首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >Prospective comparative study of dose dense neo-adjuvant chemotherapy followed by chemo-radiation and definitive chemo-radiation alone in stage IB2-IVA cervical cancer
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Prospective comparative study of dose dense neo-adjuvant chemotherapy followed by chemo-radiation and definitive chemo-radiation alone in stage IB2-IVA cervical cancer

机译:IB2-IVA期宫颈癌中剂量密集型新辅助化疗后分别进行化学放疗和确定性化学放疗的前瞻性比较研究

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Background: The standard of care for locally advanced cervical cancer is chemo-radiation. Role of neo-adjuvant chemotherapy not clear yet. Dose dense, short-term neo-adjuvant chemotherapy with early initiation of radiotherapy has shown survival benefit but randomised trials not available yet. Hence this study was done for feasibility of neo-adjuvant chemotherapy and for its comparison with the standard chemo-radiation. Methods: Cervical cancer patients not randomly assigned into two arms. Arm A received 3 cycles NACT of paclitaxel and carboplatin weekly. All patients of arm A after NACT and arm B received EBRT on linear accelerator for a dose of 4500-5000cGy in 23-25 fractions with concurrent cisplatin 40mg/m2 followed by 3 applications of HDR intracavitary brachytherapy of 700 or 800cGy respectively. All patients were assessed clinically and radiologically with MRI after completion of CTRT and at follow up of 6 weeks. Results: A total of 15 patients treated in each arm. Stage IIB and IIIB constituted 93% of the patients, well matched in both the arms. The CR rate at follow up of 6 weeks after NACT was 73% compared to only 46.7% in arm B. Neutropenia of grade 3 were seen equally in both the arms and grade 2 neutropenia was seen in about 60% patients in arm A compared to only 20% patients in arm B which was manageable without growth factors. Conclusions: Dose dense neo-adjuvant chemotherapy is a feasible and effective option in treating cancer cervix.
机译:背景:局部晚期宫颈癌的治疗标准是化学放射。新辅助化疗的作用尚不清楚。早期开始放疗的剂量密集,短期新辅助化疗已显示出生存获益,但尚无随机试验。因此,进行这项研究是为了新辅助化疗的可行性及其与标准化学放疗的比较。方法:宫颈癌患者不随机分为两组。 A组每周接受3个周期的NACT紫杉醇和卡铂。 NACT后的A组和B组的所有患者均接受线性加速器的EBRT,剂量为23-25级,剂量为4500-5000cGy,同时顺铂为40mg / m2,然后分别进行3次HDR腔内近距离放射治疗700或800cGy。在完成CTRT后以及随访6周时,对所有患者进行MRI的临床和放射学评估。结果:每组总共治疗15名患者。 IIB和IIIB期占93%的患者,两组均相配。 NACT后6周随访时的CR率为73%,而B组仅为46.7%。与A组相比,A组的3级中性粒细胞减少平均相同,A组中约60%的患者为2级中性粒细胞减少。 B组中只有20%的患者无需生长因子即可控制。结论:剂量密集的新辅助化疗是治疗宫颈癌的可行和有效的选择。

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