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Ann Arbor I期霍奇金淋巴瘤的长期治疗结果:生存及无进展生存的预后因素

Long-term outcome of treatment for Ann Arbor Stage I Hodgkin's disease: prognostic factors for survival and freedom from progression.

作者信息

Vlachaki M T, Hagemeister F B, Fuller L M, Besa P C, Hess M A, Brown B, Cabanillas F, Cox J D

机构信息

Division of Radiation Oncology, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Int J Radiat Oncol Biol Phys. 1997 Jun 1;38(3):593-9. doi: 10.1016/s0360-3016(97)00036-9.

Abstract

PURPOSE

The earliest stages of Hodgkin's disease are associated with excellent short-term survival with radiation therapy. This has led to controversies regarding pretreatment evaluation, the extent of irradiation, the role of chemotherapy, and the relative importance of prognostic factors. Long-term results were sought to address these controversies.

METHODS AND MATERIALS

A retrospective study was conducted of patients with Stage I Hodgkin's disease treated at the M. D. Anderson Cancer Center from 1967 through 1987. The median age at presentation of 145 patients was 31 years, and the male-to-female ratio was 1.8. Pretreatment evaluation included lymphangiography and bone marrow aspiration and biopsy in all patients. Laparotomy was performed in 101 of the 145 patients (70%). There were 133 patients with supradiaphragmatic presentations; 12 patients had infradiaphragmatic adenopathy. Only five patients had B symptoms (3.5%). Histologic subtypes of the disease included lymphocyte predominance 17.9%, nodular sclerosis 40.7%, mixed cellularity 40.7%, and one unclassified Hodgkin's disease with primary splenic involvement. All patients were treated with radiotherapy, and 16 (11%) also received combination chemotherapy as part of their initial treatment. Radiotherapy techniques included involved/regional field in 49%, extended field in 42.7% (mantle or inverted Y), and subtotal nodal irradiation in 8.3%. Follow-up extended from a minimum of 30-339 months, with a median period of observation of 16.5 years.

RESULTS

The median survival was 13.7 years. The 10- and 20-year survival rates were 83% and 66%, respectively. The only factor important for decreased survival was age >40 years at diagnosis (p < 0.0001). Out of 43 deaths, 11 were the result of Hodgkin's disease and the remaining 32 resulted from intercurrent disease, including treatment-related causes. Median freedom from progression was 10.5 years, and the 10- and 20-year freedom from progression were 76% and 69%, respectively. Out of 39 relapses, 5 (13%) occurred beyond 10 years. Women had higher freedom from progression (p = 0.0534) than men. Age, histology, bulk of disease, site of involvement including the mediastinal presentations, and the addition of chemotherapy did not influence the freedom of progression. Although very few patients (12 of 145) received subtotal nodal irradiation, the freedom from progression at 10 years was 91.7% for this group versus 64.7% for the group of patients who were treated with more limited techniques.

CONCLUSION

Treatment with radiation therapy for patients with Stage I Hodgkin's disease leads to an excellent outcome, but patients require long-term surveillance as late relapses are not rare. Age is the only factor that affects survival, and gender marginally affects freedom from progression. Subtotal nodal irradiation may improve freedom from progression; further investigation of this treatment is justified.

摘要

目的

霍奇金淋巴瘤的早期阶段采用放射治疗可获得出色的短期生存率。这引发了关于预处理评估、照射范围、化疗的作用以及预后因素相对重要性的争议。本研究旨在探寻长期结果以解决这些争议。

方法与材料

对1967年至1987年在MD安德森癌症中心接受治疗的I期霍奇金淋巴瘤患者进行回顾性研究。145例患者的中位就诊年龄为31岁,男女比例为1.8。所有患者的预处理评估包括淋巴管造影以及骨髓穿刺和活检。145例患者中有101例(70%)接受了剖腹探查术。有133例患者表现为膈上病变;12例患者有膈下淋巴结肿大。仅有5例患者有B症状(3.5%)。疾病的组织学亚型包括淋巴细胞为主型17.9%、结节硬化型40.7%、混合细胞型40.7%,以及1例伴有原发性脾脏受累的未分类霍奇金淋巴瘤。所有患者均接受放射治疗,16例(11%)患者在初始治疗中还接受了联合化疗。放射治疗技术包括受累/区域野照射49%、扩大野照射42.7%(斗篷野或倒Y野)以及次全淋巴结照射8.3%。随访时间最短为30 - 339个月,中位观察期为16.5年。

结果

中位生存期为13.7年。10年和20年生存率分别为83%和66%。对生存率降低有重要影响的唯一因素是诊断时年龄>40岁(p < 0.0001)。在43例死亡病例中,11例死于霍奇金淋巴瘤,其余32例死于并发疾病,包括与治疗相关的原因。中位无进展生存期为10.5年,10年和20年无进展生存率分别为76%和69%。在39例复发病例中,5例(13%)在10年后复发。女性的无进展生存率高于男性(p = 0.0534)。年龄、组织学类型、疾病体积、受累部位(包括纵隔表现)以及化疗的应用均不影响无进展生存率。尽管接受次全淋巴结照射的患者极少(145例中有12例),但该组10年无进展生存率为91.7%,而接受更有限技术治疗的患者组为64.7%。

结论

I期霍奇金淋巴瘤患者采用放射治疗可取得良好疗效,但患者需要长期监测,因为晚期复发并不罕见。年龄是影响生存的唯一因素,性别对无进展生存率有轻微影响。次全淋巴结照射可能提高无进展生存率;对这种治疗方法进行进一步研究是合理的。

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