Esophageal Squamous Cell Carcinoma Clinical Trial
Official title:
A Prospective, Phase II Study of Percutaneous Endoscopic Gastrostomy Before Definitive Concurrent Chemoradiation Therapy in Patients With Esophageal Squamous Cell Carcinoma
| Verified date | January 2023 |
| Source | Sun Yat-sen University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This Phase II randomized study is to determine the efficacy of percutaneous endoscopic gastrostomy before definitive concurrent chemoradiotherapy (CCRT) in Patients with Esophageal Squamous Cell Carcinoma(ESCC) by assessing their weight, nutritional status, performance status and treatment response.
| Status | Completed |
| Enrollment | 63 |
| Est. completion date | March 15, 2022 |
| Est. primary completion date | March 15, 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 75 Years |
| Eligibility | Inclusion Criteria: - Histologically confirmed esophageal squamous cell carcinoma - Patients have measurable or evaluable lesions based on the Response Evaluation Criteria in Solid Tumors (RECIST) criteria. - Eastern Cooperative Oncology Group (ECOG) performance status 0-1. - Estimated life expectancy of at least 6 months - No contraindications for chemotherapy or radiotherapy - Patients and their family signed the informed consents Exclusion Criteria: - Severe gastrointestinal impairment or enteral nutrition intolerance - Severe vomiting, gastrointestinal bleeding or intestinal obstruction - Severe malnutrition - Patients with contraindications for percutaneous endoscopic gastrostomy, including uncorrected coagulopathy or thrombocytopenia, varices caused by portal hypertension, or other gastric diseases - Not suitable for this study judged by researchers |
| Country | Name | City | State |
|---|---|---|---|
| China | Hui Liu | Guangzhou | Guangdong |
| Lead Sponsor | Collaborator |
|---|---|
| Sun Yat-sen University |
China,
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Cooper JS, Guo MD, Herskovic A, Macdonald JS, Martenson JA Jr, Al-Sarraf M, Byhardt R, Russell AH, Beitler JJ, Spencer S, Asbell SO, Graham MV, Leichman LL. Chemoradiotherapy of locally advanced esophageal cancer: long-term follow-up of a prospective randomized trial (RTOG 85-01). Radiation Therapy Oncology Group. JAMA. 1999 May 5;281(17):1623-7. doi: 10.1001/jama.281.17.1623. — View Citation
Lin CH, Liu NJ, Lee CS, Tang JH, Wei KL, Yang C, Sung KF, Cheng CL, Chiu CT, Chen PC. Nasogastric feeding tube placement in patients with esophageal cancer: application of ultrathin transnasal endoscopy. Gastrointest Endosc. 2006 Jul;64(1):104-7. doi: 10.1016/j.gie.2005.12.036. — View Citation
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Margolis M, Alexander P, Trachiotis GD, Gharagozloo F, Lipman T. Percutaneous endoscopic gastrostomy before multimodality therapy in patients with esophageal cancer. Ann Thorac Surg. 2003 Nov;76(5):1694-7; discussion 1697-8. doi: 10.1016/s0003-4975(02)04890-7. — View Citation
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Percentage of Recent Weight Loss | From baseline until the end of concurrent chemoradiotherapy, an average of 8 weeks | ||
| Secondary | Change in nutrition status assessed by blood test | Change in nutrition status will be assessed by hemoglobin, serum albumin, pre-albumin test. The patient-generated subjective global assessment will also be used to measure patients' nutrition status | 1 year | |
| Secondary | Quality of life measured by WHO Quality of Life-100 questionnaire | 1 year | ||
| Secondary | Rate of grade 3-4 radiation esophagitis | 1 year | ||
| Secondary | Rate of grade 3-4 radiation pneumonitis, | 1 year | ||
| Secondary | Rate of grade 3-4 bone marrow suppression | 1 year | ||
| Secondary | Objective response rate | 2 months | ||
| Secondary | Overall survival | 3 years | ||
| Secondary | Changes of participants' intestinal flora assessed by blood, urine and stool test | 1 year |
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