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Chemoradiation for Cervical Cancer

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Pelvic Cancer Surgery

Abstract

Cisplatin-based concurrent chemoradiation therapy has become the standard primary therapy in patients with locally advanced (stage IIB–IVA) or bulky early stage (IB2) cervical cancers and as an adjuvant therapy in patients with non-bulky early stage (IA2-IB1 and IIA) cervical cancer with at least one high risk factor after radical hysterectomy and pelvic lymphadenectomy. Five randomized clinical trials have shown that cisplatin-based concurrent chemoradiation is associated with 30–50 % improvement in both relative progression free survival and overall survival. This is contrast to neo-adjuvant chemotherapy administered preceding radiation therapy which in randomized trials has no survival advantage compared to radiation therapy alone in locally advanced cervical cancer. Weekly cisplatin in a dose of 40 mg/m2 for 6 weeks given during external pelvic radiation and brachytherapy represents the most widely acceptable regimen. Two current randomized clinical trials are studying the role of adjuvant chemotherapy with carboplatin and paclitaxel following standard chemoradiation in patients with locally advanced disease or early stage disease with high risk factors after radical surgery. Further, the role of biologic agents as radiation therapy sensitizers is currently being investigated either alone or in combination with cisplatin.

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Correspondence to Peter G. Rose MD .

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Mahdi, H., Rose, P.G. (2015). Chemoradiation for Cervical Cancer. In: Patel, H., Mould, T., Joseph, J., Delaney, C. (eds) Pelvic Cancer Surgery. Springer, London. https://doi.org/10.1007/978-1-4471-4258-4_36

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  • DOI: https://doi.org/10.1007/978-1-4471-4258-4_36

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