Skip to main content
Top
Published in: Cancer Chemotherapy and Pharmacology 1/2015

Open Access 01-07-2015 | Original Article

Double-blind, placebo-controlled, randomized phase II study of TJ-14 (Hangeshashinto) for infusional fluorinated-pyrimidine-based colorectal cancer chemotherapy-induced oral mucositis

Authors: Chu Matsuda, Yoshinori Munemoto, Hideyuki Mishima, Naoki Nagata, Mitsuru Oshiro, Masato Kataoka, Junichi Sakamoto, Toru Aoyama, Satoshi Morita, Toru Kono

Published in: Cancer Chemotherapy and Pharmacology | Issue 1/2015

Login to get access

Abstract

Purpose

Hangeshashinto (TJ-14, a Kampo medicine), which reduces the level of prostaglandin E2 and affects the cyclooxygenase activity, alleviates chemotherapy-induced oral mucositis (COM). We conducted a double-blind, placebo-controlled, randomized comparative trial to investigate whether TJ-14 prevents and controls COM in patients with colorectal cancer.

Methods

Ninety-three patients with colorectal cancer who developed moderate-to-severe COM (WHO grade ≧1) during any cycle of chemotherapy using FOLFOX, FOLFIRI, and/or XELOX treatment were randomly assigned to receive either TJ-14 (n = 46) or placebo (n = 47). Patients received the administration of placebo or TJ-14 for 2 weeks at the start of the next course of chemotherapy. Patients were assessed three times per week for safety and for COM incidence and its severity using the WHO grading.

Results

Ninety eligible patients (TJ-14; 43, placebo; 47) per protocol set analysis were included in the analysis after the key-opening. Although the incidence of grade ≧2 oral mucositis was lower for patients treated with TJ-14 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). No difference in other treatment toxicity was observed between the two groups, and patients exhibited high compliance in dosing administration.

Conclusion

The present study results did not meet the primary endpoint. However, TJ-14 demonstrated a significant effect in the treatment of grade ≧2 mucositis in patients with colorectal cancer compared to the placebo.
Appendix
Available only for authorised users
Literature
1.
go back to reference Keefe DM, Schubert MM, Elting LS, Sonis ST, Epstein JB, Raber-Durlacher JE et al (2007) Mucositis study section of the multinational association of supportive care in cancer and the international society for oral oncology. Updated clinical practice guidelines for the prevention and treatment of mucositis. Cancer 109:820–831PubMedCrossRef Keefe DM, Schubert MM, Elting LS, Sonis ST, Epstein JB, Raber-Durlacher JE et al (2007) Mucositis study section of the multinational association of supportive care in cancer and the international society for oral oncology. Updated clinical practice guidelines for the prevention and treatment of mucositis. Cancer 109:820–831PubMedCrossRef
2.
go back to reference Elting LS, Keefe DM, Sonis ST, Garden AS, Spijkervet FK, Barasch A et al (2008) Burden of illness head and neck writing committee. Patient-reported measurements of oral mucositis in head and neck cancer patients treated with radiotherapy with or without chemotherapy: demonstration of increased frequency, severity, resistance to palliation, and impact on quality of life. Cancer 113:2704–2713PubMedCrossRef Elting LS, Keefe DM, Sonis ST, Garden AS, Spijkervet FK, Barasch A et al (2008) Burden of illness head and neck writing committee. Patient-reported measurements of oral mucositis in head and neck cancer patients treated with radiotherapy with or without chemotherapy: demonstration of increased frequency, severity, resistance to palliation, and impact on quality of life. Cancer 113:2704–2713PubMedCrossRef
3.
go back to reference Rubenstein EB, Peterson DE, Schubert M, Keefe D, McGuire D, Epstein J et al (2004) Mucositis study section of the multinational association for supportive care in cancer; international society for oral oncology. Clinical practice guidelines for the prevention and treatment of cancer therapy-induced oral and gastrointestinal mucositis. Cancer 100:2026–2046PubMedCrossRef Rubenstein EB, Peterson DE, Schubert M, Keefe D, McGuire D, Epstein J et al (2004) Mucositis study section of the multinational association for supportive care in cancer; international society for oral oncology. Clinical practice guidelines for the prevention and treatment of cancer therapy-induced oral and gastrointestinal mucositis. Cancer 100:2026–2046PubMedCrossRef
4.
go back to reference Sonis ST, Elting LS, Keefe D, Peterson DE, Schubert M, Hauer-Jensen M et al (2004) Mucositis study section of the multinational association for supportive care in cancer; international society for oral oncology. Perspectives on cancer therapy-induced mucosal injury: pathogenesis, measurement, epidemiology, and consequences for patients. Cancer 100:1995–2025PubMedCrossRef Sonis ST, Elting LS, Keefe D, Peterson DE, Schubert M, Hauer-Jensen M et al (2004) Mucositis study section of the multinational association for supportive care in cancer; international society for oral oncology. Perspectives on cancer therapy-induced mucosal injury: pathogenesis, measurement, epidemiology, and consequences for patients. Cancer 100:1995–2025PubMedCrossRef
5.
go back to reference Sonis ST (2007) Pathobiology of oral mucositis: novel insights and opportunities. J Support Oncol 5:3–11PubMed Sonis ST (2007) Pathobiology of oral mucositis: novel insights and opportunities. J Support Oncol 5:3–11PubMed
6.
go back to reference Mahood DJ, Dose AM, Loprinzi CL, Veeder MH, Athmann LM, Therneau TM et al (1991) Inhibition of fluorouracil-induced stomatitis by oral cryotherapy. J Clin Oncol 9:449–452PubMed Mahood DJ, Dose AM, Loprinzi CL, Veeder MH, Athmann LM, Therneau TM et al (1991) Inhibition of fluorouracil-induced stomatitis by oral cryotherapy. J Clin Oncol 9:449–452PubMed
7.
go back to reference Cascinu S, Fedeli A, Fedeli SL, Catalano G (1994) Oral cooling (cryotherapy), an effective treatment for the prevention of 5-fluorouracil-induced stomatitis. Eur J Cancer B Oral Oncol 30B:234–236PubMedCrossRef Cascinu S, Fedeli A, Fedeli SL, Catalano G (1994) Oral cooling (cryotherapy), an effective treatment for the prevention of 5-fluorouracil-induced stomatitis. Eur J Cancer B Oral Oncol 30B:234–236PubMedCrossRef
8.
go back to reference Sorensen JB, Skovsgaard T, Bork E, Damstrup L, Ingeberg S (2008) Double-blind, placebo-controlled, randomized study of chlorhexidine prophylaxis for 5-fluorouracil-based chemotherapy-induced oral mucositis with nonblinded randomized comparison to oral cooling (cryotherapy) in gastrointestinal malignancies. Cancer 112:1600–1606PubMedCrossRef Sorensen JB, Skovsgaard T, Bork E, Damstrup L, Ingeberg S (2008) Double-blind, placebo-controlled, randomized study of chlorhexidine prophylaxis for 5-fluorouracil-based chemotherapy-induced oral mucositis with nonblinded randomized comparison to oral cooling (cryotherapy) in gastrointestinal malignancies. Cancer 112:1600–1606PubMedCrossRef
9.
go back to reference Anderson PM, Schroeder G, Skubitz KM (1998) Oral glutamine reduces the duration and severity of stomatitis after cytotoxic cancer chemotherapy. Cancer 83:1433–1439PubMedCrossRef Anderson PM, Schroeder G, Skubitz KM (1998) Oral glutamine reduces the duration and severity of stomatitis after cytotoxic cancer chemotherapy. Cancer 83:1433–1439PubMedCrossRef
10.
go back to reference Okuno SH, Woodhouse CO, Loprinzi CL, Sloan JA, LaVasseur BI, Clemens-Schutjer D et al (1999) Phase III controlled evaluation of glutamine for decreasing stomatitis in patients receiving fluorouracil (5-FU)-based chemotherapy. Am J Clin Oncol 22:258–261PubMedCrossRef Okuno SH, Woodhouse CO, Loprinzi CL, Sloan JA, LaVasseur BI, Clemens-Schutjer D et al (1999) Phase III controlled evaluation of glutamine for decreasing stomatitis in patients receiving fluorouracil (5-FU)-based chemotherapy. Am J Clin Oncol 22:258–261PubMedCrossRef
11.
go back to reference Jebb SA, Osborne RJ, Maughan TS, Mohideen N, Mack P, Mort D et al (1994) 5-fluorouracil and folinic acid-induced mucositis: no effect of oral glutamine supplementation. Br J Cancer 70:732–735PubMedCentralPubMedCrossRef Jebb SA, Osborne RJ, Maughan TS, Mohideen N, Mack P, Mort D et al (1994) 5-fluorouracil and folinic acid-induced mucositis: no effect of oral glutamine supplementation. Br J Cancer 70:732–735PubMedCentralPubMedCrossRef
12.
go back to reference Hejna M, Köstler WJ, Raderer M, Steger GG, Brodowicz T, Scheithauer W et al (2001) Decrease of duration and symptoms in chemotherapy-induced oral mucositis by topical GM-CSF: results of a prospective randomised trial. Eur J Cancer 37:1994–2002PubMedCrossRef Hejna M, Köstler WJ, Raderer M, Steger GG, Brodowicz T, Scheithauer W et al (2001) Decrease of duration and symptoms in chemotherapy-induced oral mucositis by topical GM-CSF: results of a prospective randomised trial. Eur J Cancer 37:1994–2002PubMedCrossRef
13.
go back to reference Wymenga AN, van der Graaf WT, Hofstra LS, Spijkervet FK, Timens W, Timmer-Bosscha H et al (1999) Phase I study of transforming growth factor-beta3 mouthwashes for prevention of chemotherapy-induced mucositis. Clin Cancer Res 5:1363–1368PubMed Wymenga AN, van der Graaf WT, Hofstra LS, Spijkervet FK, Timens W, Timmer-Bosscha H et al (1999) Phase I study of transforming growth factor-beta3 mouthwashes for prevention of chemotherapy-induced mucositis. Clin Cancer Res 5:1363–1368PubMed
14.
go back to reference Peterson DE (2006) New strategies for management of oral mucositis in cancer patients. J Support Oncol 4:9–13PubMed Peterson DE (2006) New strategies for management of oral mucositis in cancer patients. J Support Oncol 4:9–13PubMed
15.
go back to reference Wu HG, Song SY, Kim YS, Oh YT, Lee CG, Keum KC et al (2009) Therapeutic effect of recombinant human epidermal growth factor (RhEGF) on mucositis in patients undergoing radiotherapy, with or without chemotherapy, for head and neck cancer: a double-blind placebo-controlled prospective phase 2 multi-institutional clinical trial. Cancer 115:3699–3708PubMedCrossRef Wu HG, Song SY, Kim YS, Oh YT, Lee CG, Keum KC et al (2009) Therapeutic effect of recombinant human epidermal growth factor (RhEGF) on mucositis in patients undergoing radiotherapy, with or without chemotherapy, for head and neck cancer: a double-blind placebo-controlled prospective phase 2 multi-institutional clinical trial. Cancer 115:3699–3708PubMedCrossRef
16.
go back to reference Lalla RV, Pilbeam CC, Walsh SJ, Sonis ST, Keefe DM, Peterson DE (2010) Role of the cyclooxygenase pathway in chemotherapy-induced oral mucositis: a pilot study. Support Care Cancer 18:95–103PubMedCrossRef Lalla RV, Pilbeam CC, Walsh SJ, Sonis ST, Keefe DM, Peterson DE (2010) Role of the cyclooxygenase pathway in chemotherapy-induced oral mucositis: a pilot study. Support Care Cancer 18:95–103PubMedCrossRef
17.
go back to reference Morales-Rojas T, Viera N, Morón-Medina A, Alvarez CJ, Alvarez A (2012) Proinflammatory cytokines during the initial phase of oral mucositis in patients with acute lymphoblastic leukaemia. Int J Paediatr Dent 22:191–196PubMedCrossRef Morales-Rojas T, Viera N, Morón-Medina A, Alvarez CJ, Alvarez A (2012) Proinflammatory cytokines during the initial phase of oral mucositis in patients with acute lymphoblastic leukaemia. Int J Paediatr Dent 22:191–196PubMedCrossRef
18.
go back to reference Kono T, Kaneko A, Matsumoto C (2012) Amelioration of 5-Fluorouracil-Induced oral mucositis in hamsters by TJ-14 (Hangeshashinto), inhibitor of inducible prostaglandin E2 and proinflammatory cytokines. Gastroenterology 142(Suppl 1):S-673CrossRef Kono T, Kaneko A, Matsumoto C (2012) Amelioration of 5-Fluorouracil-Induced oral mucositis in hamsters by TJ-14 (Hangeshashinto), inhibitor of inducible prostaglandin E2 and proinflammatory cytokines. Gastroenterology 142(Suppl 1):S-673CrossRef
19.
go back to reference Kono T, Satomi M, Ebisawa Y (2011) Topical application of hangeshashinto (TJ-14) in the management of chemotherapy-induced oral mucositis: a preliminary study. J Clin Oncol 29: (suppl 4; abstr 603) Kono T, Satomi M, Ebisawa Y (2011) Topical application of hangeshashinto (TJ-14) in the management of chemotherapy-induced oral mucositis: a preliminary study. J Clin Oncol 29: (suppl 4; abstr 603)
20.
go back to reference Kawai K, Yokoyama Y, Kokuryo T, Watanabe K, Kitagawa T, Nagino M (2010) Inchinkoto, an herbal medicine, exerts beneficial effects in the rat liver under stress with hepatic ischemia-reperfusion and subsequent hepatectomy. Ann Surg 251:692–700PubMedCrossRef Kawai K, Yokoyama Y, Kokuryo T, Watanabe K, Kitagawa T, Nagino M (2010) Inchinkoto, an herbal medicine, exerts beneficial effects in the rat liver under stress with hepatic ischemia-reperfusion and subsequent hepatectomy. Ann Surg 251:692–700PubMedCrossRef
21.
go back to reference Yoshikawa K, Shimada M, Nishioka M, Kurita N, Iwata T, Morimoto S et al (2012) The effects of the Kampo medicine (Japanese herbal medicine) “Daikenchuto” on the surgical inflammatory response following laparoscopic colorectal resection. Surg Today 42:646–651PubMedCrossRef Yoshikawa K, Shimada M, Nishioka M, Kurita N, Iwata T, Morimoto S et al (2012) The effects of the Kampo medicine (Japanese herbal medicine) “Daikenchuto” on the surgical inflammatory response following laparoscopic colorectal resection. Surg Today 42:646–651PubMedCrossRef
22.
go back to reference Matsui T, Kono T, Hata Y (2011) Neuroprotective effects of goshajinkigan (TJ-107) in colorectal cancer patients receiving oxaliplatin-based chemotherapy: a double-blind, placebo-controlled, randomized phase II trial from the GONE Study Group. J Clin Oncol 29: (suppl; abstr e14007) Matsui T, Kono T, Hata Y (2011) Neuroprotective effects of goshajinkigan (TJ-107) in colorectal cancer patients receiving oxaliplatin-based chemotherapy: a double-blind, placebo-controlled, randomized phase II trial from the GONE Study Group. J Clin Oncol 29: (suppl; abstr e14007)
23.
go back to reference Kawashima K, Nomura A, Makino T, Saito K, Kano Y (2004) Pharmacological properties of traditional medicine (XXIX)1): effect of Hange-shashin-to and the combinations of its herbal constituents on rat experimental colitis. Biol Pharm Bull 27:1599–1603PubMedCrossRef Kawashima K, Nomura A, Makino T, Saito K, Kano Y (2004) Pharmacological properties of traditional medicine (XXIX)1): effect of Hange-shashin-to and the combinations of its herbal constituents on rat experimental colitis. Biol Pharm Bull 27:1599–1603PubMedCrossRef
24.
go back to reference Bensky D, Barolet R. Chinese Herbal Medicine (1990) Formulas and strategies (Tr. from Chinese/With resource guide to prepared medicines supplement to Chinese herbal medicine) pp 10–152 Bensky D, Barolet R. Chinese Herbal Medicine (1990) Formulas and strategies (Tr. from Chinese/With resource guide to prepared medicines supplement to Chinese herbal medicine) pp 10–152
25.
26.
go back to reference Kase Y, Hayakawa T, Aburada M, Komatsu Y, Kamataki T (1997) Preventive effects of Hange-shashin-to on irinotecan hydrochloride-caused diarrhea and its relevance to the colonic prostaglandin E2 and water absorption in the rat. Jpn J Pharmacol 75:407–413PubMedCrossRef Kase Y, Hayakawa T, Aburada M, Komatsu Y, Kamataki T (1997) Preventive effects of Hange-shashin-to on irinotecan hydrochloride-caused diarrhea and its relevance to the colonic prostaglandin E2 and water absorption in the rat. Jpn J Pharmacol 75:407–413PubMedCrossRef
27.
go back to reference Mori K, Kondo T, Kamiyama Y, Kano Y, Tominaga K (2003) Preventive effect of Kampo medicine (Hangeshashin-to) against irinotecan-induced diarrhea in advanced non-small-cell lung cancer. Cancer Chemother Pharmacol 51:403–406PubMed Mori K, Kondo T, Kamiyama Y, Kano Y, Tominaga K (2003) Preventive effect of Kampo medicine (Hangeshashin-to) against irinotecan-induced diarrhea in advanced non-small-cell lung cancer. Cancer Chemother Pharmacol 51:403–406PubMed
28.
go back to reference Sharma R, Tobin P, Clarke SJ (2005) Management of chemotherapy-induced nausea, vomiting, oral mucositis, and diarrhoea. Lancet Oncol 6:93–102PubMedCrossRef Sharma R, Tobin P, Clarke SJ (2005) Management of chemotherapy-induced nausea, vomiting, oral mucositis, and diarrhoea. Lancet Oncol 6:93–102PubMedCrossRef
30.
31.
go back to reference Epstein JB, Silverman S Jr, Paggiarino DA et al (2001) Benzydamine HCl for prophylaxis of radiation-induced oral mucositis: results from a multicenter, randomized, double-blind, placebo-controlled clinical trial. Cancer 92:875–885PubMedCrossRef Epstein JB, Silverman S Jr, Paggiarino DA et al (2001) Benzydamine HCl for prophylaxis of radiation-induced oral mucositis: results from a multicenter, randomized, double-blind, placebo-controlled clinical trial. Cancer 92:875–885PubMedCrossRef
32.
go back to reference Hanson WR, Marks JE, Reddy SP et al (1997) Protection from radiation-induced oral mucositis by a mouth rinse containing the prostaglandin E1 analog, misoprostol: a placebo controlled double blind clinical trial. Adv Exp Med Biol 400B:811–818PubMed Hanson WR, Marks JE, Reddy SP et al (1997) Protection from radiation-induced oral mucositis by a mouth rinse containing the prostaglandin E1 analog, misoprostol: a placebo controlled double blind clinical trial. Adv Exp Med Biol 400B:811–818PubMed
33.
go back to reference Sironi M, Pozzi P, Polentarutti N et al (1996) Inhibition of inflammatory cytokine production and protection against endotoxin toxicity by benzydamine. Cytokine 8(9):710–716PubMedCrossRef Sironi M, Pozzi P, Polentarutti N et al (1996) Inhibition of inflammatory cytokine production and protection against endotoxin toxicity by benzydamine. Cytokine 8(9):710–716PubMedCrossRef
34.
go back to reference Sironi M, Milanese C, Vecchi A et al (1997) Benzydamine inhibits the release of tumor necrosis factor-alpha and monocyte chemotactic protein-1 by Candida albicans-stimulated human peripheral blood cells. Int J Clin Lab Res 27:118–122PubMedCrossRef Sironi M, Milanese C, Vecchi A et al (1997) Benzydamine inhibits the release of tumor necrosis factor-alpha and monocyte chemotactic protein-1 by Candida albicans-stimulated human peripheral blood cells. Int J Clin Lab Res 27:118–122PubMedCrossRef
35.
go back to reference Duenas-Gonzalez A, Sobrevilla-Calvo P, Frias-Mendivil M et al (1996) Misoprostol prophylaxis for high-dose chemotherapy-induced mucositis: a randomized double-blind study. Bone Marrow Transplant 17:809–812PubMed Duenas-Gonzalez A, Sobrevilla-Calvo P, Frias-Mendivil M et al (1996) Misoprostol prophylaxis for high-dose chemotherapy-induced mucositis: a randomized double-blind study. Bone Marrow Transplant 17:809–812PubMed
Metadata
Title
Double-blind, placebo-controlled, randomized phase II study of TJ-14 (Hangeshashinto) for infusional fluorinated-pyrimidine-based colorectal cancer chemotherapy-induced oral mucositis
Authors
Chu Matsuda
Yoshinori Munemoto
Hideyuki Mishima
Naoki Nagata
Mitsuru Oshiro
Masato Kataoka
Junichi Sakamoto
Toru Aoyama
Satoshi Morita
Toru Kono
Publication date
01-07-2015
Publisher
Springer Berlin Heidelberg
Published in
Cancer Chemotherapy and Pharmacology / Issue 1/2015
Print ISSN: 0344-5704
Electronic ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-015-2767-y

Other articles of this Issue 1/2015

Cancer Chemotherapy and Pharmacology 1/2015 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine