Copyright
©The Author(s) 2015.
World J Meta-Anal. Jun 26, 2015; 3(3): 163-180
Published online Jun 26, 2015. doi: 10.13105/wjma.v3.i3.163
Published online Jun 26, 2015. doi: 10.13105/wjma.v3.i3.163
Table 1 The Preferred Reporting Items for Systematic Review and Meta-Analysis checklist
Section/topic | n | Checklist item | Reported on page |
Title | |||
Title | 1 | Identify the report as a systematic review, meta-analysis, or both | 1 |
Abstract | |||
Structured summary | 2 | Provide a structured summary including, as applicable: background; objectives; data sources; study eligibility criteria, participants, and interventions; study appraisal and synthesis methods; results; limitations; conclusions and implications of key findings; systematic review registration number | 2 |
Introduction | |||
Rationale | 3 | Describe the rationale for the review in the context of what is already known | 3 |
Objectives | 4 | Provide an explicit statement of questions being addressed with reference to PICOS | 3-4 |
Methods | |||
Protocol and registration | 5 | Indicate if a review protocol exists, if and where it can be accessed (e.g., Web address), and, if available, provide registration information including registration number | |
Eligibility criteria | 6 | Specify study characteristics (e.g., PICOS, length of follow-up) and report characteristics (e.g., years considered, language, publication status) used as criteria for eligibility, giving rationale | 5 |
Information sources | 7 | Describe all information sources (e.g., databases with dates of coverage, contact with study authors to identify additional studies) in the search and date last searched | 5 |
Search | 8 | Present full electronic search strategy for at least one database, including any limits used, such that it could be repeated | 5-6, Table 2 |
Study selection | 9 | State the process for selecting studies (i.e., screening, eligibility, included in systematic review, and, if applicable, included in the meta-analysis) | 6-7 |
Data collection process | 10 | Describe method of data extraction from reports (e.g., piloted forms, independently, in duplicate) and any processes for obtaining and confirming data from investigators | 7 |
Data items | 11 | List and define all variables for which data were sought (e.g., PICOS, funding sources) and any assumptions and simplifications made | 7 |
Risk of bias in individual studies | 12 | Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or outcome level), and how this information is to be used in any data synthesis | 6-7 |
Summary measures | 13 | State the principal summary measures (e.g., risk ratio, difference in means) | 7 |
Synthesis of results | 14 | Describe the methods of handling data and combining results of studies, if done, including measures of consistency (e.g., I2) for each meta-analysis | 7 |
Table 2 The PubMed searching strategy
(1) "Complementary therapies" (Mesh) |
(2) Tradition or tradition* OR china or chinese OR herb or herbal OR complement* or tcm or "zhong yi" or chm or ethno* or folk or home or indigenous or primitive or materia* or nosod* or east or eastern or orient or oriental or asian or Korea* or Tibet* or herbaceous or plant or plants or botan* or kampo or mongol* or phytogenic or phytotherapy or alternative |
(3) Medicine or medicinal or medical or remed* or therapy or therapies or therapeutic or therapeutics or therapist or treat or treatment or drug or drugs |
(4) (2) and (3) |
(5) (1) or (4) |
(6) Leukemia or lymphoma or "multiple myeloma" (mesh) |
(7) Hemotolog* or anemia or thrombocytopen* or pancytope* or "bone marrow" or transplant or "stem cell" |
(8) Leukemia OR lymphoma OR cancer OR dysplas* OR malignant OR hyperplas* OR hypoplas* or myelom* or Hodgkin or non-hodgkin or blast or blasts or "progression free survival" or "disease free survival" or "overall survival" or OS or PFS or DFS or chemotherapy or (chemical treatment) or radiotherapy or irradia* or oncolog* or monoclon* |
(9) (7) and (8) |
(10) (6) or (9) |
(11) (((((Randomized controlled trial [Publication type]) OR controlled clinical trial [Publication type]) OR (randomized or placebo[Title/Abstract])) OR drug therapy [MeSH Subheading]) OR (randomly or groups or trial [Title/Abstract])) OR rct |
(12) Animals [mh] NOT humans [mh] |
(13) (11) not (12) |
(14) (5) and (10) and (13) |
(15) (Cancer or carcinoma or sarcoma)[ti] |
(16) Carcinoma[mesh] or sarcoma[mesh] |
(17) (14) not (15) or (16) |
Table 3 Characteristics of Dian Rong 2009 study
Methods | A randomized double blind placebo controlled I multicenter study |
Participants | Refractory acute leukemia patients |
Interventions | TCM group: Combine Chinese interventions with standard chemotherapy of western medicine |
Control group: Standard chemotherapy with western medicine | |
Outcomes | The primary outcome: the response rate |
Table 4 Risk assessment of Dian Rong 2009 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Central randomized |
Comment: Probably done. Several studies published by this research group reported reliable randomization method | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Low risk | Quote: A double-blind and placebo controlled |
All outcomes | Comment: Probably done. Several studies published by this research group reported reliable method to warrant the double blindness | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: Mortality and survival time are objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 5 Characteristics of Xiu Mei 1997 study
Methods | A randomized controlled study |
Participants | Non-Hodgkin lymphoma patients |
Interventions | TCM group: Standard chemotherapy + traditional Chinese medicine |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 6 Risk assessment of Xiu Mei 1997 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: The random sequence produced by rolling the dice |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: Mortality and survival is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 7 Characteristics of Ji Hong 2011 study
Methods | A randomized controlled study |
Participants | Initial treat old AML patients |
Interventions | TCM group: HAG + TCM |
Control group: HAG | |
Outcomes | The primary outcome: The overall response rate |
Table 8 Risk assessment of Ji Hong 2011 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Use the random number table to get the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Low risk | Quote: 7 participants in 53 randomized lost to follow-up |
All outcomes | Comment | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 9 Characteristics of Ying Fei 2005 study
Methods | A multicenter double-blinded randomized controlled study |
Participants | Initial treat leukemia patients |
Interventions | TCM group: standard chemotherapy + Shen Qi Fu Zheng Ye |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 10 Risk assessment of Ying Fei 2005 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Generate randomization sequence by drawing lots |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 11 Characteristics of Wen Jiang 2010 study
Methods | A randomized placebo controlled study |
Participants | Initial treat acute leukemia patients |
Interventions | TCM group: Standard chemotherapy + Shen Qi Qing Re Ke Li |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 12 Risk assessment of Wen Jiang 2010 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Use the random number table to get the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 13 Characteristics of Su Juan 2005 study
Methods | A multicenter randomized controlled study |
Participants | Acute leukemia |
Interventions | TCM group: Standard chemotherapy + TCM Qing Re Jie Du Kang Bai Fang |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 14 Risk assessment of Su Juan 2005 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Use the random number table to get the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 15 Characteristics of Mao Sheng 2007 study
Methods | A multicenter double-blinded randomized placebo controlled study |
Participants | Acute myeloid leukemia patients with micro residual disease |
Interventions | TCM group: Standard chemotherapy + Yi Qi Jie Du Huo Xue Fang |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 16 Risk assessment of Mao Sheng 2007 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Use the random number table to get the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 17 Characteristics of Rui Rong 2004 study
Methods | A multicenter double-blinded randomized placebo controlled study |
Participants | Acute myeloid leukemia |
Interventions | TCM group: Standard chemotherapy + Yi Qi Yang Yin Qing Re Fa |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 18 Risk assessment of Rui Rong 2004 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Use the random number table to get the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 19 Characteristics of Chuan Xin 2013 study
Methods | A randomized controlled study |
Participants | Child acute myeloid leukemia patients |
Interventions | TCM group: Standard chemotherapy + traditional Chinese medicine |
Control group: Standard chemotherapy | |
Outcomes | The primary outcome: The overall response rate |
Table 20 Risk assessment of Chuan Xin 2013 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Use the random number table to get the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: The response rate is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 21 Characteristics of sWei Hong 2013 study
Methods | A randomized controlled study |
Participants | Chronic myeloid leukemia patients |
Interventions | TCM group: A-interferon or hydroxyurea + TCM |
Control group: A-interferon or hydroxyurea | |
Outcomes | The primary outcome: The response rate |
Table 22 Risk assessment of sWei Hong 2013 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: The random number table was used to generate the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: Mortality and survival is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 23 Characteristics of sHai Yan 2007 study
Methods | A randomized controlled study |
Participants | Chronic myeloid leukemia patients |
Interventions | Traditional Chinese medicine group: Hydroxyurea + traditional Chinese medicine |
Control group: Hydroxyurea | |
Outcomes | The primary outcome: The response rate |
Table 24 Risk assessment of sHai Yan 2007 study
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: The random number table was used to generate the allocation sequence |
Comment: Probably done | ||
Allocation concealment (selection bias) | Unclear | Quote: Not mentioned |
Comment: Unclear | ||
Blinding of participants and personnel (performance bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Blinding of outcome assessment (detection bias) | Low risk | Quote: Not mentioned |
All outcomes | Comment: Mortality and survival is an objective parameter. Subjective judgement can not influent the result | |
Incomplete outcome data (attrition bias) | Unclear | Quote: Not mentioned |
All outcomes | Comment: Unclear | |
Selective reporting (reporting bias) | Low risk | The primary outcome listed in the method section are all reported |
Comment: Probably done | ||
Other bias | Unclear | The study did not use the intention to treat strategy to analyze the result |
Table 25 Characteristics of included studies
Studies | Age | Sex (male:female) | Race | Disease | No. of participants | Intervention | Published | |
(TCM:control) | TCM | Control | language | |||||
Dian Rong 2009[15,21,25,31,33] | TCM 39.52 ± 18.87 | TCM 50:21 | Chinese | Acute leukemia | 71:66 | Compound Zhe Bei granule + | Placebo + standard | English |
Control 37.94 ± 18.55 | Control 39:27 | standard chemotherapy | chemotherapy | |||||
Mao Sheng 2007[26,27] | TCM 35.63 ± 6.46 | TCM 33:27 | Chinese | Acute myeloid leukemia | 60:60 | Yi Qi Jie Du Huo Xue decoction | Standard western | Chinese |
Control 36.57 ± 7.38 | Control 31:29 | + standard western mechicine | mechicine | |||||
sHai Yan 2007[22] | TCM 18-65 | TCM 5:3 | Chinese | Chronic myelogenous leukemia | 8:10 | Qu Du Hua Yu decoction | Hydroxyurea | Chinese |
Control 19-63 | Control 7:3 | + hydroxyurea | ||||||
sWei Hong 2013[23] | TCM 25-60 | TCM 22:14 | Chinese | Chronic myelogenous leukemia | 22:17 | TCM + interferon-α | Interferon-α | Chinese |
Control 25-65 | Control 17:7 | |||||||
Chuan Xin 2013[32] | TCM 4.30 ± 1.81 | TCM 12:8 | Chinese | Pediatric acute myeloid leukemia | 20:20 | TCM + standard chemotherapy | Standard chemotherapy | Chinese |
Control 4.95 ± 2.04 | Control 10:10 | |||||||
Ji Hong 2011[34] | TCM 60-71 | TCM 16:16 | Chinese | Elderly acute myeloid leukemia | 32:28 | TCM + HAG chemotherapy | HAG chemotherapy | Chinese |
Control 61-72 | Control 15:13 | |||||||
Rui Rong 2004[29] | TCM 12-78 | TCM 40:28 | Chinese | Acute myeloid leukemia | 68:46 | TCM + standard chemotherapy | Standard chemotherapy | Chinese |
Control 11-76 | Control 27:19 | |||||||
Su Juan 2005[24] | TCM 32.5 ± 12.45 | TCM 16:14 | Chinese | Acute leukemia | 30:30 | Qing Re Jie Du kang Bai decoction | Standard chemotherapy | Chinese |
Control 31.53 ± 12.41 | Control 17:13 | + standard chemotherapy | ||||||
Wen Jiang 2010[30] | TCM 47-78 | TCM 17:12 | Chinese | Acute myeloid leukemia | 29:28 | Shen Qi Qing Re Ke Li | HAG chemotherapy | Chinese |
Control 46-79 | Control 15:13 | + HAG chemotherapy | ||||||
Xiu Mei 1997[35] | TCM 6-73 | TCM 72:40 | Chinese | Non-Hodgkin lymphoma | 112:55 | TCM + standard chemotherapy | Standard chemotherapy | Chinese |
Control 6-71 | Control 36:19 | |||||||
Ying Fei 2005[28] | TCM 13-72 | TCM 22:10 | Chinese | Acute leukemia | 32:33 | Shen Qi Fu Zheng | Standard chemotherapy | Chinese |
Control 15-71 | Control 25:8 | injection + standard chemotherapy |
Table 26 Quality assessment of included studies
Studies | Random sequence generation | Allocation concealment | Blinding of participants and | Blinding of outcome | Incomplete outcome | Selective reporting | Other bias |
(selection bias) | (selection bias) | personnel (performance bias) | assessment (detection bias) | data (attrition bias) | (reporting bias) | ||
All outcomes | All outcomes | All outcomes | |||||
Dian Rong 2009[15,21,25,31,33] | Low risk | Unclear | Low risk | Low risk | Unclear | Low risk | Unclear |
Mao Sheng 2007[26,27] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
sHai Yan 2007[22] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
sWei Hong 2013[23] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
Chuan Xin 2013[32] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
Ji Hong 2011[34] | Low risk | Unclear | Unclear | Low risk | Low risk | Low risk | Unclear |
Rui Rong 2004[29] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
Su Juan 2005[24] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
Wen Jiang 2010[30] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
Xiu Mei 1997[35] | Low risk | Unclear | Unclear | Unclear | Unclear | Low risk | Unclear |
Ying Fei 2005[28] | Low risk | Unclear | Unclear | Low risk | Unclear | Low risk | Unclear |
Table 27 Summary of findings of the overall response and complete response outcomes
Outcomes | Illustrative comparative risks1 (95%CI) | Relative effect | No. of participants | Quality of the evidence | Comments | |
Assumed risk | Corresponding risk | (95%CI) | (studies) | (GRADE) | ||
Control | Overall response rate | |||||
Overall response rate | Study population | RR = 1.14 | 974 | ++-- | ||
761 per 1000 | 867 per 1000 (784-959) | (1.03-1.26) | (12 studies) | Low | ||
Moderate | ||||||
775 per 1000 | 883 per 1000 (798-976) | |||||
Complete response rate | Study population | RR = 1.21 | 974 | ++-- | ||
579 per 1000 | 701 per 1000 (579-846) | (1-1.46) | (12 studies) | Low23 | ||
Moderate | ||||||
579 per 1000 | 701 per 1000 (579-845) | |||||
Overall response rate for malignant hematologic disease | ||||||
Patient or population: Patients with malignant hematologic disease | ||||||
Settings: | ||||||
Intervention: Overall response rate |
- Citation: Qian CL, Yan F, Song YZ, Li D, Dong KZ, Zhu YM. Is the traditional Chinese medicine helpful for patients with hematologic malignant diseases? A meta-analysis of randomized controlled trials. World J Meta-Anal 2015; 3(3): 163-180
- URL: https://www.wjgnet.com/2308-3840/full/v3/i3/163.htm
- DOI: https://dx.doi.org/10.13105/wjma.v3.i3.163