Department of Obstetrics and Gynecology, University of Bonn, Bonn, Germany.
Int J Radiat Oncol Biol Phys. 2010 Jul 15;77(4):1128-33. doi: 10.1016/j.ijrobp.2009.06.088. Epub 2010 Feb 3.
Several international trials are currently investigating accelerated partial breast irradiation (APBI) for patients with early-stage breast cancer. According to existing guidelines, patients with lymphatic vessel invasion (LVI) do not qualify for APBI. D2-40 (podoplanin) significantly increases the frequency of LVI detection compared with conventional hematoxylin and eosin (HE) staining in early-stage breast cancer. Our purpose was to retrospectively assess the hypothetical change in management from APBI to whole breast radiotherapy with the application of D2-40.
Immunostaining with D2-40 was performed on 254 invasive breast tumors of 247 patients. The following criteria were used to determine the eligibility for APBI: invasive ductal adenocarcinoma of < or =3 cm, negative axillary node status (N0), and unifocal disease. Of the 247 patients, 74 with available information concerning LVI, as detected by D2-40 immunostaining and routine HE staining, formed our study population.
Using D2-40, our results demonstrated a significantly greater detection rate (p = .031) of LVI compared with routine HE staining. LVI was correctly identified by D2-40 (D2-40-positive LVI) in 10 (13.5%) of 74 tumors. On routine HE staining, 4 tumors (5.4%) were classified as HE-positive LVI. Doublestaining of these specimens with D2-40 unmasked false-positive LVI status in 2 (50%) of the 4 tumors. According to the current recommendations for APBI, immunostaining with D2-40 would have changed the clinical management from APBI to whole breast radiotherapy in 8 (10.8%) of 74 patients and from whole breast radiotherapy to APBI in 2 patients (2.7%).
These data support the implementation of D2-40 immunostaining in the routine workup to determine a patient's eligibility for APBI.
目前有几项国际试验正在研究早期乳腺癌患者的加速部分乳房照射(APBI)。根据现有指南,淋巴管浸润(LVI)患者不符合 APBI 条件。与常规苏木精和伊红(HE)染色相比,D2-40(足突蛋白)在早期乳腺癌中显著增加了 LVI 的检测频率。我们的目的是回顾性评估应用 D2-40 后从 APBI 到全乳放疗的假设治疗改变。
对 247 例患者的 254 例浸润性乳腺癌进行了 D2-40 免疫染色。APBI 合格标准为:浸润性导管腺癌<或=3cm,腋窝淋巴结状态(N0)阴性,单病灶。在 247 例患者中,有 74 例有 D2-40 免疫染色和常规 HE 染色检测 LVI 的信息,形成了我们的研究人群。
使用 D2-40,我们的结果显示 LVI 的检测率显著增加(p=0.031),与常规 HE 染色相比。D2-40 正确识别 10(13.5%)例 74 例肿瘤的 LVI(D2-40 阳性 LVI)。在常规 HE 染色中,4 例肿瘤(5.4%)被归类为 HE 阳性 LVI。对这些标本进行 D2-40 双重染色,2 例(50%)显示假阳性 LVI 状态。根据目前 APBI 的建议,D2-40 免疫染色将使 74 例患者中的 8 例(10.8%)从 APBI 改为全乳放疗,2 例(2.7%)从全乳放疗改为 APBI。
这些数据支持在常规检查中实施 D2-40 免疫染色,以确定患者是否适合 APBI。