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发表于 2007-11-6 14:50:55
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来自: 美国
心灵的歌: 1) 文献仅讨论脑癌,对原发病灶IRESSA不能停, 2) 耐药的原因是癌细胞再次变异,绕过了靶点,但仍有一部分没有变异的被挡住了,如果停了IRESSA,这部分被挡住的 癌细胞就会迅速扩散。所以耐药后,停与不停IRESSA,病情都在恶化,但恶化的“速度”是不一样的。 3) 关于反映停剂量。。没有肺癌脑转的文献,但下面文献给出的用“蒂清”和“反映停。治疗黑色素癌脑转移的剂量和效果
Cancer. 2005 Jun 15;103:2590-7 15861414 [Cited: 1]
Temozolomide plus thalidomide in patients with brain metastases from melanoma: a phase II study. 蒂清加反映停治疗,来自黑色素瘤的脑转移瘤的二期研究 Wen-Jen Hwu , Eric Lis , Jennifer H Menell , Katherine S Panageas , Lynne A Lamb , Janene Merrell , Linda J Williams , Susan E Krown , Paul B Chapman , Philip O Livingston , Jedd D Wolchok , Alan N Houghton BACKGROUND: Temozolomide plus thalidomide is a promising oral combination regimen for the treatment of metastatic melanoma. The current Phase II study examined the efficacy and safety of this combination in chemotherapy-naive patients with brain metastases. METHODS: Patients with histologically confirmed metastatic melanoma and measurable brain metastases received temozolomide (75 mg/m2 per day for 6 weeks with a 2-week break between cycles) plus concomitant thalidomide (200 mg/day escalating to 400 mg/day for patients < 70 years or 100 mg/day escalating to 250 mg/day for patients > or = 70 years). The primary end point was tumor response in the brain assessed every 8 weeks.患者经病理证实的转移性黑素瘤和可衡量的脑转移瘤,收到了蒂清( 75MG,每天2次,6周,然后休息2周) ,另加伴(反映停 200毫克/天逐步升级至400毫克/天,--对患者< 70岁,或100毫克/天逐步升级至250毫克/天,--对患者>= 70岁) 。主要终点是肿瘤在大脑中反应,每8周评估一次)(RESULTS: Twenty-six patients with a median age of 60 years were treated. All patients had progressive brain metastases: 16 were symptomatic and 25 had extensive extracranial metastases. Eight patients had received whole-brain radiotherapy, 4 had received stereotactic radiotherapy, and 8 had received craniotomy with resection of hemorrhagic lesions. Fifteen patients completed > or = 1 cycle (median, 1 cycle; range, 0-4 cycles), and 11 discontinued treatment before completing 1 cycle (7 for intracranial hemorrhage, 2 for pulmonary embolism, 1 for deep vein thrombosis, and 1 for Grade 3 rash). Of 15 patients assessable for response, 3 had a complete or partial response (12% intent to treat) and 7 had minor response or stable disease in the brain. However, 5 of these 10 patients had disease progression at extracranial sites. The median survival period was 5 months for all 26 patients and 6 months for the 15 assessable patients. CONCLUSIONS: Temozolomide plus thalidomide was an active oral regimen for patients with brain metastases from malignant melanoma. Mesh-terms: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols, therapeutic use; Brain Neoplasms, drug therapy; Brain Neoplasms, secondary; Dacarbazine, administration & dosage; Dacarbazine, analogs & derivatives; Disease-Free Survival; Female; Humans; Male; Melanoma, drug therapy; Melanoma, secondary; Middle Aged; Neoplasm Staging; Research Support, Non-U.S. Gov't; Skin Neoplasms, drug therapy; Skin Neoplasms, pathology; Survival Rate; Thalidomide, administration & dosage; Treatment Outcome;
[此贴子已经被作者于2007-11-6 15:03:01编辑过] |
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