemic anaplastic large-cell lymphoma: recommendations for diagnosis and management. Expert Rev Hematol 9 (2): 137–150.
- Escalon, M.P., Liu, N.S., Yang, Y. et al. (2005). Prognostic factors and treatment of patients with T-cell non-Hodgkin lymphoma: the M. D. Anderson Cancer Center experience. Cancer 103 (10): 2091–2098.
- Schmitz, N., Trumper, L., Ziepert, M. et al. (2010). Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group. Blood 116 (18): 3418–3425.
- Cederleuf, H., Bjerregard Pedersen, M., Jerkeman, M. et al. The addition of etoposide to CHOP is associated with improved outcome in ALK+ adult anaplastic large cell lymphoma: a Nordic Lymphoma Group study. Br J Haematol 178 (5): 739–746.
-
Shustov, A. and Soma, L. (2017). Anaplastic large cell lymphoma: contemporary concepts and optimal management. Cancer Treat Res
176: 127–144.
10.1007/978-3-319-99716-2_6 Google Scholar
- Engelina, S., Saggu, M., Yoo, J. et al. (2019). Brentuximab a novel antibody therapy: real-world use confirms efficacy and tolerability for CD30 positive cutaneous lymphoma. Br J Dermatol 182 (3): 799–800.
- Richardson, N.C., Kasamon, Y.L., Chen, H. et al. (2019). FDA approval summary: brentuximab vedotin in first-line treatment of peripheral T-cell lymphoma. Oncologist 24 (5): e180–e187.
- Horwitz, S., O'Connor, O.A., Pro, B. et al. (2019). Brentuximab vedotin with chemotherapy for CD30-positive peripheral T-cell lymphoma (ECHELON-2): a global, double-blind, randomised, phase 3 trial. Lancet 393 (10168): 229–240.
- Prince, H.M., Kim, Y.H., Horwitz, S.M. et al. (2017). Brentuximab vedotin or physician's choice in CD30-positive cutaneous T-cell lymphoma (ALCANZA): an international, open-label, randomised, phase 3, multicentre trial. Lancet 390 (10094): 555–566.
- Prokoph, N., Larose, H., Lim, M.S. et al. (2018). Treatment options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): current standard and beyond. Cancers (Basel) 10 (4): 99.
- d'Amore, F., Relander, T., Lauritzsen, G.F. et al. (2012). Up-front autologous stem-cell transplantation in peripheral T-cell lymphoma: NLG-T-01. J. Clin. Oncol. 30 (25): 3093–3099.
- National Comprehensive Cancer Network (2017). T-cell Lymphomas, (Version 2)). NCCN Clinical Practice Guidelines in Oncology. Plymouth Meeting, PA: NCCN.
- Naik, S., Martinez, C.A., Omer, B. et al. (2019). Allogeneic hematopoietic stem cell transplant for relapsed and refractory non-Hodgkin lymphoma in pediatric patients. Blood Adv 3 (18): 2689–2695.
- Vu, K. and Ai, W. (2018). Update on the treatment of anaplastic large cell lymphoma. Curr Hematol Malig Rep 13 (2): 135–141.
- Yang, Y.T., Tai, C.J., Chen, C. et al. (2016). Highly diverse efficacy of salvage treatment regimens for relapsed or refractory peripheral T-cell lymphoma: a systematic review. PLoS One 11 (10): e0161811.
- Pro, B., Advani, R., Brice, P. et al. (2012). Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol 30 (18): 2190–2196.
- Gkotzamanidou, M. and Papadimitriou, C.A. (2014). Peripheral T-cell lymphoma: the role of hematopoietic stem cell transplantation. Crit Rev Oncol Hematol 89 (2): 248–261.
- Fanin, R., Ruiz de Elvira, M.C., Sperotto, A. et al. (1999). Autologous stem cell transplantation for T and null cell CD30-positive anaplastic large cell lymphoma: analysis of 64 adult and paediatric cases reported to the European Group for Blood and Marrow Transplantation (EBMT). Bone Marrow Transplant 23 (5): 437–442.
- Jagasia, M., Morgan, D., Goodman, S. et al. (2004). Histology impacts the outcome of peripheral T-cell lymphomas after high dose chemotherapy and stem cell transplant. Leuk Lymphoma 45 (11): 2261–2267.
- Reimer, P. (2010). Impact of autologous and allogeneic stem cell transplantation in peripheral T-cell lymphomas. Adv Hematol 2010: 320624.
- Mosse, Y.P., Lim, M.S., Voss, S.D. et al. (2013). Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: a Children's Oncology Group phase 1 consortium study. Lancet Oncol 14 (6): 472–480.
- Syed, Y.Y. (2019). Lorlatinib: first global approval. Drugs 79 (1): 93–98.
- Yang, J. and Gong, W. (2019). Lorlatinib for the treatment of anaplastic lymphoma kinase-positive non-small cell lung cancer. Expert Rev Clin Pharmacol 12 (3): 173–178.
- Shimony, S., Horowitz, N., Ribakovsky, E. et al. (2019). Romidepsin treatment for relapsed or refractory peripheral and cutaneous T-cell lymphoma – real-life data from a national multicenter observational study. Hematol Oncol 37 (5): 569–577.
- Coiffier, B., Pro, B., Prince, H.M. et al. (2012). Results from a pivotal, open-label, phase II study of romidepsin in relapsed or refractory peripheral T-cell lymphoma after prior systemic therapy. J Clin Oncol 30 (6): 631–636.
- Allen, P.B. and Lechowicz, M.J. (2018). Hematologic toxicity is rare in relapsed patients treated with belinostat: a systematic review of belinostat toxicity and safety in peripheral T-cell lymphomas. Cancer Manag Res 10: 6731–6742.
- Horwitz, S.M., Kim, Y.H., Foss, F. et al. (2012). Identification of an active, well-tolerated dose of pralatrexate in patients with relapsed or refractory cutaneous T-cell lymphoma. Blood 119 (18): 4115–4122.
- O'Connor, O.A., Pro, B., Pinter-Brown, L. et al. (2011). Pralatrexate in patients with relapsed or refractory peripheral T-cell lymphoma: results from the pivotal PROPEL study. J Clin Oncol 29 (9): 1182–1189.
- Hui, J., Przespo, E., and Elefante, A. (2012). Pralatrexate: a novel synthetic antifolate for relapsed or refractory peripheral T-cell lymphoma and other potential uses. J Oncol Pharm Pract 18 (2): 275–283.
- Advani, R.H., Ansell, S.M., Lechowicz, M.J. et al. (2016). A phase II study of cyclophosphamide, etoposide, vincristine and prednisone (CEOP) alternating with Pralatrexate (P) as front line therapy for patients with peripheral T-cell lymphoma (PTCL): final results from the T- cell consortium trial. Br J Haematol 172 (4): 535–544.
- Amin, H.M., Medeiros, L.J., Ma, Y. et al. (2003). Inhibition of JAK3 induces apoptosis and decreases anaplastic lymphoma kinase activity in anaplastic large cell lymphoma. Oncogene 22 (35): 5399–5407.
- Graf, N., Li, Z., Herrmann, K. et al. (2014). Positron emission tomographic monitoring of dual phosphatidylinositol-3-kinase and mTOR inhibition in anaplastic large cell lymphoma. Onco Targets Ther 7: 789–798.
- Chan, T.S., Tse, E., and Kwong, Y.L. (2017). Chidamide in the treatment of peripheral T-cell lymphoma. Onco Targets Ther 10: 347–352.
- Luchtel, R.A., Dasari, S., Oishi, N. et al. (2018). Molecular profiling reveals immunogenic cues in anaplastic large cell lymphomas with DUSP22 rearrangements. Blood 132 (13): 1386–1398.
- Kong, J., Dasari, S., and Feldman, A.L. (2020). PD-L1 expression in anaplastic large cell lymphoma. Mod Pathol 33 (6): 1232–1233.
- Hebart, H., Lang, P., and Woessmann, W. (2016). Nivolumab for refractory anaplastic large cell lymphoma: a case report. Ann Intern Med 165 (8): 607–608.
- Rigaud, C., Abbou, S., Minard-Colin, V. et al. (2018). Efficacy of nivolumab in a patient with systemic refractory ALK+ anaplastic large cell lymphoma. Pediatr Blood Cancer 65 (4) https://doi.org/10.1002/pbc.26902.
- Wartewig, T., Kurgyis, Z., Keppler, S. et al. (2017). PD-1 is a haploinsufficient suppressor of T cell lymphomagenesis. Nature 552: 121.
- Ratner, L., Waldmann, T.A., Janakiram, M., and Brammer, J.E. (2018). Rapid progression of adult T-cell leukemia-lymphoma after PD-1 inhibitor therapy. N Engl J Med 378 (20): 1947–1948.
- Chen, J., Zhang, Y., Petrus, M.N. et al. (2017). Cytokine receptor signaling is required for the survival of ALK- anaplastic large cell lymphoma, even in the presence of JAK1/STAT3 mutations. Proc Natl Acad Sci U S A 114 (15): 3975–3980.
- Amin, H.M. and Lai, R. (2007). Pathobiology of ALK+ anaplastic large-cell lymphoma. Blood 110 (7): 2259–2267.
- Redaelli, S., Ceccon, M., Antolini, L. et al. (2016). Synergistic activity of ALK and mTOR inhibitors for the treatment of NPM-ALK positive lymphoma. Oncotarget 7 (45): 72886–72897.
- Barr, P.M., Li, H., Spier, C. et al. (2015). Phase II intergroup trial of alisertib in relapsed and refractory peripheral T-cell lymphoma and transformed mycosis fungoides: SWOG 1108. J Clin Oncol 33 (21): 2399–2404.
- Ahmed, N. and Feldman, A.L. (2020). Targeting epigenetic regulators in the treatment of T-cell lymphoma. Expert Rev Hematol 13 (2): 127–139.
- Shi, Y., Dong, M., Hong, X. et al. (2015). Results from a multicenter, open-label, pivotal phase II study of chidamide in relapsed or refractory peripheral T-cell lymphoma. Ann Oncol 26 (8): 1766–1771.
- Hassler, M.R., Klisaroska, A., Kollmann, K. et al. (2012). Antineoplastic activity of the DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine in anaplastic large cell lymphoma. Biochimie 94 (11): 2297–2307.
- Ramos, C.A., Ballard, B., Zhang, H. et al. (2017). Clinical and immunological responses after CD30-specific chimeric antigen receptor-redirected lymphocytes. J Clin Invest 127 (9): 3462–3471.
- Perera, L.P., Zhang, M., Nakagawa, M. et al. (2017). Chimeric antigen receptor modified T cells that target chemokine receptor CCR4 as a therapeutic modality for T-cell malignancies. Am J Hematol 92 (9): 892–901.
- Di Stasi, A., De Angelis, B., Rooney, C.M. et al. (2009). T lymphocytes coexpressing CCR4 and a chimeric antigen receptor targeting CD30 have improved homing and antitumor activity in a Hodgkin tumor model. Blood 113 (25): 6392–6402.
- Rothe, A., Sasse, S., Topp, M.S. et al. (2015). A phase 1 study of the bispecific anti-CD30/CD16A antibody construct AFM13 in patients with relapsed or refractory Hodgkin lymphoma. Blood 125 (26): 4024–4031.
- Wu, J., Fu, J., Zhang, M., and Liu, D. (2015). AFM13: a first-in-class tetravalent bispecific anti-CD30/CD16A antibody for NK cell-mediated immunotherapy. J Hematol Oncol 8: 96.