Anti-GD2 antibody treatment of minimal residual stage 4 neuroblastoma diagnosed at more than 1 year of age

被引:152
作者
Cheung, NKV
Kushner, BH
Cheung, IY
Kramer, K
Canete, A
Gerald, W
Bonilla, MA
Finn, R
Yeh, SJ
Larson, SM
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med Imaging, New York, NY 10021 USA
关键词
D O I
10.1200/JCO.1998.16.9.3053
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To eradicate minimal residual disease with anti-Got monoclonal antibody 3F8 in stage 4 neuroblastoma (NB) diagnosed at more than 1 year of age. Patients and Methods: Thirty-four patients were treated with 3F8 at the end of chemotherapy. Most had either bone marrow (n = 31) or distant bony metastases (n = 29). Thirteen patients were treated at second or subsequent remission (group I) and 12 patients in this group had a history of progressive/persistent disease after bone marrow transplantation (BMT); 21 patients were treated in first remission following N6 chemotherapy (group II). Results: Before 3F8 treatment, 23 patients were in complete remission CR, eight in very good partial remission (VGPR), one in partial remission (PR), and two had microscopic foci in marrow. Twenty-five had evidence of NE by at least one measurement of occult/minimal tumor (iodine 131 [I-131]-3F8 imaging, marrow immunocytology, or marrow reverse-transcriptase polymerase chain reaction [RT-PCR]). Acute self-limited toxicities of 3F8 treatment were severe pain, fever, urticaria, and reversible decreases in blood counts and serum complement levels. There was evidence of response by immunocytology (six of nine), by GAGE RT-PCR (seven of 12), and by I-131-3F8 scans (six of six). Fourteen patients are alive and 13 (age 1.8 to 7.4 years at diagnosis) are progression-free (40 to 130 months from the initiation of 3F8 treatment) without further systemic therapy, none with late neurologic complications. A transient anti-mouse response or the completion of four 3F8 cycles was associated with significantly better survival. Conclusion: Despite high-risk nature of stage 4 NB, long-term remission without autologous (A)BMT can be achieved with 3F8 treatment. Its side effects were short-lived and manageable. The potential benefits of 3F8 in consolidating remission warrant further investigations. J Clin Oncol 16:3053-3060. (C) 1998 by American Society of Clinical Oncology.
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页码:3053 / 3060
页数:8
相关论文
共 38 条
  • [1] REVISIONS OF THE INTERNATIONAL CRITERIA FOR NEUROBLASTOMA DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT
    BRODEUR, GM
    PRITCHARD, J
    BERTHOLD, F
    CARLSEN, NLT
    CASTEL, V
    CASTLEBERRY, RP
    DEBERNARDI, B
    EVANS, AE
    FAVROT, M
    HEDBORG, F
    KANEKO, M
    KEMSHEAD, J
    LAMPERT, F
    LEE, REJ
    LOOK, AT
    PEARSON, ADJ
    PHILIP, T
    ROALD, B
    SAWADA, T
    SEEGER, RC
    TSUCHIDA, Y
    VOUTE, PA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (08) : 1466 - 1477
  • [2] Cheung IY, 1997, CLIN CANCER RES, V3, P821
  • [3] CHEUNG NK, 1992, PRINCIPLES PRACTICE, P357
  • [4] REASSESSMENT OF PATIENT RESPONSE TO MONOCLONAL-ANTIBODY 3F8
    CHEUNG, NKV
    LAZARUS, H
    MIRALDI, FD
    BERGER, NA
    ABRAMOWSKY, CR
    SAARINEN, UM
    SPITZER, T
    STRANDJORD, SE
    COCCIA, PF
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (04) : 671 - 672
  • [5] CHEMOTHERAPY DOSE INTENSITY CORRELATES STRONGLY WITH RESPONSE, MEDIAN SURVIVAL, AND MEDIAN PROGRESSION-FREE SURVIVAL IN METASTATIC NEUROBLASTOMA
    CHEUNG, NKV
    HELLER, G
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (06) : 1050 - 1058
  • [6] DISIALOGANGLIOSIDE G(D2) ANTIIDIOTYPIC MONOCLONAL-ANTIBODIES
    CHEUNG, NKV
    CANETE, A
    CHEUNG, IY
    YE, JN
    LIU, CY
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1993, 54 (03) : 499 - 505
  • [7] CHEUNG NKV, 1994, CANCER RES, V54, P2228
  • [8] Cheung NKV, 1998, INT J ONCOL, V12, P1299
  • [9] DECAY-ACCELERATING FACTOR PROTECTS HUMAN-TUMOR CELLS FROM COMPLEMENT-MEDIATED CYTO-TOXICITY INVITRO
    CHEUNG, NKV
    WALTER, EI
    SMITHMENSAH, WH
    RATNOFF, WD
    TYKOCINSKI, ML
    MEDOF, ME
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (04) : 1122 - 1128
  • [10] CHEUNG NKV, 1985, CANCER RES, V45, P2642