Hara Takeshi, Tsurumi Hisashi, Goto Naoe, Kanemura Nobuhiro, Yoshikawa Takeshi, Kasahara Senji, Yamada Toshiki, Sawada Michio, Goto Hideko, Fukuno Kenji, Kitagawa Jun-Ichi, Yasuda Ichiro, Katsumura Naoki, Takemura Masao, Takahashi Takeshi, Takami Tsuyoshi, Moriwaki Hisataka
First Department of Internal Medicine, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu 501-1194, Japan.
J Cancer Res Clin Oncol. 2009 Oct;135(10):1421-8. doi: 10.1007/s00432-009-0586-4. Epub 2009 Apr 21.
We previously reported that serum concentrations of soluble Fas (sFas) predict the clinical outcome of patients with diffuse large B cell lymphoma (DLBCL) after treatment with CHOP but without rituximab (R). Here, we investigated whether the role of sFas as a prognostic factor remains valid in the R-CHOP era.
We treated 132 patients with DLBCL between October 1995 and September 2002 (group A: without rituximab), and 75 between December 2002 and March 2007 (group B: with rituximab). The patients received eight cycles of CHOP or THP (tetrahydropyranyl-adriamycin)-COP before September 2002, and R-CHOP or R-THP-COP after October 2002. The distribution of patients according to the International Prognostic Index did not significantly differ between the groups.
The 5-year overall survival (OS) rates for patients with sFas levels of > or = 3.0 and <3.0 ng/ml in group A were 19.8 and 61.9% (P < 0.0001), whereas the 3-year OS rates in group B were 54.7 and 92.2% (P < 0.01), respectively. Multivariate analysis using the proportional hazards model revealed that sFas most significantly correlated with overall survival (P < 0.05).
Serum sFas is thus a useful tool for selecting the appropriate therapeutic strategy for DLBCL.
我们之前报道过,可溶性Fas(sFas)的血清浓度可预测弥漫性大B细胞淋巴瘤(DLBCL)患者在接受CHOP方案但未联合利妥昔单抗(R)治疗后的临床结局。在此,我们研究了在R-CHOP时代,sFas作为预后因素的作用是否仍然有效。
我们在1995年10月至2002年9月期间治疗了132例DLBCL患者(A组:未使用利妥昔单抗),以及在2002年12月至2007年3月期间治疗了75例患者(B组:使用利妥昔单抗)。2002年9月之前,患者接受8个周期的CHOP或四氢吡喃阿霉素(THP)-COP方案治疗,2002年10月之后接受R-CHOP或R-THP-COP方案治疗。两组患者根据国际预后指数的分布无显著差异。
A组中sFas水平≥3.0 ng/ml和<3.0 ng/ml的患者5年总生存率(OS)分别为19.8%和61.9%(P<0.0001),而B组中3年OS率分别为54.7%和92.2%(P<0.01)。使用比例风险模型进行的多因素分析显示,sFas与总生存最显著相关(P<0.05)。
因此,血清sFas是为DLBCL选择合适治疗策略的有用工具。