J Cancer 2018; 9(23):4510-4520. doi:10.7150/jca.27611
The Efficacy and Safety of Anti-epidermal Growth Factor Receptor Monoclonal Antibodies in Nasopharyngeal Carcinoma: Literature-based Meta-analyses
1. Department of Radiation Oncology, Sun Yat-sen University Cancer Centre; State Key Laboratory of Oncology in South China; Collaborative Innovation Centre of Cancer Medicine; Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangzhou, China
2. Department of Medical Oncology, Sun Yat-sen University Cancer Centre; State Key Laboratory of Oncology in South China; Collaborative Innovation Centre of Cancer Medicine, Guangzhou, China
3. Department of Medical Statistics and Epidemiology, School of Public Health, Sun Yat-sen University, Guangzhou, China
* These authors contributed equally to this work.
Peng L, Liu ZL, Xu C, Tang LL, Liu X, Lin AH, Sun Y, Chen YP, Ma J. The Efficacy and Safety of Anti-epidermal Growth Factor Receptor Monoclonal Antibodies in Nasopharyngeal Carcinoma: Literature-based Meta-analyses. J Cancer 2018; 9(23):4510-4520. doi:10.7150/jca.27611. Available from http://www.jcancer.org/v09p4510.htm
Background: Anti-epidermal growth factor receptor monoclonal antibodies (anti-EGFR mAbs), such as cetuximab and nimotuzumab have been used in the treatment of nasopharyngeal carcinoma (NPC), yet their efficacy and safety are undetermined.
Materials and Methods: We performed two meta-analyses based on systematic searches of PubMed, EMBASE, the Cochrane Library and SinoMed: comparison 1 (standard therapy plus mAbs vs. standard therapy) and comparison 2 (radiotherapy plus concurrent mAbs vs. concurrent chemoradiotherapy) to explore the treatment value of anti-EGFR mAbs in NPC. Primary outcomes were overall survival (OS) and disease-free survival (DFS); secondary outcomes, locoregional recurrence-free survival (LRFS), distant metastasis-free survival (DMFS) and grade 3 and above acute adverse events.
Results: Four randomized controlled trials and thirteen observational studies were eligible. Comparison 1 (twelve studies): adding mAbs to standard therapy (radiotherapy or chemoradiotherapy) significantly improved OS (HR, 0.51; 95% CI, 0.39-0.66) and DFS (HR, 0.68; 95% CI, 0.54-0.86), but increased the frequency of skin rashes and mucositis. Comparison 2 (six studies): OS (HR, 1.17; 95% CI, 0.81-1.70) and DFS (HR, 1.16; 95% CI, 0.86-1.57) were not significantly different when mAbs replaced conventional cytotoxic chemotherapy concurrently with radiotherapy, with fewer hematological, gastrointestinal and renal toxicities and more skin rashes in the mAb group.
Conclusion: We recommend anti-EGFR mAbs enhance—but should not replace—current treatment paradigms for locoregionally advanced NPC. Further evidence from phase III clinical trials is required.
Keywords: nasopharyngeal carcinoma, anti-epidermal growth factor receptor, cetuximab, nimotuzumab, meta-analysis
Nasopharyngeal carcinoma (NPC) is very prevalent in endemic regions such as southern China, where the age-standardized annual incidence is 5-11 cases per 100,000 in endemic provinces, increasing to 10-27 cases in endemic counties . In early-stage NPC (stage I), radiotherapy (RT) alone has good efficacy, and leads to a 5-year overall survival rate of over 90% . However, up to 70% of patients present with locoregionally advanced (stage III-IV) disease at diagnosis ; RT combined with chemotherapy (chemoradiotherapy, CRT) is the recommended standard treatment for these patients [4, 5]. Yet, CRT fails in approximately 30% of patients; most treatment failures are due to distant metastasis [6, 7]. Moreover, conventional cytotoxic drugs (i.e., cisplatin, fluorouracil, taxol) are mainly selected for CRT, but can cause severe intolerable toxicities because of their unspecific cytotoxic effects in both normal and cancer cells .
Epidermal growth factor receptor (EGFR) is expressed in over 90% cases of NPC [9, 10], and a meta-analysis linked overexpression of EGFR to a poorer prognosis . Activation of EGFR pathways promotes tumor cell growth, invasion and metastasis, prevents apoptosis and induces chemoresistance and radioresistance [12-15]. EGFR has been evaluated as a therapeutic target in NPC. Anti-EGFR monoclonal antibodies (anti-EGFR mAbs) bind to the extra-cellular domain of EGFR and prevent activation of downstream signaling pathways, and therefore exert anti-neoplastic effects. Of the several commercialized anti-EGFR mAbs available, cetuximab and nimotuzumab have been clinically tested in NPC. Several phase II single-arm clinical trials have preliminarily investigated the efficacy and toxicity of anti-EGFR mAbs in the treatment of NPC and reported promising results [16-19]. Moreover, one randomized controlled phase II trial demonstrated combining nimotuzumab and RT improved the complete response rate compared to RT alone in NPC, but no further survival outcomes were reported . No data from phase III clinical trials is available to confirm the efficacy and toxicity of anti-EGFR mAbs in NPC; therefore, a comprehensive review of the available evidence is needed.
We conducted two separate head-to-head comparison meta-analyses in an attempt to answer the following questions: (1) whether combining anti-EGFR mAbs with the standard treatment (RT/CRT) improves efficacy without intolerable toxicities in NPC; and (2) whether anti-EGFR mAbs can replace conventional cytotoxic chemotherapy (usually platinum-based) in concurrent chemoradiotherapy (CCRT) with non-inferior efficacy and milder toxicities in NPC.
Materials and Methods
A comprehensive search was conducted of PubMed, EMBASE, the Cochrane Library and SinoMed (a Chinese database). We used the intelligent search functions provided by the electronic databases; the following terms and their synonyms provided by the intelligent search functions were used: “nasopharyngeal carcinoma” AND (“targeted therapy” OR “EGFR inhibitor” OR “anti-EGFR” OR “monoclonal antibody” OR “cetuximab” OR “nimotuzumab”). Abstracts from major cancer conferences were also considered in the EMBASE search. No restrictions on language or time of publication were applied. We also searched the US National Institutes of Health Trials Register and World Health Organization Clinical Trials Registry Platform for ongoing trials. The last search was performed on May 20th, 2018. We also manually searched the reference lists of retrieved papers or related reviews for additional studies.
We selected overall survival (OS) and disease-free survival (DFS) as primary outcomes and reported these as unadjusted hazard ratio (HR). Secondary outcomes were locoregional recurrence-free survival (LRFS) and distant metastasis-free survival (DMFS), reported as unadjusted HR, and grade 3 and above acute adverse events, reported as relative risk (RR). OS was defined as the time from treatment initiation to death from any cause; DFS, to distant metastasis, locoregional relapse or death from any cause (whichever first); LRFS, to locoregional relapse; DMFS, to distant metastasis. Acute adverse events were defined as occurring during treatment or within 90 days of treatment completion.
Studies were included if they met all of the following predefined criteria: (1) patients with a pathological diagnosis of non-metastatic NPC without previous treatment; (2) head-to-head comparisons between RT/CRT plus anti-EGFR mAbs and RT/CRT alone, or RT plus concurrent anti-EGFR mAbs and RT plus concurrent chemotherapy; (3) studies reporting at least one of the primary outcomes (OS and DFS), as HR and associated 95% confidence interval (CI) or other types of data (i.e., survival curves, numbers of events and log-rank P-values) from which we could calculate HR and 95% CI indirectly. Reviews without original data, case reports, preclinical studies and single-arm studies were excluded. When cohorts from different studies overlapped, studies with the most participants or with the most complete data were included. The eligibility of each citation was independently assessed by two reviewers (L.P. and C.X.), and disagreements were resolved by discussion.
Data extraction and quality assessment
The following data was extracted and recorded using a predesigned table: first author, year of publication, study design, recruitment period, participants' age and sex, tumor stage and histologic type, sample size (per arm), treatment protocol, follow-up time, survival outcomes, and grade 3 and above acute adverse events. RCTs were assessed using the Cochrane risk of bias assessment tool and six domains for each included study were assessed: random sequence generation, allocation concealment, blinding (of participants and outcome assessors), outcome data, selective outcome reporting and other bias . Studies were classified as having a low, unclear or high risk of bias. Observational studies were assessed with the modified Newcastle-Ottawa scale, which comprises three items: patient selection, comparability of the study groups, and assessment of outcomes . Scores range from 0 to 9; studies with scores ≥ 6 were regarded as high-quality. Two reviewers (L.P. and Z.L.L.) independently performed the extraction and assessment work and discussed any disagreements; a senior reviewer (Y.P.C.) was consulted if necessary.
For survival analysis, when unadjusted HR and associated 95% CI were unavailable, we used summary statistics or Kaplan-Meier curves to calculate the HR according to Parmar's method . For adverse events analysis, the RR and 95% CI were used as outcome measures. Heterogeneity among studies was evaluated using the Chi2 test and I2 statistic. Heterogeneity was considered statistically significant if the P-value for the Chi2 test was < 0.10 or I2 value was > 50%; if so, the random-effects model was used; otherwise, the fixed-effects model was used . We entered HR data into the meta-analysis using the inverse variance method. Subgroup analyses were based on the mAb investigated, namely cetuximab or nimotuzumab. Funnel plots and Begg's tests were generated to detect potential publication bias using Stata software 12.0 (StataCorp, College Station, TX, USA), and P > 0.05 was taken to indicate an absence of potential publication bias . The meta-analysis and forest plots were produced using Review Manager 5.3 (Cochrane Collaboration, Oxford, UK).
Characteristics of studies
Seventeen eligible studies were identified from the 1215 references retrieved [26-42]. The flow diagram of selection of the included studies is presented in Figure 1. Twelve studies [26-37] were included in the comparison between RT/CRT plus anti-EGFR mAbs and RT/CRT alone (comparison 1); six studies [29, 38-42] were included in the comparison between RT plus concurrent anti-EGFR mAbs and CCRT (comparison 2). Yin et al.  compared three cohorts: RT alone, RT plus concurrent anti-EGFR mAbs, and CCRT, so the comparison between RT alone and RT plus concurrent anti-EGFR mAb and the comparison between RT plus concurrent anti-EGFR mAb and CCRT were included in the respective meta-analyses. Among the studies included in comparison 1, two were RCTs [26, 27] and ten were observational studies [28-37], and two studies [26, 29] used RT as standard treatment while the rest used CRT. You et al.  focusing on cetuximab/nimotuzumab and Xia et al.  focusing on cetuximab were conducted at the same institution and had partially overlapping participants, so we pooled the survival data from You et al.  in the overall analysis and Xia et al.  in the subgroup analysis. With regard to toxicities, data from You et al.  was pooled in the overall and subgroup analysis as adverse events were displayed individually for cetuximab/nimotuzumab. Among the studies included in comparison 2, two were RCTs [38, 39] and four were observational studies [29, 40-42]. The characteristics of the included studies are shown in Table 1 and the treatment protocols are summarized in Table 2.
Assessment of included studies
The results of the assessment are shown in Supplementary Tables S1 and S2. Wu et al.  reported single-center results from a multicenter, randomized controlled phase II trial , and was assessed as having an unclear risk of bias, as the two groups had a small, significant difference in age. The study by Shao et al.  was assessed as having a high risk of bias as the participants were allocated by drawing lots, which may cause non-neglectable selection bias. The phase II RCT registered as NCT01614938 by Xu et al.  was assessed as having an unclear risk, as it aimed to recruit at least 86 participants, but the trial was closed ahead of schedule because of the unexpectedly high rates of grade 3/4 mucositis observed in the RT plus concurrent cetuximab arm; this trial only recruited 44 participants. Liao et al.  reported the interim results of a phase III RCT registered as NCT02012062 and was assessed as having an unclear risk of bias. Of the thirteen observational studies, nine [28, 29, 31, 32, 34-37, 40-42] were assessed as high-quality studies and two [30, 33] scored 5 indicating low quality.
Characteristics of the included studies
|Study ID||Study type||Recruitment period||Study arms||Sample size||Median or mean age (years)||Stage (%)/staging system||Histologic type (WHO)||Extractable survival outcomes||Toxicity criteria||Median follow-up time (months)|
|Comparison 1: RT/CRT + anti-EGFR mAbs versus RT/CRT alone|
|Li 2015||OB||2009-2012||CCRT+NTZ||30||57.3f||II (8.3%), III (38.3%), IV (53.4%)/ Chinese 2008 staging||II, III||OS||CTCAEv4.0||NR|
|Lou 2016||OB||2012||IC→CCRT+NTZ||22||NR||III (NR), IV (NR)/NR||NR||OS||CTCAEv3.0, RTOG/EORTC||36|
|Shao 2014||RCT||2009-2010||CCRT+NTZ||24||47g||III (58.3%), IV (41.7%)/Chinese 2008 staging||II, III||OS,DFS||CTCAEv4.0, RTOG||26|
|Tang 2012||OB||2008-2011||CCRT+NTZ→AC||63||54.2f||III (57.7%), IV (42.3%)/Chinese 2008 staging||NR||OS,DFS,LRFS,DMFS||CTCAEv3.0, RTOG/EORTC||19.5|
|Wang 2016||OB||2008-2010||CCRT+CTX||36||46.6f||I-II (80.8%), III-IV (19.2%)/NR||NR||OS, DFS||RTOG||54|
|Wang 2018||OB||2008-2014||IC→CCRT+NTZ→±AC||120||47g||III (59.6%), IV (40.4%)/AJCC 7th staging||NR||OS,DFS,LRFS,DMFS||CTCAEv3.0, RTOG||56|
|Wu 2018||OB||2010-2014||CCRT+CTX||75||47g||III (50.7%), IV (49.3%)/AJCC 7th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv3.0, RTOG||41.0|
|Wu 2007||RCT||2003-2004||RT+NTZ||18||36f||III (68.6%), IV (31.4%)/AJCC 5th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv2.0, RTOG||31.9|
|Yin 2014a||OB||2008-2012||RT+NTZ/CTX||68c||NR||II (28.0%), III (38.2%), IV (33.8%)/ NR||NR||OS,DFS,LRFS,DMFS||CTCAEv3.0||31.3a|
|You 2017||OB||2009-2013||CCRT+NTZ/CTX||189d||44.7g||II (9.2%), III (71.4%), IV (19.4%)/ AJCC 7th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv4.0, RTOG/EORTC||48.0|
|Zeng 2016||OB||2010-2012||CCRT+CTX||64||45.3f||III (47.8%), IV (52.2%)/AJCC 6th staging||NR||OS||NR||NR|
|Xia 2017b||OB||2006-2013||±IC→CCRT+CTX||96||43.9f||III (NR), IV (NR)/AJCC 7th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv4.0||62|
|Comparison 2: RT + concurrent anti-EGFR mAbs versus CCRT|
|Li 2016||OB||2008-2013||IC→RT+NTZ||52||NR||II (25.0%), III (39.4%), IV (35.6%)/ AJCC 7th staging||II, III||OS,DFS||CTCAEv4.0||50|
|Liao 2016||RCT||2012-2013||IC→RT+NTZ||28||47g||III (51.7%), IV (48.3%)/AJCC 7th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv3.0||36|
|Wu 2016||OB||2008-2012||IC→RT+CTX||56||46.2g||II (17.0%), III (49.1%), IV (33.9%)/ AJCC 7th staging||II, III||OS,DFS||CTCAEv4.0||55.4|
|Xu 2015||RCT||2010-2011||IC→RT+CTX||21||44g||III (70.5%), IV (29.5%)/AJCC 7th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv3.0||36.9|
|Yin 2014a||OB||2008-2012||RT+NTZ/CTX||68c||NR||II (28.0%), III (38.2%), IV (33.8%)/ NR||NR||OS,DFS,LRFS,DMFS||CTCAEv3.0||31.3a|
|You-Rui 2017||OB||2009-2013||±IC→RT+NTZ/CTX||143e||46g||II (11.2%), III (55.7%), IV (33.9%)/ AJCC 7th staging||II, III||OS,DFS,LRFS,DMFS||CTCAEv4.0, RTOG||50.4|
Abbreviations: OB = observational; RCT = randomized controlled trial; anti-EGFR mAbs = anti-epidermal growth factor receptor monoclonal antibodies; RT = radiotherapy; CRT = chemoradiotherapy; CCRT = concurrent chemoradiotherapy; IC = induction chemotherapy; AC = adjuvant chemotherapy; NTZ = nimotuzumab; CTX = cetuximab; NR = not reported; AJCC = American Joint Committee on Cancer; OS = overall survival; DFS = disease-free survival; LRFS = locoregional recurrence-free survival; DMFS = distant metastasis-free survival; CTCAE = Common Terminology Criteria for Adverse Events; RTOG = Radiation Therapy Oncology Group; EORTC = European Organization for Research on Treatment of Cancer. a Yin 2014 with three cohorts was split into two comparisons, and the median follow-up time was calculated based on the total three cohorts. b The cohort recruited by Xia 2017 partially overlapped with the cohort of You 2017, and was only included in cetuximab subgroup analyses for OS and DFS. c Numbers of participants treated with NTZ/CTX was 59/9. d Numbers of participants treated with NTZ/CTX was 87/102. e Numbers of participants treated with NTZ/CTX was 85/58. f Mean age.
Treatment protocols of the included studies
|Study ID||Radiotherapy||Chemotherapy||Anti-EGFR mAb during RT|
|Comparison 1: RT/CRT + anti-EGFR mAbs versus RT/CRT alone|
|Li 2015||3DCRT:60-70Gy||CCRT: NDP 40 mg qw for 6 cycles||NTZ 200 mg qw for 6 cycles|
|Lou 2016||IMRT:66-70Gy||IC: TP or TPF q3w for 1-2 cycles;|
CCRT: NDP 80 mg/m2 q3w for 2 cycles
|NTZ 100 mg or 200 mg qw for 6 cycles|
|Shao 2014||3DCRT:72-76Gy||CCRT: NDP 30 mg/m2 qw for 7 cycles||NTZ 100 mg qw for 7 cycles|
|CCRT: TP q3w for 2-3 cycles;|
AC: TP q3w for 2-4 cycles
|NTZ 100 mg qw for 6-7 cycles|
|Wu 2007||2DRT:70Gy||NA||NTZ 100 mg qw for 8 cycles|
|Wang 2016||IMRT:66Gy||CCRT: CDDP 40 mg/m2 qw for 6 cycles||CTX 40 mg/m2 qw for 6 cycles|
|Wang 2018||IMRT:66-72Gy||IC: TP or PF or TPF or GP q3w for 2-3 cycles;|
CCRT: CDDP 80 mg/m2 q3w for 2-3 cycles;
AC: PF or GP
|NTZ 200 mg qw for 6-7 cycles|
|Wu 2018||IMRT:66-75Gy||CCRT: TP or CDDP 80 mg/m2 or NDP 80 mg/m2 q3w for 2 cycles||CTX 400 mg loading, 250 mg qw for 7 cycles|
|Yin 2014||IMRT:70-74Gy||NA||CTX 400 mg loading, 250 mg qw for 7 cycles;|
NTZ 200 mg qw for 8 cycles
|You 2017||IMRT:68-72Gy||CCRT: CDDP 80-100 mg/m2 q3w for 2-3 cycles||CTX 400 mg loading, 250 mg qw for 6-7 cycles;|
NTZ 200 mg qw for 6-7 cycles
|Zeng 2016||IMRT:70Gy||CCRT: CDDP 40 mg/m2 qw for 6 cycles||CTX 400 mg loading, 250 mg qw for 7 cycles|
|CCRT: CDDP 80-100 mg/m2 q3w for 2-3 cycles or 30-40 mg/m2 qw for 5-7 cycles||CTX 400 mg loading, 250 mg qw for 6-7 cycles|
|Comparison 2: RT + concurrent anti-EGFR mAbs versus CCRT|
|Li 2016||IMRT:70-74Gy||IC: TPF q3w for 2 cycles;|
CCRT: CDDP 75 mg/m2 q3w for 2-3 cycles
|NTZ 200 mg qw for 6-8 cycles|
|Liao 2016||IMRT:70Gy||IC: TPF q3w for 3 cycles;|
CCRT: CDDP 40 mg/m2 qw for 7 cycles
|NTZ 200 mg qw for 8 cycles|
|Wu 2016||IMRT:70-74Gy||IC: TPF q3w for 2 cycles;|
CCRT: CDDP 75 mg/m2 q3w for 2-3 cycles
|CTX 400 mg loading, 250 mg qw for 8 cycles|
|Xu 2015||IMRT:66-70Gy||IC: TP q3w for 2 cycles;|
CCRT: CDDP 30 mg/m2 qw
|CTX 250 mg qw for 7 cycles|
|Yin 2014||IMRT:70-74Gy||CCRT: CDDP qw for 6 cycles or q3w for 2cycles||CTX 400 mg loading, 250 mg qw for 7 cycles;|
NTZ 200 mg qw for 8 cycles
|You-Rui 2017||IMRT:76-70Gy||IC: TP or PF or TPF q3w for 2-3 cycles;|
CCRT: CDDP 80-100 mg/m2 q3w for 2-3 cycles
|CTX 400 mg loading, 250 mg qw for 6-7 cycles;|
NTZ 200 mg qw for 6-7 cycles
Abbreviations: 3DCRT = three-dimensional conformal radiotherapy; IMRT = intensity modulated radiotherapy; 2DRT = two-dimensional radiotherapy; NDP = nedaplatin; CDDP = cisplatin; TP = taxol analog + platinum; TPF = taxol analog + platinum + 5-fluorouracil; PF = platinum + 5-fluorouracil; GP = gemcitabine + platinum; CTX = cetuximab; NTZ = nimotuzumab; anti-EGFR mAbs = anti-epidermal growth factor receptor monoclonal antibodies; RT = radiotherapy; CRT = chemoradiotherapy; CCRT = concurrent chemoradiotherapy; IC = induction chemotherapy; AC = adjuvant chemotherapy; qw = every week; q3w = every three weeks; NA = not applicable.
g Median age.
Flow diagram of selection of included and excluded studies.(Click on the image to enlarge.)
Comparison 1: RT/CRT plus anti-EGFR mAbs vs. RT/CRT alone
Pooled HR for OS showed evidence of a benefit of adding anti-EGFR mAbs to standard therapy (HR, 0.51; 95% CI, 0.39-0.66). Pooled analysis for DFS showed a benefit favoring addition of anti-EGFR mAbs (HR, 0.68; 95% CI, 0.54-0.86). Pooled analysis for LRFS also indicated a benefit favoring addition of anti-EGFR mAbs (HR, 0.66; 95% CI, 0.45-0.96). With regards to DMFS, a marginally significant effect was observed (HR, 0.64; 95% CI, 0.38-1.07). No significant heterogeneity was detected, except in the analysis of DMFS (I2 = 53%, P = 0.06; Figure 2).
Ten types of adverse event were evaluated (Table 3). Grade 3 and above skin rashes and mucositis were more frequently observed in participants treated with RT/CRT plus anti-EGFR mAbs. The pooled RR (95% CI) for skin rashes and mucositis were 4.08 (1.59-10.47) and 1.84 (1.10-3.10) respectively; both had significant heterogeneity.
In the cetuximab subgroup, OS and DFS remained significantly improved by adding cetuximab to standard therapy compared to standard therapy alone; pooled RR (95% CI) for skin rashes and mucositis were 7.28 (2.17-24.43) and 2.31 (1.04-5.15). In the nimotuzumab subgroup, OS was significantly improved by adding nimotuzumab, though the improvement in DFS was marginally significant (HR, 0.65; 95% CI, 0.41-1.03; P = 0.06); pooled RR (95% CI) for skin rashes and mucositis were 1.19 (0.51-2.78) and 1.25 (0.81-1.94; Supplementary Table S3).
Comparison 2: RT plus concurrent anti-EGFR mAbs vs. CCRT
Pooled analysis showed the survival differences between the two modalities were not significant (OS: HR, 1.17; 95% CI, 0.81-1.70; DFS: HR, 1.16; 95% CI, 0.86-1.57; LRFS: HR, 0.83; 95% CI, 0.44-1.58; DMFS: HR, 1.17; 95% CI, 0.73-1.85) and no significant heterogeneity was detected (Figure 3).
Ten types of adverse events were evaluated (Table 3). Compared to CCRT, RT plus concurrent anti-EGFR mAbs was less likely to induce grade 3 and above leucopenia (RR, 0.23; 95% CI, 0.10-0.53), thrombocytopenia (RR, 0.27; 95% CI, 0.11-0.62), anemia (RR, 0.09; 95% CI, 0.03-0.33), nausea/vomiting (RR, 0.10; 95% CI, 0.05-0.18) and renal function abnormality (RR, 0.20; 95% CI, 0.05-0.79), but more likely to cause grade 3 and above skin rashes (RR, 4.09; 95% CI, 1.21-13.87).
Forest plots of the overall analyses for comparison 1, comparing RT/CRT plus anti-EGFR mAbs and RT/CRT alone. (A) Overall survival; (B) disease-free survival; (C) locoregional recurrence-free survival; (D) distant metastasis-free survival. RT = radiotherapy; CRT = chemoradiotherapy; anti-EGFR mAbs = anti-epidermal growth factor receptor monoclonal antibodies.(Click on the image to enlarge.)
Forest plots of the overall analyses for comparison 2, comparing RT plus concurrent anti-EGFR mAbs and CCRT. (A) Overall survival; (B) disease-free survival; (C) locoregional recurrence-free survival; (D) distant metastasis-free survival. RT = radiotherapy; CCRT = concurrent chemoradiotherapy; anti-EGFR mAbs = anti-epidermal growth factor receptor monoclonal antibodies.(Click on the image to enlarge.)
In the cetuximab subgroup, OS and DFS remained non-significantly different between RT plus concurrent cetuximab and CCRT; pooled RR (95% CI) for skin rashes and mucositis were 11.13 (6.16-20.10) and 1.62 (1.33-1.98). In the nimotuzumab subgroup, pooled HR (95% CI) for OS and DFS were 2.49 (1.18-5.24) and 2.11 (1.13-3.94), indicating concurrent nimotuzumab has inferior efficacy compared to CCRT; pooled RR (95% CI) for skin rashes and mucositis were 1.32 (0.22-8.06) and 0.92 (0.72-1.18; Supplementary Table S4).
In both comparisons 1 and 2, the results of the sensitivity analyses for primary outcomes (OS and DFS) were in accordance with the overall analyses, suggesting the results were robust (Supplementary Tables S5 and S6). Additionally, no significant publication bias was detected in the overall analyses for OS and DFS (Figure 4).
Comparison 1: anti-EGFR mAbs can enhance the efficacy when combined to standard therapy in the treatment of locoregionally advanced NPC
According to the results of our meta-analyses, addition of anti-EGFR mAbs to standard therapy for NPC improved efficacy in terms of OS, DFS and LRFS compared to standard therapy alone, and sensitivity analyses confirmed the robustness of these results. This result can be explained by the synergetic anti-neoplastic effects of anti-EGFR mAbs combined with chemotherapy and radiotherapy, which renders NPC cells more sensitive to cytotoxic drugs and ionizing radiation [43, 44]. However, the improvement in DMFS was insignificant, which may be due to the between-study heterogeneity of the four studies included. When interpreting improvements in efficacy, caution is necessary due to the following constraints of the included studies: (1) most participants had advanced stage NPC (stage III and IV accounted for 90.7%); (2) the median follow-up time for the included studies ranged from 19.5 to 56 months, and only five studies [31, 32, 35-37] had a median follow-up time ≥ 36 months; (3) most studies were conducted using CRT as standard therapy, and only two studies [26, 29] employed RT. At present, there is still a lack of evidence to prove the superiority of combining anti-EGFR mAbs with RT over RT alone in stage III and IV disease. Indeed, CRT is recommended as the standard therapy for stage III and IV NPC and RT alone is sub-optimal, and only advisable if chemotherapy cannot be administered due to contraindications. For patients with stage II NPC, disagreements still exist regarding the optimal treatment modality (RT or CRT) due to the intrinsic heterogeneity of this group of patients . Therefore, whether it is suitable to add anti-EGFR mAbs to RT/CRT in stage II NPC or not is a question that needs to be addressed in the future. On the other hand, RT plus anti-EGFR mAbs could be an alternative to RT or CRT for stage II NPC (see below). When interpreting the results of subgroup analyses for survival outcomes, we should bear in mind that some studies investigating both cetuximab and nimotuzumab were not included in the subgroup analyses as detailed data was not provided separately for each mAb, and this may explain why the improvement in DFS in the nimotuzumab subgroup was not as significant as in the overall analyses.
Adding anti-EGFR mAbs to standard therapy was more likely to cause grade 3 and above skin rashes and mucositis compared with standard therapy alone. This can be explained by the fact that EGFR mAbs can bind to some normal cells, such as the epidermis and mucosal epithelium . However, such adverse events resolved after withdrawal of the mAbs due to the self-repairing ability of epithelial tissue . To some extent, subgroup analyses revealed nimotuzumab was less likely to cause such mAb-related adverse events, which can be explained by the lower EGFR-binding affinity of nimotuzumab compared to cetuximab , though this needs to be confirmed by direct or indirect comparisons between nimotuzumab and cetuximab.
Funnel plots with pseudo 95% confidence limits of overall analyses for comparison 1 (A: overall survival; B: disease-free survival) and comparison 2 (C: overall survival; D: disease-free survival). P-values were calculated by Begg's test.(Click on the image to enlarge.)
Meta-analyses of grade 3 and above adverse events for comparisons 1 and 2
|Adverse events||N of studies||N of pts in mAb group||N of pts in control group||RR (95% CI)||P-valuea||Heterogeneity|
|Comparison 1: RT/CRT + anti-EGFR mAbs versus RT/CRT alone|
|Liver dysfunction||3||294||869||1.18 (0.55-2.54)||0.68||0%||0.66|
|Renal impairment||1||189||689||0.87 (0.33-2.27)||0.77||NA||NA|
|Skin rash||4||358||943||4.08 (1.59-10.47)||0.003||70%||0.02|
|Mucositis||7||565||1152||1.84 (1.10-3.10)||0.02||89%||< 0.001|
|Weight loss||2||264||839||1.51 (0.95- 2.39)||0.08||0%||0.62|
|Comparison 2: RT + Concurrent Anti-EGFR mAbs Versus CCRT|
|Leukopenia||3||251||680||0.23 (0.10-0.53)||< 0.001||51%||0.13|
|Anemia||3||227||660||0.09 (0.03-0.33)||< 0.001||0%||0.92|
|Nausea/vomiting||4||279||712||0.10 (0.05-0.18)||< 0.001||10%||0.34|
|Renal impairment||3||227||660||0.20 (0.05-0.79)||0.02||48%||0.15|
|Skin rash||5||300||735||4.09 (1.21-13.87)||0.02||63%||0.03|
|Weight loss||3||251||680||0.96 (0.64- 1.45)||0.84||12%||0.32|
Abbreviations: N = number; pts = patients; anti-EGFR mAb = anti-epidermal growth factor receptor monoclonal antibody; RT = radiotherapy; CRT = chemoradiotherapy; CCRT = concurrent chemoradiotherapy; RR = risk ratio; CI = confidence interval; NA = not applicable. a Statistically significant results are shown in bold.
The relative efficacy of cetuximab and nimotuzumab in the treatment of NPC is still undetermined. Although several studies have demonstrated cetuximab and nimotuzumab are efficacious in NPC [16, 17, 19, 20], further comparisons between the two mAbs are needed. Considering the current evidence, cetuximab and nimotuzumab both represent good choices for combination with standard therapy in stage III and IV NPC with respect to efficacy, but nimotuzumab would be a better choice due to its more favorable toxicity profile.
Comparison 2: anti-EGFR mAbs failed to be a recommended choice to replace conventional cytotoxic regimes concurrently with RT in the treatment of locoregionally advanced NPC
When anti-EGFR mAbs were prescribed to replace conventional cytotoxic regimes concurrently with RT, we did not observe significant differences in OS, DFS, LRFS or DMFS. Of the 368 participants in the mAb group, 241 patients received induction chemotherapy (IC) before RT. IC has been proven to improve DFS, mainly by benefiting DMFS in patients with advanced NPC [49, 50]. So, we cannot exclude the possibility that benefits from IC may conceal differences between the two modalities. Subgroup analyses revealed nimotuzumab was significantly inferior to conventional cytotoxic regimes concurrent with RT in OS and DFS, while no significant differences were observed in the cetuximab subgroup. This may be due to the intrinsic pharmacological and immunological differences between the two mAbs in this clinical scenario (i.e. concurrent with RT alone) [51, 52]. More evidence is needed to support this suggestion, considering that only two studies with a small sample size were included in each subgroup analysis. With respect to adverse events, hematological, gastrointestinal and renal toxicities, such platinum-related toxicities were less likely in the RT plus mAb group, though mAb-related toxicities such as skin rashes were frequent in this group.
In the light of the current evidence, we do not recommend the replacement of platinum-based chemotherapy with anti-EGFR mAbs during RT in patients with locoregionally advanced NPC. We could not confirm the non-inferiority of RT plus anti-EGFR mAbs compared to CCRT, especially when we took the results of NCT01614938, the closed ahead-of-schedule phase II trial , and the subgroup analyses into consideration. However, for patients with stage II NPC, for whom the choice of RT or CRT is still uncertain, treatment with RT plus anti-EGFR mAbs may provide satisfactory efficacy with tolerable toxicities . Additionally, replacement of chemotherapy with anti-EGFR mAbs could be considered for elderly patients or patients with comorbidities who cannot tolerate the toxicities of platinum-based chemotherapy . The ongoing phase III clinical trial NCT02012062 should provide solid evidence in this respect.
Previous studies demonstrated that inhibition of EGFR signaling could modulate cellular sensitivity to radiation and enhance tumor cell response to radiation and established a foundation for the clinical investigation of the combination of radiation and anti-EGFR mAbs . We also noticed that most of current studies incorporated the anti-EGFR mAbs concurrently with RT in the curative setting for non-metastatic NPC. However, what are the effects of anti-EGFR mAbs when incorporated into the induction or adjuvant phase? Peng et al.  conducted a retrospective analysis suggesting that anti-EGFR mAbs in combination with IC may be a more effective and promising strategy for patients with locoregionally advanced NPC. Further investigations are required to explore the application of anti-EGFR mAbs in NPC. The phase III RTOG 0522 trial  evaluated the potential benefit of adding cetuximab to CCRT in head and neck squamous cell cancer and demonstrated no improvement in PFS or OS. However, a post hoc analysis of RTOG 0522 study  found that patients with the KRAS-variant may significantly benefit from the addition of cetuximab to CCRT. In the future, identifying reliable biomarkers that could predict the effects of anti-EGFR mAbs in NPC and optimizing the use of anti-EGFR mAbs will be a promising direction.
Several limitations of these meta-analyses need to be taken into account. Firstly, thirteen of the seventeen studies included were observational, which may introduce confounding factors into the final results. Secondly, we extracted all information from published data other than individual patient data, which may have resulted in publication and reporting bias. Thirdly, the studies adopted different criteria for evaluation of adverse events, which may cause bias to some extent.
Our meta-analyses showed that adding anti-EGFR mAbs to standard therapy can enhance OS, DFS and LRFS in NPC compared to standard therapy alone with tolerable toxicities. However, replacement of conventional platinum-based chemotherapy with anti-EGFR mAbs concurrently with RT is not supported by our analyses. In view of the limitations of our meta-analyses, further phase III RCTs are necessary to provide more solid evidences.
CCRT: concurrent chemoradiotherapy; CI: confidence interval; CRT: chemoradiotherapy; DFS: disease-free survival; DMFS: distant metastasis-free survival; EGFR: epidermal growth factor receptor; HR: hazard ratio; IC: induction chemotherapy; LRFS: locoregional recurrence-free survival; mAbs: monoclonal antibodies; NPC: nasopharyngeal carcinoma; OS: overall survival; RCT: randomized controlled trial; RR: relative risk; RT: radiotherapy.
This study was supported by grants from Natural Science Foundation of Guang Dong Province (No. 2017A030312003), Health & Medical Collaborative Innovation Project of Guangzhou City, China (201803040003), Innovation Team Development Plan of the Ministry of Education (No. IRT_17R110) and Overseas Expertise Introduction Project for Discipline Innovation (111 Project, B14035).
The authors have declared that no competing interest exists.
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Corresponding authors: Jun Ma, Department of Radiation Oncology, Sun Yat-sen University Cancer Center, No. 651 Dongfeng Road East, Guangzhou 510060, China. Tel.:+86-20-87343469; Fax:+86-20-87343295; E-mail: majun2sysu.edu.cn and Yu-Pei Chen, Department of Radiation Oncology, Sun Yat-sen University Cancer Center, No. 651 Dongfeng Road East, Guangzhou 510060, China. Tel.:+86-20-87343469; Fax: +86-20-87343295; E-mail: chenyup1org.cn