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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01732380
Other study ID # 1stPeopleLianyungang
Secondary ID
Status Recruiting
Phase Phase 2
First received November 14, 2012
Last updated November 19, 2012
Start date July 2012
Est. completion date July 2013

Study information

Verified date November 2012
Source The First People's Hospital of Lianyungang
Contact Xiaodong Jiang, Doctor
Phone 86-0518-85469074
Email jxdysy1970@163.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The aim of this study was to compare raltitrexed/oxaliplatin plus radiotherapy versus radiotherapy in subjects with inoperable esophageal cancer.


Description:

108 patients were randomized to receive Raltitrexed/Oxaliplatin Plus Radiotherapy (Raltitrexed 2.5mg/㎡ d1,Oxaliplatin 100mg/㎡ d1,q21d Plus Radiotherapy 2.0Gy/day, 5 times/week,6 weeks.)or Radiotherapy ( Radiotherapy 2.0Gy/day, 5 times/week,6 weeks) in subjects with Inoperable esophageal cancer. All patients will receive therapy of six weeks unless disease progression or unacceptable toxicity. Patients were evaluated every 3 months .Progression-Free-Survival was the primary endpoint. Response Rate, Overall survival, toxicity of the therapy are other second endpoint.


Recruitment information / eligibility

Status Recruiting
Enrollment 108
Est. completion date July 2013
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Confirmed diagnosis of inoperable esophageal cancer(squamous cell carcinoma)

- Measurable disease according to RECIST criteria

- Age > 18 years

- WHO performance score < 2

- Estimated life expectancy of > 12 weeks

- Subjects will be considered appropriate to receive systemic chemotherapy and pelvic radiotherapy

- Hematologic function: WBC = 4.0×109/L, PLT = 80×109/L, Hb = 10mg/dL

- Renal function: Cr = 1.25×UNL

- Hepatic function: BIL = 1.5×UNL, ALT/AST = 2.5×UNL

- Documented informed consent to participate in the trial

Exclusion Criteria:

- Subjects with distant metastases

- Pregnancy or breast feeding. Women of childbearing age must use effective contraception

- Serious cardiovascular disease (congestive heart failure, uncontrollable arrhythmia, unstable angina, myocardial infarction, serious heart valve disease, resistant hypertension)

- Evidence of bleeding diathesis or serious infection

- pregnant or lactating woman

- Patient participation in other studies

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:
Raltitrexed

Oxaliplatin

Radiation:
Radiotherapy


Locations

Country Name City State
China The First People`s Hospital of Lianyungang Lianyungang Jiangsu

Sponsors (4)

Lead Sponsor Collaborator
The First People's Hospital of Lianyungang Donghai People's Hospital, People's Hospital of Ganyu, The East Hospital of Lianyungang

Country where clinical trial is conducted

China, 

References & Publications (5)

Cascinu S, Graziano F, Ferraù F, Catalano V, Massacesi C, Santini D, Silva RR, Barni S, Zaniboni A, Battelli N, Siena S, Giordani P, Mari D, Baldelli AM, Antognoli S, Maisano R, Priolo D, Pessi MA, Tonini G, Rota S, Labianca R. Raltitrexed plus oxaliplatin (TOMOX) as first-line chemotherapy for metastatic colorectal cancer. A phase II study of the Italian Group for the Study of Gastrointestinal Tract Carcinomas (GISCAD). Ann Oncol. 2002 May;13(5):716-20. — View Citation

Courrech Staal EF, Aleman BM, Boot H, van Velthuysen ML, van Tinteren H, van Sandick JW. Systematic review of the benefits and risks of neoadjuvant chemoradiation for oesophageal cancer. Br J Surg. 2010 Oct;97(10):1482-96. doi: 10.1002/bjs.7175. Review. — View Citation

Gebski V, Burmeister B, Smithers BM, Foo K, Zalcberg J, Simes J; Australasian Gastro-Intestinal Trials Group. Survival benefits from neoadjuvant chemoradiotherapy or chemotherapy in oesophageal carcinoma: a meta-analysis. Lancet Oncol. 2007 Mar;8(3):226-34. — View Citation

McKenzie S, Mailey B, Artinyan A, Metchikian M, Shibata S, Kernstine K, Kim J. Improved outcomes in the management of esophageal cancer with the addition of surgical resection to chemoradiation therapy. Ann Surg Oncol. 2011 Feb;18(2):551-8. doi: 10.1245/s10434-010-1314-7. Epub 2010 Sep 14. — View Citation

Seitz JF, Bennouna J, Paillot B, Gamelin E, François E, Conroy T, Raoul JL, Becouarn Y, Bertheault-Cvitkovic F, Ychou M, Nasca S, Fandi A, Barthelemy P, Douillard JY. Multicenter non-randomized phase II study of raltitrexed (Tomudex) and oxaliplatin in non-pretreated metastatic colorectal cancer patients. Ann Oncol. 2002 Jul;13(7):1072-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Overall survival People in a study or treatment group who are still alive for a certain period of time after they were diagnosed with or started treatment for a disease, such as cancer. The overall survival is often stated as a five-year survival, which means people in a study or treatment group who are alive five years after their diagnosis or the start of treatment. up to 2 years Yes
Primary Progression-Free-Survival Progression-free survival (PFS) is the length of time during and after medication or treatment during which the disease being treated (usually cancer) does not get worse. up to 2 years Yes
Secondary Response Rate Response rate (RR) is a figure representing the percentage of patients whose cancer shrinks (termed a partial response, PR) or disappears after treatment (termed a complete response, CR) . In simpler terms RR=PR+CR. up to 2 years Yes