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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02891083
Other study ID # 2016shchest
Secondary ID
Status Recruiting
Phase Phase 3
First received September 1, 2016
Last updated September 6, 2016
Start date January 2016
Est. completion date January 2021

Study information

Verified date September 2016
Source Shanghai Chest Hospital
Contact Wentao Fang, MD
Phone +86-21-62821990
Email vwtfang12@shcheat.org
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Histological Node Negative thoracic esophageal squamous cell carcinoma(pN0 ESCC) after radical resection still carries the risk of recurrence after complete surgical resection, especially in some high-risk patients. There are still lack of knowledge on postoperative treatment indication and methods for pN0 ESCC.Our previous study has shown that risk of recurrence is associated with the location and cell differentiation of primary tumor, as well as the presence of lymphovascular invasion. This project is designed to study the efficacy of adjuvant therapies for at patients with pN0 ESCC and above mentioned risk factors of recurrence after radical surgery. We aim to compare the differences among adjuvant chemotherapy, adjuvant radiotherapy, and surgery alone for pN0 ESCC by prospective randomized controlled trial. There has been no similar studies in esophageal cancer previously reported with similar design. The results of this study is expected to have a high clinical relevance.


Description:

The study is designed to be a prospective randomized controlled trial, aiming to compare the impact of adjuvant chemotherapy with Paclitaxel and Cisplatin, adjuvant radiotherapy with IMRT of 50Gy, and surgery alone on the disease free survival (DFS) of patients with high-risk pN0 thoracic esophageal squamous cell carcinoma. Pathological staging is to be based on the 7th UICC edition, after radical resection and systemic lymph node dissection,for accurate staging.Patients with pT1b-T4a disease, proved to be pN0 upon pathological examination, meet at least one of the risk factors in the inclusion criteria, and without any exclusion criteria are to be randomized into one of the three study arms.Definition of high-risk factors for recurrence include: (1)Tumor location: in the middle or upper third thoracic esophagus; (2) Presence of LVI or submucosal metastasis; (3) Cell differentiation: poorly differentiated or undifferentiated.

Primary endpoint:

To observe and compare Disease-Free Survivals (DFS) among the three study arms.

Secondary endpoint:

To observe and compare Overall Survivals (OS) among the three study arms, and to compare adverse events between adjuvant chemotherapy and adjuvant radiation groups.

Additional instructions:

No.


Recruitment information / eligibility

Status Recruiting
Enrollment 486
Est. completion date January 2021
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. Patient: No pretreatment before surgery.Informed consent signed after screening;

2. Surgery: Complete (R0) resection of tumor, with thoraco- abdominal two-field or cervico-thoraco-abdominal three-field lymph node dissection through transthoracic esophagectomy. At least 12 stations and 12 lymph nodes should be harvested, including bilateral recurrent laryngeal nerve nodes. Both open thoracotomy and minimally invasive thoracoscopic/laparoscopic approaches are allowed and histopathological examination confirmed the diagnosis of the patients with at least cleaning more or equal to 12 stations and 12 lymph nodes;

3. Histology: Thoracic esophageal squamous cell carcinoma, with no nodal involvement (pN0) after pathological examination;

4. Staging: Tumor T stage T1b-T4a according to the 7th UICC esophageal cancer staging system;

5. Definition of high risk for recurrence: meet at least one of the three below.

A: Primary tumor located in middle or upper third of thoracic esophagus

B: Presence of lymphovascular invasion (LVI) or submucosal metastasis

C: Cell differentiation:Low grade or undifferentiated

6. Performance status: ECOG score 0-2;

7. Cardiac function:NYHA classification 1-2. Normal electrocardiogram;

8. Renal function: Normal serum creatinine level (SCr = 120mol/L) and creatinine clearance rate (CCr = 60 ml/min);

9. Hepatic function: Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) level less than or equal to 2.0 times the upper limit of normal (ULN). Serum alkaline phosphatase (ALP) level less than or equal to four times the upper limit of normal value. Serum total bilirubin level less than or equal to 1.5 times the upper limit of the normal value;

10. Hematopoietic function: White blood cell count (WBC) equal to or more than 4000 / µL,neutrophils (ANC) absolute count is more than or equal to 1500 / µ L, platelet count more than or equal to 100000/ µ L, hemoglobin equal to or more than 10.0 g / dl.

Exclusion Criteria:

1. Surgery through Left thoracic or transhiatal approach, whereby complete lymphadenectomy is not achieved;

2. Patients experienced severe postoperative complication and thus, are unable to tolerate any adjuvant therapy;

3. Patients who have concommitant other malignant tumor;

4. Patients with abnormal coagulation function, with bleeding tendencies (such as active peptic ulcer) or are currently receiving thrombolysis or anticoagulation therapies;

5. Severe cardiac comorbidities, including congestive heart failure,uncontrolled cardiac arrhythmia, unstable angina pectoris, myocardial infarction within six months,severe heart valve disease, or intractable hypertension;

6. Severe hepatic or renal insufficiency;

7. Poor mental status or mental disorders, poor compliance.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Adjuvant chemotherapy (Paclitaxel and Cisplatin)
Adjuvant chemotherapy group: three cycles: (Paclitaxel: 175mg/m2 ivgtt, 3h, d1 4week × 3 and cisplatin: 75mg/m2 ivgtt, d1 4 week × 3)
Radiation:
Adjuvant radiotherapy
Target: the upper mediastinum and bilateral supraclavicular region (Upper bound: thyrocricoid, lower bound: carina of 3cm) Dose: 50Gy Technology: strong tone Segmentation: conventional segmentation 2Gy/d
Other:
Control group (Surgery alone)


Locations

Country Name City State
China Shanghai Chest Hospital Shanghai

Sponsors (10)

Lead Sponsor Collaborator
Shanghai Chest Hospital Fudan University, Fujian Cancer Hospital, Fujian Medical University, Hunan Cancer Hospital, Qingdao University, Sichuan Cancer Hospital and Research Institute, Sun Yat-sen University, Tianjin Medical University Cancer Institute and Hospital, Wuhan TongJi Hospital

Country where clinical trial is conducted

China, 

References & Publications (5)

Ando N, Iizuka T, Ide H, Ishida K, Shinoda M, Nishimaki T, Takiyama W, Watanabe H, Isono K, Aoyama N, Makuuchi H, Tanaka O, Yamana H, Ikeuchi S, Kabuto T, Nagai K, Shimada Y, Kinjo Y, Fukuda H; Japan Clinical Oncology Group. Surgery plus chemotherapy comp — View Citation

Guo XF, Mao T, Gu ZT, Ji CY, Fang WT, Chen WH. Clinical study on postoperative recurrence in patients with pN0 esophageal squamous cell carcinoma. J Cardiothorac Surg. 2014 Aug 28;9:150. doi: 10.1186/s13019-014-0150-4. — View Citation

Shim YM, Kim HK, Kim K. Comparison of survival and recurrence pattern between two-field and three-field lymph node dissections for upper thoracic esophageal squamous cell carcinoma. J Thorac Oncol. 2010 May;5(5):707-12. doi: 10.1097/JTO.0b013e3181d3ccb2. — View Citation

Tachimori Y, Nagai Y, Kanamori N, Hokamura N, Igaki H. Pattern of lymph node metastases of esophageal squamous cell carcinoma based on the anatomical lymphatic drainage system. Dis Esophagus. 2011 Jan;24(1):33-8. doi: 10.1111/j.1442-2050.2010.01086.x. — View Citation

Wu SG, Dai MM, He ZY, Sun JY, Lin HX, Lin H, Li Q. Patterns of Regional Lymph Node Recurrence After Radical Surgery for Thoracic Esophageal Squamous Cell Carcinoma. Ann Thorac Surg. 2016 Feb;101(2):551-7. doi: 10.1016/j.athoracsur.2015.08.057. Epub 2015 O — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Disease free survival 3 years No
Secondary Overall survival 5 years No
Secondary side effect of adjuvant therapy 6 months Yes
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