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Hierbas medicinales chinas para el cáncer esofágico

Información

DOI:
https://doi.org/10.1002/14651858.CD004520.pub7Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 22 enero 2016see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Salud digestiva

Copyright:
  1. Copyright © 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Contraer

Autores

  • Xi Chen

    Department of Clinical Pharmacy and Pharmacy Administration, West China School of Pharmacy, Sichuan University, Chengdu, China

  • Linyu Deng

    National Key Laboratory of Biotherapy and Cancer Centre, West China Hospital, Sichuan University, Chengdu, China

  • Xuehua Jiang

    Department of Clinical Pharmacy and Pharmacy Administration, West China School of Pharmacy, Sichuan University, Chengdu, China

  • Taixiang Wu

    Correspondencia a: Chinese Clinical Trial Registry, Chinese Ethics Committee of Registering Clinical Trials, West China Hospital, Sichuan University, Chengdu, China

    [email protected]

Contributions of authors

Xin Wei (XW), Zhiyu Chen (ZC) and Taixiang Wu (TW) were responsible for development of the protocol.

Xi Chen (XC), Linyu Deng (LD) and TW were responsible for searching for trials, quality assessment of the trials, data extraction, data analysis and review development. TW interviewed the original trial authors of self described "RCTs" included in the initial version of this review. XC and Xuehua Jiang (XJ) interviewed the trial authors of this version of the review.

Sources of support

Internal sources

  • Chinese Cochrane Centre, West China Hospital of Sichuan University, China.

External sources

  • Chinese Medical Board of New York (CMB), USA.

Declarations of interest

XC: none known.

LD: none known.

XJ: none known.

TW: none known.

Acknowledgements

The authors would like to thank Karin Dearness, Janet Lilleyman, Iris Gordon, Cathy Bennett and Racquel Simpson of the Cochrane Upper Gastrointestinal and Pancreatic Diseases (UGPD) Group, and peer referees Professors Sheila Greenfield, Liz Gardener, Edzard Ernst, David Kirby, Miguel Sanchez Gonzalez, Weidong Lu, Chun‐Tao Che, Sarah Rhodes and Jane Blazeby for advice on writing this review. We also thank authors of the included studies who patiently discussed the trials with XC and provided information of their studies.

Version history

Published

Title

Stage

Authors

Version

2016 Jan 22

Chinese herbal medicine for oesophageal cancer

Review

Xi Chen, Linyu Deng, Xuehua Jiang, Taixiang Wu

https://doi.org/10.1002/14651858.CD004520.pub7

2009 Oct 07

Chinese herbal medicines for esophageal cancer

Review

Xin Wei, Zhiyu Chen, Xiaoyan Yang, Taixiang Wu

https://doi.org/10.1002/14651858.CD004520.pub6

2009 Jul 08

Medicinal herbs for esophageal cancer

Review

Xin Wei, Zhiyu Chen, Xiaoyan Yang, Taixiang Wu

https://doi.org/10.1002/14651858.CD004520.pub5

2007 Jul 18

Medicinal herbs for esophageal cancer

Review

W ei Xin, C hen Zhiyu, W u Taixiang, Y ang Xiaoyan, L iu Guanjian, Taixiang Wu, Guanjian Liu, Xiaoyan Yang, Xin Wei, Zhiyu Chen

https://doi.org/10.1002/14651858.CD004520.pub4

2007 Apr 18

Medicinal herbs for esophageal cancer

Review

Xin Wei, Zhiyu Chen, Xiaoyan Yang, Taixiang Wu

https://doi.org/10.1002/14651858.CD004520.pub3

2007 Jan 24

Medicinal herbs for esophageal cancer

Review

WU Taixiang, X Wei, Xiaoyan Yang, Chen Zhiyu

https://doi.org/10.1002/14651858.CD004520.pub2

2003 Oct 20

Medicinal herbs for esophageal cancer

Protocol

Zhiyu Chen, T Wu, X Yang, J Wei, Q Wang, G Liu, Wu Taixiang, LIU Guanjian, WEI Jiafu, Wang Qin, YANG Xiaoyan

https://doi.org/10.1002/14651858.CD004520

Differences between protocol and review

  1. We changed the title of the review from 'Medicinal herbs for oesophageal cancer' to 'Chinese herbal medicine for oesophageal cancer.'

  2. Types of studies: we had intended to include cross‐over trials and within‐patient studies, but limited our review to only RCTs comparing radiotherapy or chemotherapy with or without additional Chinese herbal medicine.

  3. Types of interventions: we revised and limited control treatment 'other treatments that are widely used by the doctors for oesophageal cancer' to 'active cancer therapy such as radiotherapy or chemotherapy'. We changed 'Chinese medicinal herbs are used by oral intake' to 'Water extractions of TCM were administered either orally (in capsules or as powders) or by intravenous infusion'. These revised inclusion criteria are more common in clinical studies.

  4. Types of outcome measures: we added 'Improvement, defined as complete response (CR) and partial response (PR) as clarified by Miller 1981 or short‐term therapeutic effects or TCM symptoms' to the 'Secondary outcomes'.

  5. Search strategy: we changed from the Chinese Biomedical Database and CISCOM (the Research Council for Complementary Medicine) to the VIP and Wanfang databases.

  6. We added effect of time‐to‐events data analysis to the 'Measures of treatment effect' section, and added 'GRADE and Summary of findings' tables.

  7. We revised and rewrote the 'Assessment of risk of bias in included studies', 'Subgroup analysis and investigation of heterogeneity', and 'Sensitivity analysis' sections.

Keywords

MeSH

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Study flow diagram.
Figuras y tablas -
Figure 1

Study flow diagram.

Flow diagram of telephone interviews.
Figuras y tablas -
Figure 2

Flow diagram of telephone interviews.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 3

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 4

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 1 Quality of life.
Figuras y tablas -
Analysis 1.1

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 1 Quality of life.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 2 Quality of life.
Figuras y tablas -
Analysis 1.2

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 2 Quality of life.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 3 Short‐term therapeutic effects.
Figuras y tablas -
Analysis 1.3

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 3 Short‐term therapeutic effects.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 4 TCM symptoms.
Figuras y tablas -
Analysis 1.4

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 4 TCM symptoms.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 5 Adverse events.
Figuras y tablas -
Analysis 1.5

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 5 Adverse events.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 6 Cancer bio‐markers.
Figuras y tablas -
Analysis 1.6

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 6 Cancer bio‐markers.

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 7 Weight.
Figuras y tablas -
Analysis 1.7

Comparison 1 Cancer therapy alone versus cancer therapy plus TCM, Outcome 7 Weight.

Summary of findings for the main comparison. Active cancer therapy combined with TCM compared to active cancer therapy for oesophageal cancer

Active cancer therapy combined with TCM compared to active cancer therapy for oesophageal cancer

Patient or population: patients with oesophageal cancer
Settings: inpatient, hospital in china
Intervention: active cancer therapy combined with TCM
Comparison: active cancer therapy

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Usual treatment

Usual treatment combined with TCM

All‐cause mortality ‐ not reported

See comment

See comment

Not estimable

See comment

Not investigated

Median survival times ‐ not reported

See comment

See comment

Not estimable

See comment

Not investigated

Time to progression ‐ not reported

See comment

See comment

Not estimable

See comment

Not investigated

Quality of life ‐ number experiencing improvement
Measured with Karnofsky performance status or the formulation of National Co‐operative Oncology Group quality of life scale

Study population

RR 2.2
(1.42 to 3.39)

233
(5 studies)

⊕⊕⊝⊝
low1,2,3

190 per 1000

417 per 1000
(269 to 643)

Moderate

177 per 1000

389 per 1000
(251 to 600)

Quality of life ‐ number experiencing deterioration
Measured with Karnofsky performance status or the formulation of National Co‐operative Oncology Group quality of life scale

Study population

RR 0.41
(0.27 to 0.62)

287
(6 studies)

⊕⊕⊝⊝
low1,2,3

401 per 1000

165 per 1000
(108 to 249)

Moderate

397 per 1000

163 per 1000
(107 to 246)

Quality of life ‐ Karnofsky performance status
Karnofsky status judged by clinicians. Scale: 0 to 100

See comment

See comment

Not estimable

60
(1 study)

⊕⊕⊝⊝
low2

Short‐term therapeutic effects ‐ improvement (complete response +

partial response)
Measured with the solid tumours response evaluation criteria 5

Study population

RR 1.17
(1.02 to 1.35)

450
(8 studies)

⊕⊕⊕⊝
moderate4

538 per 1000

630 per 1000
(549 to 726)

Moderate

571 per 1000

668 per 1000
(582 to 771)

Short‐term therapeutic effects ‐ progressive disease
Measured with the solid tumours response evaluation criteria 5

Study population

RR 0.73
(0.52 to 1.01)

450
(8 studies)

⊕⊕⊝⊝
low2,4

211 per 1000

154 per 1000
(110 to 213)

Moderate

172 per 1000

126 per 1000
(89 to 174)

TCM symptoms ‐

total effectiveness
Assessed with TCM clinical criteria

Study population

RR 1.84
(1.20 to 2.81)

88
(2 studies)

⊕⊝⊝⊝
very low2,6

477 per 1000

878 per 1000
(573 to 1000)

Moderate

471 per 1000

867 per 1000
(565 to 1000)

TCM symptoms ‐ ineffectiveness
Assessed with TCM clinical criteria

Study population

RR 0.22
(0.05 to 0.93)

88
(2 studies)

⊕⊝⊝⊝
very low3,6,7

523 per 1000

115 per 1000
(26 to 486)

Moderate

529 per 1000

116 per 1000
(26 to 492)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RCT: randomised controlled trial; RR: risk ratio; TCM: traditional Chinese medicine

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 The studies were parallel‐group RCTs, but not blinded. The outcome may be affected by the subjective effect of the researcher, thereby resulting in very serious limitations.
2 Studies include relatively few patients and few events and have wide confidence intervals around the estimate of the effect.
3 RR > 2.0 or RR < 0.5; the effect was large.
4 The outcome included parallel‐group RCTs, but not blinded; the result may have serious limitations.
5 One study used the WanJun evaluation criteria, five studies used the WHO Response Evaluation Criteria in Solid Tumours and two studies used the New Response Evaluation Criteria in Solid Tumours (RECIST).
6 Non‐blinding and did not conceal allocation. TCM clinical criteria was ambiguous; the outcome may be more affected by the researcher, who prepared the TCM, so the risk of bias was very serious.
7 Studies include relatively few patients and few events and there was very serious imprecision.

Figuras y tablas -
Summary of findings for the main comparison. Active cancer therapy combined with TCM compared to active cancer therapy for oesophageal cancer
Summary of findings 2. Active cancer therapy combined with TCM compared to active cancer therapy for oesophageal cancer

Active cancer therapy combined with TCM compared to active cancer therapy for oesophageal cancer

Patient or population: oesophageal cancer
Settings: inpatient, hospital in china
Intervention: active cancer therapy combined with TCM
Comparison: active cancer therapy

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Usual treatment

Usual treatment combined with TCM

Adverse events ‐ mucositis
Diagnosed by clinicians

Study population

RR 0.92
(0.80 to 1.06)

50
(1 study)

⊕⊕⊝⊝
low1

1000 per 1000

920 per 1000
(800 to 1000)

Moderate

1000 per 1000

920 per 1000
(800 to 1000)

Adverse events ‐ radiation oesophagitis
Assessed with the Common Terminology Criteria for Adverse Events

Study population

RR 0.66
(0.47 to 0.94)

160
(2 studies)

⊕⊕⊝⊝
low2,3

550 per 1000

363 per 1000
(258 to 517)

Moderate

546 per 1000

360 per 1000
(257 to 513)

Adverse events ‐ arrest of bone marrow
Assessed with the World Health Organization drug toxicity evaluation standard

Study population

RR 0.28
(0.14 to 0.58)

90
(1 study)

⊕⊕⊕⊝
moderate1,4

556 per 1000

156 per 1000
(78 to 322)

Moderate

556 per 1000

156 per 1000
(78 to 322)

Adverse events ‐ gastrointestinal reactions
Diagnosed by clinicians

Study population

RR 0.54
(0.36 to 0.81)

268
(4 studies)

⊕⊝⊝⊝
very low1,3

500 per 1000

270 per 1000
(180 to 405)

Moderate

558 per 1000

301 per 1000
(201 to 452)

Adverse events ‐ renal and hepatic impairment ‐ Fuzheng Guben granules
Assessed with the World Health Organization drug toxicity evaluation standard

Study population

RR 0.33
(0.13 to 0.84)

90
(1 study)

⊕⊕⊝⊝
low1

333 per 1000

110 per 1000
(43 to 280)

Moderate

333 per 1000

110 per 1000
(43 to 280)

Adverse events ‐ renal and hepatic impairment‐ Xiaoaiping
Diagnosed by clinicians

Study population

RR 0.90
(0.12 to 6.48)

60
(1 study)

⊕⊕⊝⊝
low1

133 per 1000

120 per 1000
(16 to 864)

Moderate

233 per 1000

210 per 1000
(28 to 1000)

Adverse events ‐ white blood cell descent
Diagnosed by clinicians

Study population

RR 0.60
(0.44 to 0.83)

224
(4 studies)

⊕⊝⊝⊝
very low1,3

486 per 1000

292 per 1000
(214 to 404)

Moderate

446 per 1000

268 per 1000
(196 to 370)

Adverse events ‐ neurotoxicity
Diagnosed by clinicians

Study population

RR 0.73
(0.34 to 1.55)

60
(1 study)

⊕⊕⊝⊝
low1

367 per 1000

268 per 1000
(125 to 568)

Moderate

367 per 1000

268 per 1000
(125 to 569)

Adverse events ‐ cardiac toxicity
Diagnosed by clinicians

Study population

RR 0.80
(0.24 to 2.69)

60
(1 study)

⊕⊕⊝⊝
low1

167 per 1000

133 per 1000
(40 to 448)

Moderate

167 per 1000

134 per 1000
(40 to 449)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RCT: randomised controlled trial; RR: Risk ratio; TCM: traditional Chinese medicine

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 The study was a parallel‐group RCT, but not blinded. The outcome may be affected by the subjective effect of the researcher, thereby resulting in very serious limitations.
2 The outcome included parallel‐group RCTs, but not blinded; the result may have serious limitations.
3 Studies include relatively few patients and few events and have wide confidence intervals around the estimate of the effect.
4 RR > 2.0 or RR < 0.5; the effect was large.

Figuras y tablas -
Summary of findings 2. Active cancer therapy combined with TCM compared to active cancer therapy for oesophageal cancer
Table 1. Traditional Chinese Medicine preparations

Study ID

TCM

Pinyin name

Latin name

English name

Preparation

Chen 2012

Fuzheng

Guben

granules

Huangqi

Dangshen

Shanzha

Chenpi

Nuzhenzi

Buguzhi

Baizhu

Gouqizi

Fuling

Shenqu

Maiya

Jixueteng

Yinchenhao

Tusizi

Radix Astragali

Radix Codonopsis

Fructus Crataegi

Pericarpium Citri Reticulatae

Fructus Ligustri Lucidi

Fructus Psoraleae

Rhizoma Atractylodis Macrocephalae

Fructus Lycii

Poria

Massa Medicata Fermentata

Fructus Hordei Germinatus

Caulis Spatholobi

Herba Artemisiae Scopariae

Semen Cuscutae

Milkvetch Root

Pilose Asiabell Root

Hawthorn Fruit

Tangerine Peel

Glossy Privet Fruit

Malaytea Scurfpea Fruit

Largehead Atractylodes Rhizome

Barbary Wolfberry Fruit

Indian Buead

Medicated Leaven

Malt

Suberect Spatholobus

Virgate Wormwood Herb

South Dodder Seed

Not described in detail

Produced by Gansu Prorincial

Wuwei Tumour Hospital

Cheng 2010

Xihuang Pill

Niuhuang

Ruxiang

Moyao

Shexiang

Calculus Bovis

Olibanum

Myrrha

Moschus

Bezoar

Frankincense

Myrrh

Musk

Frankincense and Myrrh were

treated by vinegar‐processing method

Produced by Beijing Tongrentang

Pharmaceutical Factory

He 2010a

Brucea

Javanica

oil emulsion

YadanzI

Fructus Bruceae

Java Brucea Fruit

Not described in detail

Lin 2013

Xiaoaiping

injection

Wuguteng

Radix Fissistigmae Glaucescentis

Root of Glaucescent Fissistigma

Xiaoaiping injection was extracted

from Glaucescent Fissistigma

Produced by Nanjing Shenghe

Pharmaceutical Co Ltd

Mu 2012

Ren 2013

Kangai

injection

Renshen

Huangqi

Kushen

Radix Ginseng

Radix Astragali

Radix Sophorae Flavescentis

Ginseng

Milkvetch Root

Lightyellow Sophora Root

Not described in detail

Shao2011

Yiqiyangyin

Huatanquyu

decoction

Taizishen

Nanshashen

Beishashen

Maidong

Chenpi

Banxia

Ezhu

Banzhilian

Baihuasheshecao

Zhigancao

Jineijin

Maiya

Guya

Baizhu

Shanyao

Tiandong

Wuweizi

Fuling

Yiyiren

Danggui

Radix Pseudostellariae

Radix Adenophorae

Radix Glehniae

Radix Ophiopogonis

Pericarpium Citri Reticulatae

Rhizoma Pinelliae

Rhizoma Curcumae

Herba Scutellariae Barbatae

Herba Hedyotidis Diffusae

Glycyrrhizae

Endothelium Corneum Gigeriae Galli

Fructus Hordei Germinatus

Fructus Oryzae Germinatus

Rhizoma Atractylodis Macrocephala

Rhizoma Diosscoreae

Radix Asparagi

Fructus Schisandrae

Poria

Semen Coicis

Radix Angelicae Sinensis

Heterophylly Falsestarwort Root

Ladybell Root

Coastal Glehnia Root

Dwarf Lilyturf Tuber

Tangerine Peel

Pinellia Tuber

Zedoary

Barbed Skullcap Herb

Spreading Hedyotis Herb

Radix glycyrrhizae preparata

Chicken's Gizzard‐membrane

Malt

Rice‐grain Sprout

Largehead Atractylodes Rhizome

Common Yam Rhizome

Cochinchinese Asparagus Root

Chinese Magnoliavine Fruit

Indian Buead

Coix Seed

Chinese Angelic

Modification according to symptoms:

Largehead Atractylodes Rhizome

Common Yam Rhizome

Cochinchinese Asparagus Root

Chinese Magnoliavine Fruit

Indian Buead, Coix Seed and Chinese

Angelic

Yiqiyangyin Huatanquyu decoction

was prepared by researchers

of hospital

Wang 2010c

Zhisheng

capsule

Shexiang

Ezhu

Bingpian

Renshen

Niuhuang

Dongcongxiacao

Xiyangshen

Moschus

Rhizoma Curcumae

Borneolum

Radix Ginseng

Calculus Bovis

Cordyceps

Radix Panacis Quinquefolii

Musk

Zedoary

Borneol

Ginseng

Bezoar

Chinese Caterpillar Fungus

American Ginseng

The composition of Zhisheng capsule

contained 16 traditional Chinese

medicines, only 7 of them were given

Produced by the first affiliated Hospital of Henan University of Traditional Chinese Medicine

Wu 2013a

Aidi injection

Renshen,

Ciwujia,

Bianmao,

Huangqi.

Radix Ginseng,

Radix Acanthopanacis Senticosi,

Mylabris,

Radix Astragali.

Ginseng,

Manyprickle Acanto‐Panax Root,

Blister Beetle,

Milkvetch Root.

Not described in detail

Figuras y tablas -
Table 1. Traditional Chinese Medicine preparations
Comparison 1. Cancer therapy alone versus cancer therapy plus TCM

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Quality of life Show forest plot

6

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

1.1 Number experiencing improvement

5

233

Risk Ratio (M‐H, Random, 95% CI)

2.20 [1.42, 3.39]

1.2 Number experiencing deterioration

6

287

Risk Ratio (M‐H, Random, 95% CI)

0.41 [0.27, 0.62]

2 Quality of life Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Totals not selected

2.1 Karnofsky performance status

1

Mean Difference (IV, Random, 95% CI)

0.0 [0.0, 0.0]

3 Short‐term therapeutic effects Show forest plot

8

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

3.1 Improvement

8

450

Risk Ratio (M‐H, Random, 95% CI)

1.17 [1.02, 1.35]

3.2 Progressive disease

8

450

Risk Ratio (M‐H, Random, 95% CI)

0.73 [0.52, 1.01]

4 TCM symptoms Show forest plot

2

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

4.1 Total effectiveness

2

88

Risk Ratio (M‐H, Random, 95% CI)

1.84 [1.20, 2.81]

4.2 Ineffectiveness

2

88

Risk Ratio (M‐H, Random, 95% CI)

0.22 [0.05, 0.93]

5 Adverse events Show forest plot

7

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

5.1 Mucositis

1

50

Risk Ratio (M‐H, Random, 95% CI)

0.92 [0.80, 1.06]

5.2 Radiation oesophagitis

2

160

Risk Ratio (M‐H, Random, 95% CI)

0.66 [0.47, 0.94]

5.3 Arrest of bone marrow

1

90

Risk Ratio (M‐H, Random, 95% CI)

0.28 [0.14, 0.58]

5.4 Gastrointestinal reactions

4

268

Risk Ratio (M‐H, Random, 95% CI)

0.54 [0.36, 0.81]

5.5 Renal and hepatic impairment‐Fuzheng Guben granules

1

90

Risk Ratio (M‐H, Random, 95% CI)

0.33 [0.13, 0.84]

5.6 Renal and hepatic impairment‐Xiaoaiping

1

60

Risk Ratio (M‐H, Random, 95% CI)

2.5 [0.88, 7.10]

5.7 White blood cell descent

4

224

Risk Ratio (M‐H, Random, 95% CI)

0.60 [0.44, 0.83]

5.8 Neurotoxicity

1

60

Risk Ratio (M‐H, Random, 95% CI)

0.73 [0.34, 1.55]

5.9 Cardiac toxicity

1

60

Risk Ratio (M‐H, Random, 95% CI)

0.8 [0.24, 2.69]

5.10 Anaemia

1

40

Risk Ratio (M‐H, Random, 95% CI)

1.33 [0.57, 3.14]

6 Cancer bio‐markers Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Totals not selected

6.1 Carcinoembryonic antigen

1

Mean Difference (IV, Random, 95% CI)

0.0 [0.0, 0.0]

7 Weight Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Totals not selected

7.1 Increased

1

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

7.2 Decreased

1

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 1. Cancer therapy alone versus cancer therapy plus TCM