Soper J T, Spillman M, Sampson J H, Kirkpatrick J P, Wolf J K, Clarke-Pearson D L
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Gynecol Oncol. 2007 Mar;104(3):691-4. doi: 10.1016/j.ygyno.2006.10.027. Epub 2006 Nov 29.
To report our recent experience managing four patients with brain metastases of gestational trophoblastic neoplasia (GTN), coordinating systemic chemotherapy with early neurosurgical intervention or stereotactic radiosurgery and intensive supportive care during initial therapy to prevent early mortality.
A series of four consecutive patients with brain metastases from high-risk Stage IV GTN managed at our institution in 2003 and 2005. Patients were assigned FIGO stage and risk score prospectively. Because of concern for chronic toxicity resulting from concurrent moderate dose methotrexate and whole brain radiation, an individualized multidisciplinary approach was used to manage patients.
All four women presented with brain and pulmonary metastases; one had multiple liver metastases. Neurological symptoms at presentation included grand mal seizures in 2 patients, left upper extremity hemiparesis and headache each in 1 patient, while 1 patient was asymptomatic. Index pregnancies were term pregnancies in all patients with interval from prior delivery ranging from 2 weeks to 4 years. Two had received prior chemotherapy for postmolar GTN prior to the index pregnancy with incomplete follow-up. Initial hCG values ranged from 26,400 to 137,751 mIU/ml; FIGO risk scores were > or =16 for all patients. Systemic combination chemotherapy was initiated with etoposide and cisplatin followed by moderate/high-dose (500-1000 mg/m(2)) methotrexate combinations. Craniotomy was used before or during the first chemotherapy cycle to extirpate solitary lesions in 3 patients, while stereotactic radiosurgery was administered after the first cycle to treat two brain lesions in the remaining patient. None received whole brain radiation or intrathecal methotrexate. In one patient, selective angiographic embolization was used to control hemorrhage from multiple liver metastases. Two patients required ventilator support early in treatment to allow stabilization from intrathoracic hemorrhage and neutropenic sepsis with respiratory distress syndrome, respectively. Hysterectomy was performed in one patient after completion of salvage chemotherapy. All have completed maintenance chemotherapy and are in prolonged remission (12-24 months). Neurologic sequelae include persistent left upper extremity dyskinesia and weakness in one patient, and episodic grand mal seizures and pseudoseizures in a second patient with a pre-existing seizure disorder.
This case series documents the utility for a multidisciplinary approach to the treatment of brain metastases from GTN. Using early craniotomy or stereotactic radiosurgery combined with etoposide-cisplatin and moderate/high-dose methotrexate combination chemotherapy, we were able to stabilize patients early in their treatment and avoid whole brain radiation therapy or intrathecal chemotherapy.
报告我们近期治疗4例妊娠滋养细胞肿瘤(GTN)脑转移患者的经验,在初始治疗期间协调全身化疗与早期神经外科干预或立体定向放射外科治疗以及强化支持治疗,以预防早期死亡。
2003年和2005年在我们机构治疗的一系列4例连续的高危IV期GTN脑转移患者。前瞻性地为患者分配FIGO分期和风险评分。由于担心同时使用中等剂量甲氨蝶呤和全脑放疗会导致慢性毒性,因此采用个体化多学科方法管理患者。
所有4名女性均有脑和肺转移;1例有多发肝转移。就诊时的神经症状包括2例全身性癫痫发作,1例左上肢偏瘫和头痛,另1例无症状。所有患者的索引妊娠均为足月妊娠,距上次分娩的间隔时间为2周至4年。2例在索引妊娠前曾接受过绒毛膜癌GTN的化疗,但随访不完整。初始hCG值范围为26,400至137,751 mIU/ml;所有患者的FIGO风险评分均≥16。开始使用依托泊苷和顺铂进行全身联合化疗,随后使用中/高剂量(500-1000 mg/m²)甲氨蝶呤联合化疗。3例患者在第一个化疗周期之前或期间接受开颅手术切除孤立性病变,而其余患者在第一个周期后接受立体定向放射外科治疗以治疗两处脑病变。均未接受全脑放疗或鞘内注射甲氨蝶呤。1例患者使用选择性血管造影栓塞术控制多发肝转移引起的出血。2例患者在治疗早期需要呼吸机支持,分别以稳定胸腔内出血和中性粒细胞减少性脓毒症合并呼吸窘迫综合征。1例患者在挽救性化疗完成后接受了子宫切除术。所有患者均已完成维持化疗,且处于长期缓解状态(12-24个月)。神经后遗症包括1例患者持续存在的左上肢运动障碍和无力,以及另1例原有癫痫疾病患者的全身性癫痫发作和假性癫痫发作。
本病例系列证明了多学科方法治疗GTN脑转移的实用性。通过早期开颅手术或立体定向放射外科治疗联合依托泊苷-顺铂和中/高剂量甲氨蝶呤联合化疗,我们能够在治疗早期稳定患者病情,避免全脑放疗或鞘内化疗。