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find Keyword "同步放化疗" 4 results
  • 手术加综合治疗与同步放化疗治疗ⅡB期宫颈癌的比较

    摘要:目的:对比手术为主的综合治疗及同步放化疗治疗ⅡB期宫颈癌的疗效和并发症。方法:选择2001年1月至2008年4月收治的ⅡB期宫颈鳞癌患者147例,分为以手术为主的综合治疗组(72例,术前予紫杉醇为主的化疗,根治性手术后或需补充放疗)和同步放化疗组(75例,予顺铂为主的化疗,同步给予放疗),对两组患者的疗效及并发症发生情况进行对比分析。结果:手术组化疗有效率为73.6%,同步放化疗组有效率为70.6%,其5年生存率分别为81.9%和78.6%,手术组的并发症主要为血液毒性术后尿潴留和淋巴囊肿的发生,经对症处理短时间内痊愈。同步放化疗组的并发症主要为骨髓抑制和放射性直肠炎、膀胱炎、阴道挛缩,前者可痊愈,后者严重者甚至穿孔。结论:手术为主的综合治疗ⅡB期宫颈癌可明显提高患者有效率、5年生存率及生活质量。

    Release date:2016-08-26 03:57 Export PDF Favorites Scan
  • 高强度超声聚焦刀序贯同步放化疗治疗结肠癌肝转移的临床疗效观察

    目的观察高强度超声聚焦刀序贯同步放化疗治疗结肠癌肝转移的临床疗效 方法选取笔者所在医院2011年9月至2014年12月期间收治的结肠癌肝转移患者120例,根据治疗方法的不同分为观察组与对照组,各60例,对照组给予同步放化疗治疗,观察组在对照组治疗的基础上给予高强度超声聚焦刀序贯治疗,2组均治疗观察3个月。 结果治疗后观察组与对照组的近期有效率分别为70.0%和40.0%,观察组的有效率明显高于对照组(P<0.05)。观察组治疗期间的肝肾毒性、消化道出血、骨髓抑制、感染等毒性反应情况与对照组比较差异无统计学意义(P>0.05)。所有患者随访(30.25±8.24)个月(12~48个月),观察组1年生存率与中位生存时间分别为50.0%和(12.42±2.45)个月,高于或长于对照组的33.3%和(8.98±2.87)个月,其差异有统计学意义(P<0.05)。 结论高强度超声聚焦刀序贯同步放化疗治疗结肠癌肝转移能提高近期疗效,延长生存时间,有很好的应用安全性,值得推广应用。

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  • Curative effect of XELOX/FOLFOX4 regimens as neoadjuvant concurrent chemoradiotherapy for stage Ⅱ/Ⅲ middle and low rectal cancer

    Objective To investigate efficacy and toxicity of XELOX or FOLFOX4 regimen as neoadjuvant concurrent chemoradiotherapy for stage Ⅱ/Ⅲ middle and low rectal cancer. Methods From June 2011 to March 2014, 120 patients with stage Ⅱ/Ⅲ middle and low rectal cancer who underwent the surgical treatment were enrolled in The Fifth People’s Hospital of Qinghai Province, then were randomly divided into radiotherapy+FOLFOX4 regimen group and radiotherapy+XELOX regimen group. The radiotherapy and chemotherapy were performed simultaneously before the radical resection of rectal cancer. Three-dimensional conformal radiotherapy: 1.8–2.0 Gy/times, 5 times/week, a total of 25 times, the total dose was 45.0–50.0 Gy. At the same time, 2 cycles of chemotherapy were performed according to the FOLFOX4 program (oxaliplatin+leucovorin+5-fluorouracil) or XELOX regimen (capecitabine tablet+oxaliplatin). The radical surgery was performed on 4 to 8 weeks after the preoperative chemoradiotherapy, then 8 to 12 cycles of FOLFOX4 chemotherapy and 4 to 6 cycles of XELOX chemotherapy were completed in the radiotherapy+FOLFOX4 regimen group and the radiotherapy+XELOX regimen group respectively on 1 month after the radical surgery. The curative effect and the occurrence of acute toxicity were observed. Results ① There were no significant differences in thegeneral data such as the gender, age, cT stage, cN stage, TNM stage, histological type, differentiation degree, etc. between the two groups(P>0.05). ② The reduced staging rates of cT and cN in the radiotherapy+XELOX regimen group was 63.3% (38/60) and 86.7% (52/60), respectively, which was significantly higher than that in the radiotherapy+FOLFOX4 regimen group〔38.3% (23/60) and 53.3% (32/60), respectively〕 , the differences were statistically significant (P<0.05). ③ The complete response rate and the effective rate (complete response rate+partial response rate) in the radiotherapy+XELOX regimen group were significantly higher than those in the radiotherapy+FOLFOX4 regimen group (P<0.05). ④ The overall 3-year survival rate in the radiotherapy+XELOX regimen group was significantly higher than that in the radiotherapy+FOLFOX4 regimen group (P<0.05). There were no significant differences in the 3-year disease-free survival rate, distant metastasis rate, and local recurrence rate between the two groups (P>0.05). ⑤ All the patients suffered from 3 to 4 degrees toxicities, however, the incidence rates of the overall toxicity and the diarrhea toxicity in the radiotherapy+XELOX regimen group were significantly lower than those in the radiotherapy+FOLFOX4 regimen group (P<0.05). Conclusion Preliminary results of limited cases in this study show that XELOX regimen is more effective and less acute toxicity than FOLFOX4 regimen for preoperative concurrent chemoradiotherapy for patients with stage Ⅱ/Ⅲ middle and low rectal cancer.

    Release date:2017-11-22 03:58 Export PDF Favorites Scan
  • Feasibility of neoadjuvant therapy followed by minimally invasive esophagectomy for locally advanced esophageal cancer: A case control study

    Objective To evaluate the safety and efficacy of neoadjuvant therapy followed by minimally invasive esophagectomy (MIE) for locally advanced esophageal cancer. Methods We retrospectively analyzed clinical data of 56 consecutive patients with locally advanced esophageal cancer treated by neoadjuvant therapy followed by surgery in our hospital between January 2015 and December 2016. There were 51 males and 5 females. The patients were divided into 2 groups. Neoadjuvant therapy followed by open surgery esophagectomy group was as an OE group with 25 patients aged 61 (50-73) years. And neoadjuvant therapy followed by MIE was as a MIE group with 31 patients aged 60 (55-79) years. Results The pathologic complete response (pCR) rate of 28 patients with neoadjuvant concurrent chemoradiotherapy was significantly higher than that of 28 patients with neoadjuvant chemotherapy (21.4% vs. 10.7%, P<0.05). The operation time, intraoperative blood loss, R2 rate and the number of lymph nodes dissection in the MIE group were obviously better than those of the OE group with statistical differences (P<0.05). However, there was no significant difference in the number of resected lymph nodes along the bilateral recurrent laryngeal nerves and lymph node metastasis rate (P>0.05) between the two groups. The incidence of postoperative respiratory complications in the MIE group was lower than that of the OE group (P=0.041). There was no significant difference between the two groups in the incidence of other complications, re-operation, re-entry to ICU, median length of stay or perioperative deaths (P>0.05). There was only one patient with neoadjuvant concurrent chemoradiotherapy in the OE group died due to gastric fluid asphyxia caused by trachea-esophageal fistula. Conclusion Neoadjuvant therapy followed by MIE for locally advanced esophageal cancer is safe and feasible. The oncological outcomes seem comparable regardless of OE.

    Release date:2018-03-05 03:32 Export PDF Favorites Scan
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