Treatment of primary progressive Hodgkin's and aggressive non-Hodgkin's lymphoma: Is there a chance for cure?

被引:82
作者
Josting, A [1 ]
Reiser, M [1 ]
Rueffer, U [1 ]
Salzberger, B [1 ]
Diehl, V [1 ]
Engert, A [1 ]
机构
[1] Univ Hosp, Dept Internal Med 1, D-50924 Cologne, Germany
关键词
D O I
10.1200/JCO.2000.18.2.332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine differences in prognosis between primary progressive Hodgkin's disease (HD) and aggressive non-Hodgkin's lymphoma (NHL), we retrospectively analyzed patients with progressive lymphoma who were treated with different salvage chemotherapy regimens including high-dose chemotherapy (HDCT) followed by autologous stem-cell support (ASCT), Patients and Methods: One hundred thirty-one patients with primary progressive lymphoma (HD, n = 67; NHL, n = 64) were enrolled. Primary progressive disease was defined as disease progression during first-line chemotherapy or only transient response (complete or partial response lasting less than or equal to 90 days) after induction treatment. patients 60 years or younger with progressive lymphoma were eligible to receive HDCT with ASCT. Results: The overall response rate after salvage chemotherapy for patients with primary progressive HD and NHL was 33% and 15%, respectively, Twenty-five HD patients (37%) received HDCT. Most patients with NHL had progressive disease under salvage treatment, with only six patients (10%) receiving HDCT. Of those, only two patients were alive and in continuous complete remission 3 and 12 months after HDCT. No patient with NHL survived longer than 26 months after first diagnosis. Actuarial OS after 5 years was 19% for all HD patients; 53% for HD patients receiving HDCT, and 0% for patients who did not receive HDCT. In HD patients, multivariate regression analysis identified chemosensitive disease on salvage treatment (P = .0001) and HDCT (P = .031) as significant prognostic factors for freedom from treatment failure. Significant prognostic factors for OS are chemosensitive disease (P = .0005). HDCT (P = .039), and 8 symptoms at the time of progress: (P = .046). Conclusion: There are striking differences in the prognosis of patients with progressive HD and aggressive NHL. The prognosis of progressive NHL patients is dismal. Most patients have rapidly progressive disease after salvage treatment and are therefore, excluded from HDCT programs. In contrast, progressive HD patients can achieve long-term survival after HDCT. (C) 2000 by American Society of Clinical Oncology.
引用
收藏
页码:332 / 339
页数:8
相关论文
共 32 条
  • [1] ALLOGENEIC, SYNGENEIC, AND AUTOLOGOUS MARROW TRANSPLANTATION FOR HODGKINS-DISEASE - THE 21-YEAR SEATTLE EXPERIENCE
    ANDERSON, JE
    LITZOW, MR
    APPELBAUM, FR
    SCHOCH, G
    FISHER, LD
    BUCKNER, CD
    PETERSEN, FB
    CRAWFORD, SW
    PRESS, OW
    SANDERS, JE
    BENSINGER, WI
    MARTIN, PJ
    STORB, R
    SULLIVAN, KM
    HANSEN, JA
    THOMAS, ED
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (12) : 2342 - 2350
  • [2] Comparison of high-dose therapy and autologous stem-cell transplantation with conventional therapy for Hodgkin's disease induction failure:: A case-control study
    André, M
    Henry-Amar, M
    Pico, JL
    Brice, P
    Blaise, D
    Kuentz, M
    Coiffier, B
    Colombat, P
    Cahn, JY
    Attal, M
    Fleury, J
    Milpied, N
    Nedellec, G
    Biron, P
    Tilly, H
    Jouet, JP
    Gisselbrecht, C
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (01) : 222 - 229
  • [3] Outcome of patients with Hodgkin's disease failing after primary MOPP-ABVD
    Bonfante, V
    Santoro, A
    Viviani, S
    Devizzi, L
    Balzarotti, M
    Soncini, F
    Zanini, M
    Valagussa, P
    Bonadonna, G
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) : 528 - 534
  • [4] CABANILLAS F, 1988, SEMIN HEMATOL, V25, P47
  • [5] CHEMOTHERAPY OF ADVANCED HODGKINS-DISEASE WITH MOPP, ABVD, OR MOPP ALTERNATING WITH ABVD
    CANELLOS, GP
    ANDERSON, JR
    PROPERT, KJ
    NISSEN, N
    COOPER, MR
    HENDERSON, ES
    GREEN, MR
    GOTTLIEB, A
    PETERSON, BA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (21) : 1478 - 1484
  • [6] CHOPRA R, 1993, BLOOD, V81, P1137
  • [7] AUTOLOGOUS VERSUS ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR NON-HODGKINS-LYMPHOMA - A CASE-CONTROLLED ANALYSIS OF THE EUROPEAN-BONE-MARROW-TRANSPLANT-GROUP REGISTRY DATA
    CHOPRA, R
    GOLDSTONE, AH
    PEARCE, R
    PHILIP, T
    PETERSEN, F
    APPELBAUM, F
    DEVOL, E
    ERNST, P
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (11) : 1690 - 1695
  • [8] Coiffier B, 1998, BLOOD, V92, P1927
  • [9] COX DR, 1972, J R STAT SOC B, V34, P187
  • [10] HIGH-DOSE ETOPOSIDE AND MELPHALAN, AND AUTOLOGOUS BONE-MARROW TRANSPLANTATION FOR PATIENTS WITH ADVANCED HODGKINS-DISEASE - IMPORTANCE OF DISEASE STATUS AT TRANSPLANT
    CRUMP, M
    SMITH, AM
    BRANDWEIN, J
    COUTURE, F
    SHERRET, H
    SUTTON, DMC
    SCOTT, JG
    MCCRAE, J
    MURRAY, C
    PANTALONY, D
    SUTCLIFFE, SB
    KEATING, A
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (04) : 704 - 711