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. 2021 Feb 25:11:626145.
doi: 10.3389/fonc.2021.626145. eCollection 2021.

The Most Efficacious Induction Chemotherapy Regimen for Locoregionally Advanced Nasopharyngeal Carcinoma: A Network Meta-Analysis

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The Most Efficacious Induction Chemotherapy Regimen for Locoregionally Advanced Nasopharyngeal Carcinoma: A Network Meta-Analysis

Horace Cheuk-Wai Choi et al. Front Oncol. .

Abstract

Background: Induction chemotherapy (IC) followed by concurrent chemoradiotherapy (CCRT) for non-metastatic locoregionally advanced nasopharyngeal carcinoma (NPC) has gained considerable attention. However, the most efficacious IC regimens remain investigational. We aimed to compare the survival benefits of all available IC regimens followed by CCRT in this network meta-analysis.

Methods: All randomized-controlled trials of CCRT with or without IC in non-metastatic locoregionally advanced NPC were included, with an overall nine trials of 2,705 patients counted in the analysis. CCRT alone was the reference category. Eight IC regimens followed by CCRT were analyzed: docetaxel + cisplatin (DC), gemcitabine + carboplatin + paclitaxel (GCP), gemcitabine + cisplatin (GP), mitomycin + epirubicin + cisplatin + fluorouracil + leucovorin (MEPFL), cisplatin + epirubicin + paclitaxel (PET), cisplatin + fluorouracil (PF), cisplatin + capecitabine (PX) and cisplatin + fluorouracil (PF), cisplatin + capecitabine (PX). Fixed-effects frequentist network meta-analysis models was applied and P-score was used to rank the treatments.

Results: DC, GP, and PX were the top three IC regimens with the highest probability of benefit on overall survival (OS). Their corresponding hazard ratios (HRs) (95% CIs) compared with CCRT alone were of 0.24 (0.08-0.73), 0.43 (0.24-0.77), and 0.54 (0.27-1.09) and the respective P-scores were 94%, 82%, and 68%. The first three IC regimens showing significantly improved progression-free survival (PFS) were PX, followed by GP and DC with respective HRs of 0.46 (0.24-0.88), 0.51 (0.34-0.77), and 0.49 (0.20-1.20), and P-scores of 82%, 78%, and 74%. Among the studies in the intensity-modulated radiation therapy (IMRT) era, GP and PX were the best performed IC regimens, whilst DC performed the best among non-IMRT studies. Doublet and gemcitabine-based IC regimens had better survival benefits compared to triplet and taxane-based IC regimens, respectively.

Conclusions: Given its consistent superiority in both OS and PFS, DC, GP, and PX ranked among the three most efficacious IC regimens in both the overall and subgroup analysis of IMRT or non-IMRT studies. Exploratory analyses suggested that doublet and gemcitabine-based IC regimens showed better survival performance.

Keywords: efficacy; induction chemotherapy; nasopharyngeal carcinoma; network meta-analysis; survival outcome.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Schematic of the network of evidence used in network meta-analysis for induction chemotherapy. The size of the nodes is proportional to the number of patients in each induction chemotherapy regimen category. The width of the lines is proportional to the number of comparisons. Two trials were included in the comparison of CCRT vs TPF. CCRT, concurrent chemoradiation; DC, docetaxel + cisplatin; PET, cisplatin + epirubicin + paclitaxel; GCP, gemcitabine + carboplatin + paclitaxel; TPF, docetaxel + cisplatin + fluorouracil; MEPFL, mitomycin + epirubicin + cisplatin + fluorouracil + leucovorin; PF, cisplatin + fluorouracil; PX, cisplatin + capecitabine; GP, gemcitabine + cisplatin.
Figure 2
Figure 2
Forest plot for overall survival (left) and progression-free survival (right) showing results comparing IC regimens against CCRT from network meta-analysis. HR<1 is in favor of CCRT alone. 95% CI, 95% confidence interval; HR, hazard ratio; PFS, progression-free survival; OS, overall survival; regimens analyzed: CCRT, concurrent chemoradiation; DC, docetaxel + cisplatin; PET, cisplatin + epirubicin + paclitaxel; GCP, gemcitabine + carboplatin + paclitaxel; IC, induction-concurrent; TPF, docetaxel + cisplatin + fluorouracil; MEPFL, mitomycin + epirubicin + cisplatin + fluorouracil + leucovorin; PF, cisplatin + fluorouracil; PX, cisplatin + capecitabine; GP, gemcitabine + cisplatin.

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