From the Division of Gynecologic Oncology, Department of Reproductive Medicine, and Division of Hematology-Oncology, Department of Medicine, UC San Diego Moores Cancer Center, La Jolla, California; Foundation Medicine, Inc., Cambridge, Massachusetts; and Division of Surgical Oncology, Department of Surgery, UC San Diego Moores Cancer Center, La Jolla, California.
J Natl Compr Canc Netw. 2018 Mar;16(3):238-242. doi: 10.6004/jnccn.2017.7039.
Gastrointestinal stromal tumors (GISTs) are rare in pregnancy, with only 11 reported cases. Adjuvant imatinib therapy, which targets the most common driver mutations in GIST ( and , is recommended for patients with high-risk GIST, but it has known teratogenicity in the first trimester. A 34-year-old G3P2 woman underwent exploratory laparotomy at 16 weeks' gestation for a presumed adnexal mass. Surgical findings included normal adnexa and a 14-cm solid small bowel mass. The mass was resected en bloc with a segment of jejunum followed by a primary anastomosis. Histopathology and genomic analyses demonstrated a GIST with high-risk features but lack of mutations and identified the presence of a previously unreported, pathogenic gene fusion. Given her tumor profile, adjuvant therapy with imatinib was not recommended. GIST is rare in pregnancy, but can masquerade as an adnexal mass in women of childbearing age. Because neoadjuvant/adjuvant imatinib has risks of teratogenicity, tumor molecular profiling is critical as we identified a previously unreported gene fusion of with that is predicted to be imatinib-resistant. In this case, testing provided the rationale for not offering adjuvant imatinib to avoid unnecessary toxicity to the patient and fetus.
胃肠道间质瘤(GIST)在妊娠中罕见,仅有 11 例报道。针对 GIST 中最常见驱动突变(和)的辅助伊马替尼治疗被推荐用于高危 GIST 患者,但它在孕早期具有已知的致畸性。一位 34 岁的 G3P2 女性在 16 周妊娠时因疑似附件肿块接受剖腹探查术。手术发现包括正常附件和 14cm 实性小肠肿块。肿块整块切除并切除一段空肠,然后进行一期吻合。组织病理学和基因组分析显示具有高危特征的 GIST,但缺乏突变,并发现了以前未报道的致病性基因融合。鉴于她的肿瘤特征,不建议进行伊马替尼辅助治疗。GIST 在妊娠中罕见,但在育龄妇女中可能表现为附件肿块。由于新辅助/辅助伊马替尼有致畸风险,肿瘤分子谱分析至关重要,因为我们发现了以前未报道的基因融合,与 预测对伊马替尼耐药。在这种情况下,检测提供了不提供辅助伊马替尼的理由,以避免对患者和胎儿的不必要毒性。