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早期局部区域高剂量放疗与鼻和鼻咽局限性原发性血管中心性淋巴瘤的长期疾病控制相关。

Early locoregional high-dose radiotherapy is associated with long-term disease control in localized primary angiocentric lymphoma of the nose and nasopharynx.

作者信息

Ribrag V, Ell Hajj M, Janot F, Girinsky T, Domenge C, Schwaab G, Fenaux P, Bosq J

机构信息

Département de Médecine, Institut Gustave-Roussy, Villejuif, France.

出版信息

Leukemia. 2001 Jul;15(7):1123-6. doi: 10.1038/sj.leu.2402148.

Abstract

Nasal NK/T cell is a rare form of usually localized non-Hodgkin's lymphoma (NHL) which generally carries a poor prognosis when treated with conventional NHL chemotherapy protocols. We reviewed 20 consecutive localized stage I/II nasal NK/T cell lymphomas treated at our institution over a 29 year period. Median age was 44 (range 23-71). Front-line therapy was generally radiotherapy alone (35-70 Gy) before 1980 and combination chemotherapy after 1980. Six patients were treated with first-line radiotherapy and they achieved complete remission (CR). Two subsequently received combination chemotherapy. Five of those patients remained in complete remission, after 97+ to 277+ months. Twelve patients were treated with first-line chemotherapy including CHOP or CHOP-like regimen in seven cases, and COP in five cases. Only three of them achieved CR, five had partial response and four had progressive disease. Five of the seven patients treated with CHOP did not achieve complete remission. The nine patients who failed to achieve CR with chemotherapy subsequently received salvage radiotherapy but only two of them obtained CR. Finally, two patients were treated with alternated chemotherapy and radiotherapy and achieved CR, which persisted after 14+ and 26+ months. Median survival was not reached in patients who received front-line radiotherapy, and was 35 months in patients who received front-line chemotherapy. These findings confirm that chemotherapy gives a low complete remission rate in localized nasal NK/T cell lymphoma. By contrast, first-line radiotherapy seems to give favorable results, whereas its results are poorer when administered after resistance to chemotherapy. Whether the use of chemotherapy after radiotherapy, or alternated chemotherapy-radiotherapy regimens give better clinical results than radiotherapy alone will have to be evaluated prospectively in this type of NHL.

摘要

鼻型NK/T细胞淋巴瘤是一种罕见的通常为局限性的非霍奇金淋巴瘤(NHL),采用传统的NHL化疗方案治疗时,其预后通常较差。我们回顾了29年间在我院接受治疗的20例连续性局限性I/II期鼻型NK/T细胞淋巴瘤患者。中位年龄为44岁(范围23 - 71岁)。1980年前一线治疗通常仅采用放疗(35 - 70 Gy),1980年后采用联合化疗。6例患者接受一线放疗并获得完全缓解(CR)。其中2例随后接受了联合化疗。这些患者中有5例在97 +至277 +个月后仍处于完全缓解状态。12例患者接受一线化疗,其中7例采用CHOP或CHOP类似方案,5例采用COP方案。他们中只有3例达到CR,5例部分缓解,4例疾病进展。采用CHOP方案治疗的7例患者中有5例未达到完全缓解。9例化疗未达到CR的患者随后接受了挽救性放疗,但其中只有2例获得CR。最后,2例患者接受了化疗与放疗交替治疗并获得CR,在14 +和26 +个月后仍持续缓解。接受一线放疗的患者未达到中位生存期,接受一线化疗的患者中位生存期为35个月。这些结果证实,化疗在局限性鼻型NK/T细胞淋巴瘤中的完全缓解率较低。相比之下,一线放疗似乎能取得较好的效果,而在对化疗耐药后进行放疗,效果则较差。放疗后使用化疗或化疗与放疗交替方案是否比单纯放疗能取得更好的临床效果,还需对这类NHL进行前瞻性评估。

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