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06.12.2024 | REVIEW

Measurable Residual Disease in Mantle Cell Lymphoma: The Unbearable Lightness of Being Undetectable

verfasst von: Julio Cartagena, Anagha Deshpande, Allison Rosenthal, Mazie Tsang, Talal Hilal, Lisa Rimsza, Razelle Kurzrock, Javier Munoz

Erschienen in: Current Oncology Reports | Ausgabe 12/2024

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Abstract

Purpose of review

This paper evaluates the benefits and limitations of detecting measurable residual disease (MRD) in mantle cell lymphoma (MCL) and assesses its prognostic value. It also aims to highlight the importance of detecting low MRD levels post-treatment and their application in clinical practice.

Recent findings

Recent studies show that MRD levels predict relapse and survival outcomes in hematologic neoplasms, including MCL. RT-qPCR is currently the most used method due to its high reproducibility and sensitivity. Ideal MRD detection should be highly sensitive, cost-effective, and applicable to a wide demographic of patients.

Summary

This paper concludes that MRD detection has prognostic value in MCL but faces limitations in sensitivity and specificity. Further research is needed to establish the significance of low MRD levels before integrating these methods into clinical practice. Improved MRD detection technologies and understanding their impact on clinical outcomes will guide better patient management in MCL.
Literatur
1.
Zurück zum Zitat Wang M, Sun L, Qian J, et al. Cyclin D1 as a universally expressed mantle cell lymphoma-associated tumor antigen for immunotherapy. Leukemia. 2009;23:1320–8.PubMedPubMedCentralCrossRef Wang M, Sun L, Qian J, et al. Cyclin D1 as a universally expressed mantle cell lymphoma-associated tumor antigen for immunotherapy. Leukemia. 2009;23:1320–8.PubMedPubMedCentralCrossRef
2.
Zurück zum Zitat Wu X, Lu H, Pang T, et al. Association of minimal residual disease levels with clinical outcomes in patients with mantle cell lymphoma: a meta-analysis. Leuk Res. 2021;108:106605.PubMedCrossRef Wu X, Lu H, Pang T, et al. Association of minimal residual disease levels with clinical outcomes in patients with mantle cell lymphoma: a meta-analysis. Leuk Res. 2021;108:106605.PubMedCrossRef
3.
Zurück zum Zitat Smith A, Howell D, Patmore R, Jack A, Roman E. Incidence of haematological malignancy by sub-type: a report from the Haematological Malignancy Research Network. Br J Cancer. 2011;105:1684–92.PubMedPubMedCentralCrossRef Smith A, Howell D, Patmore R, Jack A, Roman E. Incidence of haematological malignancy by sub-type: a report from the Haematological Malignancy Research Network. Br J Cancer. 2011;105:1684–92.PubMedPubMedCentralCrossRef
4.
Zurück zum Zitat Lew TE, Minson A, Dickinson M, et al. Treatment approaches for patients with TP53-mutated mantle cell lymphoma. Lancet Haematol. 2023;10:e142–54.PubMedCrossRef Lew TE, Minson A, Dickinson M, et al. Treatment approaches for patients with TP53-mutated mantle cell lymphoma. Lancet Haematol. 2023;10:e142–54.PubMedCrossRef
5.
Zurück zum Zitat Ying ZT, Zheng W, Wang XP, et al. The clinical features, therapeutic responses, and prognosis of the patients with mantle cell lymphoma. Chin J Cancer. 2012;31:348–53.PubMedPubMedCentralCrossRef Ying ZT, Zheng W, Wang XP, et al. The clinical features, therapeutic responses, and prognosis of the patients with mantle cell lymphoma. Chin J Cancer. 2012;31:348–53.PubMedPubMedCentralCrossRef
6.
Zurück zum Zitat Hermine O, Hoster E, Walewski J, et al. Addition of high-dose cytarabine to immunochemotherapy before autologous stem-cell transplantation in patients aged 65 years or younger with mantle cell lymphoma (MCL Younger): a randomised, open-label, phase 3 trial of the European Mantle Cell Lymphoma Network. Lancet. 2016;388:565–75.PubMedCrossRef Hermine O, Hoster E, Walewski J, et al. Addition of high-dose cytarabine to immunochemotherapy before autologous stem-cell transplantation in patients aged 65 years or younger with mantle cell lymphoma (MCL Younger): a randomised, open-label, phase 3 trial of the European Mantle Cell Lymphoma Network. Lancet. 2016;388:565–75.PubMedCrossRef
7.
Zurück zum Zitat Le Gouill S, Thieblemont C, Oberic L, et al. Rituximab after autologous stem-cell transplantation in mantle-cell lymphoma. N Engl J Med. 2017;377:1250–60.PubMedCrossRef Le Gouill S, Thieblemont C, Oberic L, et al. Rituximab after autologous stem-cell transplantation in mantle-cell lymphoma. N Engl J Med. 2017;377:1250–60.PubMedCrossRef
8.
Zurück zum Zitat Hilal T, Wang Z, Almader-Douglas D, Rosenthal A, Reeder CB, Jain T. Rituximab maintenance therapy for mantle cell lymphoma: a systematic review and meta-analysis. Am J Hematol. 2018;93:1220–6.PubMedCrossRef Hilal T, Wang Z, Almader-Douglas D, Rosenthal A, Reeder CB, Jain T. Rituximab maintenance therapy for mantle cell lymphoma: a systematic review and meta-analysis. Am J Hematol. 2018;93:1220–6.PubMedCrossRef
9.
Zurück zum Zitat Rummel MJ, Niederle N, Maschmeyer G, et al. Bendamustine plus rituximab versus CHOP plus rituximab as first-line treatment for patients with indolent and mantle-cell lymphomas: an open-label, multicentre, randomised, phase 3 non-inferiority trial. Lancet. 2013;381:1203–10.PubMedCrossRef Rummel MJ, Niederle N, Maschmeyer G, et al. Bendamustine plus rituximab versus CHOP plus rituximab as first-line treatment for patients with indolent and mantle-cell lymphomas: an open-label, multicentre, randomised, phase 3 non-inferiority trial. Lancet. 2013;381:1203–10.PubMedCrossRef
10.
Zurück zum Zitat Dreyling M, Doorduijn JK, Gine E, et al. Efficacy and safety of ibrutinib combined with standard first-line treatment or as substitute for autologous stem cell transplantation in younger patients with mantle cell lymphoma: results from the randomized triangle trial by the european MCL network. Blood. 2022;140:1–3.CrossRef Dreyling M, Doorduijn JK, Gine E, et al. Efficacy and safety of ibrutinib combined with standard first-line treatment or as substitute for autologous stem cell transplantation in younger patients with mantle cell lymphoma: results from the randomized triangle trial by the european MCL network. Blood. 2022;140:1–3.CrossRef
11.
12.
Zurück zum Zitat Cliff ERS, Hilal T, Kesselheim AS. Complicated regulatory decision-making following inconsistent trial results: the issue with ibrutinib for mantle cell lymphoma. Nat Rev Clin Oncol. 2024;21:1–2.PubMedCrossRef Cliff ERS, Hilal T, Kesselheim AS. Complicated regulatory decision-making following inconsistent trial results: the issue with ibrutinib for mantle cell lymphoma. Nat Rev Clin Oncol. 2024;21:1–2.PubMedCrossRef
13.
Zurück zum Zitat Wang M, Rule S, Zinzani P, et al. Acalabrutinib monotherapy in patients with relapsed/refractory mantle cell lymphoma: long-term efficacy and safety results from a phase 2 study. Blood. 2020;136:38–9.CrossRef Wang M, Rule S, Zinzani P, et al. Acalabrutinib monotherapy in patients with relapsed/refractory mantle cell lymphoma: long-term efficacy and safety results from a phase 2 study. Blood. 2020;136:38–9.CrossRef
14.
15.
Zurück zum Zitat Martin P, Maddocks K, Leonard JP, et al. Postibrutinib outcomes in patients with mantle cell lymphoma. Blood. 2016;127:1559–63.PubMedCrossRef Martin P, Maddocks K, Leonard JP, et al. Postibrutinib outcomes in patients with mantle cell lymphoma. Blood. 2016;127:1559–63.PubMedCrossRef
16.
Zurück zum Zitat Porter DL, Levine BL, Kalos M, Bagg A, June CH. Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia. N Engl J Med. 2011;365:725–33.PubMedPubMedCentralCrossRef Porter DL, Levine BL, Kalos M, Bagg A, June CH. Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia. N Engl J Med. 2011;365:725–33.PubMedPubMedCentralCrossRef
17.
18.
Zurück zum Zitat Deshpande A, Wang Y, Munoz J, Jain P. Brexucabtagene autoleucel: a breakthrough in the treatment of mantle cell lymphoma. Drugs Today (Barc). 2022;58:283–98.PubMedCrossRef Deshpande A, Wang Y, Munoz J, Jain P. Brexucabtagene autoleucel: a breakthrough in the treatment of mantle cell lymphoma. Drugs Today (Barc). 2022;58:283–98.PubMedCrossRef
19.
Zurück zum Zitat Wang M, Munoz J, Goy A, et al. Three-year follow-up of kte-x19 in patients with relapsed/refractory mantle cell lymphoma, including high-risk subgroups, in the zuma-2 study. J Clin Oncol. 2023;41:555–67.PubMedCrossRef Wang M, Munoz J, Goy A, et al. Three-year follow-up of kte-x19 in patients with relapsed/refractory mantle cell lymphoma, including high-risk subgroups, in the zuma-2 study. J Clin Oncol. 2023;41:555–67.PubMedCrossRef
20.
Zurück zum Zitat Jain P, Nastoupil L, Westin J, et al. Outcomes and management of patients with mantle cell lymphoma after progression on brexucabtagene autoleucel therapy. Br J Haematol. 2021;192:e38–42.PubMedCrossRef Jain P, Nastoupil L, Westin J, et al. Outcomes and management of patients with mantle cell lymphoma after progression on brexucabtagene autoleucel therapy. Br J Haematol. 2021;192:e38–42.PubMedCrossRef
21.
Zurück zum Zitat Wang ML, Jurczak W, Zinzani PL, et al. Pirtobrutinib in covalent bruton tyrosine kinase inhibitor pretreated mantle-cell lymphoma. J Clin Oncol. 2023;41:3988–97.PubMedPubMedCentralCrossRef Wang ML, Jurczak W, Zinzani PL, et al. Pirtobrutinib in covalent bruton tyrosine kinase inhibitor pretreated mantle-cell lymphoma. J Clin Oncol. 2023;41:3988–97.PubMedPubMedCentralCrossRef
22.
Zurück zum Zitat Wu S, Blombery P, Westerman D, Tam CS. Utility of measurable residual disease (MRD) assessment in mantle cell lymphoma. Curr Treat Options Oncol 2023. Wu S, Blombery P, Westerman D, Tam CS. Utility of measurable residual disease (MRD) assessment in mantle cell lymphoma. Curr Treat Options Oncol 2023.
23.
Zurück zum Zitat Hummel M, Tamaru J, Kalvelage B, Stein H. Mantle cell (previously centrocytic) lymphomas express VH genes with no or very little somatic mutations like the physiologic cells of the follicle mantle. Blood. 1994;84:403–7.PubMedCrossRef Hummel M, Tamaru J, Kalvelage B, Stein H. Mantle cell (previously centrocytic) lymphomas express VH genes with no or very little somatic mutations like the physiologic cells of the follicle mantle. Blood. 1994;84:403–7.PubMedCrossRef
24.
Zurück zum Zitat Flohr T, Schrauder A, Cazzaniga G, et al. Minimal residual disease-directed risk stratification using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the international multicenter trial AIEOP-BFM ALL 2000 for childhood acute lymphoblastic leukemia. Leukemia. 2008;22:771–82.PubMedCrossRef Flohr T, Schrauder A, Cazzaniga G, et al. Minimal residual disease-directed risk stratification using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the international multicenter trial AIEOP-BFM ALL 2000 for childhood acute lymphoblastic leukemia. Leukemia. 2008;22:771–82.PubMedCrossRef
25.
Zurück zum Zitat van Dongen JJM, van der Velden VHJ, Brüggemann M, Orfao A. Minimal residual disease diagnostics in acute lymphoblastic leukemia: need for sensitive, fast, and standardized technologies. Blood. 2015;125:3996–4009.PubMedPubMedCentralCrossRef van Dongen JJM, van der Velden VHJ, Brüggemann M, Orfao A. Minimal residual disease diagnostics in acute lymphoblastic leukemia: need for sensitive, fast, and standardized technologies. Blood. 2015;125:3996–4009.PubMedPubMedCentralCrossRef
26.
Zurück zum Zitat Drandi D, Alcantara M, Benmaad I, et al. Droplet digital PCR quantification of mantle cell lymphoma follow-up samples from four prospective trials of the european MCL network. Hemasphere. 2020;4:e347.PubMedPubMedCentralCrossRef Drandi D, Alcantara M, Benmaad I, et al. Droplet digital PCR quantification of mantle cell lymphoma follow-up samples from four prospective trials of the european MCL network. Hemasphere. 2020;4:e347.PubMedPubMedCentralCrossRef
27.
Zurück zum Zitat Shirai R, Osumi T, Keino D, et al. Minimal residual disease detection by mutation-specific droplet digital PCR for leukemia/lymphoma. Int J Hematol. 2023;117:910–8.PubMedPubMedCentralCrossRef Shirai R, Osumi T, Keino D, et al. Minimal residual disease detection by mutation-specific droplet digital PCR for leukemia/lymphoma. Int J Hematol. 2023;117:910–8.PubMedPubMedCentralCrossRef
28.
Zurück zum Zitat Rimokh R, Berger F, Delsol G, et al. Detection of the chromosomal translocation t(11;14) by polymerase chain reaction in mantle cell lymphomas. Blood. 1994;83:1871–5.PubMedCrossRef Rimokh R, Berger F, Delsol G, et al. Detection of the chromosomal translocation t(11;14) by polymerase chain reaction in mantle cell lymphomas. Blood. 1994;83:1871–5.PubMedCrossRef
29.
Zurück zum Zitat Pott C, Schrader C, Gesk S, et al. Quantitative assessment of molecular remission after high-dose therapy with autologous stem cell transplantation predicts long-term remission in mantle cell lymphoma. Blood. 2006;107:2271–8.PubMedCrossRef Pott C, Schrader C, Gesk S, et al. Quantitative assessment of molecular remission after high-dose therapy with autologous stem cell transplantation predicts long-term remission in mantle cell lymphoma. Blood. 2006;107:2271–8.PubMedCrossRef
30.
Zurück zum Zitat Pott C, Hoster E, Delfau-Larue MH, et al. Molecular remission is an independent predictor of clinical outcome in patients with mantle cell lymphoma after combined immunochemotherapy: a European MCL intergroup study. Blood. 2010;115:3215–23.PubMedCrossRef Pott C, Hoster E, Delfau-Larue MH, et al. Molecular remission is an independent predictor of clinical outcome in patients with mantle cell lymphoma after combined immunochemotherapy: a European MCL intergroup study. Blood. 2010;115:3215–23.PubMedCrossRef
31.
Zurück zum Zitat Bottcher S, Ritgen M, Buske S, et al. Minimal residual disease detection in mantle cell lymphoma: methods and significance of four-color flow cytometry compared to consensus IGH-polymerase chain reaction at initial staging and for follow-up examinations. Haematologica. 2008;93:551–9.PubMedCrossRef Bottcher S, Ritgen M, Buske S, et al. Minimal residual disease detection in mantle cell lymphoma: methods and significance of four-color flow cytometry compared to consensus IGH-polymerase chain reaction at initial staging and for follow-up examinations. Haematologica. 2008;93:551–9.PubMedCrossRef
32.
Zurück zum Zitat Cheminant M, Derrieux C, Touzart A, et al. Minimal residual disease monitoring by 8-color flow cytometry in mantle cell lymphoma: an EU-MCL and LYSA study. Haematologica. 2016;101:336–45.PubMedPubMedCentralCrossRef Cheminant M, Derrieux C, Touzart A, et al. Minimal residual disease monitoring by 8-color flow cytometry in mantle cell lymphoma: an EU-MCL and LYSA study. Haematologica. 2016;101:336–45.PubMedPubMedCentralCrossRef
33.
Zurück zum Zitat Bayly E, Nguyen V, Binek A, et al. Validation of a modified pre-lysis sample preparation technique for flow cytometric minimal residual disease assessment in multiple myeloma, chronic lymphocytic leukemia, and B-non Hodgkin lymphoma. Cytometry B Clin Cytom. 2020;98:385–98.PubMedCrossRef Bayly E, Nguyen V, Binek A, et al. Validation of a modified pre-lysis sample preparation technique for flow cytometric minimal residual disease assessment in multiple myeloma, chronic lymphocytic leukemia, and B-non Hodgkin lymphoma. Cytometry B Clin Cytom. 2020;98:385–98.PubMedCrossRef
34.
Zurück zum Zitat Smith M, Jegede O, Parekh S, et al. Minimal residual disease (MRD) Assessment in the ecog1411 randomized phase 2 trial of front-line bendamustine-rituximab (br)-based induction followed by rituximab (r) ± lenalidomide (l) consolidation for mantle cell lymphoma (MCL). Blood. 2019;134:751.CrossRef Smith M, Jegede O, Parekh S, et al. Minimal residual disease (MRD) Assessment in the ecog1411 randomized phase 2 trial of front-line bendamustine-rituximab (br)-based induction followed by rituximab (r) ± lenalidomide (l) consolidation for mantle cell lymphoma (MCL). Blood. 2019;134:751.CrossRef
35.
Zurück zum Zitat Morgane C, Coralie D, Aurore T, et al. Minimal residual disease monitoring by 8-color flow cytometry in mantle cell lymphoma: an EU-MCL and LYSA study. Haematologica. 2016;101:336–45.CrossRef Morgane C, Coralie D, Aurore T, et al. Minimal residual disease monitoring by 8-color flow cytometry in mantle cell lymphoma: an EU-MCL and LYSA study. Haematologica. 2016;101:336–45.CrossRef
36.
Zurück zum Zitat Ching T, Duncan ME, Newman-Eerkes T, et al. Analytical evaluation of the clonoSEQ Assay for establishing measurable (minimal) residual disease in acute lymphoblastic leukemia, chronic lymphocytic leukemia, and multiple myeloma. BMC Cancer. 2020;20:612.PubMedPubMedCentralCrossRef Ching T, Duncan ME, Newman-Eerkes T, et al. Analytical evaluation of the clonoSEQ Assay for establishing measurable (minimal) residual disease in acute lymphoblastic leukemia, chronic lymphocytic leukemia, and multiple myeloma. BMC Cancer. 2020;20:612.PubMedPubMedCentralCrossRef
37.
Zurück zum Zitat Ladetto M, Bruggemann M, Monitillo L, et al. Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders. Leukemia. 2014;28:1299–307.PubMedCrossRef Ladetto M, Bruggemann M, Monitillo L, et al. Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders. Leukemia. 2014;28:1299–307.PubMedCrossRef
38.
Zurück zum Zitat Epstein-Peterson ZD, Batlevi CL, Caron P, et al. Frontline sequential immunochemotherapy plus lenalidomide for mantle cell lymphoma incorporating MRD evaluation: phase ii, investigator-initiated. Single-Center Study Blood. 2020;136:11–2. Epstein-Peterson ZD, Batlevi CL, Caron P, et al. Frontline sequential immunochemotherapy plus lenalidomide for mantle cell lymphoma incorporating MRD evaluation: phase ii, investigator-initiated. Single-Center Study Blood. 2020;136:11–2.
39.
Zurück zum Zitat Rezazadeh A, Pruett J, Detzner A, et al. Immunoglobulin high throughput sequencing (Ig-HTS) minimal residual disease (MRD) analysis is an effective surveillance tool in patients with mantle cell lymphoma. Clin Lymphoma Myeloma Leuk. 2024;24:254–9.PubMedCrossRef Rezazadeh A, Pruett J, Detzner A, et al. Immunoglobulin high throughput sequencing (Ig-HTS) minimal residual disease (MRD) analysis is an effective surveillance tool in patients with mantle cell lymphoma. Clin Lymphoma Myeloma Leuk. 2024;24:254–9.PubMedCrossRef
40.
Zurück zum Zitat Furqan F, Fenske T, Longo W, Johnson B, Hamadani M, Shah N. MRD Status by clonoseq ® is a poor predictor of long-term outcomes after bispecific lv20.19 CAR t-cell therapy for relapsed. Refractory B-Cell NHL Blood. 2022;140:6407–8. Furqan F, Fenske T, Longo W, Johnson B, Hamadani M, Shah N. MRD Status by clonoseq ® is a poor predictor of long-term outcomes after bispecific lv20.19 CAR t-cell therapy for relapsed. Refractory B-Cell NHL Blood. 2022;140:6407–8.
41.
Zurück zum Zitat Ananth S, Su Y-J, Hamilton MP, et al. Post-CAR-T minimal residual disease (MRD) monitoring in mantle cell lymphoma enables early relapse detection. Blood. 2023;142:1673.CrossRef Ananth S, Su Y-J, Hamilton MP, et al. Post-CAR-T minimal residual disease (MRD) monitoring in mantle cell lymphoma enables early relapse detection. Blood. 2023;142:1673.CrossRef
42.
Zurück zum Zitat Wan JCM, Massie C, Garcia-Corbacho J, et al. Liquid biopsies come of age: towards implementation of circulating tumour DNA. Nat Rev Cancer. 2017;17:223–38.PubMedCrossRef Wan JCM, Massie C, Garcia-Corbacho J, et al. Liquid biopsies come of age: towards implementation of circulating tumour DNA. Nat Rev Cancer. 2017;17:223–38.PubMedCrossRef
43.
Zurück zum Zitat Diehl F, Schmidt K, Choti MA, et al. Circulating mutant DNA to assess tumor dynamics. Nat Med. 2008;14:985–90.PubMedCrossRef Diehl F, Schmidt K, Choti MA, et al. Circulating mutant DNA to assess tumor dynamics. Nat Med. 2008;14:985–90.PubMedCrossRef
45.
Zurück zum Zitat Kato S, Li B, Adashek JJ, et al. Serial changes in liquid biopsy-derived variant allele frequency predict immune checkpoint inhibitor responsiveness in the pan-cancer setting. Oncoimmunology. 2022;11:2052410.PubMedPubMedCentralCrossRef Kato S, Li B, Adashek JJ, et al. Serial changes in liquid biopsy-derived variant allele frequency predict immune checkpoint inhibitor responsiveness in the pan-cancer setting. Oncoimmunology. 2022;11:2052410.PubMedPubMedCentralCrossRef
46.
Zurück zum Zitat Adashek JJ, Janku F, Kurzrock R. Signed in blood: circulating tumor DNA in cancer diagnosis treatment and screening. Cancers. 2021;13:3600.PubMed Adashek JJ, Janku F, Kurzrock R. Signed in blood: circulating tumor DNA in cancer diagnosis treatment and screening. Cancers. 2021;13:3600.PubMed
47.
Zurück zum Zitat Goodman AM, Holden KA, Jeong AR, et al. Assessing CAR t-cell therapy response using genome-wide sequencing of cell-free dna in patients with b-cell lymphomas. Transplant Cell Ther. 2022;28(30):e1–7. Goodman AM, Holden KA, Jeong AR, et al. Assessing CAR t-cell therapy response using genome-wide sequencing of cell-free dna in patients with b-cell lymphomas. Transplant Cell Ther. 2022;28(30):e1–7.
48.
Zurück zum Zitat Agarwal R, Chan YC, Tam CS, et al. Dynamic molecular monitoring reveals that SWI-SNF mutations mediate resistance to ibrutinib plus venetoclax in mantle cell lymphoma. Nat Med. 2019;25:119–29.PubMedCrossRef Agarwal R, Chan YC, Tam CS, et al. Dynamic molecular monitoring reveals that SWI-SNF mutations mediate resistance to ibrutinib plus venetoclax in mantle cell lymphoma. Nat Med. 2019;25:119–29.PubMedCrossRef
49.
Zurück zum Zitat Tam CS, Anderson MA, Pott C, et al. Ibrutinib plus venetoclax for the treatment of mantle-cell lymphoma. N Engl J Med. 2018;378:1211–23.PubMedCrossRef Tam CS, Anderson MA, Pott C, et al. Ibrutinib plus venetoclax for the treatment of mantle-cell lymphoma. N Engl J Med. 2018;378:1211–23.PubMedCrossRef
50.
Zurück zum Zitat Stewart CM, Michaud L, Whiting K, et al. Phase I/Ib study of the efficacy and safety of buparlisib and ibrutinib therapy in MCL, FL, and DLBCL with serial cell-free DNA monitoring. Clin Cancer Res. 2022;28:45–56.PubMedCrossRef Stewart CM, Michaud L, Whiting K, et al. Phase I/Ib study of the efficacy and safety of buparlisib and ibrutinib therapy in MCL, FL, and DLBCL with serial cell-free DNA monitoring. Clin Cancer Res. 2022;28:45–56.PubMedCrossRef
51.
Zurück zum Zitat Lakhotia R, Melani C, Dunleavy K, et al. Circulating tumor DNA predicts therapeutic outcome in mantle cell lymphoma. Blood Adv. 2022;6:2667–80.PubMedPubMedCentralCrossRef Lakhotia R, Melani C, Dunleavy K, et al. Circulating tumor DNA predicts therapeutic outcome in mantle cell lymphoma. Blood Adv. 2022;6:2667–80.PubMedPubMedCentralCrossRef
52.
Zurück zum Zitat Zheng Z, Liebers M, Zhelyazkova B, et al. Anchored multiplex PCR for targeted next-generation sequencing. Nat Med. 2014;20:1479–84.PubMedCrossRef Zheng Z, Liebers M, Zhelyazkova B, et al. Anchored multiplex PCR for targeted next-generation sequencing. Nat Med. 2014;20:1479–84.PubMedCrossRef
53.
Zurück zum Zitat Yang Y, Wang C, Yang Q, et al. Distinct mechanisms define murine B cell lineage immunoglobulin heavy chain (IgH) repertoires. eLife. 2015;4:e09083.PubMedPubMedCentralCrossRef Yang Y, Wang C, Yang Q, et al. Distinct mechanisms define murine B cell lineage immunoglobulin heavy chain (IgH) repertoires. eLife. 2015;4:e09083.PubMedPubMedCentralCrossRef
54.
55.
56.
Zurück zum Zitat Paiva B, Puig N, Cedena MT, et al. Measurable residual disease by next-generation flow cytometry in multiple myeloma. J Clin Oncol. 2020;38:784–92.PubMedCrossRef Paiva B, Puig N, Cedena MT, et al. Measurable residual disease by next-generation flow cytometry in multiple myeloma. J Clin Oncol. 2020;38:784–92.PubMedCrossRef
57.
Zurück zum Zitat Munshi NC, Avet-Loiseau H, Anderson KC, et al. A large meta-analysis establishes the role of MRD negativity in long-term survival outcomes in patients with multiple myeloma. Blood Adv. 2020;4:5988–99.PubMedPubMedCentralCrossRef Munshi NC, Avet-Loiseau H, Anderson KC, et al. A large meta-analysis establishes the role of MRD negativity in long-term survival outcomes in patients with multiple myeloma. Blood Adv. 2020;4:5988–99.PubMedPubMedCentralCrossRef
58.
Zurück zum Zitat Paiva B, San-Miguel J, Avet-Loiseau H. MRD in multiple myeloma: does CR really matter? Blood. 2022;140:2423–8.PubMedCrossRef Paiva B, San-Miguel J, Avet-Loiseau H. MRD in multiple myeloma: does CR really matter? Blood. 2022;140:2423–8.PubMedCrossRef
59.
Zurück zum Zitat Soumerai JD, Mato AR, Dogan A, et al. Zanubrutinib, obinutuzumab, and venetoclax with minimal residual disease-driven discontinuation in previously untreated patients with chronic lymphocytic leukaemia or small lymphocytic lymphoma: a multicentre, single-arm, phase 2 trial. The Lancet Haematology. 2021;8:e879–90.PubMedPubMedCentralCrossRef Soumerai JD, Mato AR, Dogan A, et al. Zanubrutinib, obinutuzumab, and venetoclax with minimal residual disease-driven discontinuation in previously untreated patients with chronic lymphocytic leukaemia or small lymphocytic lymphoma: a multicentre, single-arm, phase 2 trial. The Lancet Haematology. 2021;8:e879–90.PubMedPubMedCentralCrossRef
60.
Zurück zum Zitat Thompson PA, Srivastava J, Peterson C, et al. Minimal residual disease undetectable by next-generation sequencing predicts improved outcome in CLL after chemoimmunotherapy. Blood. 2019;134:1951–9.PubMedPubMedCentralCrossRef Thompson PA, Srivastava J, Peterson C, et al. Minimal residual disease undetectable by next-generation sequencing predicts improved outcome in CLL after chemoimmunotherapy. Blood. 2019;134:1951–9.PubMedPubMedCentralCrossRef
61.
Zurück zum Zitat Molica S, Giannarelli D, Montserrat E. Minimal residual disease and survival outcomes in patients with chronic lymphocytic leukemia: a systematic review and meta-analysis. Clin Lymphoma Myeloma Leuk. 2019;19:423–30.PubMedCrossRef Molica S, Giannarelli D, Montserrat E. Minimal residual disease and survival outcomes in patients with chronic lymphocytic leukemia: a systematic review and meta-analysis. Clin Lymphoma Myeloma Leuk. 2019;19:423–30.PubMedCrossRef
62.
Zurück zum Zitat Munir T, Moreno C, Owen C, et al. Impact of minimal residual disease on progression-free survival outcomes after fixed-duration ibrutinib-venetoclax versus chlorambucil-obinutuzumab in the glow study. J Clin Oncol. 2023;41:3689–99.PubMedPubMedCentralCrossRef Munir T, Moreno C, Owen C, et al. Impact of minimal residual disease on progression-free survival outcomes after fixed-duration ibrutinib-venetoclax versus chlorambucil-obinutuzumab in the glow study. J Clin Oncol. 2023;41:3689–99.PubMedPubMedCentralCrossRef
63.
Zurück zum Zitat Saygin C, Cannova J, Stock W, Muffly L. Measurable residual disease in acute lymphoblastic leukemia: methods and clinical context in adult patients. Haematologica. 2022;107:2783–93.PubMedPubMedCentralCrossRef Saygin C, Cannova J, Stock W, Muffly L. Measurable residual disease in acute lymphoblastic leukemia: methods and clinical context in adult patients. Haematologica. 2022;107:2783–93.PubMedPubMedCentralCrossRef
64.
Zurück zum Zitat Logan AC. Measurable residual disease in acute lymphoblastic leukemia: How low is low enough? Best Pract Res Clin Haematol. 2022;35:101407.PubMedCrossRef Logan AC. Measurable residual disease in acute lymphoblastic leukemia: How low is low enough? Best Pract Res Clin Haematol. 2022;35:101407.PubMedCrossRef
65.
Zurück zum Zitat Berry DA, Zhou S, Higley H, et al. Association of minimal residual disease with clinical outcome in pediatric and adult acute lymphoblastic leukemia: a meta-analysis. JAMA Oncol. 2017;3:e170580.PubMedPubMedCentralCrossRef Berry DA, Zhou S, Higley H, et al. Association of minimal residual disease with clinical outcome in pediatric and adult acute lymphoblastic leukemia: a meta-analysis. JAMA Oncol. 2017;3:e170580.PubMedPubMedCentralCrossRef
66.
Zurück zum Zitat Freedman A. Follicular lymphoma: 2015 update on diagnosis and management. Am J Hematol. 2015;90:1171–8.PubMedCrossRef Freedman A. Follicular lymphoma: 2015 update on diagnosis and management. Am J Hematol. 2015;90:1171–8.PubMedCrossRef
67.
Zurück zum Zitat Luminari S, Manni M, Galimberti S, et al. Response-adapted postinduction strategy in patients with advanced-stage follicular lymphoma: the foll12 study. J Clin Oncol. 2022;40:729–39.PubMedCrossRef Luminari S, Manni M, Galimberti S, et al. Response-adapted postinduction strategy in patients with advanced-stage follicular lymphoma: the foll12 study. J Clin Oncol. 2022;40:729–39.PubMedCrossRef
68.
Zurück zum Zitat Chase ML, Armand P. Minimal residual disease in non-Hodgkin lymphoma - current applications and future directions. Br J Haematol. 2018;180:177–88.PubMedCrossRef Chase ML, Armand P. Minimal residual disease in non-Hodgkin lymphoma - current applications and future directions. Br J Haematol. 2018;180:177–88.PubMedCrossRef
69.
Zurück zum Zitat Pott C, Jurinovic V, Trotman J, et al. Minimal residual disease status predicts outcome in patients with previously untreated follicular lymphoma: a prospective analysis of the phase III GALLIUM study. J Clin Oncol. 2024;42:550–61.PubMedCrossRef Pott C, Jurinovic V, Trotman J, et al. Minimal residual disease status predicts outcome in patients with previously untreated follicular lymphoma: a prospective analysis of the phase III GALLIUM study. J Clin Oncol. 2024;42:550–61.PubMedCrossRef
70.
Zurück zum Zitat Merryman RW, Redd RA, Taranto E, et al. Minimal residual disease in patients with diffuse large B-cell lymphoma undergoing autologous stem cell transplantation. Blood Adv. 2023;7:4748–59.PubMedCrossRef Merryman RW, Redd RA, Taranto E, et al. Minimal residual disease in patients with diffuse large B-cell lymphoma undergoing autologous stem cell transplantation. Blood Adv. 2023;7:4748–59.PubMedCrossRef
71.
Zurück zum Zitat Miles B, Mao D, Vardhanabhuti S, et al. Circulating tumor DNA (ctDNA) by clonoSEQ to monitor residual disease after axicabtagene ciloleucel (axi-cel) in large B-cell lymphoma (LBCL). Journal of Clinical Oncology. 2023;41:7547.CrossRef Miles B, Mao D, Vardhanabhuti S, et al. Circulating tumor DNA (ctDNA) by clonoSEQ to monitor residual disease after axicabtagene ciloleucel (axi-cel) in large B-cell lymphoma (LBCL). Journal of Clinical Oncology. 2023;41:7547.CrossRef
72.
Zurück zum Zitat Munoz J, Deshpande A, Rimsza L, Nowakowski GS, Kurzrock R. Navigating between Scylla and Charybdis: A roadmap to do better than Pola-RCHP in DLBCL. Cancer Treat Rev. 2024;124:102691.PubMedCrossRef Munoz J, Deshpande A, Rimsza L, Nowakowski GS, Kurzrock R. Navigating between Scylla and Charybdis: A roadmap to do better than Pola-RCHP in DLBCL. Cancer Treat Rev. 2024;124:102691.PubMedCrossRef
74.
Zurück zum Zitat Furqan F, Fenske TS, Longo WL, Johnson B, Hamadani M, Shah NN. MRD Status By Clonoseq ® is a poor predictor of long-term outcomes after bispecific lv20.19 CAR t-cell therapy for relapsed. Refractory B-Cell NHL Blood. 2022;140:6407–8. Furqan F, Fenske TS, Longo WL, Johnson B, Hamadani M, Shah NN. MRD Status By Clonoseq ® is a poor predictor of long-term outcomes after bispecific lv20.19 CAR t-cell therapy for relapsed. Refractory B-Cell NHL Blood. 2022;140:6407–8.
Metadaten
Titel
Measurable Residual Disease in Mantle Cell Lymphoma: The Unbearable Lightness of Being Undetectable
verfasst von
Julio Cartagena
Anagha Deshpande
Allison Rosenthal
Mazie Tsang
Talal Hilal
Lisa Rimsza
Razelle Kurzrock
Javier Munoz
Publikationsdatum
06.12.2024
Verlag
Springer US
Erschienen in
Current Oncology Reports / Ausgabe 12/2024
Print ISSN: 1523-3790
Elektronische ISSN: 1534-6269
DOI
https://doi.org/10.1007/s11912-024-01620-8

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