Concurrent cisplatin-based chemotherapy and radiotherapy (CCRT) plus brachytherapy is standard treatment for locally advanced cervical cancer. Platinumbased neoadjuvant chemotherapy (NACT) followed by radical hysterectomy has been proposed as an alternative approach, especially for patients with stage Ib2-IIb disease. This review analyzes the most commonly used combination regimens in this clinical setting and the randomized trials comparing chemo-surgery versus definitive radiotherapy or CCRT. The combination of paclitaxel plus ifosfamide plus cisplatin (TIP regimen) obtained the highest rates of optimal pathological response, associated with elevated hematological toxicity. In a recent phase II study, a dose-dense regimen consisting of weekly paclitaxel plus carboplatin for 9 cycles has achieved optimal pathological response rates similar to those of TIP with better toxicity profile. Further studies are strongly warranted to better define the optimal regimen for the patients selected to receive NACT followed by radical surgery. GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries have shown 569,874 new cases of cervical cancer and 311,365 deaths due to this malignancy in 2018 (1). Concurrent cisplatin (CDDP)-based chemotherapy and radiotherapy (CCRT) plus brachytherapy represents the standard of care in patients with locally advanced disease, i.e. in stage FIGO 2009 Ib2-IIa2-IIb-III-IVa (2-6). A meta-analysis of 13 randomized trials showed that CCRT significantly improved 5year overall disease-free survival (DFS) [hazard ratio (HR)=0.78, 95% confidence interval (CI)=0.70-0.87], 5-year loco-regional disease-free survival (HR=0.76, 95%CI=0.68-0.86), 5-year metastases-free survival (HR=0.81, 95%CI=0.72-0.91) and 5year overall survival (OS) (HR=0.81, 95%CI=0.71-0.91) compared to radiotherapy alone (7). A larger survival advantage emerged for the two further trials in which adjuvant chemotherapy was administered after CCRT. An additional trial appeared to confirm the clinical benefit of this adjuvant treatment (8). In in vitro studies gemcitabine (GEM) was found to synergize with CDDP and have a radiosensitizing effect in six cervical cancer cell lines (9). A Mexican phase III trial randomized 515 patients with stage IIb-IVa cervical cancer to receive either CCRT (with CDDP 40 mg/m 2 + GEM 125 mg/m 2 weekly) plus brachytherapy followed by two cycles of adjuvant chemotherapy with CDDP (50 mg/m 2 day 1) + GEM 1000 mg/m 2 (days 1 and 8) every 3 weeks or the standard CCRT (with CDDP 40 mg/m 2 weekly) plus brachytherapy (8). The former arm experienced a trend significantly lower distant recurrence rate (8.1% versus 16.4%, p=0.005) a trend to a lower local recurrence rate (11.2% versus 16.4%, p=0.097), a significantly better progression-free survival (PFS) (HR=0.68, 95%CI=0.49-0.95) and a significantly better OS (HR=0.68, 95%CI=0.49-0.95), associated with increased, but manageable toxicity. Further investigations are needed to clarify the role of adjuvant chemotherapy after CCRT, especia...