Chronic Thalidomide and Chemoembolization for Hepatocellular Carcinoma. (31st October 2014)
- Record Type:
- Journal Article
- Title:
- Chronic Thalidomide and Chemoembolization for Hepatocellular Carcinoma. (31st October 2014)
- Main Title:
- Chronic Thalidomide and Chemoembolization for Hepatocellular Carcinoma
- Authors:
- Wu, Jennifer
Ng, Jennifer
Christos, Paul J.
Goldenberg, Alec S.
Sparano, Joseph
Sung, Max W.
Hochster, Howard S.
Muggia, Franco M. - Abstract:
- Abstract : Background: Transcatheter arterial chemoembolization (TACE) has been used to curtail tumor vasculature and delay tumor progression in hepatocellular carcinoma (HCC). We conducted a phase I trial to evaluate the efficacy and toxicity of thalidomide when combined with TACE in patients with advanced HCC. Methods: Between June 2000 and November 2003, 56 patients with unresectable HCC and amenable to TACE were enrolled. The starting dose of thalidomide was 200 mg/day and was escalated every 2 weeks as tolerated to a maximum dose of 1, 000 mg/day. Dose reductions and discontinuation were determined by toxicity. TACE was performed 4 weeks after initiation of thalidomide therapy and repeated as necessary. Results: Overall, 47 and 55 patients were evaluable for response and toxicity, respectively; the median dose of thalidomide given was 200 mg/day. Three patients (6.38%) patients achieved complete responses, whereas 10 (21.3%) had partial responses, for an overall response rate of 27.7%, and 27 (57.5%) had stable disease. Median progression‐free survival was 7 months (95% confidence interval [CI]: 5–10 months), and median OS was 21 months (95% CI: 16–28 months) (Fig. 1 ). Fatigue and lethargy (49.1%), constipation (47.3%), and nausea (43.6%) were common. Grade 3–4 toxicities consisted mostly of increased aspartate aminotransferase (43.6%) and elevated alanine aminotransferase (38.2%) (Table 1 ). Conclusion: Thalidomide and TACE were commonly associated with nonhematologicAbstract : Background: Transcatheter arterial chemoembolization (TACE) has been used to curtail tumor vasculature and delay tumor progression in hepatocellular carcinoma (HCC). We conducted a phase I trial to evaluate the efficacy and toxicity of thalidomide when combined with TACE in patients with advanced HCC. Methods: Between June 2000 and November 2003, 56 patients with unresectable HCC and amenable to TACE were enrolled. The starting dose of thalidomide was 200 mg/day and was escalated every 2 weeks as tolerated to a maximum dose of 1, 000 mg/day. Dose reductions and discontinuation were determined by toxicity. TACE was performed 4 weeks after initiation of thalidomide therapy and repeated as necessary. Results: Overall, 47 and 55 patients were evaluable for response and toxicity, respectively; the median dose of thalidomide given was 200 mg/day. Three patients (6.38%) patients achieved complete responses, whereas 10 (21.3%) had partial responses, for an overall response rate of 27.7%, and 27 (57.5%) had stable disease. Median progression‐free survival was 7 months (95% confidence interval [CI]: 5–10 months), and median OS was 21 months (95% CI: 16–28 months) (Fig. 1 ). Fatigue and lethargy (49.1%), constipation (47.3%), and nausea (43.6%) were common. Grade 3–4 toxicities consisted mostly of increased aspartate aminotransferase (43.6%) and elevated alanine aminotransferase (38.2%) (Table 1 ). Conclusion: Thalidomide and TACE were commonly associated with nonhematologic side effects, with fatigue and constipation being prominent. With a lack of clear therapeutic benefit, this combination is unlikely to be pursued for HCC. Abstract : 摘要 背景 . 经导管肝动脉化疗栓塞术(TACE)在肝细胞癌(HCC)的治疗中用于减少肿瘤血供和延缓肿瘤进展。我们开展了一项 I 期试验,旨在评价沙利度胺联合 TACE 在进展期 HCC 患者中的有效性和毒性。 方法 . 2000 年 6 月∼ 2003 年 11 月,共入组 56 例不可手术切除且适于行 TACE 的 HCC 患者。沙利度胺的起始剂量为 200 mg/天,视耐受情况每 2 周上调一次剂量,直至最大剂量 1000 mg/天。根据毒性决定下调给药剂量和停药。TACE 于开始沙利度胺治疗 4 周后实施,并且按需重复实施。 结果 . 总体而言,47 例患者可评估治疗反应,55 例可评估毒性;中位沙利度胺剂量为 200 mg/天。3 例患者(6.38%)达到完全缓解,10 例(21.3%)达到部分缓解,总缓解率为 27.7%。27 例患者(57.5%)疾病稳定。中位无进展生存为 7 个月[95% 可信区间(CI):5 ∼ 10 个月],中位总生存(OS)为 21 个月(95%CI:16 ∼ 28 个月)(图 1)。疲乏及嗜睡(49.1%)、便秘(47.3%)和恶心(43.6%)较为常见。3/4 级毒性事件主要包括天门冬氨酸氨基转移酶水平升高(43.6%)和丙氨酸氨基转移酶水平升高(38.2%)(表 1)。 结论 . 沙利度胺和 TACE 多与非血液学不良事件相关,主要是疲乏和便秘。由于缺乏明显的治疗获益,这一联合方案不太推荐用于 HCC 治疗。 The Oncologist 2014;19:1229–1230 … (more)
- Is Part Of:
- Oncologist. Volume 19:Number 12(2014)
- Journal:
- Oncologist
- Issue:
- Volume 19:Number 12(2014)
- Issue Display:
- Volume 19, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 19
- Issue:
- 12
- Issue Sort Value:
- 2014-0019-0012-0000
- Page Start:
- 1229
- Page End:
- 1230
- Publication Date:
- 2014-10-31
- Subjects:
- Oncology -- Periodicals
Tumors -- Periodicals
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Oncology
Tumors
Neoplasms
Electronic journals
Periodicals
Periodicals
616.994 - Journal URLs:
- https://academic.oup.com/oncolo ↗
https://theoncologist.onlinelibrary.wiley.com/journal/1549490x ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1634/theoncologist.2014-0283 ↗
- Languages:
- English
- ISSNs:
- 1083-7159
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- Legaldeposit
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