Abstract
The aim of the present analysis was to compare the efficacy and safety profile of S-1-based chemotherapy (SBCT) versus capecitabine-based chemotherapy (CBCT) for advanced gastric cancer (AGC) and advanced colorectal cancer (ACRC). A meta-analysis was performed, which included eligible randomized controlled trials (RCTs) that were identified using RevMan 5.1.0 software. A total of 1,064 patients from 11 RCTs, comprising of 527 patients in the SBCT group and 537 patients in the CBCT group, were included in the analysis. For AGC, the meta-analysis of overall survival (OS) [hazard ratio (HR), 0.98; 95% confidence interval (CI), 0.85–1.12], time to progression (HR, 0.95; 95% CI, 0.80–1.12) and overall response rate (ORR) [odds ratio (OR), 1.06; 95% CI, 0.72–1.55] of patients in the SBCT group indicated no statistical significance when compared with those in the CBCT group. Furthermore, for ACRC, a pooled analysis demonstrated no significant difference between the SBCT and CBCT groups (OS: HR, 0.82; 95% CI, 0.61–1.10; progression-free survival: HR, 0.79; 95% CI=0.60–1.04; ORR: OR, 1.27; 95% CI, 0.91–1.78). The statistically significant differences identified in the overall meta-analysis indicated a low incidence of grade 3–4 hand-foot-syndrome (OR, 0.15; 95% CI, 0.06–0.36) in the SBCT group; however no statistically significant difference was observed in the incidence of grade 3–4 anemia, thrombocytopenia, leucopenia, neutropenia, diarrhea, stomatitis or nausea/vomiting. The SBCT treatment exhibited similar efficacy and an approximately equivalent safety profile compared with the CBCT treatment and was an alternative to CBCT for patients with AGC or ACRC; however, further investigation is required to provide confirmation.
Keywords: S-1, capecitabine, advanced gastric cancer, advanced colorectal cancer, meta-analysis
Introduction
Regardless of advances in their diagnosis and treatment, gastric and colorectal cancer remain a common cause of cancer-related mortality worldwide (1,2). Acquiring curative therapy by surgery or radiotherapy is complex for patients with advanced gastric cancer (AGC) or advanced colorectal cancer (ACRC); therefore, systemic chemotherapy is considered to be the primary effective treatment.
Traditional continuous infusion of 5-fluorouracil (5-FU) in combination with folinic acid has been the primary chemotherapeutic treatment for AGC and ACRC. However, continuous infusion requires an indwelling central venous catheter; thus, there is an increased risk of infection and thrombosis, in addition to the requirement for regular hospital visits. Therefore, administration of the traditional 5-FU-based chemotherapy (FBCT) is time-consuming, uncomfortable and inconvenient for patients.
Recently, oral fluoropyrimidines have been developed as a substitution for 5-FU infusion therapy. Capecitabine is an oral fluoropyrimidine that was designed to simulate a continuous intravenous infusion of 5-FU (3) and has been approved for the treatment of patients with AGC and ACRC. S-1 is another treatment, which is a combination of three pharmacological compounds: Tegafur, gimeracil and oteracil potassium at a molar ratio of 1:0.4:1, respectively (4), which has been identified as a suitable alternative to 5-FU for the treatment of patients with ACRC or AGC (5,6).
As the efficacy and safety of oral fluoropyrimidines, capecitabine and S-1, have been confirmed, it is necessary to identify which treatment exhibits a greater efficacy and safety profile for AGC and ACRC patients. To date, there have been a series of trials comparing S-1 with capecitabine as part of a mono or combined therapeutic treatment (7–17); however, a single study may not be sufficient to comprehensively assess their efficacy and safety. Moreover, to the best of our knowledge, a meta-analysis of S-1-based chemotherapy (SBCT) versus capecitabine-based chemotherapy (CBCT) for ACRC or AGC has not been conducted. Therefore, the present meta-analysis of eligible studies was performed to compare the two treatment approaches and evaluate their clinical efficacy and safety in patients with AGC and ACRC.
Materials and methods
Literature search
A comprehensive search was conducted using PubMed (http://www.ncbi.nlm.nih.gov/pubmed), Embase (https://www.embase.com), the Cochrane Library (http://www.thecochranelibrary.com) and the Chinese Biological Medical Database (http://www.sinomed.ac.cn/zh/) to identify randomized controlled trials (RCTs) from inception of the databases to August 31st 2013. Various combinations of different terms, such as ‘gastric cancer’, ‘colorectal cancer’, ‘capecitabine’, ‘S-1’, ‘randomized’ and their synonyms served as search terms. The following search strategy of Embase was used: i) ‘gastric neoplasm’: ab, ti OR ‘gastric cancer’: ab, ti OR ‘gastric carcinoma’: ab, ti OR ‘stomach cancer’: ab, ti OR ‘cancer of stomach’: ab, ti OR ‘stomach neoplasm’: ab, ti OR ‘stomach cancer’/exp OR ‘colorectal carcinoma’: ab, ti OR ‘colorectal cancer’: ab, ti OR ‘colorectal neoplasm’: ab, ti OR ‘rectal cancer’: ab, ti OR ‘colon cancer’: ab, ti OR ‘intestinal cancer’: ab, ti OR ‘colorectal carcinoma’/exp. ii) ‘tegafur gimeracil oteracil potassium’: ab, ti OR ‘S-1’: ab, ti OR ‘TS-1’: ab, ti OR ‘gimeracil plus oteracil potassium plus tegafur’/exp. iii) ‘capecitabine’: ab, ti OR ‘xeloda’: ab, ti OR ‘capecitabine’/exp. iv) random*: ab, ti OR ‘randomized controlled trial’: ab, ti OR ‘controlled clinical trial’: ab, ti OR ‘randomized controlled trial’/exp OR ‘randomized controlled trial (topic)’/exp. v) #1 AND #2 AND #3 AND #4. This strategy was applied to the search of other databases.
In addition, all of the abstracts from the American Society of Clinical Oncology conferences (http://meetinglibrary.asco.org/) that were held between 2003 and 2013 were searched to identify the relevant RCTs and references that were cited in the identified articles were searched manually. The search was conducted without any restriction on language.
Inclusion and exclusion criteria
The inclusion and exclusion criteria were delineated prior to commencement of the literature search. The eligible studies were included in the present meta-analysis if they met all of the following criteria: i) Participants were patients with histologically confirmed, advanced, recurrent or metastatic colorectal or gastric cancer and did not present with severe, basic diseases which may affect the treatment effect of patients (including cardiovascular and cerebrovascular diseases); ii) only RCTs were considered; iii) trials compared SBCT with CBCT, particularly mono- or combined therapy of S-1 versus capecitabine, without confusion resulting from the administration of additional drugs or interventions (for example, experimental and control arms exhibited differences between S-1 and capecitabine components alone within a combination therapy). Accordingly, the following exclusion criteria were used: i) Cross-over studies; ii) non-randomized or single-arm phase II trials; iii) any review, letter, case report or comment; iv) for repeated published articles or the same study of a different follow-up period, the study with the strictest methodology and most complete data was selected and the other excluded.
Data extraction
The essential data was independently extracted from the eligible studies by two investigators and any discrepancies were resolved by a consensus between the two. Information was collected from each study as follows: The first author’s name, publishing year, country/region of origin, study design, characteristics of the participants, interventions conducted and outcomes. When the hazard ratio (HR) of overall survival (OS), progression-free survival (PFS) and time to progression (TTP) could not be directly extracted from the original reports, they were extracted from Kaplan-Meier curves as reported by Tierney et al (18).
Quality assessment of the included studies
The quality of the eligible studies was assessed by two investigators independently and any disagreements were resolved by a third investigator. According to the Cochrane Collaboration’s tool for assessing risk of bias of RCTs (5.1.0) (19), the following criteria were used to appraise the RCTs included in full texts: Random sequence generation, allocation concealment, binding of participants and personnel, binding of outcome assessments, incomplete outcome data, selective reporting and other bias. In all cases, high, low or unclear risk was used to evaluate the risk of bias; when there was insufficient detail included in the study, the judgment was that the risk of bias was unclear.
Statistical analysis
Statistical analysis of the HR and 95% confidence interval (CI) for OS, PFS and TTP, in addition to the odds ratio (OR) and 95% CI for the overall response rate (ORR) and grade 3 or 4 adverse events (AEs) were calculated using RevMan 5.1.0 software. The ORR was defined as the sum of the partial and complete response rates according to the Response Evaluation Criteria in Solid Tumors (20). A fixed-effects model was initially used and the Q test and I2 statistical test were subsequently performed to assess the heterogeneity between studies; P<0.1 was considered to indicate a statistically significant difference. When there was heterogeneity across the trials, sensitivity analysis or a randomized-effect model was applied to overcome this shortcoming, and the process of sensitivity analysis excluding the study firstly according to different inclusion criteria and then re-analyzing the remaining studies. For the results mentioned above (not including the heterogeneity test): P<0.05 was considered to indicate a statistically significant difference. OR>1 indicated a favorable outcome in the S-1-based group; however, it indicated a greater level of toxicity and a HR>1 demonstrated a greater number of fatalities or progression with S-1-based regimens for OS or TTP and PFS, respectively.
Results
Literature search
The search strategy yielded 288 records, of these, 11 duplicates were eliminated and 265 articles were excluded due to irrelevancy or failing to meet the inclusion criteria, which was determined by a review of the titles and abstracts. Further evaluation of the remaining 12 studies revealed that one study was ongoing (21). Thus, 11 studies (7–17) qualified for inclusion in the present meta-analysis (Fig. 1). Table I displays the characteristics of the 11 individual studies with respect to author, year, country, demographic data, interventions and the study outcomes.
Figure 1.
Flow chart displaying the process of study selection for the present meta-analysis. ASCO, American Society of Clinical Oncology.
Table I.
Predominant characteristics of the studies included in the present meta-analysis.
| Study (ref.) | Country/tumor type | No. of patientsa | PS (score) | SBCT regimen | CBCT regimen | Outcome measures |
|---|---|---|---|---|---|---|
| Kim et al 2012 (8) | Korea/AGC | 65/64 | 0–2 | S-1: 80 mg/m2 d1–14, oxaliplatin: 130 mg/m2 d1, q3w | Capecitabine: 2,000 mg/m2 d1–14 oxaliplatin: 130 mg/m2 d1, q3w |
ORR, OS, TTP, QOL, toxicities |
| Lee et al 2008 (9) | Korea/AGC | 45/46 | 0–2 | S-1: 40–60 mg, bid, according to body surface area, d1–28, q6w | Capecitabine: 1,250 mg/m2, bid, d1–14, q3w | ORR, TTP, OS, toxicities |
| Xiong et al 2013 (15) | China/AGC | 42/44 | >70b | Docetaxel: 25 mg/m2 d1 d8 d15, S-1: 80 mg/m2, d1–14, q4w | Docetaxel: 25 mg/m2 d1 d8 d15, capecitabine: 1250 mg/m2 d1–14, q4w | ORR, MST, toxicities |
| Zhang et al 2010 (17) | China/AGC | 17/19 | ≥60b | S-1: 80 mg/m2, d1–28, q6w | Capecitabine: 2500 mg/m2 d1–14, q3w | ORR, toxicities |
| Ba et al 2012 (11) | China/AGC | 18/19 | 0–1 | S-1: 80 mg/m2 d1–14, cisplatin: 75 mg/m2 d1, q3w | Capecitabine: 2000 mg/m2 d1–14; cisplatin: 75 mg/m2 d1, q3w | ORR, TTP, OS, toxicities |
| Yan et al 2012 (16) | China/AGC | 21/21 | - | S-1: 40 mg/m2, bid, d1–14, cisplatin: 75 mg/m2 d1, q3w | Capecitabine: 1000 mg/m2, bid, d1–14; cisplatin: 75 mg/m2 d1, q3w | ORR, toxicities |
| Qiu et al 2011 (13) | China/AGC | 28/28 | ≥60b | S-1: 40 mg/m2, bid, d1–28, q5w | Capecitabine: 1,250 mg/m2, bid, d1–14, q3w | ORR, toxicities |
| Hong et al 2012 (7) | Korea/ACRC | 168/172 | 0–2 | S-1: 40 mg/m2, bid, d1–14, oxaliplatin: 130 mg/m2 d1, q3w | Capecitabine: 1000 mg/m2, bid, d1–14, oxaliplatin: 130 mg/m2 d1, q3w | ORR, TTF, PFS, OS, toxicities |
| Sun et al 2013 (14) | China/ACRC | 54/52 | >70b | S-1: 80 mg/m2, d1–14, q3w | Capecitabine: 2000 mg/m2, d1–14, q3w | ORR, MST, toxicities |
| Lu et al 2012 (12) | China/ACRC | 26//27 | 0–2 | S-1: 80 mg/m2 d1–14; oxaliplatin: 130 mg/m2 d1, q3w | Capecitabine: 2000 mg/m2 d1–14, oxaliplatin: 130 mg/m2 d1, q3w | ORR, toxicities |
| Zang et al 2012 (10) | Korea/ACRC | 43/45 | 0–2 | S-1: 80 mg/m2 d1–14, oxaliplatin: 130 mg/m2 d1, q3w | Capecitabine: 2000 mg/m2 d1–14, oxaliplatin: 130 mg/m2 d1, q3w | ORR, TTP, MST, toxicities |
SBCT/CBCT regimen patients,
Karnofsky method.
PS, performance status; SBCT, S-1-based chemotherapy; CBCT, capecitabine-based chemotherapy; AGC, advanced gastric cancer; ORR, overall response rate; OS, overall survival; TTP, time to progression; QOL, quality of life; MST, median survival time; PFS, progression-free survival; ACRC, advanced colorectal cancer; TTF, time to treatment failure; d1–14, days 1–14; q3w, every 3 weeks; q4w, every 4 weeks; q6w, every 6 weeks.
Quality of eligible studies
The present meta-analysis included 11 RCTs and all of the studies included the term ‘random’, however, only three studies (7,8,14) specifically reported the methods that were utilized for random sequence generation. Furthermore, only two studies (7,9) adequately reported the reliability-determined allocation concealment. Three trials (7,9,10) were open-labeled and the other studies did not state whether a blind method was adopted; however, these were unlikely to affect the quality assessment results. One trial was an abstract and included insufficient information regarding the outcome data, selective reporting and other bias (10), additional trials satisfied the criteria for complete outcome data and did not include selective reporting or other bias (Table II).
Table II.
Risk of bias for each study.
| Risk of bias | |||||||
|---|---|---|---|---|---|---|---|
|
|
|||||||
| Study (ref.) | A | B | C | D | E | F | G |
| Kim et al, 2012 (8) | Low | Unclear | Low | Low | Low | Low | Low |
| Lee et al, 2008 (9) | Unclear | Low | Low | Low | Low | Low | Low |
| Xiong et al, 2013 (15) | Unclear | Unclear | Low | Low | Low | Low | Low |
| Zhang et al, 2010 (17) | Unclear | Unclear | Low | Low | Low | Low | Low |
| Ba et al, 2012 (11) | Unclear | Unclear | Low | Low | Low | Low | Low |
| Yan et al, 2012 (16) | Unclear | Unclear | Low | Low | Low | Low | Low |
| Qiu et al, 2011 (13) | Unclear | Unclear | Low | Low | Low | Low | Low |
| Hong et al, 2012 (7) | Low | Low | Low | Low | Low | Low | Low |
| Sun et al, 2013 (14) | Low | Unclear | Low | Low | Low | Low | Low |
| Lu et al, 2012 (12) | Unclear | Unclear | Low | Low | Low | Low | Low |
| Zang et al, 2012 (10) | Unclear | Unclear | Low | Low | Unclear | Unclear | Unclear |
A, random sequence generation; B, allocation concealment; C, binding of participants and personnel; D, binding of outcome assessment; E, incomplete outcome data; F, selective reporting; G, other bias.
Tumor response
All of the included studies provided the information on ORR and the pooled OR of ORR for AGC of the fixed-effect model was 1.06 (95% CI, 0.72 and 1.55) with no heterogeneity (P=0.94, I2=0%; Fig. 2). For ACRC, there was no heterogeneity identified across the trials (P=0.30, I2=17%) and the pooled OR of ORR using the fixed-effect model was 1.27 (95% CI, 0.91 and 1.78). The OR indicated that there was no significant difference between the SBCT and CBCT group.
Figure 2.
Forest plot of the odds ratio of the overall response rate. CI, confidence interval.
TTP or PFS
Regarding AGC, four trials provided TTP information (8,9,11,15), of which the TTP HR of the trial reported by Xiong et al (15) was extracted from the Kaplan-Meier curves that were presented in the study. The pooled HR of TTP indicated that there was no significant difference between the SBCT and CBCT group (HR=0.95, 95% CI, 0.80–1.12) and the pooled HR was performed using a fixed-effect model, with no heterogeneity observed (P=0.92, I2=0%). Concerning ACRC, no trials provided the HR of TTP and only one trial provided PFS data (7); moreover, the HR of PFS identified no significant difference between the SBCT and CBCT group (HR=0.79, 95% CI, 0.60–1.04; Fig. 3).
Figure 3.
Forest plot of the hazard ratio of time to progression or progression-free survival. CI, confidence interval.
OS data
Five of the 12 trials provided OS data (7–9,11,15), of which the OS HR of the trial, reported by Xiong et al (15), was extracted from the Kaplan-Meier curves that were presented in the study. Regarding AGC, there was no significant heterogeneity observed between the studies (P=0.86, I2=0%), the pooled HR of OS obtained using a fixed-effect model showed no significant difference between the SBCT and CBCT group, yielding a HR of 0.98 (95% CI, 0.85–1.12). Concerning ACRC, only one trial provided the HR of OS (HR=0.82, 95% CI, 0.61–1.10) (7), which demonstrated that there was no significant difference between the two groups (Fig. 4).
Figure 4.
Forest plot of the hazard ratio of overall survival. CI, confidence interval.
Safety profile
Neutropenia in hematologic toxicities
A meta-analysis of seven trials (7–11,15,16) regarding grade 3–4 neutropenia, which included 398 patients in the SBCT group and 399 patients in the CBCT group, identified no significant difference between the two groups (OR=1.17, 95%CI, 0.81–1.70), with significant heterogeneity observed across the trials (P=0.02, I2=61%) and as the sensitivity analysis did not identify the source of the heterogeneity, a random-effect model was applied. The result of the random-effect model showed that there was no significant difference between the two groups (OR=0.79, 95% CI, 0.37–1.69).
Leucopenia
A meta-analysis of seven trials (7–9,12–14,17) regarding grade 3–4 leucopenia, which included 401 patients in the SBCT group and 400 patients in the CBCT group, showed no significant difference between the two groups (OR=0.91, 95% CI, 0.37–2.24) and there was no significant heterogeneity identified across the trials (P=0.72, I2=0%).
Thrombocytopenia
Nine trials (7–12,15–17) reported grade 3–4 thrombocytopenia from the assessment of 889 participants (SBCT, n=441; CBCT, n=445). The pooled analysis showed no significant difference between the two groups (OR=1.34, 95% CI, 0.89–2.02) and significant heterogeneity was demonstrated across the trials (P=0.01, I2=62%). As the heterogeneity could not be eliminated by conducting a sensitivity analysis, a random-effect model was performed (OR=0.85, 95% CI, 0.36–1.97).
Anemia
Data concerning anemia was available from nine trials (7–13,15,16), which included 906 participants (SBCT, n=452; CBCT, n=454) in the meta-analysis. The pooled OR of the nine trials indicated no significant difference between the two groups (OR=1.61, 95% CI, 0.93–2.80) and there was no heterogeneity noted between the studies (P=0.88, I2=0.0%).
Hand-foot syndrome (HFS) in non-hematologic toxicities
Ten trials (7–13,15–17) reported grade 3–4 HFS (SBCT, n=469; CBCT, n=473). The pooled OR of grade 3–4 HFS (OR=0.15, 95% CI, 0.06–0.36) showed that there was a statistically significant difference between the SBCT and CBCT groups, with no significant heterogeneity observed across the trials (P=0.99, I2=0%), which indicated that grade 3–4 HFS was less likely to occur in SBCT patients.
Diarrhea and nausea/vomiting
Ten studies (7–9,11–17) that included 482 patients in the SBCT group and 484 patients in the CBCT group, provided information on cases of grade 3–4 diarrhea and nausea/vomiting. The meta-analysis of the 10 trials showed no significant difference between the two groups (diarrhea: OR=1.00, 95% CI, 0.56–1.78; nausea/vomiting: OR=0.83, 95% CI, 0.48–1.43) and there was no heterogeneity identified.
Stomatitis
Eight trials (7,9,11,13–17) reported grade 3–4 stomatitis, these trials included 391 patients in the SBCT group and 393 patients in the CBCT group. The meta-analysis of the fixed-effects model indicated no significant difference between the two groups (OR=1.23, 95% CI, 0.37–4.12; heterogeneity: P=0.88, I2=0%).
The results of the grade 3 and 4 AE analyses are displayed in Table III.
Table III.
Outcome of the toxicity meta-analysis comparing SBCT with CBCT in advanced gastric and colorectal cancer.
| Heterogenity | ||||||||
|---|---|---|---|---|---|---|---|---|
|
|
||||||||
| Toxicity | Trials | SBCT | CBCT | P-value | I2 (%) | OR (95% CI) | Model | References |
| Grade 3–4 anemia | 9 | 35/452 | 23/454 | 0.88 | 0 | 1.61 (0.93, 2.80) | Fixed | (7–13,15,16) |
| Grade 3–4 leucopenia | 7 | 9/401 | 10/400 | 0.72 | 0 | 0.91 (0.37, 2.24) | Fixed | (7–9,12–14,17) |
| Grade 3–4 neutropenia | 7 | 72/398 | 63/399 | 0.02 | 61 | 0.79 (0.37, 1.69) | Random | (7–11,15,16) |
| Grade 3–4 thrombocytopenia | 9 | 61/441 | 47/445 | 0.01 | 62 | 0.85 (0.36, 1.97) | Random | (7–12,15–17) |
| Grade 3–4 diarrhea | 10 | 21/482 | 21/484 | 0.42 | 2 | 1.00 (0.56, 1.78) | Fixed | (7–9,11–17) |
| Grade 3–4 nausea/vomiting | 10 | 23/482 | 28/484 | 0.69 | 0 | 0.83 (0.48,1.43) | Fixed | (7–9,11–17) |
| Grade 3–4 stomatitis | 8 | 5/391 | 4/393 | 0.88 | 0 | 1.23 (0.37, 4.12) | Fixed | (7,9,11,13–17) |
| Grade 3–4 HFS | 10 | 3/469 | 33/473 | 0.99 | 0 | 0.15 (0.06, 0.36) | Fixed | (7–13,15–17) |
HFS, hand-foot syndrome; SBCT, S-1-based chemotherapy; CBCT, capecitabine-based chemotherapy; OR, odds ratio; CI, confidence interval.
Discussion
To the best of our knowledge, this was the first meta-analysis to evaluate the efficacy and safety profile of SBCT versus CBCT for AGC or ACRC. A total of 1,064 patients from 11 RCTs, including 527 patients in the SBCT group and 537 patients in the CBCT group were analyzed. On the basis of intention-to-treat analysis, with respect to ORR, TTP and OS, the present meta-analysis showed no significant differences between the SBCT and CBCT group for AGC, which suggested that SBCT was not inferior to CBCT for patients with AGC. With regards to ACRC, the pooled analysis indicated that there was no significant difference between the SBCT and CBCT groups concerning the ORR, PFS and OS, which indicated that SBCT exhibited similar efficacy to CBCT for patients with ACRC.
With regard to the safety profile, although the present meta-analysis indicated that grade 3–4 HFS was less likely to occur in SBCT patients (OR=0.15, 95% CI, 0.06–0.36), grade 3–4 toxicities, such as anemia, leucopenia, neutropenia, thrombocytopenia, nausea/vomiting, diarrhea and stomatitis were identified to be similarly prevalent between the two groups. The types of toxicities were deemed to be manageable, predictable and tolerable. Therefore, compared with CBCT, SBCT exhibited an approximately equivalent safety profile for patients with AGC and ACRC.
Owing to the significant heterogeneity observed between grade 3–4 neutropenia and grade 3–4 thrombocytopenia, a sensitivity analysis was performed; however, the factors contributing to the heterogeneity could not be identified, therefore, they may be associated with variations in age, performance status of patients, dose and the regimen of therapy between the trials. Thus, a random-effects model was applied to compensate for this and the conclusion did not alter relative to the result of the fixed-effects model, which confirmed the reliability of our outcome.
Of note, the patient population included in the present meta-analysis was markedly heterogeneous, i.e. the patients exhibited metastatic colorectal or advanced gastric cancer. Thus, subgroup analysis by tumor type was performed on ORR, TTP and OS; the findings of which indicated that the non-inferiority of SBCT versus CBCT could be applied to all of the patient subgroups that were considered within the present analysis. However, as the type of toxicity was not specific to a certain type of tumor for the same drug and AGC and ACRC are gastrointestinal cancers, a greater significance was determined from the results of the overall meta-analysis of grade 3–4 AEs for all of the patients, rather than the results from the subgroup population analysis.
In 2009, a meta-analysis of individual patient data was conducted by Okines et al (22) and demonstrated that OS was superior in patients with AGC that were treated with CBCT compared with the patients with AGC that were treated with FBCT (HR=0.87, 95% CI, 0.77–0.98). Similarly, a meta-analysis was performed by Huang et al (23) comparing the use of FBCT, which identified a significant OS benefit in favor of SBCT for patients with AGC (HR=0.87, 95% CI, 0.79–0.96). The data from these two meta-analyses indirectly showed that SBCT exhibited a similar efficacy to CBCT for AGC patients, which was in line with the present study.
In addition, S-1 and capecitabine possess different optimal doses, efficacy and safety among patients that are from different regions. Based on the metabolic pathway, capecitabine exhibited no obvious racial difference concerning the dose and efficacy regardless of a lower grade 3–4 gastrointestinal toxicity when compared with FBCT in Asian patients (24). However, as the polymorphic variants of the liver enzyme gene, cytochrome P450 (CYP) 2A6, which converts tegafur to 5-FU, were more frequent in Asians than in Caucasians, there were certain racial differences identified regarding S-1 tolerance, which results in varying optimal doses of S-1 for different races (25). The study by Kong et al showed that the CYP2A6 genotype was associated with the treatment efficacy of SBCT in AGC patients (26) and it may result in certain racial differences in S-1 efficacy. In 2009, the updated results of a randomized phase III study, conducted by Fuse et al (27), demonstrated that S-1 was associated with an increased OS compared with 5-FU in Japanese patients with AGC (HR=0.83, 95% CI, 0.68–1.00, P=0.02). However, in 2010 the findings of a RCT conducted by Ajani et al (28) showed that SBCT did not prolong the OS of Western patients with AGC when compared with FBCT (HR=0.92, 95% CI, 0.80–1.05, P=0.20).
There were certain limitations in the present meta-analysis. As all of the studies included were from Asia, the present results require confirmation from studies conducted on patients from a Western population. Moreover, the quantity of included studies was small and there may have been publication bias. The quality of the studies was not considered to be high, with just three studies (7,8,14) reporting the specific methods of random sequence generation and two studies (7,9) reporting with adequate reliability the method by which the allocation concealment was determined; thus, a greater number of RCTs with improved methodologies are required to update the present study. Furthermore, information was not obtained from individual patients for each trial, which would have resulted in a more comprehensive analysis and, finally, heterogeneous results were included.
In conclusion, the present meta-analysis indicated that SBCT exhibited a comparable efficacy and approximately equivalent safety profile in patients with AGC and ACRC compared with CBCT; therefore, it was considered to be an effective alternative to CBCT. However, further investigation, which includes large-scale prospective studies with an adequate methodological quality and legitimate control measures that account for possible confounding factors are required to confirm or update the present study, particularly including patients from a Western population.
References
- 1.Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893–2917. doi: 10.1002/ijc.25516. [DOI] [PubMed] [Google Scholar]
- 2.Meyerhardt JA, Mayer RJ. Systemic therapy for colorectal cancer. N Engl J Med. 2005;352:476–487. doi: 10.1056/NEJMra040958. [DOI] [PubMed] [Google Scholar]
- 3.Miwa M, Ura M, Nishida M, et al. Design of a novel oral fluoropyrimidine carbamate, capecitabine, which generates 5-fluorouracil selectively in tumours by enzymes concentrated in human liver and cancer tissue. Eur J Cancer. 1998;34:1274–1281. doi: 10.1016/s0959-8049(98)00058-6. [DOI] [PubMed] [Google Scholar]
- 4.Shirasaka T, Shimamato Y, Ohshimo H, et al. Development of a novel form of an oral 5-fluorouracil derivative (S-1) directed to the potentiation of the tumor selective cytotoxicity of 5-fluorouracil by two biochemical modulators. Anticancer Drugs. 1996;7:548–557. doi: 10.1097/00001813-199607000-00010. [DOI] [PubMed] [Google Scholar]
- 5.Xu RH, Sun GP, Lu HS, et al. A phase III study of S-1 plus cisplatin versus fluorouracil plus cisplatin in patients with advanced gastric or gastroesophageal junction adenocarcinoma. Journal of Clinical Oncology. 2013;31 [Google Scholar]
- 6.Muro K, Boku N, Shimada Y, et al. Irinotecan plus S-1 (IRIS) versus fluorouracil and folinic acid plus irinotecan (FOLFIRI) as second-line chemotherapy for metastatic colorectal cancer: a randomised phase 2/3 non-inferiority study (FIRIS study) Lancet Oncol. 2010;11:853–860. doi: 10.1016/S1470-2045(10)70181-9. [DOI] [PubMed] [Google Scholar]
- 7.Hong YS, Park YS, Lim HY, et al. S-1 plus oxaliplatin versus capecitabine plus oxaliplatin for first-line treatment of patients with metastatic colorectal cancer: a randomised, non-inferiority phase 3 trial. Lancet Oncol. 2012;13:1125–1132. doi: 10.1016/S1470-2045(12)70363-7. [DOI] [PubMed] [Google Scholar]
- 8.Kim GM, Jeung HC, Rha SY, et al. A randomized phase II trial of S-1-oxaliplatin versus capecitabine-oxaliplatin in advanced gastric cancer. Eur J Cancer. 2012;48:518–526. doi: 10.1016/j.ejca.2011.12.017. [DOI] [PubMed] [Google Scholar]
- 9.Lee JL, Kang YK, Kang HJ, et al. A randomised multicentre phase II trial of capecitabine vs S-1 as first-line treatment in elderly patients with metastatic or recurrent unresectable gastric cancer. Br J Cancer. 2008;99:584–590. doi: 10.1038/sj.bjc.6604536. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Zang DY, Chung IJ, Oh HS, Park KU, Lee KH, Han B, Choi DR, Kim HS, Kim JH. Randomized phase II study of oxaliplatin and S-1 (OS) versus oxaliplatin and capecitabine (XELOX) in patients with metastatic or recurrent colorectal cancer. J Clin Oncol. 2012;30:595. [Google Scholar]
- 11.Ba Z, Wu M, Wang LJ, Zhang HQ. Curative effect analysis of S-1 combined with cisplatin or capecitabine combined with cisplatin in the treatment of advanced gastric cancer. Chinese General Practice. 2012;15:672–676. [Google Scholar]
- 12.Lu HM, Zhou LL, Liu JJ, Liu SH. Clinical study of oxaliplatin plus TS-1 or capecitabine in the treatment of advanced colon cancer. Cancer Research and Clinic. 2012;24:613–615. [Google Scholar]
- 13.Qiu GQ, Xu LZ, Lin ZC, Chen YQ. Clinical observation of S-1 in the treatment of old patients with advanced gastric carcinoma. Chin J Clin Oncol Rehabil. 2011;18:61–63. [Google Scholar]
- 14.Sun DS, Zhang GR, Ma LG, Zou YH. The comparative effect of capecitabine and tegafur/gimeracil/oteracil(S-1) on advanced colorectal cancer. Chin J Prim Med Pharm. 2013;20:826–827. [Google Scholar]
- 15.Xiong HL, Liu XQ, Sun AH, He Y, Li J, Yuan X. Clinical comparison of docetaxel combined with S-1 or Capicitabine in treating advanced gastric carcinoma. Modern Oncology. 2013;21:581–584. [Google Scholar]
- 16.Yan Z, Zhao TX, Xing Y, Chen D, He LL. Curative effect analysis of S-1 combined with cisplatin in the treatment of advanced gastric cancer. Progress in Modern Biomedicine. 2012;12:5324–5326. [Google Scholar]
- 17.Zhang HY, Sun LZ. The clinical study of domestic compound Tegafur capsule first-line Therapy for patients with elderly advanced gastric cancer. Medical Innovation of China. 2010;7:94–96. [Google Scholar]
- 18.Tierney JF, Stewart LA, Ghersi D, Burdett S, Sydes MR. Practical methods for incorporating summary time-to-event data into meta-analysis. Trials. 2007;8:16. doi: 10.1186/1745-6215-8-16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Higgins J, Green S. [Accessed August 31, 2013];The Chochrane Collaboration: Cochrane Handbook for Systematic Reviews of Interventions. 2011 http://www.cochranehandbook.org.
- 20.Therasse P, Arbuck SG, Eisenhauer EA, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000;92:205–216. doi: 10.1093/jnci/92.3.205. [DOI] [PubMed] [Google Scholar]
- 21.Tsuburaya A, Morita S, Kodera Y, et al. A randomized phase II trial to elucidate the efficacy of capecitabine plus cisplatin (XP) and S-1 plus cisplatin (SP) as a first-line treatment for advanced gastric cancer: XP ascertainment vs. SP randomized PII trial (XParTS II) BMC Cancer. 2012;12:307. doi: 10.1186/1471-2407-12-307. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Okines AFC, Norman AR, McCloud P, Kang YK, Cunningham D. Meta-analysis of the REAL-2 and ML17032 trials: evaluating capecitabine-based combination chemotherapy and infused 5-fluorouracil-based combination chemotherapy for the treatment of advanced oesophago-gastric cancer. Ann Oncol. 2009;20:1529–1534. doi: 10.1093/annonc/mdp047. [DOI] [PubMed] [Google Scholar]
- 23.Huang J, Cao Y, Wu L, Liao C, He Y, Gao F. S-1-based therapy versus 5-FU-based therapy in advanced gastric cancer: a meta-analysis. Med Oncol. 2011;28:1004–1011. doi: 10.1007/s12032-010-9594-0. [DOI] [PubMed] [Google Scholar]
- 24.Ma Y, Tang L, Wang HX, Xu YC, Ma Y, Zhang FC. Capecitabine for the treatment for advanced gastric cancer: efficacy, safety and ethnicity. J Clin Pharm Ther. 2012;37:266–275. doi: 10.1111/j.1365-2710.2011.01289.x. [DOI] [PubMed] [Google Scholar]
- 25.Ajani JA, Faust J, Ikeda K, et al. Phase I pharmacokinetic study of S-1 plus cisplatin in patients with advanced gastric carcinoma. J Clin Oncol. 2005;23:6957–6965. doi: 10.1200/JCO.2005.01.917. [DOI] [PubMed] [Google Scholar]
- 26.Kong SY, Lim HS, Nam BH, et al. Association of CYP2A6 polymorphisms with S-1 plus docetaxel therapy outcomes in metastatic gastric cancer. Pharmacogenomics. 2009;10:1147–1155. doi: 10.2217/pgs.09.48. [DOI] [PubMed] [Google Scholar]
- 27.Fuse N, Fukuda H, Yamada Y, et al. Updated results of randomized phase III study of 5-fluorouracil (5-FU) alone versus combination of irinotecan and cisplatin (CP) versus S-1 alone in advanced gastric cancer (JCOG 9912) J Clin Oncol (ASCO Annual Meeting abstracts) 2009;27:4514. [Google Scholar]
- 28.Ajani JA, Rodriguez W, Bodoky G, et al. Multicenter phase III comparison of cisplatin/S-1 with cisplatin/infusional fluorouracil in advanced gastric or gastroesophageal adenocarcinoma study: the FLAGS trial. J Clin Oncol. 2010;28:1547–1553. doi: 10.1200/JCO.2009.25.4706. [DOI] [PubMed] [Google Scholar]