The Value of Concurrent Chemoradiotherapy for Stage II Nasopharyngeal Carcinoma
Primary Purpose
Nasopharyngeal Carcinoma
Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
cisplatin
Sponsored by
About this trial
This is an interventional treatment trial for Nasopharyngeal Carcinoma focused on measuring Nasopharyngeal carcinoma, Stage II, Intensity-modulated radiotherapy, Concurrent chemoradiotherapy, Cisplatin
Eligibility Criteria
Inclusion Criteria:
- pathological confirmed squamous cell carcinoma, WHO II-III type,
- clinical stage II (UICC 7th edition, 2009)
- Karnovsky performance score > 70
- first course of radiotherapy, without radiotherapy and chemotherapy history for other head and neck cancer.
- anticipated life span more than 6 month
- Hemoglobin > 120g/L, WBC > 4.0x10*9/L, Plt > 100x10*9/L
- liver and renal function under the 1.25 normal upper limit
- with written consent information
Exclusion Criteria:
- have other cancer history
- have chemotherapy history
- have radiotherapy history
- have head and neck surgery history(exclusion lymph node biopsy)
- evidence showed distant metastasis or other cancer
- other severe medical comorbidity
Sites / Locations
- Cancer hospital, Sun Yat-sen University
- Zhejiang province cancer hospital
- Cancer hospital, Chinese Academy of Medical Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Arm1-radical radiotherapy alone group
Arm2-concurrent chemoradiotherapy group
Arm Description
Arm1-radical radiotherapy alone group, the eligibility patients will received radical intensity-modulated radiotherapy alone
Arm2-concurrent chemoradiotherapy group, the eligibility patients will received radiotherapy the same as radical radiotherapy arm,and also will received the concurrent chemotherapy wiht the regimen consist of cisplatin 40mg/m2, weekly for 7weeks.
Outcomes
Primary Outcome Measures
Acute toxicities
Acute toxicity will be measured by CTCAE3.0
Secondary Outcome Measures
Long term treatment results
1-, 3-year local-regional control, overall survival, disease-free survival, distant metastasis-free survival will be observed.
Full Information
NCT ID
NCT01187238
First Posted
August 18, 2010
Last Updated
July 14, 2020
Sponsor
Chinese Academy of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT01187238
Brief Title
The Value of Concurrent Chemoradiotherapy for Stage II Nasopharyngeal Carcinoma
Official Title
A Randomized Multicenter Phase II Study of Intensity-modulated Radiotherapy Combined With Chemotherapy Versus Intensity-modulated Radiotherapy Alone for Stage II Nasopharyngeal Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
October 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese Academy of Medical Sciences
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to verify the role of adding cisplatin chemotherapy to the intensity-modulated radiotherapy (IMRT) for stage II nasopharyngeal carcinoma.
Detailed Description
Clinical Stage II nasopharyngeal carcinoma consisted of T2N0M0, T1N1M0, T2N1M0 three subgroups, the data came from conventional radiotherapy era showed that the prognosis of this three subgroups were different, the N1 groups suffered more distant metastasis than N0 group, and some literature showed that combined chemotherapy with radiotherapy in stage II patients can improve the treatment results.
Intensity-modulated radiotherapy (IMRT)now is an widely used technique in the treatment of nasopharyngeal carcinoma, the preliminary results showed that IMRT can improve the quality of life in nasopharyngeal through salivary gland preservation.
Compared IMRT alone with IMRT plus cisplatin concurrent chemotherapy in the treatment of stageII nasopharyngeal carcinoma, we hope to confirm whether stage II (and which subgroup) nasopharyngeal carcinoma will be benefit from concurrent chemoradiotherapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma
Keywords
Nasopharyngeal carcinoma, Stage II, Intensity-modulated radiotherapy, Concurrent chemoradiotherapy, Cisplatin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm1-radical radiotherapy alone group
Arm Type
No Intervention
Arm Description
Arm1-radical radiotherapy alone group, the eligibility patients will received radical intensity-modulated radiotherapy alone
Arm Title
Arm2-concurrent chemoradiotherapy group
Arm Type
Experimental
Arm Description
Arm2-concurrent chemoradiotherapy group, the eligibility patients will received radiotherapy the same as radical radiotherapy arm,and also will received the concurrent chemotherapy wiht the regimen consist of cisplatin 40mg/m2, weekly for 7weeks.
Intervention Type
Drug
Intervention Name(s)
cisplatin
Other Intervention Name(s)
DDP
Intervention Description
in experimental arm, the eligibility patients will be received the same radiotherapy as radical radiotherapy alone group, and also will received concurrent chemotherapy with the regimen of cisplatin 40mg/m2, weekly,from week 1 to week 7
Primary Outcome Measure Information:
Title
Acute toxicities
Description
Acute toxicity will be measured by CTCAE3.0
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Long term treatment results
Description
1-, 3-year local-regional control, overall survival, disease-free survival, distant metastasis-free survival will be observed.
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
pathological confirmed squamous cell carcinoma, WHO II-III type,
clinical stage II (UICC 7th edition, 2009)
Karnovsky performance score > 70
first course of radiotherapy, without radiotherapy and chemotherapy history for other head and neck cancer.
anticipated life span more than 6 month
Hemoglobin > 120g/L, WBC > 4.0x10*9/L, Plt > 100x10*9/L
liver and renal function under the 1.25 normal upper limit
with written consent information
Exclusion Criteria:
have other cancer history
have chemotherapy history
have radiotherapy history
have head and neck surgery history(exclusion lymph node biopsy)
evidence showed distant metastasis or other cancer
other severe medical comorbidity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Li Gao, MD
Organizational Affiliation
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cancer hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
Facility Name
Zhejiang province cancer hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310022
Country
China
Facility Name
Cancer hospital, Chinese Academy of Medical Sciences
City
Beijing
ZIP/Postal Code
100021
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
17971582
Citation
Kam MK, Leung SF, Zee B, Chau RM, Suen JJ, Mo F, Lai M, Ho R, Cheung KY, Yu BK, Chiu SK, Choi PH, Teo PM, Kwan WH, Chan AT. Prospective randomized study of intensity-modulated radiotherapy on salivary gland function in early-stage nasopharyngeal carcinoma patients. J Clin Oncol. 2007 Nov 1;25(31):4873-9. doi: 10.1200/JCO.2007.11.5501.
Results Reference
background
PubMed Identifier
12833458
Citation
Chua DT, Sham JS, Kwong DL, Au GK. Treatment outcome after radiotherapy alone for patients with Stage I-II nasopharyngeal carcinoma. Cancer. 2003 Jul 1;98(1):74-80. doi: 10.1002/cncr.11485.
Results Reference
background
PubMed Identifier
16750333
Citation
Chua DT, Ma J, Sham JS, Mai HQ, Choy DT, Hong MH, Lu TX, Au GK, Min HQ. Improvement of survival after addition of induction chemotherapy to radiotherapy in patients with early-stage nasopharyngeal carcinoma: Subgroup analysis of two Phase III trials. Int J Radiat Oncol Biol Phys. 2006 Aug 1;65(5):1300-6. doi: 10.1016/j.ijrobp.2006.02.016. Epub 2006 Jun 5.
Results Reference
result
PubMed Identifier
10811668
Citation
Cheng SH, Tsai SY, Yen KL, Jian JJ, Chu NM, Chan KY, Tan TD, Cheng JC, Hsieh CY, Huang AT. Concomitant radiotherapy and chemotherapy for early-stage nasopharyngeal carcinoma. J Clin Oncol. 2000 May;18(10):2040-5. doi: 10.1200/JCO.2000.18.10.2040.
Results Reference
result
PubMed Identifier
32850414
Citation
Huang X, Chen X, Zhao C, Wang J, Wang K, Wang L, Miao J, Cao C, Jin T, Zhang Y, Qu Y, Chen X, Liu Q, Zhang S, Zhang J, Luo J, Xiao J, Xu G, Gao L, Yi J. Adding Concurrent Chemotherapy to Intensity-Modulated Radiotherapy Does Not Improve Treatment Outcomes for Stage II Nasopharyngeal Carcinoma: A Phase 2 Multicenter Clinical Trial. Front Oncol. 2020 Aug 7;10:1314. doi: 10.3389/fonc.2020.01314. eCollection 2020.
Results Reference
derived
Learn more about this trial
The Value of Concurrent Chemoradiotherapy for Stage II Nasopharyngeal Carcinoma
We'll reach out to this number within 24 hrs