The interval between progression and therapy initiation is the key prognostic parameter in relapsing diffuse large B cell lymphoma: analysis from the Czech Lymphoma Study Group database (NIHIL)
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
AZV16-31092A
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
32506244
DOI
10.1007/s00277-020-04099-y
PII: 10.1007/s00277-020-04099-y
Knihovny.cz E-resources
- Keywords
- Diffuse large B cell lymphoma, Prognosis, Relapse, Therapy,
- MeSH
- Time-to-Treatment * statistics & numerical data MeSH
- Cyclophosphamide therapeutic use MeSH
- Databases, Factual MeSH
- Lymphoma, Large B-Cell, Diffuse diagnosis epidemiology pathology therapy MeSH
- Adult MeSH
- Doxorubicin therapeutic use MeSH
- Cohort Studies MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Neoadjuvant Therapy methods statistics & numerical data MeSH
- Prednisone therapeutic use MeSH
- Prognosis MeSH
- Disease Progression MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Recurrence MeSH
- Retrospective Studies MeSH
- Rituximab administration & dosage MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Vincristine therapeutic use MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic epidemiology MeSH
- Names of Substances
- Cyclophosphamide MeSH
- Doxorubicin MeSH
- Prednisone MeSH
- Rituximab MeSH
- Vincristine MeSH
Relapsing diffuse large B cell lymphomas (rDLBCL) represent a heterogeneous disease. This heterogeneity should be recognized and reflected, because it can deform the interpretation of clinical trial results. DLBCL patients with the first relapse and without CNS involvement were identified in the Czech Lymphoma Study Group (CLSG) database. Interval-to-therapy (ITT) was defined as the time between the first manifestation of rDLBCL and the start of any treatment. The overall survival (OS) of different ITT cohorts (< 7 vs. 7-21 vs. > 21 days) was compared. In total, 587 rDLBCLs (51.8% males) progressed with a median of 12.8 months (range 1.6 to 152.3) since the initial diagnosis (2000-2017). At the time of relapse, the median age was 67 years (range 22-95). First-line therapy was administered in 99.3% of the patients; CHOP and anti-CD20 were given to 69.2% and 84.7% of the patients, respectively. The salvage immune/chemotherapy was administered in 88.1% of the patients (39.2% platinum-based regimen). The median ITT was 20 days (range 1-851), but 23.2% of patients initiated therapy within 7 days. The 5-year OS was 17.4% (range 10-24.5%) vs. 20.5% (range 13.5-27.4%) vs. 42.2% (range 35.5-48.8%) for ITT < 7 vs. 7-21 vs. > 21 days (p < 0.001). ITT was associated with B symptoms (p 0.004), ECOG (p < 0.001), stage (p 0.002), bulky disease (p 0.005), elevated LDH (p < 0.001), and IPI (p < 0.001). The ITT mirrors the real clinical behavior of rDLBCL. There are patients (ITT < 7 days) with aggressive disease and a poor outcome. Conversely, there are rDLBCLs with ITT ≥ 21 days who survive for a long time.
Department of Clinical Hematology Teaching Hospital Ostrava Ostrava Czech Republic
Department of Hematology University Hospital Olomouc Olomouc Czech Republic
Department of Oncology Hospital Ceske Budejovice Ceske Budejovice Czech Republic
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
See more in PubMed
Al-Hamadani M, Habermann TM, Cerhan JR et al (2015) Non-Hodgkin lymphoma subtype distribution, geodeomographic patterns, and survival in the US: a longitudinal analysis of the national cancer data base from 1998 to 2011. Am J Hematol 90:790–795 DOI
Habermann TM, Weller EA, Morisson VA et al (2006) Rituximab-CHOP versus CHOP alone or with maintenance rituximab in older patients with diffuse large B-cell lymphoma. J Clin Oncol 24:3121–3127 DOI
Pfreundschuh M, Trumpel L, Osterborg A et al (2006) CHOP-like chemotherapy plus rituximab versus CHOP-like chemotherapy alone in young patients with good-prognosis diffuse large B-cell lymphoma: a randomised controlled trial by the MabThera International (MInT) group. Lancet Oncol 7:379–391 DOI
Sehn LH, Donaldson J, Chhanabhai M, Fitzgerald C, Gill K, Klasa R, MacPherson N, O'Reilly S, Spinelli JJ, Sutherland J, Wilson KS, Gascoyne RD, Connors JM (2005) Introduction of combined CHOP plus rituximab dramatically improved outcome of diffuse large B-cell lymphoma in British Columbia. J Clin Oncol 23:5027–5033 DOI
Howlander N, Mariotto AB, Besson C et al (2017) Cancer-specific mortality, cure fraction, and noncancer causes of death among diffuse large B-cell lymphoma patients in the immunochemotherapy era. Cancer 123:3326–3334 DOI
Coiffier B, Lepage E, Briére J et al (2002) CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. NEJM 346:235–242 DOI
Coiffier B, Thieblemont C, Den Van Neste E et al (2010) Long-term outcome of patients in the LNH-98.5 trial, the first randomized study comparing rituximab-CHOP to standard CHOP chemotherapy in DLBCL patients: a study by the Groupe d’Etudes des Lymphomes de l'Adulte. Blood 116:2040–2045 DOI
Farooq U, Maurer MJ, Thompson CA, Thanarajasingam G, Inwards DJ, Micallef I, Macon W, Syrbu S, Lin T, Lin Y, Ansell SM, Nowakowski GS, Habermann TM, Cerhan JR, Link BK (2017) Clinical heterogeneity of diffuse large B cell lymphoma following failure of front-line immunochemotherapy. Br J Haematol 179:50–60 DOI
https://www.clinical.trials.gov
Kahan BC, REhal S, Cro S (2015) Risk of selection bias in randomised trials. Trials 16:405. https://doi.org/10.1186/s13063-015-0920-x PubMed DOI PMC
Maurer MJ, Ghesquiéres H, Link BK et al (2018) Diagnosis-to-treatment interval is an important clinical factor in newly diagnosed diffuse large B-cell lymphoma and has implication for Bias in clinical trials. J Clin Oncol 36:1603–1610 DOI
Kochenderfer JN, Sommerville RPT, Lu T et al (2017) Lymphoma remissions caused by anti-CD19 chimeric antigen receptor T cells are associated with high serum interleukin-15 levels. J Clin Oncol 35(16):1803–1813 DOI
Abramson J, Gordon L, Palomba ML et al (2018) Updated safety and long-term clinical outcomes in TRANSCEND NHL 001, pivotal trial of lisocabtagen maraleucel (JCAR017) in R/R aggressive NHL. J Clin Oncol 36(15suppl):7505 DOI
https://www.uzis.cz/cz/mkn/C81-C96.html
Swerdlow SH, Campo E, Harris NL et al (2008) WHO classification of tumours of haematopoietic and lymphoid tissues. In: International Agency for Research on Cancer (IARC), 4th edn. Lyon
Hans CP, Weisenburger DD, Greiner TC et al (2004) Confirmation of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray. Blood 103:275–282 DOI
Carbone PP, Kaplan HS, Musshoff K, Smithers DW, Tubiana M (1971) Report of the committee on no Hodgkin’s disease staging classification. Cancer Res 31:1860–1861 PubMed
Sykorova A, Belada D, Smolej L et al (2010) Staging of non-Hodgkin’s lymphoma –recommendations of the Czech Lymphoma Study Group. Klin Onkol 23:146–154 PubMed
Cheson BD, Horning SJ, Coiffier B et al (1999) Report of an international workshop to standardize response criteria for non-Hodgkin’s lymphomas. NCI Sponsored International Working Group. J Clin Oncol 17(4):1244 DOI
Cheson BD, Pfistner B, Juweid ME et al (2007) International Harmonization Project on lymphoma. Revised response criteria for malignant lymphoma. J Clin Oncol 25(5):579–586 DOI
Shi Q, Schmitz N, Ou FS, Dixon JG, Cunningham D, Pfreundschuh M, Seymour JF, Jaeger U, Habermann TM, Haioun C, Tilly H, Ghesquieres H, Merli F, Ziepert M, Herbrecht R, Flament J, Fu T, Coiffier B, Flowers CR (2018) Progression-free survival as a surrogate end point for overall survival in first-line diffuse large B-cell lymphoma: an individual patient-level analysis of multiple randomized trials (SEAL). J Clin Oncol 36:2593–2602 DOI
Crump M, Neelapu SS, Farooq U, van den Neste E, Kuruvilla J, Westin J, Link BK, Hay A, Cerhan JR, Zhu L, Boussetta S, Feng L, Maurer MJ, Navale L, Wiezorek J, Go WY, Gisselbrecht C (2017) Outcomes in refractory diffuse large B-cell lymphoma: results from the international SCHOLAR-1 study. Blood 130:1800–1808 DOI
Blunt DN, Smyth L, Gatov E, Nagamuthu C, Buckstein R, Croxford R, Cheung M (2018) Diagnosis to treatment interval in DLBCL is predictive of overal survival in a large, population-based registry. Blood 132:1700 DOI
Yelland LN, Kahan BC, Dent E, Lee KJ, Voysey M, Forbes AB, Cook JA (2018) Prevalence and reporting of recruitment, randomisation and treatment errors in clinical trials: a systematic review. Clin Trials 15(3):278–285 DOI
Fatola T, Rutherford SC, Allan JN, Ruan J, Furman RR, Zhengming C, Garcia A, Kong C, Bhavsar EB, Falsenfeld J, Leonard JP, Martin P (2018) Understanding the differences between clinical trial participants and real-world patients with non-Hodgkin lymphoma. Blood 132:2970 DOI
Maurer MJ, Farooq U, Wahlen MM et al (2018) Short time between progression after immunochemotherapy and initiation of salvage therapy (PTI) is associated with inferior long-term outcomes in patients with relapsed/refractory DLBCL. ASH Annual Meeting; Abstract No 4204
Harrysson S, Eloranta S, Ekberg S, Enblad G, Jerkeman M, Hasselblom S, Wahlin BE, Andersson PO, Smedby KE (2018) Incidence and outcome of relapsed/refractory diffuse large B-cell lymphoma (DLBCL) in a population-based cohort of 3165 patients in Sweden. Blood 132:2975 DOI
Galaznik A, Way N (2018) Patient characteristics and treatment paterns in the first-line and second-line treatment of diffuse large B-cell lymphoma and follicular lymphoma in the United Kingdom, France, and Germany. Blood 132:4232 DOI
Locke FL, Ghobaldi A, Jacobskon CA et al (2019) Long-term safety and activity of axicabtabene ciloleucel in refractory large B-cell lymphoma (ZUMA-1): a single-arm, multicentre, phase 1-2 trial. Lancet Oncol 20:31–42 DOI
Neelapu SS, Locke FL, Bertlett et al (2017) Axicabtagene Ciloleucel CAR T-cell therapy in refractory large B-cell lymphoma. N Engl J Med 377:2531–2544 DOI
Schuster SJ, Bishop M, Tam C, Waller EK, Borchmann P, McGuirk J, Jäger U, Jaglowski S, Andreadis C, Westin JR, Fleury I, Bachanova V, Foley SR, Ho PJ, Mielke S, Magenau JM, Holte H, Pantano S, Pacaud LB, Awasthi R, Chu J, Anak Ö, Salles G, Maziarz RT, JULIET Investigators (2019) Tisagenlecleucel in adult relapsed and refractory diffuse large B-cell lymphoma. N Engl J Med 380:45–56 DOI
Veldman-Jones MH, Lai Z, Wappett M, Harbron CG, Barrett JC, Harrington EA, Thress KS (2015) Reproducible, quantitative, and flexible molecular subtyping of clinical DLBCL samples using the nanostring Countersystem. Clin Cancer Res 21:2367–2378 DOI
Greenawalt D, Liang WS, Saif S et al (2017) Comparative analysis of primary versus relapse/refractory DLBCL identifies shifts in mutation spectrum. Oncotarget 8:99237–99244 DOI