Magomedova A U, Kravchenko S K, Kremenetskaia A M, Zvonkov E A, Bariakh E A, Mangasarova Ia K, Kaplanskaia I B, Samoĭlova R S, Vorob'ev I A, Obukhova T N, Karagiulian S R, Shulutko E M, Galstian G M, Mar'in D S, Gabeeva N G, Vorob'ev A I
Ter Arkh. 2011;83(7):5-10.
To ascertain indications to standard (CHOP-21/R-CHOP-21) and intensive (mNHL-BFM-90) treatment in patients with diffuse large B-cell lymphosarcoma (DLBCL) with involvement of lymphoid organs.
The trial, performed from January 2002 to December 2010, enrolled 139 DLBCL patients with affected lymph nodes (LN), tonsils, spleen, bone marrow (BM). The diagnosis was made according to WHO criteria. The patients were examined according to the protocol of lymphoproliferative diseases. Biopsy material from all 139 patients was studied immunohistochemically on paraffin blocks (LN, tonsils, spleen, BM) using a wide panel of antibodies. The same examinations of BM were made in all 18 cases of BM involvement. Cytogenetic examination was performed in 106 patients: 48 standard cytogenetic tests, 139 - FISH for t (14;18) as well as rearrangement of locus 3q27. Patients with a poor prognosis (n = 86, 61.8%) received intensive therapy according to mNHL-BFM-90 program. The signs of a poor prognosis were the following: massive tumor (tumor size more than 7.5 cm), invasion into the adjacent organs or tissues, stage III-IV disease by Enn-Erbor, high concentration of LDG. Patients without a poor prognosis (n = 53, 38.2%) received standard treatment CHOP-21 (n = 28) or R-CHOP-21 (n = 25).
A complete remission without recurrences was achieved in all 53 patients without signs of unfavourable prognosis (100%). Overall 5-year survival was 96%, 2 patients died in remission of other causes. Of 86 patients with a poor prognosis a complete remission was achieved in 64 (74.4%) patients. Overall and recurrence-free 5-year survival was 65 and 86%, respectively.
Standard treatment provided long-term complete remission in all the patients without poor prognosis. Intensive (mNHL-BFM-90) treatment produced the best results in generalized lesion without BM involvement. Overall 5-year survival was 84% in these patients and 12% in patients with BM involvement.
确定弥漫性大B细胞淋巴瘤(DLBCL)累及淋巴器官患者接受标准治疗(CHOP-21/R-CHOP-21)和强化治疗(mNHL-BFM-90)的指征。
该试验于2002年1月至2010年12月进行,纳入了139例患有受累淋巴结(LN)、扁桃体、脾脏、骨髓(BM)的DLBCL患者。诊断依据世界卫生组织标准。患者按照淋巴增殖性疾病方案进行检查。使用多种抗体对139例患者石蜡块(LN、扁桃体、脾脏、BM)中的活检材料进行免疫组织化学研究。对所有18例骨髓受累患者进行相同的骨髓检查。对106例患者进行了细胞遗传学检查:48例进行标准细胞遗传学检测,139例进行t(14;18)以及3q27位点重排的荧光原位杂交(FISH)检测。预后不良的患者(n = 86,61.8%)根据mNHL-BFM-90方案接受强化治疗。预后不良的体征如下:巨大肿瘤(肿瘤大小超过7.5 cm)、侵犯相邻器官或组织、根据恩恩-埃尔伯分期为III-IV期疾病、乳酸脱氢酶(LDG)浓度高。预后良好的患者(n = 53,38.2%)接受标准治疗CHOP-21(n = 28)或R-CHOP-21(n = 25)。
所有53例无不良预后体征的患者均实现了无复发的完全缓解(100%)。总体5年生存率为96%,2例患者在缓解期因其他原因死亡。86例预后不良的患者中,64例(74.4%)实现了完全缓解。总体5年生存率和无复发生存率分别为65%和86%。
标准治疗使所有预后良好的患者获得了长期完全缓解。强化治疗(mNHL-BFM-90)在无骨髓受累的广泛性病变患者中取得了最佳效果。这些患者的总体5年生存率为84%,骨髓受累患者为12%。