School of Health and Care Professions, University of Portsmouth, Portsmouth, UK.
Center for Integrative Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Cochrane Database Syst Rev. 2022 Nov 29;11(11):CD012053. doi: 10.1002/14651858.CD012053.pub2.
Radiotherapy and chemotherapy are used to improve survival in colorectal cancer but adverse effects can be a problem. Severe adverse effects may result in dose reduction or cessation of treatment, which have an impact on survival. Coriolus versicolor (Trametes versicolor or 'Turkey Tail') mushroom and its extracts have been used by cancer patients to help with adverse effects.
To assess the effects of adjunctive Coriolus versicolor (Trametes versicolor) and its extracts on adverse effects and on survival during colorectal cancer treatment (chemotherapy and radiotherapy) compared with no adjunctive treatment.
We searched databases including CENTRAL, MEDLINE, Embase, AMED and CINAHL, Chinese and Japanese databases, and trials registers to 12th April 2022 without restriction of language or publication status. We screened reference lists and attempted to contact researchers in the field to identify additional studies.
We included randomised controlled trials (RCTs) investigating the efficacy and safety of Coriolus versicolor and its extracts in adult participants with a confirmed diagnosis of colorectal cancer, in addition to conventional treatment. Interventions included any preparation of Coriolus versicolor (raw, decoction, capsule, tablet, tincture, extract, injection), any part of the fungus (cap, stem, mycelium or whole), in any dose or regimen. Outcomes included adverse events rates, survival, disease progression and recurrence, response rates and quality of life.
Two review authors independently screened and selected studies, extracted outcome data, and assessed risk of bias. We evaluated the overall certainty of evidence using the GRADE approach.
We included seven parallel RCTs (1569 participants). Six studies (1516 participants) were conducted in Japan and one study (53 participants) in China. Studies included both male and female participants with colorectal cancer (five studies), colon cancer (one study) or rectal cancer (one study). Participants were diagnosed with cancer ranging from stage II to stage IV. Coriolus was used in the form of an extract in all seven studies and was generally used after curative resection, although in one study it was used preoperatively. Duration of treatment with the extract varied between four weeks and three years. Chemotherapeutic regimens in six studies consisted of an oral fluoropyrimidine which was preceded by weekly intravenous 5-Fluorouracil (5-FU) in one study, by mitomycin C in two studies, and which was combined with folinic acid (Leucovorin) in two studies and with radiotherapy preoperatively in one study. XELOX (oxaliplatin intravenous infusion and capecitabine) was used in the remaining study. We found very low-certainty evidence of little to no effect of adjunctive treatment with Coriolus (in the form of an extract, polysaccharide-Krestin, PSK) on withdrawal from treatment due to adverse events (risk ratio (RR) 1.03, 95% confidence interval (CI) 0.45 to 2.34; 703 participants; 3 studies;). We are uncertain whether adjunctive Coriolus versicolor and its extracts compared to usual care alone resulted in a difference in adverse events including neutropenia (RR 0.41, 95% CI 0.24 to 0.71; 133 participants; 3 studies; very low certainty), oral cavity disorders such as oral dryness and mucositis (RR 0.37, 95% CI 0.13 to 1.03; 1022 participants; 5 studies; very low certainty), nausea (RR 0.73, 95% CI 0.44 to 1.22; 969 participants; 4 studies; very low certainty), diarrhoea (RR 0.77, 95% CI 0.32 to 1.86; 1022 participants; 5 studies; very low certainty), and fatigue (RR 0.76; 95% CI 0.33 to 1.78; 133 participants; 3 studies; very low certainty). We found low-certainty evidence of a small effect of adjunctive Coriolus on improved survival at five years compared with no adjunctive care (RR 1.08, 95% CI 1.01 to 1.15; 1094 participants; 3 studies; number needed to benefit (NNTB) = 16 (95% Cl 9 to 70). The effect at earlier time points was unclear.
AUTHORS' CONCLUSIONS: Due to the very low certainty of evidence, we were uncertain about the effect of adjunctive Coriolus (in the form of an extract PSK) on adverse events resulting from conventional chemotherapy for colorectal cancer. This includes effects on withdrawal of treatment due to adverse events and on specific adverse outcomes such as neutropenia and nausea. The uncertainty in the evidence also means that it was unclear whether any adverse events were due to the chemotherapy or to the extract itself. While there was low-certainty evidence of a small effect on overall survival at five years, the influence of reduced adverse effects on this could not be determined. In addition, chemotherapy regimens used in assessing this outcome do not reflect current preferred practice.
放疗和化疗可用于提高结直肠癌患者的生存率,但也可能出现不良反应。严重的不良反应可能导致剂量减少或治疗中断,从而影响生存。云芝(彩绒革盖菌或“土耳其尾巴”)蘑菇及其提取物已被癌症患者用于缓解不良反应。
评估辅助云芝(彩绒革盖菌)及其提取物对结直肠癌(化疗和放疗)治疗期间不良反应和生存的影响,与无辅助治疗相比。
我们检索了包括 CENTRAL、MEDLINE、Embase、AMED 和 CINAHL 在内的数据库,以及中国和日本的数据库和试验注册处,检索截至 2022 年 4 月 12 日,不限制语言或出版状态。我们筛选了参考文献列表,并试图联系该领域的研究人员以确定其他研究。
我们纳入了随机对照试验(RCT),这些试验调查了常规治疗外加云芝及其提取物对成人确诊结直肠癌患者的疗效和安全性。干预措施包括任何形式的云芝(生、煮、胶囊、片剂、酊剂、提取物、注射液),任何部分的真菌(帽、茎、菌丝体或全株),任何剂量或方案。结局包括不良反应发生率、生存、疾病进展和复发、反应率和生活质量。
两名综述作者独立筛选和选择研究,提取结局数据,并评估偏倚风险。我们使用 GRADE 方法评估证据的总体确定性。
我们纳入了 7 项平行 RCT(1569 名参与者)。其中 6 项研究(1516 名参与者)在日本进行,1 项研究(53 名参与者)在中国进行。这些研究包括结直肠癌(5 项研究)、结肠癌(1 项研究)或直肠癌(1 项研究)的男性和女性参与者。参与者的癌症诊断为 II 期至 IV 期。云芝在所有 7 项研究中均以提取物的形式使用,通常在根治性切除术后使用,但在一项研究中,它在术前使用。提取物治疗的持续时间在四周至三年之间不等。在 6 项研究中,化疗方案包括口服氟嘧啶,其中一项研究每周静脉注射 5-氟尿嘧啶(5-FU),两项研究使用丝裂霉素 C,两项研究联合使用叶酸(亚叶酸),一项研究在术前联合放疗。另一项研究使用 XELOX(奥沙利铂静脉输注和卡培他滨)。我们发现,辅助治疗(以提取物、多糖 Krestin、PSK 的形式)对因不良反应而停止治疗的影响,证据质量非常低,几乎没有效果(风险比(RR)1.03,95%置信区间(CI)0.45 至 2.34;703 名参与者;3 项研究)。我们不确定与单独使用常规治疗相比,辅助使用云芝及其提取物是否会导致不良反应(包括中性粒细胞减少症、口腔干燥和粘膜炎、恶心、腹泻和疲劳)的差异(RR 0.41,95%CI 0.24 至 0.71;133 名参与者;3 项研究;非常低的确定性)。
由于证据的确定性非常低,我们不确定辅助使用云芝(以提取物 PSK 的形式)对结直肠癌常规化疗引起的不良反应是否有影响。这包括因不良反应而停止治疗以及中性粒细胞减少症和恶心等特定不良反应的影响。证据的不确定性也意味着,尚不清楚任何不良反应是由化疗还是提取物本身引起的。虽然有低确定性证据表明,在五年时总体生存率有较小的影响,但无法确定减少不良反应对这一结果的影响。此外,用于评估这一结果的化疗方案并不反映当前的首选治疗方法。