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改良三联化疗在高危转移性妊娠滋养细胞肿瘤治疗中的应用

Modified triple chemotherapy in the management of high-risk metastatic gestational trophoblastic tumors.

作者信息

Berkowitz R S, Goldstein D P, Bernstein M R

出版信息

Gynecol Oncol. 1984 Oct;19(2):173-81. doi: 10.1016/0090-8258(84)90177-x.

DOI:10.1016/0090-8258(84)90177-x
PMID:6208089
Abstract

Modified triple chemotherapy (MAC III: methotrexate with citrovorum factor, actinomycin D, and cyclophosphamide) was administered as primary treatment to 14 patients with high-risk metastatic gestational trophoblastic tumors (GTT). Ten (71.4%) patients attained complete remission with 1 to 4 courses of MAC III (mean = 2.7 courses). Three of the remaining patients subsequently achieved remission with the modified Bagshawe regimen or vinblastine, bleomycin, and cis-platinum. Following 38 courses of MAC III, moderate hepatotoxicity (SGOT greater than or equal to 150 U) developed after 1 (2.6%) course. Marked thrombocytopenia (platelets less than 50,000/mm3) and marked granulocytopenia (granulocytes less than 500/mm3) developed after 7 (18.4%) and 19 (50%) of the courses, respectively. Platelet transfusions were administered after 4 (10.5%) courses of MAC III and no patient required granulocyte transfusions. MAC III is an effective alternative treatment for patients with high-risk metastatic GTT.

摘要

改良三联化疗(MAC III:甲氨蝶呤联合亚叶酸钙、放线菌素D和环磷酰胺)作为初始治疗方案应用于14例高危转移性妊娠滋养细胞肿瘤(GTT)患者。10例(71.4%)患者接受1至4个疗程的MAC III治疗后达到完全缓解(平均2.7个疗程)。其余3例患者随后采用改良的巴格肖方案或长春碱、博来霉素和顺铂治疗后获得缓解。在38个疗程的MAC III治疗后,1个疗程(2.6%)后出现中度肝毒性(血清谷草转氨酶≥150 U)。分别在7个疗程(18.4%)和19个疗程(50%)后出现明显血小板减少(血小板<50,000/mm³)和明显粒细胞减少(粒细胞<500/mm³)。4个疗程(10.5%)的MAC III治疗后进行了血小板输注,无患者需要粒细胞输注。MAC III是高危转移性GTT患者的一种有效替代治疗方法。

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1
Modified triple chemotherapy in the management of high-risk metastatic gestational trophoblastic tumors.改良三联化疗在高危转移性妊娠滋养细胞肿瘤治疗中的应用
Gynecol Oncol. 1984 Oct;19(2):173-81. doi: 10.1016/0090-8258(84)90177-x.
2
Etoposide and cisplatin/etoposide, methotrexate, and actinomycin D (EMA) chemotherapy for patients with high-risk gestational trophoblastic tumors refractory to EMA/cyclophosphamide and vincristine chemotherapy and patients presenting with metastatic placental site trophoblastic tumors.对于对EMA/环磷酰胺和长春新碱化疗难治的高危妊娠滋养细胞肿瘤患者以及出现转移性胎盘部位滋养细胞肿瘤的患者,采用依托泊苷和顺铂/依托泊苷、甲氨蝶呤及放线菌素D(EMA)化疗。
J Clin Oncol. 2000 Feb;18(4):854-9. doi: 10.1200/JCO.2000.18.4.854.
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Methotrexate with citrovorum factor rescue as primary therapy for gestational trophoblastic disease.以甲氨蝶呤加亚叶酸解救作为妊娠滋养细胞疾病的主要治疗方法。
Cancer. 1982 Nov 15;50(10):2024-7. doi: 10.1002/1097-0142(19821115)50:10<2024::aid-cncr2820501008>3.0.co;2-4.
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Management of low-risk metastatic gestational trophoblastic tumors.
J Reprod Med. 1991 Jan;36(1):36-9.
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Actinomycin D as the primary agent for gestational trophoblastic disease.放线菌素D作为妊娠滋养细胞疾病的主要治疗药物。
Cancer. 1975 Sep;36(3):863-6. doi: 10.1002/1097-0142(197509)36:3<863::aid-cncr2820360306>3.0.co;2-g.
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Methotrexate with citrovorum factor rescue for gestational trophoblastic neoplasms.甲氨蝶呤联合亚叶酸解救治疗妊娠滋养细胞肿瘤。
Obstet Gynecol. 1978 Jan;51(1):93-6.
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Treatment of low-risk metastatic gestational trophoblastic tumors with single-agent chemotherapy.采用单药化疗治疗低危转移性妊娠滋养细胞肿瘤。
Am J Obstet Gynecol. 1996 Jun;174(6):1917-23; discussion 1923-4. doi: 10.1016/s0002-9378(96)70229-6.
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Cisplatin, vinblastine, and bleomycin combination therapy in resistant gestational trophoblastic disease.顺铂、长春碱和博来霉素联合治疗耐药性妊娠滋养细胞疾病。
Cancer. 1986 Oct 1;58(7):1407-10. doi: 10.1002/1097-0142(19861001)58:7<1407::aid-cncr2820580704>3.0.co;2-2.
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Vinblastine, cisplatin and bleomycin as salvage therapy for refractory high-risk metastatic gestational trophoblastic disease.长春碱、顺铂和博来霉素作为难治性高危转移性妊娠滋养细胞疾病的挽救治疗。
J Reprod Med. 1989 Mar;34(3):189-92.
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[Therapeutic evaluation of cisplatin, etoposide, and bleomycin chemotherapy regimen in high-risk gestational trophoblastic neoplasia].顺铂、依托泊苷和博来霉素化疗方案治疗高危妊娠滋养细胞肿瘤的疗效评估
Zhonghua Fu Chan Ke Za Zhi. 2012 Aug;47(8):571-6.

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