Skip to main content
Log in

Prognostic factors in patients with aggressive non-Hodgkin’s lymphoma without complete response to first-line therapy

  • Published:
Advances in Therapy Aims and scope Submit manuscript

Abstract

This study was conducted to retrospectively identify the prognostic factors that specifically predict survival rates of patients with aggressive non-Hodgkin’s lymphoma who did not achieve a complete response (CR) to first-line therapy. Prognostic factors in terms of survival were analyzed in 76 adult patients with non-Hodgkin’s lymphoma who had failed to achieve CR to first-line chemotherapy (CT) regimens administered at Istanbul University, Institute of Oncology, between February 1989 and October 1998. A total of 41 patients were female, and median age was 60 y (range, 18–87 y). Twenty-seven patients (35%) had primary refractory disease (stable disease + progressive disease). A partial response (PR) was demonstrated in 49 (65%). In all, 92% had been administered anthracycline on the basis of computed tomography findings. Of 27 patients with primary refractory disease, 20 died because of initial CT toxicity or disease progression. A total of 10 patients with primary refractory disease underwent second-line CT. CR was observed in only 1 of those patients. Of the 49 patients who had a PR to first-line therapy, 31 died because of disease progression. Of those patients, 14 underwent second-line CT. Four patients were observed to have a CR. Median overall survival (OS) in all patients was established at 15 mo (range, 11–19 mo), and 5-y OS was 25%. On the other hand, median OS in patients with primary refractory disease was 7.6 mo (range, 5.7–9.4 mo) and was observed to be 17.8 mo (range, 9.4–26.1 mo) in patients with a PR. The difference in survival rates between patients with primary refractory disease and those with a PR was significant (P=.005). Although median OS was 18.1 mo (range, 8.4–27.8 mo) in patients with intermediategrade histology, it was 6.1 mo (range, 1–11.7 mo) in patients with high-grade histology (P=.001). As a result of univariate analysis, significant prognostic factors associated with OS included histologic grade (intermediate/high) (P=.001), response to initial therapy (primary refractory disease/PR) (P=.005), performance status (0–2/2–4) (P=.024), and International Prognostic Index risk groups (low/low intermediate/intermediate-high/high risk) (P=.004). Multivariate analysis revealed that independent prognostic parameters associated with OS included response to initial therapy (P=.009) and histologic grade (P=.001). Although prognosis is rather poor in patients with high histologic grade and primary refractory disease, patients with a PR have a slightly better prognosis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Armitage JO, Cheson BD. Interpretation of clinical trials in diffuse large-cell lymphoma.J Clin Oncol. 1988;6:1335–1347.

    PubMed  CAS  Google Scholar 

  2. Cavalli F. Treatment of lymphomas.Baillieres Clin Haematol. 1991;4:157–179.

    Article  PubMed  CAS  Google Scholar 

  3. Fisher RI, Gaynor ER, Dahlberg MS, et al. Comparison of a standard regimen (CHOP) with three intensive chemotherapy regimens for advanced non-Hodgkin’s lymphoma.N Engl J Med. 1993;328:1002–1006.

    Article  PubMed  CAS  Google Scholar 

  4. Davidson KL, Devaney MB, Tighe JE, et al. A pilot study of CODOX-M/IVAC in primary refractory or relapsed high-grade non-Hodgkin’s lymphoma: a Scotland and Newcastle Lymphoma Group Study.Haematologia. 2003;88:1366–1371.

    Google Scholar 

  5. Cabanillas F, Velasquez WS, McLaughlin P, et al. Results of recent salvage chemotherapy regimens for lymphoma and Hodgkin’s disease.Semin Hematol. 1988;25:47–50.

    PubMed  CAS  Google Scholar 

  6. Cabanillas F, Hagemeister F, Bodey GP, Freireich EJ. IMVP-16, an effective regimen for patients with lymphoma who have relapsed after initial combination chemotherapy.Blood. 1982;60:693–697.

    PubMed  CAS  Google Scholar 

  7. Cabanillas F, Hagemeister FB, McLaughlin P, et al. Results of MIME salvage regimen for recurrent or refractory lymphoma.J Clin Oncol. 1987;5:407–412.

    PubMed  CAS  Google Scholar 

  8. Velasquez WS, Cabanillas F, Salvador P, et al. Effective salvage therapy for lymphoma with cisplatinum in combination with high doses of Ara-C and dexamethasone (DHAP).Blood. 1988;71:117–122.

    PubMed  CAS  Google Scholar 

  9. Velasquez WS, McLaughlin P, Tucker S, et al. ESHAP-an effective chemotherapy regimen in refractory and relapsing lymphoma: a 4 year follow-up study.J Clin Oncol. 1994;12:1169–1176.

    PubMed  CAS  Google Scholar 

  10. Rodríguez MA, Cabanillas FC, Velasquez W, et al. Results of a salvage treatment program for relapsing lymphoma: MINE consolidated with ESHAP.J Clin Oncol. 1995;13:1734–1741.

    PubMed  Google Scholar 

  11. Kimby E, Brandt L, Nygren P, Glimelius B, for the SBU-group. Swedish Council of Technology Assessment in Health Care: a systematic overview of chemotherapy effects in aggressive non-Hodgkin’s lymphoma.Acta Oncol. 2001;40:198–212.

    Article  PubMed  CAS  Google Scholar 

  12. Non-Hodgkin’s Lymphoma Pathologic Classification Project. National Cancer Institute sponsored study of classifications of non-Hodgkin’s lymphomas: summary and description of a working formulation for clinical usage.Cancer. 1982;49:2112–2135.

    Article  Google Scholar 

  13. Carbone PP, Kaplan HS, Musshoff K, Smithers DW, Tubiana M. Report of the Committee on Hodgkin’s disease staging classification.Cancer Res. 1971;31:1860–1861.

    PubMed  CAS  Google Scholar 

  14. Miller AB, Hoogstraten B, Staquet M, et al. Reporting results of cancer treatment.Cancer. 1981;47:207–214.

    Article  PubMed  CAS  Google Scholar 

  15. The international non-Hodgkin’s lymphoma prognostic factors project: a predictive model for aggressive non-Hodgkin’s lymphoma.N Engl J Med. 1993;329:987–994.

  16. Kaplan EL, Meier P. Nonparametric estimation from incomplete observations.J Am Stat Assoc. 1958;53:457–481.

    Article  Google Scholar 

  17. Mantel N. Evaluation of survival data and two new rank order statistics arising in its consideration.Cancer Chemother Rep. 1966;50:163–170.

    PubMed  CAS  Google Scholar 

  18. Cox DR.The Analysis of Binary Data. New York: Chapman and Hall; 1970.

    Google Scholar 

  19. Coiffier B, Gisselbrecht C, Herbrecht R, Tilly H, Bosly A, Brousse N. LNH-84 regimen: a multicenter study of intensive chemotherapy in 737 patients with aggressive malignant lymphoma.J Clin Oncol. 1989;7:1018–1026.

    PubMed  CAS  Google Scholar 

  20. Josting A, Reiser M, Rueffer U, Salzberger B, Diehl V, Engert A. Treatment of primary progressive Hodgkin’s and aggressive non-Hodgkin’s lymphoma: is there a chance for cure?J Clin Oncol. 2000;18:332–339.

    PubMed  CAS  Google Scholar 

  21. Villela L, López-Guillermo A, Montoto S, et al. Prognostic features and outcome in patients with diffuse large B-cell lymphoma who do not achieve a complete response to first-line regimens.Cancer. 2001;91:1557–1562.

    Article  PubMed  CAS  Google Scholar 

  22. Vose JM, Rowling PA, Lazarus HM, Phillips GL, Armitage JO, Horowitz MM. Multivariate analysis of autotransplant for patients with aggressive non-Hodgkin’s lymphoma failing primary induction therapy.Blood. 1997;90(suppl 1):594a.

    Google Scholar 

  23. Shipp MA, Abeloff MD, Antman KH, et al. International consensus conference on high-dose therapy with hematopoietic stem-cell transplantation in aggressive non-Hodgkin’s lymphomas: report of the jury.Ann Oncol. 1999;10:13–19.

    Article  PubMed  CAS  Google Scholar 

  24. Conde E, Sierra J, Iriondo A, et al. Prognostic factors in patients who received autologous bone marrow transplantation for non-Hodgkin’s lymphoma: report of 104 patients from the Spanish Cooperative Group GEL/TAMO.Bone Marrow Trans. 1994;14:279–286.

    CAS  Google Scholar 

  25. Philip T, Guglielmi C, Hagenbeek A, et al. Autologous bone marrow transplantation as compared with salvage chemotherapy in relapses of chemotherapy sensitive non-Hodgkin’s lymphoma.N Engl J Med. 1995;333:1540–1545.

    Article  PubMed  CAS  Google Scholar 

  26. Haq R, Sawka CA, Franssen E, Berinstein NL. Significance of a partial or slow response to front-line chemotherapy in the management of intermediate-grade or high-grade non-Hodgkin’s lymphoma: a literature review.J Clin Oncol. 1994;12:1074–1084.

    Google Scholar 

  27. Prince HM, Crump M, Imrie K, et al. Intensive therapy and autotransplant for patients with an incomplete response to front-line therapy for lymphoma.Ann Oncol. 1996;7:1043–1049.

    PubMed  CAS  Google Scholar 

  28. Engelhard M, Brittinger G, Huhn D, Gerhartz HH, Meuses P, Siegert W. Subclassification of diffuse large B-cell lymphoma according to the Kiel classification: distinction of centroblastic and immunoblastic lymphomas is a significant prognostic risk factor.Blood. 1997;89:2291–2297.

    PubMed  CAS  Google Scholar 

  29. Baars JW, De Jong D, Willensem EM, Gras L, Dalesio O, Heerde P. Diffuse large B-cell non-Hodgkin’s lymphoma: the clinical relevance of histological subclassification.Br J Cancer. 1999;79:1770–1776.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Alici, S., Bavbek, S., Basaran, M. et al. Prognostic factors in patients with aggressive non-Hodgkin’s lymphoma without complete response to first-line therapy. Adv Therapy 23, 534–542 (2006). https://doi.org/10.1007/BF02850042

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02850042

Keywords

Navigation