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非转移性可见残留神经母细胞瘤的术后治疗:一项儿科肿瘤学组的研究。

Postoperative treatment of nonmetastatic visible residual neuroblastoma: a Pediatric Oncology Group study.

作者信息

Nitschke R, Smith E I, Altshuler G, Altmiller D, Shuster J, Green A, Castleberry R, Hayes F A, Golembe B, Ducos R

机构信息

Oklahoma University Health Sciences Center, Oklahoma City.

出版信息

J Clin Oncol. 1991 Jul;9(7):1181-8. doi: 10.1200/JCO.1991.9.7.1181.

Abstract

The Pediatric Oncology Group (POG) evaluated in a prospective study the hypothesis that patients who had localized, visible residual neuroblastoma without regional lymph node involvement after surgery (POG stage B) have a favorable prognosis when treated with moderate intensive chemotherapy. Eligible patients were initially treated with five courses of Cytoxan (cyclophosphamide; Bristol-Myers Squibb Co., Evansville, IN) and Adriamycin (doxorubicin; Adria Laboratories, Columbus, OH) followed by surgery (CY/AD +/- surgery). Those patients not achieving a complete remission (CR) crossed over to five courses of cisplatin and teniposide (PL/VM) +/- surgery. Radiation therapy (XRT) was given to selected patients who still were not in CR after the crossover therapy. Of the 61 eligible patients, 38 (62%) patients achieved CR after CY/AD proven by clinical (31) or surgical (seven) evaluation. One (2%) patient in clinical partial remission (PR-C) entered CR without further therapy. Nineteen (31%) patients achieved CR with the following salvage therapies: surgery (five), PL/VM +/- surgery (five) followed by XRT (three) or autologous bone marrow transplant (ABMT) (one) and further courses of CY/AD +/- PL/VM instead of courses of PL/VM (five). The overall CR rate was 95% (58 of 61). Four patients had recurrence of the disease. The probability of being disease-free at 3 years after initial or salvage therapy was estimated at 84% (SE, 5%). The overall prognosis of children older than 1 year and younger than 1 year was similar (P = .26). If, however, the three remission deaths (all younger than 1 year) were censored, there was only one other failure in 32 children younger than one versus seven of 29 children older than 1 year (P = .018). These results confirm the excellent prognosis for patients with POG stage B neuroblastoma and indicate that most patients are curable with CY/AD +/- surgery, and those not achieving CR with this therapy are curable with alternate therapy.

摘要

儿童肿瘤研究组(POG)在一项前瞻性研究中评估了以下假设:对于术后有局限性、可见残留神经母细胞瘤且无区域淋巴结受累的患者(POG B期),采用中等强度化疗治疗时预后良好。符合条件的患者最初接受五个疗程的环磷酰胺(Cytoxan;布里斯托-迈尔斯·斯奎布公司,印第安纳州埃文斯维尔)和阿霉素(阿霉素;阿德里亚实验室,俄亥俄州哥伦布)治疗,随后进行手术(CY/AD +/- 手术)。那些未达到完全缓解(CR)的患者转而接受五个疗程的顺铂和替尼泊苷(PL/VM)治疗 +/- 手术。对交叉治疗后仍未达到CR的部分选定患者给予放射治疗(XRT)。在61名符合条件的患者中,38名(62%)患者经临床(31名)或手术(7名)评估证实CY/AD治疗后达到CR。1名(2%)处于临床部分缓解(PR-C)的患者未接受进一步治疗即进入CR状态。19名(31%)患者通过以下挽救治疗达到CR:手术(5名)、PL/VM +/- 手术(5名),随后进行XRT(3名)或自体骨髓移植(ABMT)(1名),以及采用CY/AD +/- PL/VM疗程替代PL/VM疗程(5名)。总体CR率为95%(61名中的58名)。4名患者疾病复发。初次或挽救治疗后3年无病概率估计为84%(标准误,5%)。1岁以上和1岁以下儿童的总体预后相似(P = 0.26)。然而,如果剔除3例缓解期死亡患者(均小于1岁),则1岁以下的32名儿童中仅有1例其他治疗失败,而1岁以上的29名儿童中有7例(P = 0.018)。这些结果证实了POG B期神经母细胞瘤患者的良好预后,并表明大多数患者可通过CY/AD +/- 手术治愈,而那些该治疗未达到CR的患者可通过替代治疗治愈。

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