Next Article in Journal
Cost-Effectiveness in Alternative Treatment Options for Pancreatic Pseudocysts
Previous Article in Journal
Postural Orthostatic Tachycardia Syndrome (POTS) as an Adverse Event to the Human Papilloma Virus (HPV) Vaccine and Its Relationship with Ehlers–Danlos Syndrome (EDS)
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Reports
Volume 7
Issue 2
10.3390/reports7020037
reports-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Trophoblast Cell Surface Antigen 2 (Trop2) Is Expressed in Cases of EBV-Positive Diffuse Large B-Cell Lymphoma Emerging from Angioimmunoblastic T-Cell Lymphoma

by
Susanne Ghandili
1,*,
Judith Dierlamm
1,
Carsten Bokemeyer
1,
Clara Marie von Bargen
2,
Anne Menz
2,† and
Sören Alexander Weidemann
2,†
1
Department of Oncology, Hematology and Bone Marrow Transplantation with Section Pneumology, University Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany
2
Institute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Reports 2024, 7(2), 37; https://doi.org/10.3390/reports7020037
Submission received: 27 March 2024 / Revised: 9 May 2024 / Accepted: 10 May 2024 / Published: 14 May 2024
(This article belongs to the Special Issue Cyto-Histological Correlations in Pathology Diagnostics)
Browse Figures
Review Reports Versions Notes

Abstract

:
Although trophoblast cell surface antigen 2 (Trop2)-targeting drugs are already approved or under investigation in various solid tumors, the significance of Trop2 in lymphoma is unknown. Thus, our objective was to investigate the expression of Trop2 in diffuse large B-cell lymphoma (DLBCL) through a systemic immunohistochemistry screening. We constructed a tissue microarray comprising tissue from 92 DLBCL patients, each diagnosed at the University Medical Center Hamburg-Eppendorf (2020–2022). Trop2-immunohistochemistry was carried out, and positive staining was deemed a specific membranous positivity. Four samples were derived from Epstein-Barr virus (EBV)-positive DLBCL, with one case of EBV-positive DLBCL following angioimmunoblastic T-cell lymphoma (AITL). Strong Trop2 immunostaining was detectable in 1 of 91 analyzable samples, originating from a patient with a composite EBV-positive DLBCL emerging from AITL. Therefore, we performed an additional database search to identify all cases of composite EBV-positive DLBCL emerging from AITL since 2015. Five additional cases were identified and stained for Trop2, revealing two cases with strong B-blast positivity. Our preliminary data imply that Trop2 appears absent in de novo DLBCL, whereas Trop2 is strongly expressed in cases of a rare variant of EBV-positive DLBCL. Further investigations are needed to confirm our results, particularly on the subset of EBV-positive DLBCL emerging from AITL.

1. Introduction

Non-Hodgkin lymphoma comprises a heterogeneous group of nodal, extranodal, or disseminated B- or T-cell malignancies; worldwide diffuse large B-cell lymphoma (DLBCL) accounts for approximately every third to fourth non-Hodgkin lymphoma [1,2,3,4]. Even though most DLBCL can be classified as primary DLBCL based on a de novo origin, a significant percentage of DLBCL originates or emerges from indolent B-cell lymphoma. Progression rates are in the range 2–8% in chronic lymphatic leukemia up to 14.3% in follicular lymphoma [5,6]. Moreover, DLBCL can originate within nodular lymphocyte predominant B-cell lymphoma or peripheral T-cell lymphoma (e.g., angioimmunoblastic T-cell lymphoma (AITL) [7,8,9,10,11,12]. Current treatment regimens that e.g., Pola-R-CHP or R-CHOP (consisting of polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisolone and rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone, respectively), have shown curability rates of up to 60–70% in patients with previously untreated DLBCL [3,13]. Yet, for chemotherapy-insensitive primary refractory or early relapsing DLBCL, promising newly developed treatment approaches, including CD19-directed CAR-T-cell therapies and T-cell-engaging bi-specific CD3xCD20-directed antibodies, have recently been approved, changing the treatment landscape of refractory and relapsing DLBCL [14,15,16,17,18,19]. However, a precision medicine strategy based on identifying potentially targetable driver mutations might provide additional treatment options in a subset of patients.
The tumor-associated calcium signal transducer 2, also referred to as trophoblast cell surface antigen 2 (Trop2), is a cell-surface glycoprotein, first elucidated as a transmembrane calcium signal transducer, encoded by the TACSTD2 gene [20]. Trop2 expression was initially delineated in non-cancerous trophoblasts and fetal tissues and is physiologically expressed in the stratified squamous epithelium of the skin, tonsillar crypts, esophagus, and uterine cervix [20,21,22]. Overexpression of Trop2 has been reported in glioma, basal cell carcinoma, squamous cell cancer of the skin, squamous cell cancer of the oral cavity, head, and neck, thyroid, lung, esophageal, gastric, colorectal, pancreatic, renal, breast, uterine, and ovarian cancer [23,24]. Moreover, in several solid malignancies such as pancreatic, hilar cholangiocarcinoma, cervical and gastric cancer, high Trop2 expression correlates with poor prognosis [19]. Furthermore, Trop2 interacts with several molecular signaling pathways associated with tumor development and progression (e.g., MAPK, PI3K/AKT). Levels of Trop2-mRNA expression correlate with tumor size and, in some cancer entities, with the extent of metastasis, whereas Trop2 knockdown or antibody-based inhibition leads to decreasing in vitro cancer cell proliferation, invasion, colony formation, and migration [24]. Since Trop2 is a transmembrane protein with an extra-cellular domain overexpressed in various solid malignancies compared to normal tissues, it has been the subject of targeted therapy. Sacituzumab govitecan is a first-in-class Trop2-directed antibody-drug-conjugate delivering SN38 (an irinotecan metabolite), first approved in 2021 “for the treatment of patients with unresectable locally advanced or metastatic triple-negative breast cancer who have received two or more prior systemic therapies, at least one of them for metastatic disease”, shortly after “for locally advanced or metastatic urothelial cancer who have previously received platinum-containing chemotherapy and either programmed death receptor-1 or programmed death-ligand 1 inhibitor”, and most recently “for patients with unresectable locally advanced or metastatic hormone receptor-positive, HER2-negative breast cancer who have received endocrine-based therapy and at least two additional systemic therapies in the metastatic setting” [24,25,26,27]. Another promising Trop2-directed antibody-drug conjugated is datopotamab deruxtecan, which is currently part of clinical trials (e.g., NCT04526691, NCT05555732, NCT05489211, and NCT05374512). Even though Trop2 has been widely investigated in preclinical and clinical trials in the setting of solid tumors, studies on its role in hematological malignancies, particularly lymphoma, remain rare [28,29,30]. Thus, up to now, Trop2 expression in lymphoma and DLBCL has yet to be investigated.
Since sacituzumab govitecan, an approved Trop2-targeting drug, is now available, we sought to examine the expression of Trop2 by performing a systemic immunohistochemistry (IHC) screening on a tissue microarray (TMA) derived from 92 patients with newly diagnosed or refractory or relapsed (r/r) DLBCL.

2. Materials and Methods

2.1. Patients

In this observational, single-center study, we examined 92 consecutive DLBCL patients aged 18 years or older who were immunohistochemically tested for Trop2 overexpression. This analysis adds to our previously published research, in which we performed a systematic immunohistochemical screening for NTRK fusion proteins on the same DLBCL cohort and accordingly using the same DLBCL-TMA. Details regarding the patient cohort can be found in Ghandili et al. [2]. As previously described, samples of all patients included in this analysis were derived from the Institute of Pathology of the University Medical Center Hamburg-Eppendorf, Germany, during the years 2020, 2021, and 2022. All patients were diagnosed with DLBCL as part of the clinical routine. The study design is presented in Figure 1. For disease staging assessment, we used the Ann Arbor classification [31]. For the calculation of prognostic risk scores, we used the International Prognostic Index (IPI) [32].
The date 21 December 2022 marked the data cutoff. Five additional cases date from 2017–2022. Representative tumor material was stained on large-area sections using the identical protocol, as explained for the TMA block below.
The use of archived remnants of diagnostic tissues for manufacturing of tissue microarrays (TMA) and their analysis for research purposes, as well as patient data collection and analysis, were reviewed and approved according to local legal requirements (HmbKHG, §12) and by the local ethics committee (Ethics Commission Hamburg, WF-049/09). Moreover, all analyses were carried out in compliance with the Declaration of Helsinki.

2.2. Tissue Microarray (TMA)

An already existing TMA of 92 DLBCLs was utilized. For the years 2020–2022, the institutional pathology database included a total of 414 samples of diagnosed DLBCL. Thereof, 92 samples were suitable for the TMA construction. Tissue samples of deficient sample size were excluded. The leading causes for deficient tissue sample size were either entirely or nearly completely utilized tissue during diagnostic workup or samples gained by small needle biopsy containing too little material for tissue extraction. Furthermore, we excluded all bone marrow biopsies since they are generally unsuitable for TMA construction.
TMA construction has already been discussed in detail [33]. Briefly, tissue cylinders, each 0.6 mm in diameter, were taken from tumor-containing areas of “donor” tissue blocks and placed into empty recipient paraffin blocks. The squamous epithelium of the skin served as a positive control.

2.3. Immunohistochemistry (IHC)

A freshly cut slide of the TMA block was deparaffinized with xylol and rehydrated through an alcohol series. A heat-induced antigen retrieval for 5 min was performed in an autoclave at 121 °C in pH 7.8 using DakoTarget Retrieval SolutionTM (Agilent, Santa Clara, CA, USA; #S2367). Endogenous peroxidase activity was blocked with Dako Peroxidase-Blocking SolutionTM (Agilent, Santa Clara, CA, USA; #52023) for 10 min. A primary antibody specific against TROP2 protein (recombinant rabbit monoclonal, MSVA-733R, MS Validated Antibodies, Hamburg, Germany) was applied at 37 °C for 60 min with a dilution of 1:150. According to the manufacturer’s protocol, the bound antibody was visualized using the EnVision KitTM (Agilent, Santa Clara, CA, USA; #K5007). The slide was then counterstained with haemalaun. The percentage of Trop2-positive lymphoma cells for each spot was estimated, and the staining intensity was semiquantitatively recorded (no staining = 0, weak staining = 1+, moderate staining = 2+, strong staining = 3+).

2.4. Endpoints

The primary objective of this study was to assess the frequency and intensity of immunohistochemical Trop2 expression in tumor samples of DLBCL patients.

2.5. Statistical Analysis

The statistical analyses were conducted using Microsoft Excel for Mac, version 16.38 (Microsoft Cooperation, Redmon, WA, USA). Continuous values are expressed as median, and nominal variables are presented as numbers.

3. Results

3.1. Patient Characteristics

Details of patient characteristics have been previously reported. In summary, all samples of 91 consecutive patients diagnosed with DLBCL were included in the analysis. Patient demographics and characteristics are presented in Table 1. Most samples originated from lymph nodes (38%), followed by testes (9%). The remaining samples were derived from other extranodal organs, such as the small intestine, colon, skin, spleen, liver, nasal, and buccal mucosa. The median age was 74, ranging from 32 to 90, and predominantly male (60%). In 13 patients, DLBCL derived or emerged from another preexisting lymphoma, including follicular lymphoma, lymphoplasmacytic lymphoma, chronic lymphatic lymphoma, and one case of AITL.

3.2. Immunohistochemical Findings

Based on identifying one case of strongly stainable Trop2-positive EBV-positive DLBCL (Figure 2 and Figure 3) that emerged from AITL, next, we performed an additional systemic search in the pathology reports database to identify all cases of EBV-positive DLBCL that emerged from AITL. A total of five other patients were identified. Characteristics and IHC results of these additional five patients are presented in Table 2. Two cases had strong membranous staining on the B-blasts, while all T-cells remained negative (Figure 4).

4. Discussion

Up to now, the role of Trop2 in lymphoma, especially in DLBCL, has been sparsely examined. Thus, our objective was to investigate the frequency and intensity of Trop2 expression in DLBCL by performing a systemic immunohistochemical screening for Trop2 expression in a sizeable cohort of DLBCL samples. Trop2 expression was detectable in only 1 of 91 TMA samples. Remarkably, the positive sample originated from a patient with secondary EBV-positive DLBCL developed in the background of AITL. By supplementary investigation of five additional samples of EBV-positive DLBCL emerging from AITL available at our department, we could observe strong Trop2 expression in two of these cases.
Based on a suspected dysfunction of both B- and T-cells, AITL is characterized by the development of concomitant autoimmune disorders and a particular tendency of patients to develop opportunistic infections. Thus, the systemic immunological dysfunction observed in AITL is reminiscent of the late stages of infection by the human immunodeficiency virus [11]. Furthermore, chemotherapy protocols impair the immune system and inhibit cellular immunity, favoring the growth of latent EBV-infected B cells. EBV-positive immunoblasts are a common diagnostic finding in AITL. Thirty percent of AITL cases develop clonal IgG rearrangements, and up to 5% of AITL cases have a morphologically perceptible EBV-positive B-cell lymphoproliferation. Nevertheless, transformation to a high-grade lymphoma, e.g., secondary DLBCL, is possible but rarely occurs [12,34]. Unsurprisingly, in immunohistochemistry, only a few blasts seemed to stain positive. In all positive cases, several follow-up bone marrow and lymph node biopsies were taken within a few months. First, a clonal B-cell lymphoproliferation of unclear significance was detected, which was considered to progress to a DLBCL after persisting in follow-up biopsies. Naturally, in such cases there were no dense, homogenous areas of blasts, but rather small clusters of blasts. Therefore, the expected number of positive B-blasts was lower than in de novo DLBCL.
The fact that an immunosuppressive environment contributes to the clonal proliferation of EBV-positive cells from which high-grade lymphomas can arise is already well described in the literature for the post-transplant scenario [35,36,37]. The current edition of the WHO has dedicated a separate chapter to this phenomenon and replaced the former term post-transplant lymphoproliferations (PTLD) with the broader term lymphoproliferations and lymphomas associated with immunodeficiency and dysregulation (IDD lymphomas). We consider it appropriate to classify the cases of EBV-positive secondary DLBCL described here in this category and to assume a similar pathogenesis of insufficient immune regulation within the tumor environment of AITL.
Regarding de novo EBV negative DLBCL, our results generally align with those previously published by Dum and colleagues [28]. Dum et al. report one of the few studies of immunohistochemically screening for Trop2, among others, in a large cohort of different lymphoma entities, including 108 samples of DLBCL. Interestingly, Trop2 was neither detectable in DLBCL nor in any other lymphoma entity, including Hodgkin, indolent B-cell, mantle cell, and T-cell lymphoma [28]. Another analysis investigating the expression of Trop2 in lymphoma is a Chinese study reported by Chen et al. The authors demonstrated a high immunohistochemical Trop2 expression in 14 of 26 tissue samples of extranodal NK/T cell lymphoma, nasal-type patients [30].
Albeit we performed a systemic immunohistology screening for Trop2, our study has limitations, since there remains a residual risk of a potential selection bias of the used DLBCL samples gained from a single center cohort. In addition, data on patients’ clinical characteristics were only available for a subset of patients since even though all patients were diagnosed, they were not compulsively treated at our university medical center.
Since we observed no space-filling but rather sporadic Trop-2 positive blast population, predictions regarding potentially Trop2-directed treatment response remain content of further research.

5. Conclusions

In conclusion, even though Trop2 was not detectable in EBV-negative de novo DLBCL, we were able to immunohistochemically detect high Trop2 expression in a total of three samples of EBV-positive DLBCL transformed from AITL. To our knowledge, this is the first analysis reporting high Trop2 expression in secondary EBV-positive DLBCL. Nevertheless, additional studies of Trop2 in cohorts of EBV-positive DLBCL, particularly those emerging from AITL of similar or larger size, are necessary to confirm our results.

Author Contributions

Conceptualization, S.G. and S.A.W.; methodology, S.A.W.; validation, S.A.W.; formal analysis, S.G. and S.A.W.; investigation, S.G. and S.A.W.; resources, S.A.W.; data curation, S.G. and S.A.W.; writing—original draft preparation, S.G. and S.A.W.; writing—review and editing, S.G., J.D., C.B., C.M.v.B., A.M. and S.A.W., visualization, S.G. and S.A.W.; supervision, J.D. and C.B.; project administration, S.G. and S.A.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki. The use of archived remnants of diagnostic tissues for manufacturing of tissue microarrays (TMA) and their analysis for research purposes, as well as patient data collection and analysis, were reviewed and have been approved by local legal requirements (HmbKHG, §12) and by the local ethics committee (Ethics Commission Hamburg, WF-049/09).

Informed Consent Statement

Informed consent was waived by the ethics committee since only pseudonymous data were analyzed and published.

Data Availability Statement

The data generated in this study are available upon request from the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Armitage, J.O.; Gascoyne, R.D.; Lunning, M.A.; Cavalli, F. Non-Hodgkin lymphoma. Lancet 2017, 390, 298–310. [Google Scholar] [CrossRef] [PubMed]
  2. Ghandili, S.; Dierlamm, J.; Bokemeyer, C.; von Bargen, C.M.; Weidemann, S.A. NTRK fusion protein expression is absent in a large cohort of diffuse large B-cell lymphoma. Front. Oncol. 2023, 13, 1146029. [Google Scholar] [CrossRef] [PubMed]
  3. Melchardt, T.; Egle, A.; Greil, R. How I treat diffuse large B-cell lymphoma. ESMO Open 2023, 8, 100750. [Google Scholar] [CrossRef]
  4. Hui, D.; Proctor, B.; Donaldson, J.; Shenkier, T.; Hoskins, P.; Klasa, R.; Savage, K.; Chhanabhai, M.; Gascoyne, R.D.; Connors, J.M.; et al. Prognostic implications of extranodal involvement in patients with diffuse large B-cell lymphoma treated with rituximab and cyclophosphamide, doxorubicin, vincristine, and prednisone. Leuk. Lymphoma 2010, 51, 1658–1667. [Google Scholar] [CrossRef] [PubMed]
  5. Rossi, D.; Spina, V.; Gaidano, G. Biology and treatment of Richter syndrome. Blood 2018, 131, 2761–2772. [Google Scholar] [CrossRef]
  6. Wagner-Johnston, N.D.; Link, B.K.; Byrtek, M.; Dawson, K.L.; Hainsworth, J.; Flowers, C.R.; Friedberg, J.W.; Bartlett, N.L. Outcomes of transformed follicular lymphoma in the modern era: A report from the National LymphoCare Study (NLCS). Blood 2015, 126, 851–857. [Google Scholar] [CrossRef] [PubMed]
  7. Biasoli, I.; Stamatoullas, A.; Meignin, V.; Delmer, A.; Reman, O.; Morschhauser, F.; Coiffier, B.; Bosly, A.; Divine, M.; Brice, P. Nodular, lymphocyte-predominant Hodgkin lymphoma: A long-term study and analysis of transformation to diffuse large B-cell lymphoma in a cohort of 164 patients from the Adult Lymphoma Study Group. Cancer 2010, 116, 631–639. [Google Scholar] [CrossRef] [PubMed]
  8. Hartmann, S.; Eray, M.; Doring, C.; Lehtinen, T.; Brunnberg, U.; Kujala, P.; Vornanen, M.; Hansmann, M.-L. Diffuse large B cell lymphoma derived from nodular lymphocyte predominant Hodgkin lymphoma presents with variable histopathology. BMC Cancer 2014, 14, 332. [Google Scholar] [CrossRef] [PubMed]
  9. Xu, Y.; McKenna, R.W.; Hoang, M.P.; Collins, R.H.; Kroft, S.H. Composite angioimmunoblastic T-cell lymphoma and diffuse large B-cell lymphoma: A case report and review of the literature. Am. J. Clin. Pathol. 2002, 118, 848–854. [Google Scholar] [CrossRef]
  10. Yang, Q.X.; Pei, X.J.; Tian, X.Y.; Li, Y.; Li, Z. Secondary cutaneous Epstein-Barr virus-associated diffuse large B-cell lymphoma in a patient with angioimmunoblastic T-cell lymphoma: A case report and review of literature. Diagn. Pathol. 2012, 7, 7. [Google Scholar] [CrossRef]
  11. Dunleavy, K.; Wilson, W.H.; Jaffe, E.S. Angioimmunoblastic T cell lymphoma: Pathobiological insights and clinical implications. Curr. Opin. Hematol. 2007, 14, 348–353. [Google Scholar] [CrossRef] [PubMed]
  12. Attygalle, A.D.; Kyriakou, C.; Dupuis, J.; Grogg, K.L.; Diss, T.C.; Wotherspoon, A.C.; Chuang, S.S.; Cabeçadas, J.; Isaacson, P.G.F.; Du, M.-Q.M.; et al. Histologic evolution of angioimmunoblastic T-cell lymphoma in consecutive biopsies: Clinical correlation and insights into natural history and disease progression. Am. J. Surg. Pathol. 2007, 31, 1077–1088. [Google Scholar] [CrossRef] [PubMed]
  13. Pavlovsky, M.; Cubero, D.; Agreda-Vasquez, G.P.; Enrico, A.; Mela-Osorio, M.J.; San Sebastian, J.A.; Fogliatto, L.; Ovilla, R.; Avendano, O.; Machnicki, G.; et al. Clinical Outcomes of Patients With B-Cell Non-Hodgkin Lymphoma in Real-World Settings: Findings from the Hemato-Oncology Latin America Observational Registry Study. JCO Glob. Oncol. 2022, 8, e2100265. [Google Scholar] [CrossRef] [PubMed]
  14. Bishop, M.R.; Dickinson, M.; Purtill, D.; Barba, P.; Santoro, A.; Hamad, N.; Kato, K.; Sureda, A.; Greil, R.; Thieblemont, C.; et al. Second-Line Tisagenlecleucel or Standard Care in Aggressive B-Cell Lymphoma. N. Engl. J. Med. 2022, 386, 629–639. [Google Scholar] [CrossRef] [PubMed]
  15. Hutchings, M.; Mous, R.; Clausen, M.R.; Johnson, P.; Linton, K.M.; Chamuleau, M.E.D.; Lewis, D.J.; Balari, A.S.; Cunningham, D.; Oliveri, R.S.; et al. Dose escalation of subcutaneous epcoritamab in patients with relapsed or refractory B-cell non-Hodgkin lymphoma: An open-label, phase 1/2 study. Lancet 2021, 398, 1157–1169. [Google Scholar] [CrossRef] [PubMed]
  16. Dickinson, M.J.; Carlo-Stella, C.; Morschhauser, F.; Bachy, E.; Corradini, P.; Iacoboni, G.; Khan, C.; Wróbel, T.; Offner, F.; Trněný, M.; et al. Glofitamab for Relapsed or Refractory Diffuse Large B-Cell Lymphoma. N. Engl. J. Med. 2022, 387, 2220–2231. [Google Scholar] [CrossRef]
  17. Hutchings, M.; Morschhauser, F.; Iacoboni, G.; Carlo-Stella, C.; Offner, F.C.; Sureda, A.; Salles, G.; Martínez-Lopez, J.; Crump, M.; Thomas, D.N.; et al. Glofitamab, a Novel, Bivalent CD20-Targeting T-Cell-Engaging Bispecific Antibody, Induces Durable Complete Remissions in Relapsed or Refractory B-Cell Lymphoma: A Phase I Trial. J. Clin. Oncol. 2021, 39, 1959–1970. [Google Scholar] [CrossRef] [PubMed]
  18. Locke, F.L.; Miklos, D.B.; Jacobson, C.A.; Perales, M.A.; Kersten, M.J.; Oluwole, O.O.; Ghobadi, A.; Rapoport, A.P.; McGuirk, J.; Pagel, J.M.; et al. Axicabtagene Ciloleucel as Second-Line Therapy for Large B-Cell Lymphoma. N. Engl. J. Med. 2022, 386, 640–654. [Google Scholar] [CrossRef] [PubMed]
  19. Kamdar, M.; Solomon, S.R.; Arnason, J.; Johnston, P.B.; Glass, B.; Bachanova, V.; Ibrahimi, S.; Mielke, S.; Mutsaers, P.; Hernandez-Ilizaliturri, F.; et al. Lisocabtagene maraleucel versus standard of care with salvage chemotherapy followed by autologous stem cell transplantation as second-line treatment in patients with relapsed or refractory large B-cell lymphoma (TRANSFORM): Results from an interim analysis of an open-label, randomised, phase 3 trial. Lancet 2022, 399, 2294–2308. [Google Scholar]
  20. Zaman, S.; Jadid, H.; Denson, A.C.; Gray, J.E. Targeting Trop-2 in solid tumors: Future prospects. Onco Targets Ther. 2019, 12, 1781–1790. [Google Scholar] [CrossRef]
  21. Vranic, S.; Gatalica, Z. Trop-2 protein as a therapeutic target: A focused review on Trop-2-based antibody-drug conjugates and their predictive biomarkers. Bosn. J. Basic. Med. Sci. 2022, 22, 14–21. [Google Scholar] [CrossRef]
  22. Lipinski, M.; Parks, D.R.; Rouse, R.V.; Herzenberg, L.A. Human trophoblast cell-surface antigens defined by monoclonal antibodies. Proc. Natl. Acad. Sci. USA 1981, 78, 5147–5150. [Google Scholar] [CrossRef] [PubMed]
  23. Stepan, L.P.; Trueblood, E.S.; Hale, K.; Babcook, J.; Borges, L.; Sutherland, C.L. Expression of Trop2 cell surface glycoprotein in normal and tumor tissues: Potential implications as a cancer therapeutic target. J. Histochem. Cytochem. 2011, 59, 701–710. [Google Scholar] [CrossRef]
  24. Goldenberg, D.M.; Stein, R.; Sharkey, R.M. The emergence of trophoblast cell-surface antigen 2 (TROP-2) as a novel cancer target. Oncotarget 2018, 9, 28989–29006. [Google Scholar] [CrossRef] [PubMed]
  25. FDAUS. FDA Approves Sacituzumab Govitecan-Hziy for HR-Positive Breast Cancer 2023. Available online: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-sacituzumab-govitecan-hziy-hr-positive-breast-cancer (accessed on 23 June 2023).
  26. FDA US. FDA Grants Regular Approval to Sacituzumab Govitecan for Triple-Negative Breast Cancer 2021. Available online: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-regular-approval-sacituzumab-govitecan-triple-negative-breast-cancer (accessed on 23 June 2023).
  27. FDA US. FDA Grants Accelerated Approval to Sacituzumab Govitecan for Advanced Urothelial Cancer 2021. Available online: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-sacituzumab-govitecan-advanced-urothelial-cancer (accessed on 23 June 2023).
  28. Dum, D.; Taherpour, N.; Menz, A.; Hoflmayer, D.; Volkel, C.; Hinsch, A.; Gorbokon, N.; Lennartz, M.; Hube-Magg, C.; Fraune, C.; et al. Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors. Pathobiology 2022, 89, 245–258. [Google Scholar] [CrossRef] [PubMed]
  29. Bobos, M.; Kotoula, V.; Kaloutsi, V.; Karayannopoulou, G.; Papadimitriou, C.S.; Kostopoulos, I. Aberrant CCND1 copies and cyclin D1 mRNA expression do not result in the production of functional cyclin D1 protein in anaplastic large cell lymphoma. Histol. Histopathol. 2009, 24, 1035–1048. [Google Scholar]
  30. Chen, R.; Lu, M.; Wang, J.; Zhang, D.; Lin, H.; Zhu, H.; Zhang, W.; Xiong, L.; Ma, J.; Mao, Y.; et al. Increased expression of Trop2 correlates with poor survival in extranodal NK/T cell lymphoma, nasal type. Virchows Arch. 2013, 463, 713–719. [Google Scholar] [CrossRef]
  31. Lister, T.A.; Crowther, D.; Sutcliffe, S.B.; Glatstein, E.; Canellos, G.P.; Young, R.C.; Rosenberg, S.A.; Coltman, C.A.; Tubiana, M. Report of a committee convened to discuss the evaluation and staging of patients with Hodgkin’s disease: Cotswolds meeting. J. Clin. Oncol. 1989, 7, 1630–1636. [Google Scholar] [CrossRef] [PubMed]
  32. International Non-Hodgkin’s Lymphoma Prognostic Factors P. A predictive model for aggressive non-Hodgkin’s lymphoma. N. Engl. J. Med. 1993, 329, 987–994. [Google Scholar] [CrossRef]
  33. Kononen, J.; Bubendorf, L.; Kallioniemi, A.; Barlund, M.; Schraml, P.; Leighton, S.; Torhorst, J.; Mihatsch, M.J.; Sauter, G.; Kallionimeni, O.-P. Tissue microarrays for high-throughput molecular profiling of tumor specimens. Nat. Med. 1998, 4, 844–847. [Google Scholar] [CrossRef]
  34. Zettl, A.; Lee, S.S.; Rudiger, T.; Starostik, P.; Marino, M.; Kirchner, T.; Ott, M.; Muller-Hermelink, H.K.; Ott, G. Epstein-Barr virus-associated B-cell lymphoproliferative disorders in angloimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, unspecified. Am. J. Clin. Pathol. 2002, 117, 368–379. [Google Scholar] [CrossRef]
  35. Petit, B.; Le Meur, Y.; Jaccard, A.; Paraf, F.; Robert, C.L.; Bordessoule, D.; Labrousse, F.; Drouet, M. Influence of host-recipient origin on clinical aspects of posttransplantation lymphoproliferative disorders in kidney transplantation. Transplantation 2002, 73, 265–271. [Google Scholar] [CrossRef]
  36. Martinez, O.M.; Krams, S.M. The Immune Response to Epstein Barr Virus and Implications for Posttransplant Lymphoproliferative Disorder. Transplantation 2017, 101, 2009–2016. [Google Scholar] [CrossRef]
  37. Leblond, V.; Choquet, S. Lymphoproliferative disorders after liver transplantation. J. Hepatol. 2004, 40, 728–735. [Google Scholar] [CrossRef]
Reports 07 00037 g001
Figure 1. Flow chart of study design and population, as previously published by Ghandili et al. 2023 [2].
Figure 1. Flow chart of study design and population, as previously published by Ghandili et al. 2023 [2].
Reports 07 00037 g001
Reports 07 00037 g002
Figure 2. (200×): Strong (3+) immunohistology Trop2 expression in a case of composite EBV-positive DLBCL emerging from AITL.
Figure 2. (200×): Strong (3+) immunohistology Trop2 expression in a case of composite EBV-positive DLBCL emerging from AITL.
Reports 07 00037 g002
Reports 07 00037 g003
Figure 3. (200×): Trop2 positive control tested on a skin sample.
Figure 3. (200×): Trop2 positive control tested on a skin sample.
Reports 07 00037 g003
Reports 07 00037 g004aReports 07 00037 g004b
Figure 4. (A,B) (200×): Case 1 (A) and Case 4 (B): Most cells are T-cells of angioimmunoblastic T-cell lymphoma as well as reactive background cells. Single cells and incipient groups of B-blasts were consistently found to moderately to strongly express Trop2. In additional studies, these blasts showed strong positivity for CD30 and EBV-encoding RNA (EBER) (not shown) as well as a clonal IgH-genre arrangement and indicated a transition from a clonal B-lymphoproliferation into high-grade EBV-positive B-cell lymphoma.
Figure 4. (A,B) (200×): Case 1 (A) and Case 4 (B): Most cells are T-cells of angioimmunoblastic T-cell lymphoma as well as reactive background cells. Single cells and incipient groups of B-blasts were consistently found to moderately to strongly express Trop2. In additional studies, these blasts showed strong positivity for CD30 and EBV-encoding RNA (EBER) (not shown) as well as a clonal IgH-genre arrangement and indicated a transition from a clonal B-lymphoproliferation into high-grade EBV-positive B-cell lymphoma.
Reports 07 00037 g004aReports 07 00037 g004b
Table 1. Patient characteristics of the TMA cohort [1].
Table 1. Patient characteristics of the TMA cohort [1].
Total number of analyzable patients, n91
Age at DLBCL diagnosis, median (range)74 (32–90)
Female sex, n (%)37 (40)
Subtypes, n (%)
Cell of origin type: Germinal center B-cell-like41 (45)
Epstein-Barr-virus positivity4 (4)
Double hit2 (2)
Triple hit0
Ann Arbor stage, n (%)
1A or 1B and 2A or 2B18 (20)
3A or 3B5 (5)
4A or 4B14 (15)
Not evaluable59 (65)
International Prognostic Index, n (%)
0–112 (13)
2–313 (14)
4–54 (4)
Not evaluable62 (68)
Table 2. Characteristics and IHC results of additional five patients/tissue samples of composite EBV-positive DLBCL emerging AITL. All cases of composite EBV-positive DLBCL were confirmed by reference pathology.
Table 2. Characteristics and IHC results of additional five patients/tissue samples of composite EBV-positive DLBCL emerging AITL. All cases of composite EBV-positive DLBCL were confirmed by reference pathology.
Age in YearsSexTissue OriginTrop2 Staining IntensityRefer to Figure
Case 156FemaleLymph node3+4A
Case 284FemaleLymph node0NA
Case 348FemaleLymph node0NA
Case 481FemaleLymph node3+4B
Case 548FemaleSkin0NA
NA: Not applicable.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Ghandili, S.; Dierlamm, J.; Bokemeyer, C.; von Bargen, C.M.; Menz, A.; Weidemann, S.A. Trophoblast Cell Surface Antigen 2 (Trop2) Is Expressed in Cases of EBV-Positive Diffuse Large B-Cell Lymphoma Emerging from Angioimmunoblastic T-Cell Lymphoma. Reports 2024, 7, 37. https://doi.org/10.3390/reports7020037

AMA Style

Ghandili S, Dierlamm J, Bokemeyer C, von Bargen CM, Menz A, Weidemann SA. Trophoblast Cell Surface Antigen 2 (Trop2) Is Expressed in Cases of EBV-Positive Diffuse Large B-Cell Lymphoma Emerging from Angioimmunoblastic T-Cell Lymphoma. Reports. 2024; 7(2):37. https://doi.org/10.3390/reports7020037

Chicago/Turabian Style

Ghandili, Susanne, Judith Dierlamm, Carsten Bokemeyer, Clara Marie von Bargen, Anne Menz, and Sören Alexander Weidemann. 2024. "Trophoblast Cell Surface Antigen 2 (Trop2) Is Expressed in Cases of EBV-Positive Diffuse Large B-Cell Lymphoma Emerging from Angioimmunoblastic T-Cell Lymphoma" Reports 7, no. 2: 37. https://doi.org/10.3390/reports7020037

Article Metrics

Back to TopTop