Escalón Maricer P, Liu Nina S, Yang Ying, Hess Mark, Walker Pamela L, Smith Terry L, Dang Nam H
Department of Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer. 2005 May 15;103(10):2091-8. doi: 10.1002/cncr.20999.
T-cell non-Hodgkin lymphomas (T-NHL) are more aggressive and patients have a poorer prognosis compared with patients with the corresponding B-cell lymphomas. Although intensive treatments have been developed, it is unknown whether they are more effective than CHOP chemotherapy (cyclophosphamide, doxorubicin, oncovorin, and prednisone).
The authors' retrospective study evaluated the clinical outcome of 135 previously untreated patients with T-NHL who were treated at The University of Texas M. D. Anderson Cancer Center (Houston, TX) between 1996 and 2002. Lymphomas with T-cell histologies with the exception of mycosis fungoides were included.
The estimated median overall survival was 46 months. Thirty-seven percent of the patients received CHOP therapy, 48% received intensive therapy, and 15% received other therapy. The estimated 3-year overall survival rates were 62% for the patients treated with CHOP therapy and 56% for the patients who received intensive therapy. After the exclusion of patients with anaplastic large cell lymphoma (ALCL), who are known to have a better prognosis than patients with other T-NHLs, the estimated 3-year overall survival rates were 43% for the patients treated with CHOP therapy and 49% for the patients who received intensive therapy. Parameters that may be independent prognostic factors for survival in T-NHL, excluding ALCL, included ECOG performance status > or = 2, beta-2-microglobulin level > 2 mg/L, lactate dehydrogenase level higher than normal, bulky disease > or = 7 cm, and a higher international prognostic index and tumor score.
The current study data suggested that patients treated with intensive therapies did not fare better than those treated with CHOP therapy. New treatment regimens need to be developed for patients with T-NHL.
与相应的B细胞淋巴瘤患者相比,T细胞非霍奇金淋巴瘤(T-NHL)侵袭性更强,患者预后更差。尽管已经研发出强化治疗方案,但尚不清楚这些方案是否比CHOP化疗(环磷酰胺、阿霉素、长春新碱和泼尼松)更有效。
作者进行的回顾性研究评估了1996年至2002年间在德克萨斯大学MD安德森癌症中心(德克萨斯州休斯顿)接受治疗的135例未经治疗的T-NHL患者的临床结局。纳入除蕈样霉菌病外具有T细胞组织学特征的淋巴瘤。
估计的中位总生存期为46个月。37%的患者接受了CHOP治疗,48%接受了强化治疗,15%接受了其他治疗。接受CHOP治疗的患者估计3年总生存率为62%,接受强化治疗的患者为56%。排除已知预后比其他T-NHL患者更好的间变性大细胞淋巴瘤(ALCL)患者后,接受CHOP治疗的患者估计3年总生存率为43%,接受强化治疗的患者为49%。在不包括ALCL的T-NHL中,可能是生存独立预后因素的参数包括东部肿瘤协作组(ECOG)体能状态≥2、β2微球蛋白水平>2mg/L、乳酸脱氢酶水平高于正常、大包块病变≥7cm,以及更高的国际预后指数和肿瘤评分。
当前研究数据表明,接受强化治疗的患者并不比接受CHOP治疗的患者预后更好。需要为T-NHL患者研发新的治疗方案。