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