Heidemann Jan, Ogawa Hitoshi, Otterson Mary F, Shidham Vinod B, Binion David G
Division of Gastroenterology and Hepatology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.
Dis Colon Rectum. 2004 Jan;47(1):118-22. doi: 10.1007/s10350-003-0019-4. Epub 2004 Jan 14.
Desmoid tumors are uncommon, benign, fibrous lesions occurring sporadically and in association with familial adenomatous polyposis. Typical clinical features include a locally aggressive behavior, an unpredictable course, and a high propensity for recurrence after surgical resection. There are no standard medical or surgical approaches, and no markers for monitoring medical therapy of desmoid tumors.
We report two cases of mesenteric desmoid tumors treated with interferon alfa-2b and toremifene, a novel regimen devised to block angiogenesis. Pre- and posttreatment desmoid tumor tissues were obtained in one patient during a repeat resection for recurrent stenosing Crohn's disease and examined for mean vessel count and cellular proliferation levels by immunostaining for the endothelial surface antigen CD31 and the proliferation associated nuclear antigen, Ki-67, respectively. We assessed plasma D-dimers, a potential marker of angiogenic activity, and followed this throughout the course of antiangiogenic therapy in our two patients.
Examination of posttreatment tissue revealed a significant decrease in microvessel density (P<0.02) and Ki-67-positive nuclei (P<0.0001) compared with pretreatment tissue. Both patients demonstrated a prompt and sustained drop in previously elevated plasma D-dimer levels, which correlated clinically with lesion regression and sustained remission.
Treatment with toremifene and interferon alfa-2b was successful and well tolerated in our two patients. Our data suggest a combined antiangiogenic and antiproliferative mechanism of action. Furthermore, normalization of previously elevated plasma D-dimers may emerge as a strategy to monitor treatment efficacy in mesenteric desmoid tumors.
硬纤维瘤是一种罕见的良性纤维性病变,可散发出现,也可与家族性腺瘤性息肉病相关。典型的临床特征包括局部侵袭性生长行为、不可预测的病程以及手术切除后高复发倾向。目前尚无标准的内科或外科治疗方法,也没有用于监测硬纤维瘤内科治疗的标志物。
我们报告了两例肠系膜硬纤维瘤患者,采用干扰素α-2b和托瑞米芬治疗,这是一种旨在阻断血管生成的新方案。其中一名患者在因复发性狭窄性克罗恩病再次切除时获取了治疗前后的硬纤维瘤组织,分别通过内皮表面抗原CD31免疫染色和增殖相关核抗原Ki-67免疫染色检测平均血管计数和细胞增殖水平。我们评估了血浆D-二聚体这一血管生成活性的潜在标志物,并在两名患者的抗血管生成治疗过程中全程进行跟踪。
与治疗前组织相比,治疗后组织检查显示微血管密度显著降低(P<0.02),Ki-67阳性核显著减少(P<0.0001)。两名患者先前升高的血浆D-二聚体水平均迅速且持续下降,这在临床上与病变消退和持续缓解相关。
托瑞米芬和干扰素α-2b治疗在我们的两名患者中取得成功且耐受性良好。我们的数据提示了一种联合的抗血管生成和抗增殖作用机制。此外,先前升高的血浆D-二聚体恢复正常可能成为监测肠系膜硬纤维瘤治疗疗效的一种策略。