Overview

Phase II/III Study Comparing Chemoradiotherapy With Radiotherapy in Elderly Patients With Esophageal or Esophagogastric Cancer - 3JECROG P-01

Status:
Completed
Trial end date:
2020-04-01
Target enrollment:
0
Participant gender:
All
Summary
Ratiotherapy alone is the current standard treatment for elderly esophageal or esophagogastric cancer in China. And Little is known about chemoradiotherapy (CRT) in elderly patients. This study aimed to assess the efficiency and safety of simultaneous integrated boost (SIB) intensity modulated radiation therapy (IMRT) with S1 based SIB-IMRT followed by adjuvant chemotherapy with S1 in in elderly (age ≥70 years) esophageal or esophagogastric cancer patients
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Chinese Academy of Medical Sciences
Collaborators:
Affiliated Hospital of Hebei University
Anyang Tumor Hospital
Fujian Cancer Hospital
Hebei Medical University Fourth Hospital
Sichuan Cancer Hospital and Research Institute
Tengzhou Central People's Hospital
The Affiliated Hospital of Inner Mongolia Medical University
The First Affiliated Hospital of Zhengzhou University
The First Affiliated Hospital with Nanjing Medical University
Tianjin Medical University Cancer Institute and Hospital
Criteria
Inclusion Criteria:

- ≥70 years

- Esophageal or Esophagogastric cancer

- Histologically proven squamous cell carcinoma or adenocarcinoma in patients staged as
IIa-IVb (UICC 2002, IVb only with supraclavicular or celiac trunk lymph nodes
metastasis)

- Karnofsky performance status(KPS)≥ 70 and Charlson score ≤3

- No distant metastasis other than supraclavicular lymph nodes

- No prior history of thoracic radiation

- Patients must have normal organ and marrow function as defined below: Leukocytes:
greater than or equal to 3,500 G/L; Platelets: greater than or equal to 100,000/mm3
.Hemoglobin:greater than or equal to 10g/L .Total bilirubin: within normal
institutional limits; AST/ALT: less than or equal to 1.5 times the upper limit;
Creatinine within normal upper limits

- Informed consent

Exclusion Criteria:

- Patients with other cancer history except cervical carcinoma in situ and non-malignant
melanoma skin cancer

- With any distant metastasis out of regional lymphatic drainage or in
liver,lung,bone,CNS,etc

- History of allergic reactions attributed to similar chemical or biologic complex to
S-1

- With esophageal fistula, perforation, cachexia prior to treatment

- Uncontrolled illness including, but not limited to, active infection, symptomatic
heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness

- History of myocardial infarction within the past 6 months or history of ventricular
arrhythmia

- Pregnant or lactating females