Nakata Eiji, Kunisada Toshiyuki, Hasei Joe, Nakahara Ryuichi, Yanai Hiroyuki, Toji Tomohiro, Inoue Ct Hirofumi, Ozaki Toshifumi
E. Nakata, T. Kunisada, J. Hasei, R. Nakahara, T. Ozaki, Department of Orthopedic Surgery, Okayama University Hospital, Okayama, Japan.
H. Yanai, T. Toji, H. Inoue, Department of Pathology, Okayama University Hospital, Okayama, Japan.
Clin Orthop Relat Res. 2020 Nov;478(11):2550-2561. doi: 10.1097/CORR.0000000000001338.
Dedifferentiated liposarcoma (DDLPS) is a rare malignancy that transitions from an atypical lipomatous tumor to a sarcoma with a variable morphologic appearance. The behavior of this tumor in the retroperitoneum is aggressive, but the behavior of DDLPS in the extremities is less well-defined because it is rare. Few reports have assessed the imaging features and clinical outcomes of primary DDLPS in the extremities.
QUESTIONS/PURPOSES: In patients with primary DDLPS of the extremity, we asked the following questions: (1) How frequently do additional primary malignancies occur in patients with DDLPS? (2) What is the rate of overall survival, metastases, and local recurrence in DDLPS? (3) What factors are associated with metastasis-free survival and local recurrence in DDLPS?
We defined DDLPS as a biphasic neoplasm that transitions from an atypical lipomatous tumor (ALT) to a sarcoma of variable morphologic appearance and histologic grades. We retrospectively evaluated the medical records of patients with DDLPS of the extremities who underwent surgery in our institution between 2003 and 2017. During that time, 16 patients were treated for this diagnosis; one was excluded from this study because the patient did not have an MRI, leaving 15 patients (nine men, six women; their median [range] age was 67 years [42 to 87]) for evaluation. All had a minimum of 2 years follow-up (median [range] 54 months [25 to 136]); 14 of 15 have been seen in the last 5 years (one patient, who was doing well at the time, was lost after 9 years of follow-up). In 11 patients, MRI demonstrated two components: an ALT component with high intensity on both T1-weighed and T2-weighted sequences and a dedifferentiated component low-to-intermediate intensity on T1-weighed and heterogeneous hyperintensity on T2-weighted sequence. Nine patients were evaluated using 2-deoxy-2-18F-fluoro-D-glucose positron emission tomography (FDG-PET) combined with CT (PET/CT). PET/CT showed a biphasic pattern with a close relationship to MRI findings. The dedifferentiated component presented with high FDG uptake (median [range] maximum standardized uptake value 5.1 [1.9 to 22.6]), while the atypical lipomatous tumor component showed almost no FDG uptake. In all patients, immunohistochemical studies of p16 and cyclin-dependent kinase-4 (CDK4) were investigated. Positive staining for both p16 and CDK4 were seen in 13 of 15 patients.We retrospectively evaluated the electronic medical records of all patients in our institution for the presence of additional primary malignancies, local recurrence-free survival, metastasis-free survival, and overall survival. The survival rate was estimated using the Kaplan-Meier method. The Wilcoxon exact test was used to determine the prognostic importance of the following survival variables: age, sex, maximum tumor size, radiotherapy, and surgical margin.
Seven additional primary malignancies developed in five of 15 patients (two lung cancers, two sarcomas, one renal cell cancer, one uterine cancer, and one non-Hodgkin lymphoma). The 3- and 5-year metastasis-free survival rates were 86% (95% CI 0.67 to 1.00) and 75% (95% CI 0.49 to 1.00), respectively. With the numbers available, we found no factors associated with metastasis-free survival. The 3- and 5-year overall survival rates were 100% (95% CI 1.00 to 1.00) and 88% (95% CI 0.65 to 1.00), respectively. Three of 15 patients had local recurrence. The 3- and 5-year local recurrence-free survival rates were 86% (95% CI 0.67 to 1.00) and 75% (95% CI 0.49 to 1.00), respectively. Large (> 15 cm) tumors were more likely to have a local recurrence (p = 0.04).
In this small series, we found that the extremities are a favorable site for DDLPS compared with the retroperitoneum, although we did not directly compare the two sites. This rare tumor has a relatively high likelihood of being associated with other malignancies. We believe patients should be assessed and monitored carefully for this possibility. In the future, larger studies are needed to better define predictors of local recurrence, although the tumor's size may be associated with a greater propensity for local recurrence.
Level II, prognostic study.
去分化脂肪肉瘤(DDLPS)是一种罕见的恶性肿瘤,由非典型脂肪瘤性肿瘤转变为具有多种形态学表现的肉瘤。这种肿瘤在腹膜后的行为具有侵袭性,但在四肢的行为则不太明确,因为其较为罕见。很少有报告评估四肢原发性DDLPS的影像学特征和临床结果。
问题/目的:对于四肢原发性DDLPS患者,我们提出以下问题:(1)DDLPS患者中额外原发性恶性肿瘤的发生频率如何?(2)DDLPS的总生存率、转移率和局部复发率是多少?(3)与DDLPS无转移生存和局部复发相关的因素有哪些?
我们将DDLPS定义为一种双相性肿瘤,它从非典型脂肪瘤性肿瘤(ALT)转变为具有多种形态学表现和组织学分级的肉瘤。我们回顾性评估了2003年至2017年在我们机构接受手术的四肢DDLPS患者的病历。在此期间,有l6例患者接受了该诊断治疗;其中1例因未进行MRI检查而被排除在本研究之外,剩下15例患者(9例男性,6例女性;中位[范围]年龄为67岁[42至87岁])进行评估。所有患者至少随访2年(中位[范围]54个月[25至136个月]);15例患者中有14例在过去5年中接受了随访(1例患者在随访9年后失访,当时情况良好)。11例患者的MRI显示有两个成分:在T1加权和T2加权序列上均为高强度的ALT成分,以及在T1加权上为低至中等强度且在T2加权序列上为不均匀高信号的去分化成分。9例患者接受了2-脱氧-2-18F-氟-D-葡萄糖正电子发射断层扫描(FDG-PET)联合CT(PET/CT)检查。PET/CT显示出双相模式,与MRI结果密切相关。去分化成分表现为高FDG摄取(中位[范围]最大标准化摄取值5.1[1.9至22.6]),而非典型脂肪瘤性肿瘤成分几乎没有FDG摄取。对所有患者均进行了p16和细胞周期蛋白依赖性激酶-4(CDK4)免疫组化研究。15例患者中有13例p16和CDK4均呈阳性染色。我们回顾性评估了我们机构所有患者的电子病历,以了解是否存在其他原发性恶性肿瘤、无局部复发生存率、无转移生存率和总生存率。生存率采用Kaplan-Meier方法估计。采用Wilcoxon确切检验来确定以下生存变量的预后重要性:年龄、性别、最大肿瘤大小、放疗和手术切缘。
15例患者中有5例发生了7种额外的原发性恶性肿瘤(2例肺癌、2例肉瘤、1例肾细胞癌、1例子宫癌和1例非霍奇金淋巴瘤)。3年和5年无转移生存率分别为86%(95%CI0.67至1.00)和75%(95%CI0.49至1.00)。根据现有数据,我们未发现与无转移生存相关的因素。3年和5年总生存率分别为l00%(95%CI1.00至1.00)和88%(95%CI0.65至1.00)。15例患者中有3例发生了局部复发。3年和5年无局部复发生存率分别为86%(95%CI0.67至1.00)和75%(95%CI0.49至1.00)。肿瘤较大(>15cm)的患者更易发生局部复发(p=0.04)。
在这个小系列研究中,我们发现与腹膜后相比,四肢是DDLPS的一个较好发病部位,尽管我们没有直接比较这两个部位。这种罕见肿瘤与其他恶性肿瘤相关的可能性相对较高。我们认为应对患者进行仔细评估和监测以排查这种可能性。未来,需要更大规模的研究来更好地确定局部复发的预测因素,尽管肿瘤大小可能与更高的局部复发倾向相关。
II级,预后研究。