Survival from locally invasive or widespread neuroblastoma without cytotoxic therapy

被引:82
作者
Kushner, BH
Cheung, NKV
LaQuaglia, MP
Ambros, PF
Ambros, IM
Bonilla, MA
Gerald, WL
Ladanyi, M
Gilbert, F
Rosenfield, NS
Yeh, SDJ
机构
[1] MEM SLOAN KETTERING CANC CTR, DEPT MED IMAGING, 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 SURG, NEW YORK, NY 10021 USA
[4] NEW YORK HOSP, DEPT PEDIAT, NEW YORK, NY 10021 USA
[5] ST ANNA CHILDRENS HOSP, CHILDRENS CANC RES INST, VIENNA, AUSTRIA
关键词
D O I
10.1200/JCO.1996.14.2.373
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To test the hypothesis that cytotoxic therapy is not needed at diagnosis to assure the survival of most patients with non-stage 4 neuroblastoma. Methods: Patients with non-stage 4 disease received no cytotoxic therapy in the absence of N-myc amplification. The International Neuroblastoma Staging System (INSS) was used. Results: Of 84 consecutive patients with previously untreated, newly diagnosed neuroblastoma, 31 (37%) had non-stage 4 disease. All 31 patients initially received no cytotoxic therapy because none of them had N-myc amplification. Nine stage 1 patients are relapse-free. This report focuses on the 22 patients with locally invasive or distant disease: two stage SA with gross residual tumor postsurgery, 11 stage 2B with ipsilateral or midline lymph node involvement, four stage 3, and five stage 4S. Eight of the 22 patients were older than 1 year. Postsurgery, 13 patients had visible residual disease, and two others had markedly increased urinary catecholamine levels for more than 1 year, Recurrent or enlarging tumors regressed spontaneously (n = 2) or were excised 5 to 39 months after diagnosis (n = 4). One of the latter had chromosome 1p deletions (common in poor-risk neuroblastoma) that were not detected in the patient's original tumor resected 23 months earlier-findings consistent with clonal evolution or multifocal disease. The patient received chemotherapy. All 22 patients are alive 24 to 98 months (median, 64) from diagnosis. Conclusion: Our results suggest that non-stage 4 patient without N-myc amplification can be spared cytotoxic therapy because (1) residual postsurgical or recurrent biologically favorable neuroblastoma rarely evolves into lethal stage 4 disease; and (2) neuroblastoma in lymph nodes has no prognostic significance. These findings are remarkable because no other cancer includes subtypes that are curable without therapy to ablate residual disease. (C) 1996 by American Society of Clinical Oncology.
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页码:373 / 381
页数:9
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