Kampo (Traditional Japanese Herbal) Formulae for Treatment of Stomatitis and Oral Mucositis
Abstract
1. Introduction
2. Clinical Applications
3. Clinical Studies
4. Basic Studies of HST
5. Conclusions
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
Abbreviations
BKN | Byakkokaninjinto |
COM | chemotherapy-induced oral mucositis |
COX | cyclooxygenase |
HET | Hochuekkito |
HST | Hangeshashinto |
ICT | Inchinkoto |
IL | interleukin |
JTT | Juzentaihoto |
OGT | Orengedokuto |
ORT | Orento |
PG | prostaglandin |
RCT | randomized controlled trial |
ROS | reactive oxygen species |
SST | Shosaikoto |
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Kampo Formulae | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Crude Drug/Japanese Name | Hangeshashinto (HST) | Orento (ORT) | Orengedokuto (OGT) | Byakkokaninjinto (BKN) | Shosaikoto (SST) | Inchinkoto (ICT) | Heiisan (HIS) | Juzentaihoto (JTT) | Hochuekkito (HET) | Antioxidant [7] (mmol/100 g) | Chief Ingredient | Principal Effects | |
Cinnamomi Cortex | Keihi | ◯ | ◯ | ◯ | 120.2 | cinnamaldehyde | antipyresis, perspiration, analgesia | ||||||
Scutellariae Radix | Ogon | ◯ | ◯ | ◯ | 111.5 | baicalin | anti-inflammation, antipyresis, laxative | ||||||
Cimicifugae Rhizoma | Shoma | ◯ | 64.3 | cimigenol | anti-inflammation, antipyresis, analgesia, antiedema | ||||||||
Paeoniae Radix | Shakuyaku | ◯ | ◯ | 55.1 | paeoniflorin | analgesia, spasmolysis, anti-inflammation | |||||||
Aurantii Nobilis Pericarpium | Chinpi | ◯ | ◯ | 17.5 | hesperidin | stomachic, antitussive | |||||||
Glycyrrhizae Radix | Kanzo | ◯ | ◯ | ◯ | ◯ | ◯ | ◯ | ◯ | 11.6 | glycyrrhizin | anti-inflammation, analgesia, detoxification | ||
Zingiberis Rhizoma | Shokyo | ◯ | ◯ | ◯ | 7.5 | gingerol | stomachic, antinausea | ||||||
Atractylodis Lanceae Rhizoma | Sojutsu | ◯ | ◯ | ◯ | 7.4 | atractylodin | anti-inflammation, stomachic, diuresis | ||||||
Cnidii Rhizoma | Senkyu | ◯ | 6.7 | cnidilide | analeptic, nourishing, anti-inflammation, analgesia | ||||||||
Zizyphi Fructus | Taiso | ◯ | ◯ | ◯ | ◯ | ◯ | 5.9 | zizyphus saponin | analeptic, nourishing, stomachic | ||||
Bupleuri Radix | Saiko | ◯ | ◯ | 5.7 | saikosaponin | anti-inflammation, antipyresis | |||||||
Astragali Radix | Ogi | ◯ | ◯ | 4.9 | formononetin | anti-inflammation, analeptic, diuresis, hypotensive | |||||||
Rhemanniae Radix | Jio | ◯ | 3.9 | catalpol | nourishing, diuresis | ||||||||
Angelicae Radix | Toki | ◯ | ◯ | 3.0 | ligustilide | analeptic, nourishing, anti-inflammation, analgesia | |||||||
Hoelen | Bukuryo | ◯ | 2.8 | eburicoic acid | antiedema, stomachic | ||||||||
Ginseng Radix | Ninjin | ◯ | ◯ | ◯ | ◯ | ◯ | ◯ | 1.5 | ginsenoside | stomachic, nourishing, antinausea | |||
Pinelliae Tuber | Hange | ◯ | ◯ | ◯ | 0.3 | homogentisic acid | sedation, antinausea, antitussive | ||||||
Zingiberis Rhizoma Processum | Kankyo | ◯ | ◯ | shogaol | warming, analgesia | ||||||||
Coptidis Rhizoma | Oren | ◯ | ◯ | ◯ | berberine | anti-inflammation, stomachic, antibacterial, spasmolysis | |||||||
Phellodendri Cortex | Obaku | ◯ | berberine | anti-inflammation, stomachic | |||||||||
Gardeniae Fructus | Sanshishi | ◯ | ◯ | geniposide | anti-inflammation, antipyresis, choleresis | ||||||||
Artemisiae Capillaris Flos | Inchinko | ◯ | capillarisin | anti-inflammation, antipyresis, choleresis | |||||||||
Rhei Rhizoma | Daio | ◯ | sennoside | laxative, blood fluidity improving | |||||||||
Magnoliae Cortex | Koboku | ◯ | magnolol | stomachic, analgesia, spasmolysis | |||||||||
Gypsum | Sekko | ◯ | calcium sulfate | anti-inflammation, antipyresis, sedation | |||||||||
Oryzae Fructus | Kobei | ◯ | starch | stomachic, nourishing | |||||||||
Anemarrhenae Rhizoma | Chimo | ◯ | timosaponin AIII | antipyresis, hypoglycemia |
Kampo Formulae | Pathognomonic Symptoms |
---|---|
Hangeshashinto (HST) | multiple stomatitis irritation, anxiety, insomnia, rush of blood to the head, anorexia, diarrhea, epigastric discomfort and resistance |
Orento (ORT) | multiple stomatitis rush of blood to the head, anorexia, decrease in digestive function, abdominal chill symptom, abdominalgia due to chill, epigastric discomfort and resistance |
Orengedokuto (OGT) | multiple stomatitis irritation, insomnia, rush of blood to the head |
Byakkokaninjinto (BKN) | thirstiness, dry mouth hyperidrosis, polyuria |
Shosaikoto (SST) | bitter in the mouth irritation, depression, anorexia, hypochondriac discomfort and distension, nausea |
Inchinkoto (ICT) | multiple stomatitis, dry mouth irritation, insomnia, constipation, oliguria |
Heiisan (HIS) | multiple stomatitis anorexia, decrease in digestive function, abdominal distension |
Juzentaihoto (JTT) | chronic and repetitive stomatitis, dry mouth depressed, fatigue, dullness, macies, hot sensation, night sweat, anemia, anorexia, decrease in digestive function |
Hochuekkito (HET) | chronic and repetitive stomatitis depressed, fatigue, dullness, anorexia, decrease in digestive function |
No. | First Author, Year [Reference No.] | Kampo Formula | Study Design | Target Patient | Principal Result |
---|---|---|---|---|---|
1 | Ogino, 1992 [11] | Shosaikoto (SSK) | case series study | cryptogenic stomatitis (n = 10) | Efficacy rate was 80%. (very effective = 2, effective = 4, slightly effective = 2, no change = 2) |
2 | Oka, 2007 [12] | Orento (ORT) | RCT | acute aphthous stomatitis (n = 39) > non-treated (n = 6), steroid ointment-treated (n = 6) and ORT-treated (n = 27) groups | The administration of Orento reduced the number of days until the disappearance of pain and the complete cure compared to other groups. |
3 | Yuki, 2003 [13] | Orengedokuto (OGT) | case-control (retrospective) study | chemotherapy-induced stomatitis in patients with acute leukemia (n = 40) > ORG-treated (n = 15) and gargling (n = 25) groups | Incidence of stomatitis was 27.9% in the ORG-treated group, which was significantly lower compared with 71.6% in those who received a gargle consisting of allopurinol, sodium gualenate, and povidone-iodine (p < 0.0001). |
4 | Kono, 2010 [14] | Hangeshashinto (HST) | case series study | chemotherapy-induced oral mucositis during mFOLFOX6 or FOLFIRI treatment for metastasis of advanced colorectal cancer (n = 14) | Thirteen patients (92.8%) showed improvements in oral mucositis, with significantly decreased mean CTCAE grades (p = 0.0012). |
5 | Aoyama, 2014 [18] | RCT | gastric cancer chemotherapy-induced oral mucositis (COM) (n = 91) > HST-treated (n = 45) and placebo (n = 46) groups | Although HST treatment did not reduce the incidence of ≥grade 2 COM, a trend was observed in which HST reduced the risk of COM in the patients who developed grade 1 COM. | |
6 | Matsuda, 2015 [15] | RCT | infusional fluorinated-pyrimidine-based colorectal cancer chemotherapy-induced oral mucositis (n = 93) > HST-treated (n = 46) and placebo (n = 47) groups | Although the incidence of grade ≥2 mucositis was lower for patients treated with HST compared to those treated with placebo, there was no significant difference (48.8 vs. 57.4%; p = 0.41). The median duration of grade ≥2 mucositis was 5.5 versus 10.5 days (p = 0.018). | |
7 | Yoshida, 2017 [16] | case series study | cancer chemotherapy-induced oral mucositis (grade ≥ 2) (n = 50) | Thirty-seven patients (74%) showed improvements in oral mucositis, with significantly decreased mean NRS and CTC-grade (p < 0.001). | |
8 | Nishikawa, 2018 [17] | RCT | chemotherapy-induced oral mucositis (COM) in patients with gastric cancer and colorectal cancer (n = 181) > HST-treated (n = 88) and placebo (n = 93) groups | The incidence of grade ≥2 COM in the HST group was 55.7%, while that in the placebo group was 53.8% (p = 0.796). The median time to remission of grade ≥ 2 COM to grade < 1 was 8 days in the HST group and 15 days in the placebo group (p = 0.072). | |
9 | Ohoka, 2018 [19] | RCT | sunitinib-induced oral mucositis (OM) in patients with metastatic renal cancer (n = 22) > HST-gargling (n = 12) and non-gargling (n = 10) groups | The gargling with HST significantly improved OM grade and eating status (Global self assessment) (p = 0.002). | |
10 | Wada, 2004 [20] | Juzentaihoto (JTT) | RCT | radiation (40 Gy >)-induced stomatitis in patients with oral cancer (n = 15) > JTT-treated (n = 8) and non-treated (n = 7) groups | The mean period that patients could not ingest orally was 17.9 ± 7.1 days in the JTT-treated group, while that in the non-treated group was 26.0 ± 11.6 day (p = 0.121). |
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Sunagawa, M.; Yamaguchi, K.; Tsukada, M.; Ebihara, N.; Ikemoto, H.; Hisamitsu, T. Kampo (Traditional Japanese Herbal) Formulae for Treatment of Stomatitis and Oral Mucositis. Medicines 2018, 5, 130. https://doi.org/10.3390/medicines5040130
Sunagawa M, Yamaguchi K, Tsukada M, Ebihara N, Ikemoto H, Hisamitsu T. Kampo (Traditional Japanese Herbal) Formulae for Treatment of Stomatitis and Oral Mucositis. Medicines. 2018; 5(4):130. https://doi.org/10.3390/medicines5040130
Chicago/Turabian StyleSunagawa, Masataka, Kojiro Yamaguchi, Mana Tsukada, Nachi Ebihara, Hideshi Ikemoto, and Tadashi Hisamitsu. 2018. "Kampo (Traditional Japanese Herbal) Formulae for Treatment of Stomatitis and Oral Mucositis" Medicines 5, no. 4: 130. https://doi.org/10.3390/medicines5040130
APA StyleSunagawa, M., Yamaguchi, K., Tsukada, M., Ebihara, N., Ikemoto, H., & Hisamitsu, T. (2018). Kampo (Traditional Japanese Herbal) Formulae for Treatment of Stomatitis and Oral Mucositis. Medicines, 5(4), 130. https://doi.org/10.3390/medicines5040130