Skip to main content
NCBI home page
Medicine logoLink to Medicine
. 2020 Mar 6;99(10):e19360. doi: 10.1097/MD.0000000000019360

The efficacy and toxicity of induction chemotherapy plus concurrent chemoradiotherapy in locoregionally advanced nasopharyngeal carcinoma

A meta-analysis of randomized controlled trials

Peirong Wang 1, Mingwei Zhang 1, Chunlin Ke 1, Chuanshu Cai 1,∗
Editor: Surinder Kumar1
PMCID: PMC7478529  PMID: 32150078

Supplemental Digital Content is available in the text

Keywords: combined IC and CCRT therapy, concurrent chemoradiotherapy, improved survival, induction chemotherapy, locally advanced nasopharyngeal carcinoma

Abstract

Background:

A systemic review and meta-analysis of randomized controlled trials (RCTs) was performed to compare the efficacy, toxicity and safety of concurrent chemoradiotherapy (CCRT) with or without induction chemotherapy (IC) for locoregionally advanced nasopharyngeal carcinoma (NPC).

Methods:

Research searching was performed in Web of Science, PubMed, The Cochrane Library, Embase, Chinese Biomedical Database, Chinese National Knowledge Infrastructure, Chongqing VIP Database for Chinese Technical Periodicals and Wanfang Database. RCTs including patients diagnosed with locoregionally advanced NPC without metastasis and randomly treated with IC plus CCRT and CCRT alone were included. Survival and outcome data were extracted and meta-analysis was performed using the Revman 5.3.0 software.

Results:

Ten RCTs (2280 patients) were selected and used for pooled meta-analysis. In comparison with CCRT, IC plus CCRT treatment significantly improved the overall survival (OS; HR = 0.70, 95%CI 0.56–0.87, P = .002), progression-free survival (PFS; HR = 0.75, 95%CI 0.65–0.87, P < .0001), distant metastasis failure-free survival (DMFS; HR = 0.71, 95%CI 0.58–0.85, P = .0003) and loco-regional failure-free survival (LFES; HR = 0.72, 95%CI 0.59–0.88, P = .002) of patients with locoregionally advanced NPC. Patients treated with IC and CCRT had higher incidence of grade 3–4 leucopenia and thrombocytopenia than patients treated with CCRT alone (P < .0001). No significant difference in other grade 3–4 adverse events and radiation toxicity was observed between the two groups. IC combined with CCRT improved the survival of patients with locoregionally advanced NPC.

Conclusions:

Combined IC and CCRT therapy was an efficacy treatment regimen for locoregionally advanced NPC.

1. Introduction

Nasopharyngeal carcinoma (NPC) is an epidermoid original cancer which distinctly from head and neck cancers. Epstein-Barr virus (EBV) infection is a major character of NPC.[1] NPC is regionally distributed and the high incidences are reported in Eastern Asia, Northern Africa, Southern China, Micronesia and Polynesia.[2] The incidence of NPC is reported in 60.6 thousand people in China in 2015, with higher proportion (71.45%) in males and a mortality of 56.27%.[3] An urgent problem that desperately needs to be solved is the survival and quality of patients with locoregionally advanced NPC.

Radiotherapy is the first preferred alternative treatment for NPC. Concurrent chemoradiotherapy (CCRT) is an unquestionable treatment for early NPC.[4] The contribution of induction chemotherapy (IC) after CCRT, however, remains controversial for the treatment of locoregionally advanced NPC.[5–8] On the one hand, there were two different trial outcomes on the benefit of IC to CCRT (effective or noneffective). Some studies showed IC plus CCRT improved patients survival rate significantly, while the others showed no improvement on overall survival (OS).[5–8] On the other hand, IC resulted into higher incidence of grade 3–4 adverse events, including neutropenia, leucopenia and stomatitis.[5–9]

This meta-analysis will give us a summary on the efficacy of using IC plus CCRT in locoregionally advanced NPC and provide a reference for clinical management for locoregionally advanced NPC.

2. Materials and methods

This review of RCTs was designed and conducted following the guidelines of PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses).[10] This study does not include human tissue samples, and therefore an ethics committee approval is not applicable.

2.1. Search strategy

Eligible studies published in Web of Science, PubMed, The Cochrane Library, Embase, Chinese Biomedical Database (CBD), Chinese National Knowledge Infrastructure (CNKI), Chongqing VIP Database for Chinese Technical Periodicals (CQVIP) and Wanfang Database with the searching terms: “nasopharyngeal neoplasms” OR “nasopharyngeal tumors” OR “nasopharyngeal cancers” AND “clinical trials” OR “randomized controlled trial”. Publications in both Chinese and English languages from the earliest record of the databases to July 15, 2018 were included. Publications with insufficient data were excluded, while additional eligible studies in references were identified and included as alternatives.

2.2. Inclusion and exclusion criteria

Inclusion criteria were patients

  • (1)

    diagnosed with locoregionally advanced NPC without metastasis;

  • (2)

    treated with IC plus with CCRT or CCRT alone;

  • (3)

    recruited in RCTs.

Publications were excluded if they were:

  • (1)

    duplicated publications;

  • (2)

    low quality reports or with incomplete information;

  • (3)

    RCTs only published as abstracts;

  • (4)

    cohort study;

  • (5)

    comments, reviews, case reports, or letters.

Three experts independently assessed the abstracts of studies that met the inclusion criteria. If there are different opinions, the three experts agree to be approved.

2.3. Data extraction and outcomes

Publication data including the title, first author information and publication data were collected. RCT quality was obtained. The baseline data of patients [including sex, age, (Tumor Node Metastasis (TNM) classification, histology stage, Eastern Cooperative Oncology Group (ECOG) performance status], treatment regimens (IC plus with CCRT or CCRT alone) and follow-up times were extracted. Outcome data, including overall survival (OS), progression-free survival (PFS), distant metastasis failure-free survival (DMFS), loco-regional failure-free survival (LFFS), radiation toxicity and advent events, were extracted from eligible studies. All data extracted from included RCTs were pooled separately for meta-analysis.

2.4. Quality assessment

The quality evaluation of the data extracted from the included studies was independently performed using the Cochrane Collaboration's tool for assessing risk of publication bias[11] and 5-point Jadad score system.[12]

2.5. Statistical analysis

Meta-analysis for the extracted data was performed using Revman 5.3.0 software. The 95% confidence interval (95% CI) and Peto odds ratio were used for meta-analysis. The number of incident events and total people was recorded. The expected number of deaths (O-E) was calculated based on the 5-year age groups and calendar periods as well as mortality rates of locoregionally advanced NPC patients. Publications’ heterogeneity was assessed using I-square (I2) test with χ2 test. I2 ≥50% and P < .1were set as the threshold for heterogeneity, and homogeneity otherwise (I2 < 50% and P ≥ .1). Sensitivity analysis was performed for heterogeneity studies. Meta-analysis was conducted using fixed-effect and random-effect model of extracted data in homogeneity (I2 < 50%) and heterogeneity (I2 ≥50%), respectively.

3. Results

3.1. Included studies

A total of 484 English and Chinese publications were searched from databases and 3 articles were obtained by manual retrieval the reference lists. After removing duplicated publications (n = 132) or publications met the exclusion criteria (meeting abstract, case reports and reviews, not RCTs or patients not assigned into treatment with IC and CCRT vs CCRT, n = 345), only 10 eligible studies[1,6–9,13–17] were included for the meta-analysis (Table 1). The PRISMA flow diagram of publication selection is shown in Figure 1. No publication bias was found in these publications (Fig. 2 and Figure S1).

Table 1.

Characteristics of the 10 eligible studies included in this review.

3.1.

Open in a new tab

Figure 1.

Figure 1

Open in a new tab

The PRISMA flow diagram of the identification and selection of relevant articles for this meta-analysis.

Figure 2.

Figure 2

Open in a new tab

Publication bias of the 10 included articles.

3.2. Baseline characteristics of included studies

A total of 2280 patients were randomly assigned into IC combined with CCRT treatment (n = 1145) and CCRT alone (n = 1135). Patients had locoregionally advanced NPC at TNM classification IIB ∼ IVB or WHO classification I ∼ IVA and were followed up for 23.7 to 72 median months. For CCRT, patients were mainly received cisplatin (30∼100 mg/m2 for one day, followed with different regimens). Nine drugs, including paclitaxel, carboplatin, gemcitabine, cisplatin, epirubicin, docetaxel, fluorouracil, mitomycin and leucovorin, were mentioned as the IC regimens in different articles, with different combinations (Table 1).

3.3. IC + CCRT treatment has higher efficacy than CCRT alone on locoregionally advanced NPC

All the 2280 patients in the selected 10 articles were used for the OS meta-analysis. Of which, 2206 (9 articles except for He[14]) were used for the PFS meta-analysis. And 2199 (9 articles except for Frikha[7]) patients were available for the DMFS and LFFS meta-analysis, respectively. In comparison with CCRT alone, locoregionally advanced NPC patients treated with combined treatment showed significantly higher rates of OS (HR = 0.70, 95% CI 0.56–0.87, P = .002, I2 = 0.0%, Fixed model; Fig. 3A), PFS (HR = 0.75, 95% CI 0.65–0.87, P < .0001, I2 = 0.0%, Fixed model; Fig. 3B), DMFS (HR = 0.71, 95% CI, 0.58 – 0.85, P = .0003; I2 = 0.0%, Fixed model; Fig. 3C) and LFFS (HR = 0.72, 95% CI, 0.59–0.88, P = .002; I2 = 0.0%, Fixed model; Fig. 3D). These results suggested that IC was in favor of the survival rate of CCRT-treated patients with locoregionally advanced NPC.

Figure 3.

Figure 3

Open in a new tab

The forest plots for the effect of different therapies on induction chemotherapy the survival of patients with locoregionally advanced nasopharyngeal carcinoma. A to D, the overall survival (OS), progression-free survival (PFS), distant metastasis failure-free survival (DMFS) and loco-regional failure-free survival (LFFS) of patients with LA-NPC (locoregionally advanced nasopharyngeal carcinoma). Experiment group was treated with induction chemotherapy combined with concurrent chemoradiotherapy (IC + CCRT) and control group was treated with (concurrent chemoradiotherapy), respectively. CI = confidence interval, O-E = observed minus expected events.

3.4. IC + CCRT improves adverse events than CCRT

No treatment-related death was reported in the two groups during the follow up. According to the Common Terminology Criteria for Adverse Events (CTCAE), the frequently recorded adverse events (grade 3–4) following IC prior to CCRT treatment were neutropenia (32%, available in 3 articles), leucopenia (30%, available in 3 articles), thrombocytopenia (12%, available in 3 articles) and nausea or vomiting (9%, available in 4 articles, Table 2). During the phase of CCRT, the incidences of grade 3–4 adverse events, including leucopenia (P < .0001) and thrombocytopenia (P = .0006), in patients treated with IC + CCRT were higher than that treated with CCRT alone (Table 3). No differences were seen in other adverse grade 3–4 adverse events (Table 3) and late radiation morbidity (Table 4) between the two groups.

Table 2.

Adverse events induction chemotherapy treatment.

3.4.

Open in a new tab

Table 3.

The pooled analyses of the grade 3–4adverse events during concurrent chemoradiotherapy between experimental and control groups.

3.4.

Open in a new tab

Table 4.

Late radiation toxicities (grade 3–4) according to RTOG morbidity grading.

3.4.

Open in a new tab

4. Discussion

The addition of IC to CCRT could improve the survival time and rates of patients with advanced cancers.[18] Our meta-analysis study, including 10 eligible studies, showed that IC plus CCRT-treated patients with locoregionally advanced NPC had higher survival rates (OS, PFS, DMFS and LFFS) than patients only treated with CCRT. Although there were higher occurrence of grade 3–4 leucopenia and thrombocytopenia in IC and CCRT group, no difference in treatment-related death was found between the 2 groups. These results systemically suggested the efficacy and survival benefit of IC and CCRT for locoregionally advanced NPC.

Song et al[19] and Chen et al[20] separately performed a meta-analysis in 2015 enrolling 798 (4 RCTs) and 1988 (9 RCTs) patients with locoregionally advanced NPC randomly treated with IC or IC and CCRT, respectively. They both showed that the addition of IC to CCRT had no significant improvement in OS.[19,20] However, Song et al showed the benefit of IC addition for improving the DFS and DMFS of patients with locoregionally advanced NPC.[19] Yan et al performed a review of 25 RCTs and confirmed that IC did not favor CCRT in view of OS, but it favored radiotherapy (RT).[21] In addition, Yan showed that adjuvant chemotherapy (A) plus CCRT, IC plus CCRT, CCRT and IC+RT+A had similar probability (28%, 25%, 24%, and 21%, respectively) of being the best regimen, using a network meta-analysis.[21] Similar results were reported by Ribassin-Majed et al.[22] In comparison with these meta-analyses,[19–21] our study (enrolled 2280 patients in 10 eligible publications in both Chinese and English) confirmed that the addition of IC to CCRT showed significant benefit for the OS, PFS, DMFS, and LFFS of patients with locoregionally advanced NPC compared with CCRT alone (Fig. 3). We found patients showed higher survival rate when treated with IC plus CCRT, compared with CCRT alone. These might due to the inclusion of three latest publications published in 2016,[9] 2017,[8] and 2018.[6]

Of the 3 latest published articles, Hong et al (n = 479) showed the addition of IC showed significant benefit to DFS and LFFS[6]; Sun et al (n = 480) showed the significant benefit of IC addition to OS, DFS and LFFS[9]; and Cao et al (n = 476) showed IC addition significantly improved DFS and a marginal significance in DMFS (P < .056).[8] A recently reported meta-analysis of RCTs and observational studies by Tan et al showed the similar significantly benefit of IC addition to CCRT for improving DFS and OS.[23] These data showed that the IC addition to CCRT is being advanced into clinical treatment of locoregionally advanced NPC. It has been widely reported that IC offers favor to eradicating the micrometastasis and improving patients’ tolerability,[5,22] which might benefit for the better prognosis of patients treated with IC and CCRT.

Most of the included studies[6,8,9,13–17] and others[24] showed that the addition of IC regimens to CCRT induced higher rates of grade 3–4 adverse events, including leucopenia, neutropenia, thrombocytopenia and stomatitis/mucositis. These data suggested that the investigational IC arm showed more grade 3–4 toxicities. However, no difference was seen in the radiation toxicity between the two groups. Frikha et al[7] even showed there was no difference in the grade 3–4 adverse events between the two groups, suggesting the adjustable incidence of adverse events by adding different IC regimens.

5. Limitations

Several limitations exist in our study. First, 7 IC regimens were used in the 10 included studies, including TPF (docetaxel, cisplatin, and fluorouracil),[7,9] PF (cisplatin and fluorouracil),[8,13,14] DC (cisplatin and docetaxel ),[16] CF (carboplatin and fluorouracil),[15] GCP (gemcitabine, carboplatin, and paclitaxel),[17] PET (epirubicin, paclitaxel and cisplatin)[1] and MEPFL (mitomycin C, epirubicin, cisplatin, and 5-fluorouracil (5-FU)/leucovorin).[6] The advantages of TPF to PF regimen had been reported in chemotherapy NPC and in other cancers.[6] TPF regimen showed significant benefit for the OS and DMFS of patients with locally advanced locoregionally advanced NPC[25] or other cancers.[26] In addition, TPF regimen is a standard induction regimen for locally advanced unresectable head and neck cancer[27,28] and larynx preservation.[29] These results suggested that different IC regimens might affect the prognosis of patients with locoregionally advanced NPC. The unification of IC regimens might confirm a more reliable efficacy of IC addition on CCRT survival years. Second, the follow-up period in some studies was less than 5 years,[13,14] which resulted into the limit data for the analysis of the long-time efficacy and safety of IC. Third, the frequencies of late radiation toxicities (grade 3–4) were only reported in few studies, which limited the evaluation for the long-term safety of using IC regimens in NPC.

6. Conclusion

This meta-analysis suggested the IC addition to CCRT improved the OS, DFS, DMFS and LFFS of patients with locoregionally advanced NPC significantly. Leucopenia, neutropenia, and mucositis were the most grade 3–4 adverse events in IC and CCRT arm. No difference was seen in the radiation toxicity between the two groups. The meta-analysis showed that IC addition arm significantly benefitted to the survival of patients with locoregionally advanced NPC in comparison with CCRT alone. This study provided important reference for clarifying the precise value of IC and CCRT in treatment of locoregionally advanced NPC.

Acknowledgments

This research was guided by Cai Chuanshu's technical guidance.

Author contributions

Conceptualization: Peirong Wang, Chuanshu Cai.

Data curation: Peirong Wang, Chuanshu Cai.

Formal analysis: Peirong Wang, Chuanshu Cai.

Funding acquisition: Peirong Wang, Chuanshu Cai.

Investigation: Peirong Wang, Chuanshu Cai.

Methodology: Peirong Wang, Chuanshu Cai.

Project administration: Peirong Wang, Chuanshu Cai.

Resources: Peirong Wang, Mingwei Zhang, Chunlin Ke, Chuanshu Cai.

Software: Peirong Wang, Mingwei Zhang, Chunlin Ke, Chuanshu Cai.

Supervision: Peirong Wang, Chuanshu Cai.

Validation: Peirong Wang, Chuanshu Cai.

Visualization: Peirong Wang, Chuanshu Cai.

Writing – original draft: Peirong Wang.

Writing – review & editing: Peirong Wang, Chuanshu Cai.

Supplementary Material

Supplemental Digital Content
medi-99-e19360-s001.doc (151.5KB, doc)

Footnotes

Abbreviations: CBD = Chinese Biomedical Database, CCRT = concurrent chemoradiotherapy, CNKI = Chinese National Knowledge Infrastructure, CQVIP = Chongqing VIP Database for Chinese Technical Periodicals, CTCAE = common terminology criteria for adverse events, DMFS = distant metastasis failure-free survival, DMFS = distant metastasis failure-free survival, EBV = Epstein–Barr virus, ECOG = Eastern Cooperative Oncology Group, IC = induction chemotherapy, LFES = locoregional failure-free survival, LFES = loco-regional failure-free survival, NPC = nasopharyngeal carcinoma, OS = overall survival, PFS = progression-free survival, PFS = progression-free survival, RCTs = randomized controlled trials, RT = favored radiotherapy, TNM = tumor node metastasis.

How to cite this article: Wang P, Zhang M, Ke C, Cai C. The efficacy and toxicity of induction chemotherapy plus concurrent chemoradiotherapy in locoregionally advanced nasopharyngeal carcinoma: A meta-analysis of randomized controlled trials. Medicine. 2020;99:10(e19360).

The authors certify that there is no conflict of interest with any individual/organization for the present work. This article does not contain any studies with animals performed by any of the authors. Informed consent was obtained from all individual participants included in the study.

The authors have no funding and conflicts of interest to disclose

Supplemental Digital Content is available for this article.

References

  • [1].Fountzilas G, Ciuleanu E, Bobos M, et al. Induction chemotherapy followed by concomitant radiotherapy and weekly cisplatin versus the same concomitant chemoradiotherapy in patients with nasopharyngeal carcinoma: a randomized phase II study conducted by the Hellenic Cooperative Oncology Group (HeCOG) with biomarker evaluation. Ann Oncol 2012;23:427–35. [DOI] [PubMed] [Google Scholar]
  • [2].Torre LA, Bray F, Siegel RL, et al. Global cancer statistics, 2012. CA Cancer J Clin 2015;65:87–108. [DOI] [PubMed] [Google Scholar]
  • [3].Chen W, Zheng R, Baade PD, et al. Cancer statistics in China, 2015. CA Cancer J Clin 2016;66:115–32. [DOI] [PubMed] [Google Scholar]
  • [4].Lee AWM, Ma BBY, Wai Tong N, et al. Management of nasopharyngeal carcinoma: current practice and future perspective. J Clin Oncol 2015;33:3356–64. [DOI] [PubMed] [Google Scholar]
  • [5].Lei C, Chao-Su H, Xiao-Zhong C, et al. Concurrent chemoradiotherapy plus adjuvant chemotherapy versus concurrent chemoradiotherapy alone in patients with locoregionally advanced nasopharyngeal carcinoma: a phase 3 multicentre randomised controlled trial. Lancet Oncol 2012;13:163–71. [DOI] [PubMed] [Google Scholar]
  • [6].Hong RL, Hsiao CF, Ting LL, et al. Final results of a randomized phase III trial of induction chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in patients with stage IVA and IVB nasopharyngeal carcinoma-Taiwan Cooperative Oncology Group (TCOG). Ann Oncol 2018;29:1972–9. [DOI] [PubMed] [Google Scholar]
  • [7].Frikha M, Auperin A, Tao Y, et al. A randomized trial of induction docetaxel-cisplatin-5FU followed by concomitant cisplatin-RT versus concomitant cisplatin-RT in nasopharyngeal carcinoma (GORTEC 2006-02). Ann Oncol 2017;29:731–6. [DOI] [PubMed] [Google Scholar]
  • [8].Cao SM, Yang Q, Guo L, et al. Neoadjuvant chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in locoregionally advanced nasopharyngeal carcinoma: A phase III multicentre randomised controlled trial. Eur J Cancer 2017;75:14–23. [DOI] [PubMed] [Google Scholar]
  • [9].Sun Y, Li WF, Chen NY, et al. Induction chemotherapy plus concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in locoregionally advanced nasopharyngeal carcinoma: a phase 3, multicentre, randomised controlled trial. Lancet Oncol 2016;17:1509–20. [DOI] [PubMed] [Google Scholar]
  • [10].Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Rev Esp Nutr Hum Diet 2009;339:b2535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [11].Julian H, Douglas A, Peter Gt, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. Br Med J 2011;343:889–93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [12].McCormick F, Cvetanovich GL, Kim JM, et al. An assessment of the quality of rotator cuff randomized controlled trials: utilizing the Jadad score and CONSORT criteria. J Shoulder Elbow Surg 2013;22:1180–5. [DOI] [PubMed] [Google Scholar]
  • [13].Gao J, Gao T, Dong Z, et al. A prospective and randomized study of induction chemotherapy combined with concurrent chemoradiotherapy in the treatment for nasopharyngeal carcinoma stage T 3∼4 N 2∼3 M 0. J Chin Oncol 2013;19:161–4. [Google Scholar]
  • [14].He Q, Yang L, Nie Y, et al. A phase II study of neoadjuvant chemotherapy followed by concurrent chemoradiotherapy in locally advanced nasopharyngeal carcinoma. Chin Clin Oncol 2009;14:1011–4. [Google Scholar]
  • [15].Huang S, Deng G, Huang G, et al. Efficacy of induction chemotherapy combined with concurrent chemoradiotherapy for advanced nasopharyngeal carcinoma. Chin J Clin Oncol 2012;39:788–91. [Google Scholar]
  • [16].Hui EP, Ma BB, Leung SF, et al. Randomized phase II trial of concurrent cisplatin-radiotherapy with or without neoadjuvant docetaxel and cisplatin in advanced nasopharyngeal carcinoma. J Clin Oncol 2009;27:242–9. [DOI] [PubMed] [Google Scholar]
  • [17].Tan T, Lim W-T, Fong K-W, et al. Concurrent chemo-radiation with or without induction gemcitabine, Carboplatin, and Paclitaxel: a randomized, phase 2/3 trial in locally advanced nasopharyngeal carcinoma. Int J Radiat Oncol Biol Phys 2015;91:952–60. [DOI] [PubMed] [Google Scholar]
  • [18].Alan KB, Nigel HR, Robert KH, et al. Addition of gemtuzumab ozogamicin to induction chemotherapy improves survival in older patients with acute myeloid leukemia. J Clin Oncol 2012;30:3924–31. [DOI] [PubMed] [Google Scholar]
  • [19].Song Y, Wang W, Tao G, et al. Survival benefit of induction chemotherapy in treatment for locally advanced nasopharyngeal carcinoma-A time-to-event meta-analysis. Oral Oncol 2015;51:764–9. [DOI] [PubMed] [Google Scholar]
  • [20].Chen YP, Rui G, Na L, et al. Efficacy of the additional neoadjuvant chemotherapy to concurrent chemoradiotherapy for patients with locoregionally advanced nasopharyngeal carcinoma: a bayesian network meta-analysis of randomized controlled trials. J Cancer 2015;6:883–92. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [21].Yan M, Kumachev A, Siu LL, et al. Chemoradiotherapy regimens for locoregionally advanced nasopharyngeal carcinoma: a Bayesian network meta-analysis. Eur J Cancer 2015;51:1570–9. [DOI] [PubMed] [Google Scholar]
  • [22].Ribassin-Majed L, Marguet S, Lee AW, et al. What is the best treatment of locally advanced nasopharyngeal carcinoma? An individual patient data network meta-analysis. J Clin Oncol 2017;35:498–505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [23].Teng HT, Yu YS, Cheo T, et al. Induction chemotherapy for locally advanced nasopharyngeal carcinoma treated with concurrent chemoradiation: a systematic review and meta-analysis. Radiother Oncol 2018;129:10–7. [DOI] [PubMed] [Google Scholar]
  • [24].Mei L, Chen C, Huang Y, et al. Neoadjuvant chemotherapy followed by concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in nasopharyngeal carcinoma patients with cervical nodal necrosis. Sci Rep 2017;7:42624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [25].Liu GY, Lv X, Wu YS, et al. Effect of induction chemotherapy with cisplatin, fluorouracil, with or without taxane on locoregionally advanced nasopharyngeal carcinoma: a retrospective, propensity score-matched analysis. Cancer Commun 2018;38:21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [26].Yamasaki M, Yasuda T, Yano M, et al. Multicenter randomized phase II study of cisplatin and fluorouracil plus docetaxel (DCF) compared with cisplatin and fluorouracil plus Adriamycin (ACF) as preoperative chemotherapy for resectable esophageal squamous cell carcinoma (OGSG1003). Ann Oncol 2016;28:116–21. [DOI] [PubMed] [Google Scholar]
  • [27].Vermorken JB, Remenar E, Van HC, et al. Cisplatin, fluorouracil, and docetaxel in unresectable head and neck cancer. N Engl J Med 2007;357:1695–704. [DOI] [PubMed] [Google Scholar]
  • [28].Schrijvers D, Van HC, Kerger J, et al. Docetaxel, cisplatin and 5-fluorouracil in patients with locally advanced unresectable head and neck cancer: a phase I-II feasibility study. Ann Oncol 2004;15:638–45. [DOI] [PubMed] [Google Scholar]
  • [29].Pointreau Y, Garaud PS, Sire C, et al. Randomized trial of induction chemotherapy with cisplatin and 5-fluorouracil with or without docetaxel for larynx preservation. J Natl Cancer Inst 2009;101:1157–8. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplemental Digital Content
medi-99-e19360-s001.doc (151.5KB, doc)

Articles from Medicine are provided here courtesy of Wolters Kluwer Health

RESOURCES