利用单个中心收集的38年数据确定妊娠期间诊断的骨和软组织肉瘤的处理方法

Chee Leong Choong , Vineet Kurisunkal , Jonathan Stevenson , Lee Jeys
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引用次数: 0

摘要

背景骨骼或软组织肉瘤的诊断并不常见,在怀孕期间出现的几率也很低。因此,妊娠期肉瘤的治疗更为复杂,迄今为止,没有一个单一的指导方针适合所有人。方法从我们的骨科肿瘤学数据库中回顾性确定1983年至2021年期间诊断为骨或软组织肉瘤或妊娠期转移性肉瘤进展的患者。收集了有关其管理的人口统计学和相关信息,包括孕产妇和新生儿结局、转移进展和生存率。结果共纳入30例妊娠期诊断为肉瘤的患者;骨肉瘤16例(53.33%),软组织肉瘤9例(30%)。其中5例(16.67%)在妊娠期间出现骨或软组织肉瘤的转移进展。诊断时的中位年龄为31岁,最小的18岁,最大的38岁。肉瘤多学科团队(MDT)和产科团队在每位患者的妊娠随访期间进行了详细的讨论。7人接受了终止妊娠,6人在妊娠期间接受了手术治疗,没有产妇或新生儿并发症的报告。8例早期引产,4例早期剖腹产,以便在没有任何新生儿并发症的情况下进行分期和最终治疗。骨肉瘤的母亲一年和五年生存率分别为100%和73.68%,软组织肉瘤的母亲一周和五年存活率分别为10%和70%。其中一例在转移性进展组中存活了五年以上,但在第7年因脑转移而死亡。结论在集体知识和专业知识的基础上,通过肉瘤MDT治疗妊娠期骨和软组织肉瘤,可获得与非妊娠人群的产妇生存率相当的良好新生儿或产妇结局。治疗计划应基于患者的个人期望,具体取决于妊娠期、病理类型和肉瘤的位置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defining the management of bone and soft tissue sarcoma diagnosed during pregnancy using 38-year data collected in a single centre

Background

Diagnosis of a bone or soft tissue sarcomas is uncommon, and the odds of being present during pregnancy are rare. Hence, the management of sarcoma during pregnancy is more complicated, and to date, no single guideline suits all.

Method

Patients diagnosed with either bone or soft-tissue sarcomas or metastatic sarcoma progression during pregnancy were identified retrospectively between 1983 and 2021 from our orthopaedic oncology database. Demographic and relevant information regarding their management was collected, including maternal and neonatal outcomes, metastatic progression, and survival rates.

Results

A sum of 30 patients diagnosed with sarcoma during pregnancy were included; 16 (53.33%) with bone sarcoma and nine (30%) with soft-tissue sarcoma. Five (16.67%) had metastatic progression of their bone or soft-tissue sarcoma during pregnancy. The median age at diagnosis is 31 years old, youngest at 18 and eldest at 38 years old. Detailed discussions between the sarcoma multidisciplinary team (MDT) and obstetric teams took place throughout each patient's pregnancy follow-up. Seven underwent termination of pregnancy, and six underwent surgical treatment during pregnancy with no maternal or neonatal complications reported. Eight were induced early and four underwent early caesarean section to allow for staging and definitive management without any neonatal complications. Maternal one-year and five-year survival rates for bone sarcomas were 100% and 73.68%, respectively, and 100% and 70%, respectively, for soft-tissue sarcomas. One survived more than five years in the metastatic progression group but succumbed at 7th year due to cerebral metastasis.

Conclusion

The management of bone and soft-tissue sarcomas during pregnancy by sarcoma MDT with collective knowledge and expertise led to good neonatal or maternal outcomes comparable to maternal survival rates of the non-pregnant population. The treatment plan should be based on individual expectations from the patient depending on the gestational period of the pregnancy, the type of pathology, and the location of the sarcoma.

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