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采用LSA2L2方案化疗后,腹腔内非霍奇金淋巴瘤患儿的预后得到改善。

Improved prognosis in children with intra-abdominal non-Hodgkin's lymphoma following LSA2L2 protocol chemotherapy.

作者信息

Wollner N, Wachtel A E, Exelby P R, Centore D

出版信息

Cancer. 1980 Jun 15;45(12):3034-9. doi: 10.1002/1097-0142(19800615)45:12<3034::aid-cncr2820451226>3.0.co;2-7.

DOI:10.1002/1097-0142(19800615)45:12<3034::aid-cncr2820451226>3.0.co;2-7
PMID:7388747
Abstract

Thirty-five consecutive, previously untreated patients with intra-abdominal non-Hodgkin's lymphoma (IANHL), seen between January 1971 and June 1978, were entered on the LSA2-L2 protocol. Six patients had Stage II disease, 23 Stage III and six Stage IV. The prevalent histologic types were diffuse lymphocytic poorly differentiated (13 patients) and diffuse undifferentiated (13 patients) followed by diffuse histiocytic (5 patients) and diffuse lymphoblastic (2 patients). All patients received LSA2-L2 protocol chemotherapy. Three of 4 patients with gross residual disease following initial surgery, who were seen prior to 1974, received radiation therapy during induction chemotherapy; there were no survivors among these 3 patients. Our treatment plan was revised in 1974 to include a "second-look" laparotomy during the third week of induction chemotherapy for all patients with gross residual intra-abdominal disease following their initial surgery. The disease-free actuarial survival for the total group of 35 patients is 72%. Fifteen of the 26 surviving patients are off therapy and have shown no evidence of recurrence or metastases (median observation time 26 + months). Fifteen of 26 patients seen after 1973 underwent the second laparotomy and only two were found to have residual disease. The LSA2-L2 protocol has significantly improved the disease-free survival rate of children with IANHL, even with widespread intra-abdominal and extra-abdominal disease at diagnosis. Further, the "second-look" laparotomy in patients with large unresectable disease at presentation has proved a useful method of unequivocal evaluation of response, thus eliminating unnecessary extensive abdominal irradiation in many of these children.

摘要

1971年1月至1978年6月期间,连续收治了35例未经治疗的腹腔内非霍奇金淋巴瘤(IANHL)患者,并采用LSA2-L2方案进行治疗。6例为Ⅱ期疾病,23例为Ⅲ期,6例为Ⅳ期。常见的组织学类型为弥漫性淋巴细胞低分化型(13例)和弥漫性未分化型(13例),其次为弥漫性组织细胞型(5例)和弥漫性淋巴母细胞型(2例)。所有患者均接受LSA2-L2方案化疗。1974年前接受初次手术且有肉眼可见残留病灶的4例患者中,有3例在诱导化疗期间接受了放射治疗;这3例患者均无存活。1974年,我们修订了治疗方案,对所有初次手术后腹腔内有肉眼可见残留病灶的患者,在诱导化疗的第三周进行“二次探查”剖腹手术。35例患者的无病精算生存率为72%。26例存活患者中有15例已停止治疗,且无复发或转移迹象(中位观察时间26 + 个月)。1973年后就诊的26例患者中有15例接受了二次剖腹手术,只有2例发现有残留病灶。LSA2-L2方案显著提高了IANHL患儿的无病生存率,即使在诊断时腹腔内和腹腔外疾病广泛的情况下也是如此。此外,对于初诊时患有无法切除的大面积疾病的患者,“二次探查”剖腹手术已被证明是一种明确评估反应的有用方法,从而避免了许多此类儿童不必要的广泛腹部照射。

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引用本文的文献

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Advanced primary non-Hodgkin's lymphoma of the small intestine in childhood: report of four cases.儿童晚期原发性小肠非霍奇金淋巴瘤:4例报告
Surg Today. 1994;24(11):1023-7. doi: 10.1007/BF02215819.
3
Burkitt-type lymphoma in France among non-Hodgkin malignant lymphomas in Caucasian children.
法国白人儿童非霍奇金恶性淋巴瘤中的伯基特型淋巴瘤。
Br J Cancer. 1982 May;45(5):670-8. doi: 10.1038/bjc.1982.107.
4
Characteristics of Burkitt's lymphoma in India.印度伯基特淋巴瘤的特征。
Indian J Pediatr. 1987 Nov-Dec;54(6):859-62. doi: 10.1007/BF02761011.