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Palliative chemotherapy in recurrent carcinoma cervix: experience from a regional cancer centre in southern India

机译:复发性子宫颈姑息化疗:印度南部地区癌症中心的经验

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Aims: To evaluate the clinical outcome and complications with two different palliative chemotherapy regimens in recurrent cervical carcinoma. Methods and materials: Forty (40) women with recurrent cervical squamous cell carcinoma were treated with palliative chemotherapy using paclitaxel plus cisplatin or single-agent docetaxel. Clinical outcome and toxicities were analysed. The parameters in two arms were compared using Student’s t-test and statistical analysis was done using R software. Results: At a median follow up of 1.35 years the clinical outcome was complete response/partial response in 50% and 60% and progressive disease in 20% and 10% of the patients with either paclitaxel/cisplatin or docetaxel, respectively, which was not statistically significant. Stable disease (SD) was 30% in both arms. Toxicity included nausea, seen in all the patients in both arms, and diarrhoea, seen in 90% and 70% of the patients in the two arms, respectively. Grade II to III neutropenia was seen in 10% of patients with paclitaxel/cisplatin and none with docetaxel. Hypersensitivity was encountered in 40% and 30% in the two arms, respectively. Conclusion: There was no significant difference in clinical outcome and morbidity in patients with either paclitaxel/cisplatin or single-agent docetaxel. Further prospective clinical trials with larger study groups and longer follow-up are required to substantiate these claims. (Full text available online at www.medpharm.tandfonline.com/ojgo) South Afr J Gynaecol Oncol 2016; DOI: 10.1080/20742835.2016.1175152.
机译:目的:评估两种不同的姑息化疗方案治疗复发性宫颈癌的临床结果和并发症。方法和材料:四十(40)例复发性宫颈鳞癌妇女接受紫杉醇联合顺铂或单药多西紫杉醇的姑息化疗。临床结果和毒性进行了分析。使用Student的t检验比较了两个臂中的参数,并使用R软件进行了统计分析。结果:在1.35年的中位随访中,紫杉醇/顺铂或多西他赛的患者分别有50%和60%的完全缓解/部分缓解和20%和10%的进展性疾病,但没有具有统计意义。两只手臂的稳定疾病(SD)为30%。毒性包括在所有患者中均见到的恶心和腹泻,分别在两个患者中分别见于90%和70%的腹泻。紫杉醇/顺铂患者中有10%的患者出现II至III级中性粒细胞减少,而多西他赛则无。两组中分别有40%和30%出现超敏反应。结论:紫杉醇/顺铂或单药多西他赛患者的临床结局和发病率均无显着差异。需要进一步的前瞻性临床试验与更大的研究组和更长的随访来证实这些说法。 (全文可在线访问www.medpharm.tandfonline.com/ojgo)South Afr J Gynaecol Oncol 2016; DOI:10.1080 / 20742835.2016.1175152。

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