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      Association of Chemoradiotherapy Regimens and Survival Among Patients With Nasopharyngeal Carcinoma : A Systematic Review and Meta-analysis

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          Abstract

          This systematic review and meta-analysis assesses whether concurrent chemoradiotherapy is associated with improvement in survival outcomes for patients with locoregionally advanced nasopharyngeal carcinoma.

          Key Points

          Question

          Is induction chemotherapy or adjuvant chemotherapy associated with additional survival benefit in locoregionally advanced nasopharyngeal carcinoma?

          Findings

          In a systematic review and meta-analysis of 28 randomized clinical trials of 8036 patients, concurrent chemoradiotherapy was associated with substantial improvement in survival outcomes for patients with locoregionally advanced nasopharyngeal carcinoma. Survival benefit was also associated with the addition of induction chemotherapy but not adjuvant chemotherapy to concurrent chemoradiotherapy.

          Meaning

          For locoregionally advanced nasopharyngeal carcinoma, concurrent chemoradiotherapy should be recommended as the standard treatment strategy, with the addition of induction chemotherapy but not adjuvant chemotherapy.

          Abstract

          Importance

          The role of induction chemotherapy (IC) or adjuvant chemotherapy (AC) in the treatment of locoregionally advanced nasopharyngeal carcinoma (NPC) remains controversial.

          Objectives

          To update meta-analyses on the association of survival outcomes with IC and AC regimens in patients with locoregionally advanced NPC and assess whether the current evidence is conclusive by a trial sequential analysis (TSA) approach.

          Data Sources

          PubMed, Embase, and Web of Science were searched for articles published from inception until June 1, 2019.

          Study Selection

          Randomized clinical trials that assessed the efficacy of radiotherapy with or without chemotherapy among previously untreated patients and patients with nondistant metastatic NPC.

          Data Extraction and Synthesis

          Data were extracted by 2 investigators from each trial independently and synthesized by the 2 investigators. All trial results were combined and analyzed by a fixed- or random-effects model.

          Main Outcomes and Measures

          Overall survival (OS), progression-free survival (PFS), distant metastasis–free survival (DMFS), and locoregional recurrence-free survival (LRFS).

          Results

          A total of 8036 patients (median age, 46.5 years; 5872 [73.1%] male) from 28 randomized clinical trials were included in the analysis. Pooled analyses revealed that concurrent chemoradiotherapy (CCRT) was significantly associated with improved OS, PFS, DMFS, and LRFS compared with radiotherapy across all subgroups. The TSA confirmed the treatment outcomes of CCRT compared with radiotherapy. The additional IC regimen was associated with an improvement in OS (hazard ratio [HR], 0.84; 95% CI, 0.74-0.95), PFS (HR, 0.73; 95% CI, 0.64-0.84), DMFS (HR, 0.67; 95% CI, 0.59-0.78), and LRFS (HR, 0.74; 95% CI, 0.64-0.85). These findings were consistent in subgroup analyses of multicenter trials with sample sizes greater than 250, years of survival rate of 5 or greater, median follow-up longer than 5 years, or low risk of bias. However, the additional AC regimen was not associated with a survival benefit in OS (HR, 0.98; 95% CI, 0.78-1.23), PFS (HR, 0.86; 95% CI, 0.70-1.07), DMFS (HR, 0.84; 95% CI, 0.64-1.10), or LRFS (HR, 0.80, 95% CI, 0.59-1.09). The TSA provided sound evidence on the additional benefit of IC but not AC.

          Conclusions and Relevance

          These data suggest a significant association of survival outcomes with CCRT in patients with locoregionally advanced NPC. The addition of IC instead of AC could achieve survival benefits. The potential therapeutic gain of AC should be explored in the future.

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          Most cited references40

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          Chemoradiotherapy versus radiotherapy in patients with advanced nasopharyngeal cancer: phase III randomized Intergroup study 0099.

          The Southwest Oncology Group (SWOG) coordinated an Intergroup study with the participation of Radiation Therapy Oncology Group (RTOG), and Eastern Cooperative Oncology Group (ECOG). This randomized phase III trial compared chemoradiotherapy versus radiotherapy alone in patients with nasopharyngeal cancers. Radiotherapy was administered in both arms: 1.8- to 2.0-Gy/d fractions Monday to Friday for 35 to 39 fractions for a total dose of 70 Gy. The investigational arm received chemotherapy with cisplatin 100 mg/m2 on days 1, 22, and 43 during radiotherapy; postradiotherapy, chemotherapy with cisplatin 80 mg/m2 on day 1 and fluorouracil 1,000 mg/m2/d on days 1 to 4 was administered every 4 weeks for three courses. Patients were stratified by tumor stage, nodal stage, performance status, and histology. Of 193 patients registered, 147 (69 radiotherapy and 78 chemoradiotherapy) were eligible for primary analysis for survival and toxicity. The median progression-free survival (PFS) time was 15 months for eligible patients on the radiotherapy arm and was not reached for the chemo-radiotherapy group. The 3-year PFS rate was 24% versus 69%, respectively (P < .001). The median survival time was 34 months for the radiotherapy group and not reached for the chemo-radiotherapy group, and the 3-year survival rate was 47% versus 78%, respectively (P = .005). One hundred eighty-five patients were included in a secondary analysis for survival. The 3-year survival rate for patients randomized to radiotherapy was 46%, and for the chemoradiotherapy group was 76% (P < .001). We conclude that chemoradiotherapy is superior to radiotherapy alone for patients with advanced nasopharyngeal cancers with respect to PFS and overall survival.
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            Phase III study of concurrent chemoradiotherapy versus radiotherapy alone for advanced nasopharyngeal carcinoma: positive effect on overall and progression-free survival.

            Nasopharyngeal carcinoma (NPC) is a radiosensitive and chemosensitive tumor. This randomized phase III trial compared concurrent chemoradiotherapy (CCRT) versus radiotherapy (RT) alone in patients with advanced NPC. From December 1993 to April 1999, 284 patients with 1992 American Joint Committee on Cancer stage III to IV (M0) NPC were randomly allocated into two arms. Similar dosage and fractionation of RT was administered in both arms. The investigational arm received two cycles of concurrent chemotherapy with cisplatin 20 mg/m(2)/d plus fluorouracil 400 mg/m(2)/d by 96-hour continuous infusion during the weeks 1 and 5 of RT. Survival analysis was estimated by the Kaplan-Meier method and compared by the log-rank test. Baseline patient characteristics were comparable in both arms. After a median follow-up of 65 months, 26.2% (37 of 141) and 46.2% (66 of 143) of patients developed tumor relapse in the CCRT and RT-alone groups, respectively. The 5-year overall survival rates were 72.3% for the CCRT arm and 54.2% for the RT-only arm (P =.0022). The 5-year progression-free survival rates were 71.6% for the CCRT group compared with 53.0% for the RT-only group (P =.0012). Although significantly more toxicity was noted in the CCRT arm, including leukopenia and emesis, compliance with the combined treatment was good. The second cycle of concurrent chemotherapy was refused by nine patients and was delayed for > or = 1 week for another nine patients. There were no treatment-related deaths in either arm. We conclude that CCRT is superior to RT alone for patients with advanced NPC in endemic areas.
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              • Abstract: found
              • Article: not found

              Randomized trial of radiotherapy versus concurrent chemoradiotherapy followed by adjuvant chemotherapy in patients with American Joint Committee on Cancer/International Union against cancer stage III and IV nasopharyngeal cancer of the endemic variety.

              The Intergroup 00-99 Trial for nasopharyngeal cancer (NPC) showed a benefit of adding chemotherapy to radiotherapy. However, there were controversies regarding the applicability of the results to patients in endemic regions. This study aims to confirm the findings of the 00-99 Trial and its applicability to patients with endemic NPC. Between September 1997 and May 2003, 221 patients were randomly assigned to receive radiotherapy (RT) alone (n = 110) or chemoradiotherapy (CRT; n = 111). Patients in both arms received 70 Gy in 7 weeks using standard RT portals and techniques. Patients on CRT received concurrent cisplatin (25 mg/m2 on days 1 to 4) on weeks 1, 4, and 7 of RT and adjuvant cisplatin (20 mg/m2 on days 1 to 4) and fluorouracil (1,000 mg/m2 on days 1 to 4) every 4 weeks (weeks 11, 15, and 19) for three cycles after completion of RT. All patients were analyzed by intent-to-treat analysis. The median follow-up time was 3.2 years. Distant metastasis occurred in 38 patients on RT alone and 18 patients on CRT. The difference in 2-year cumulative incidence was 17% (95% CI, 14% to 20%; P = .0029). The hazard ratio (HR) for disease-free survival was 0.57 (95% CI, 0.38 to 0.87; P = .0093). The 2- and 3-year overall survival (OS) rates were 78% and 85% and 65% and 80% for RT alone and CRT, respectively. The HR for OS was 0.51 (95% CI, 0.31 to 0.81; P = .0061). This report confirms the findings of the Intergroup 00-99 Trial and demonstrates its applicability to endemic NPC. This study also confirms that chemotherapy improves the distant metastasis control rate in NPC.
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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                18 October 2019
                October 2019
                18 October 2019
                : 2
                : 10
                : e1913619
                Affiliations
                [1 ]Department of Radiology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China
                [2 ]Department of Radiation Oncology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China
                [3 ]Department of Oncology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China
                [4 ]Big Data Decision Institute, Jinan University, Guangzhou, Guangdong, China
                [5 ]Department of Catheterization Laboratory, Guangdong Cardiovascular Institute, Guangdong Provincial Key Laboratory of South China Structural Heart Disease, Guangdong Provincial People’s Hospital/Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China
                [6 ]Department of Epidemiology and Biostatistics, School of Public Health, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China
                [7 ]Department of Head and Neck Cancer, Guangdong Provincial People’s Hospital/Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China
                [8 ]Guangdong Provincial People’s Hospital/Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China
                [9 ]Key Laboratory of Molecular Imaging, Chinese Academy of Sciences, Beijing, China
                Author notes
                Article Information
                Accepted for Publication: September 3, 2019.
                Published: October 18, 2019. doi:10.1001/jamanetworkopen.2019.13619
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2019 Zhang B et al. JAMA Network Open.
                Corresponding Authors: Jie Tian, MD, PhD, Key Laboratory of Molecular Imaging, Chinese Academy of Sciences, No. 95 Zhongguancun E Rd, Beijing 100190, China ( jie.tian@ 123456ia.ac.cn ); Shui Xing Zhang, MD, PhD, Department of Radiology, The First Affiliated Hospital of Jinan University, No. 613 Huangpu W Rd, Tianhe District, Guangzhou, Guangdong 510627, China ( shui7515@ 123456126.com ).
                Author Contributions: Drs B. Zhang and Li contributed equally to this work. Drs B. Zhang and S. X. Zhang had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: B. Zhang, Li, W. H. Chen, Zhao, S. X. Zhang.
                Acquisition, analysis, or interpretation of data: B. Zhang, Li, W. H. Chen, W. Q. Chen, Dong, Gong, Q. Y. Chen, L. Zhang, Mo, Luo, Tian.
                Drafting of the manuscript: B. Zhang.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: B. Zhang, W. Q. Chen, Gong.
                Obtained funding: B. Zhang, S. X. Zhang.
                Administrative, technical, or material support: B. Zhang, Dong, Q. Y. Chen, L. Zhang, Mo, S. X. Zhang.
                Supervision: B. Zhang, Tian, S. X. Zhang.
                Conflict of Interest Disclosures: None reported.
                Funding/Support: This research was supported by grants 81571664 (Dr S. X. Zhang), 81871323 (Dr S. X. Zhang), and 81801665 (Dr B. Zhang) from the National Natural Science Foundation of China; grant 2018B030311024 from the National Natural Science Foundation of Guangdong Province (Dr S. X. Zhang); grant 201707010328 from the Scientific Research General Project of Guangzhou Science Technology and Innovation Commission (Dr S. X. Zhang); and grant 2016M600145 from the China Postdoctoral Science Foundation (Dr S. X. Zhang).
                Role of the Funder/Sponsor: The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and the decision to submit the manuscript for publication.
                Additional Contributions: Jiang Hu, BS (Nanchang Foryodoo Technology Co Ltd, Nanchang, China), assisted in editing the manuscript and was not compensated for the work.
                Article
                zoi190520
                10.1001/jamanetworkopen.2019.13619
                6813597
                31626318
                5f79f996-ff24-4b7b-94d4-9e1a4b436275
                Copyright 2019 Zhang B et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 11 July 2019
                : 3 September 2019
                Categories
                Research
                Original Investigation
                Online Only
                Oncology

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