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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03607656
Other study ID # LONGHUA-2018-SH
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date June 8, 2018
Est. completion date November 30, 2023

Study information

Verified date December 2023
Source Shanghai University of Traditional Chinese Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a randomized, open-label study done in 3 hospitals in China. Patients with stage IIIB and IIIC gastric cancer who undergo curative D2 gastrostomy will be randomly assigned after surgery to receive adjuvant chemotherapy with oxaliplatin and capecitabine, or adjuvant chemotherapy combined Traditional Chinese treatment. The primary outcome was disease-free survival and 3-year disease-free survival rate in the intention-to-treat population.


Description:

The purpose of this study is to evaluate the Traditional Chinese Medicine combined adjuvant chemotherapy in the treatment of stage IIIb and IIIc gastric cancer through randomized controlled trial. Metastasis and recurrence is the primary cause in decreasing the survival time of gastric cancer patients who experienced radical operation. Among whom, patients with stage IIIB and IIIC are especially in high risk of metastasis and recurrence, result in a significant poor survival time than patients with earlier stages. Oxaliplatin with capecitabine is the standard adjuvant chemotherapy for curative D2 gastrostomy gastric cancer, contribute the 3-year disease free survival rate of 74% in ITT, and 61% in stage IIIB sub-group. Meanwhile, Traditional Chinese Medicine (TCM) treatment has been used for thousands of years in Chinese clinical practices. In China, the clinical curative effect of TCM in the treatment of gastric cancer has been part of affirmation. Some reports with large samples of clinical research show that the TCM is effective and safety for gastric cancer.In order to evaluate efficacy on TCM combined adjuvant chemotherapy in IIIB and IIIC gastric cancer, we design this randomized, open-label study.


Recruitment information / eligibility

Status Completed
Enrollment 270
Est. completion date November 30, 2023
Est. primary completion date October 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Histologically proven gastric carcinoma with radical operation, TNM (primary tumor, regional nodes, metastasis) stage IIIb or IIIc (The Eighth Edition American Joint Committee on Cancer [AJCC] gastric cancer staging); - Karnofsky performance status higher than 70; - Adequate hepatic, renal, cardio and hematologic function; - With patients' consent and comply to long term follow-up. Exclusion Criteria: - Gastrectomy beyond D2, or TNM stage beyond ?b and ?c; - Histological type beyond gastric carcinoma; - Conversion chemotherapy before surgery; - Concurrent cancer; - Women of gravid or lactating; patients with mental illness; - Uncontrolled significant comorbid conditions.

Study Design


Intervention

Drug:
Oxaliplatin
Oxaliplatin powder injection
Capecitabine
Capecitabine tablet
Other:
TCM
TCM decoction orally taken twice a day for at least 3 months
Drug:
S-1
S-1 capsule
Docetaxel
Docetaxel injection
5-FU
5-FU injection

Locations

Country Name City State
China Longhua Hospital Shanghai Shanghai

Sponsors (3)

Lead Sponsor Collaborator
Shanghai University of Traditional Chinese Medicine Jiangsu Province Hospital of Traditional Chinese Medicine, RenJi Hospital

Country where clinical trial is conducted

China, 

References & Publications (2)

Bang YJ, Kim YW, Yang HK, Chung HC, Park YK, Lee KH, Lee KW, Kim YH, Noh SI, Cho JY, Mok YJ, Kim YH, Ji J, Yeh TS, Button P, Sirzen F, Noh SH; CLASSIC trial investigators. Adjuvant capecitabine and oxaliplatin for gastric cancer after D2 gastrectomy (CLASSIC): a phase 3 open-label, randomised controlled trial. Lancet. 2012 Jan 28;379(9813):315-21. doi: 10.1016/S0140-6736(11)61873-4. Epub 2012 Jan 7. — View Citation

Xu Y, Zhao AG, Li ZY, Zhao G, Cai Y, Zhu XH, Cao ND, Yang JK, Zheng J, Gu Y, Han YY, Zhu YJ, Yang JZ, Gao F, Wang Q. Survival benefit of traditional Chinese herbal medicine (a herbal formula for invigorating spleen) for patients with advanced gastric cancer. Integr Cancer Ther. 2013 Sep;12(5):414-22. doi: 10.1177/1534735412450512. Epub 2012 Jul 9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 3-year Disease Free Survival rate The rate refers to cases that see first tumor metastasis or recurrence or death of any cause from randomization. 36 months
Secondary Safety (adverse effects) Using NCI-CTC standard to record adverse effects of chemotherapy and treatments. 36 months
Secondary EORTC QLQ-C30 scale Using the EORTC QLQ-C30 scale (European Organization for Research on Treatment of Cancer Quality of Life Questionnaire-Core 30) to evaluate the quality of life of patients. The scale includes 14 aspects: physical functioning, role functioning, emotional functioning, cognitive functioning, social functioning, fatigue, nausea/vomiting, pain, dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial problem, with each aspect scores from one point to four points (lower points represent a better quality of life), and a general quality of life scores from one point to seven points (higher points represent a better quality of life). 36 months
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