Dolmans M M, Iwahara Y, Donnez J, Soares M, Vaerman J L, Amorim C A, Poirel H
Pôle de Recherche en Gynécologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain (UCL), Brussels, Belgium Gynecology Department, Cliniques Universitaires Saint-Luc, Brussels, Belgium
Pôle de Recherche en Gynécologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain (UCL), Brussels, Belgium.
Hum Reprod. 2016 Oct;31(10):2292-302. doi: 10.1093/humrep/dew193. Epub 2016 Sep 2.
What is the risk of finding malignant cells in cryopreserved ovarian tissue from sarcoma patients?
Minimal disseminated disease (MDD) was not detected in frozen-thawed ovarian tissue from 26 patients by any of the sensitive methods applied.
In case of leukemia, the risk of malignant cell transmission through the graft is well known and widely documented. However, for bone cancer, like Ewing sarcoma or osteosarcoma, only a small number of case reports, have been published. These cancers often affect prepubertal girls, in whom ovarian tissue cryopreservation and transplantation is the only option to preserve fertility.
STUDY DESIGN, SIZE, DURATION: The presence of malignant cells in cryopreserved ovarian tissue from patients with bone/soft tissue sarcoma was investigated with disease-specific markers for each patient, using immunohistochemistry (IHC), FISH and real-time quantitative RT-PCR (qPCR), with the original tumor serving as a positive control.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Forty-eight sarcoma patients were enrolled in the study, 12 of whom subsequently died. In each case, tissue from the primary tumor was investigated in order to identify markers (immunohistochemical and/or molecular) to analyze the ovarian tissue case by case. Ovarian tissue from osteosarcoma (n = 15), liposarcoma (n = 1) and undifferentiated sarcoma (n = 5) patients could not be evaluated, as no specific markers were detected by FISH or sensitive IHC in any of their primary tumoral tissue. One patient with Li-Fraumeni syndrome was also excluded from the study. IHC analyses were therefore performed on ovarian tissue from 26 patients and qPCR on 19. The primary tumors involved were Ewing sarcoma family of tumors (n = 14), rhabdomyosarcoma (n = 7), synovial sarcoma (n = 2), clear cell sarcoma (n = 2) and a malignant peripheral nerve sheath tumor (n = 1).
MDD was not detected in any of the 26 analyzed samples using sensitive techniques in this largest reported series, even from patients who subsequently died and/or those who presented with metastasis (11/26), hence the most aggressive forms of bone cancer. Indeed, anti-CD99 IHC and PCR performed on patients presenting with Ewing sarcoma family of tumors (n = 14) was negative in all cases. In patients with soft tissue sarcoma (n = 12) primitive tumor markers were detected by IHC and were negative in ovarian tissue. PCR could only be performed in 6/12 of these patients, again proving negative.
LIMITATIONS, REASONS FOR CAUTION: Cryopreserved ovarian fragments to be transplanted cannot be tested, so this analysis of malignant cells cannot guarantee that all cryopreserved fragments will not contain any disseminated disease. Moreover, molecular markers are not readily available for all types of tumors.
These results are reassuring regarding the risk of malignant cells in the ovary for transplantation, as the study involves a large series including different types of sarcomas. We believe this will help clinicians in their patient counseling for fertility preservation and restoration.
STUDY FUNDING/COMPETING INTERESTS: This work was supported by the Fonds National de la Recherche Scientifique de Belgique-FNRS under Grants Nos 7.4578.14 (Télévie to MS) and 5/4/150/5 to MMD. The authors declare no competing financial interests.
在肉瘤患者的冷冻保存卵巢组织中发现恶性细胞的风险有多大?
通过所应用的任何敏感方法,在26例患者的冻融卵巢组织中均未检测到微小播散性疾病(MDD)。
对于白血病,通过移植物传播恶性细胞的风险是众所周知且有大量文献记载的。然而,对于骨癌,如尤因肉瘤或骨肉瘤,仅发表了少数病例报告。这些癌症常影响青春期前女孩,对她们而言,卵巢组织冷冻保存和移植是保留生育能力的唯一选择。
研究设计、规模、持续时间:使用免疫组织化学(IHC)、荧光原位杂交(FISH)和实时定量逆转录聚合酶链反应(qPCR),针对每位患有骨/软组织肉瘤的患者,采用疾病特异性标志物研究冷冻保存卵巢组织中恶性细胞的存在情况,以原发肿瘤作为阳性对照。
参与者/材料、环境、方法:48例肉瘤患者纳入本研究,其中12例随后死亡。每例均对原发肿瘤组织进行研究,以确定标志物(免疫组织化学和/或分子标志物),从而逐例分析卵巢组织。骨肉瘤(n = 15)、脂肪肉瘤(n = 1)和未分化肉瘤(n = 5)患者的卵巢组织无法评估,因为在其任何原发肿瘤组织中,FISH或敏感的免疫组织化学均未检测到特异性标志物。一名患有李-弗劳梅尼综合征的患者也被排除在研究之外。因此,对26例患者的卵巢组织进行了免疫组织化学分析,对19例进行了qPCR分析。所涉及的原发肿瘤包括尤因肉瘤家族性肿瘤(n = 14)、横纹肌肉瘤(n = 7)、滑膜肉瘤(n = 2)、透明细胞肉瘤(n = 2)和恶性外周神经鞘瘤(n = 1)。
在这个最大规模的报道系列中,使用敏感技术在26例分析样本中均未检测到MDD,即使是来自随后死亡和/或出现转移的患者(11/26),即最具侵袭性的骨癌类型。实际上,对患有尤因肉瘤家族性肿瘤的患者(n = 14)进行的抗CD99免疫组织化学和PCR检测在所有病例中均为阴性。在软组织肉瘤患者(n = 12)中,通过免疫组织化学检测到原发肿瘤标志物,而在卵巢组织中为阴性。PCR仅能在其中6/12例患者中进行,结果同样为阴性。
局限性、谨慎原因:待移植的冷冻卵巢碎片无法进行检测,因此这种对恶性细胞的分析不能保证所有冷冻保存的碎片都不含有任何播散性疾病。此外,并非所有类型的肿瘤都有现成的分子标志物。
这些结果对于卵巢移植中恶性细胞的风险而言是令人安心的,因为该研究纳入了包括不同类型肉瘤的大量病例系列。我们相信这将有助于临床医生为患者提供关于生育力保存和恢复的咨询。
研究资金/利益冲突:这项工作得到了比利时国家科学研究基金(FNRS)的资助,资助编号分别为7.4578.14(Télévie资助给MS)和5/4/150/5资助给MMD。作者声明不存在相互竞争的财务利益。