Endostatin in Combination With Chemotherapy for Metastatic Nasopharyngeal Carcinoma

NCT01915134 — Phase 3, Unknown, 362 participants, Zhejiang Cancer Hospital

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A Prospective,Randomized,Controlled,Multicenter,Phase III Study of Stage Ⅲ Study of Gemcitabine Plus Cisplatin With or Without Endostatin to the Metastatic Nasopharyngeal Carcinoma

RegistryNCT01915134
StatusUnknown
PhasePhase 3
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment362 (Estimated)
SponsorZhejiang Cancer Hospital (Other); collaborators: Zhejiang University, Second Affiliated Hospital, Zhejiang University, School of Medicine, Sir Run Run Shaw Hospital
ConditionsEffects of Chemotherapy, Stage IVC Nasopharyngeal Carcinoma
InterventionsRecombinant Human Endostatin plus gemcitabine and cisplatin, Gemcitabine and cisplatin (Drug)
Datesstart 2013-08-01, primary completion 2016-01-01 (estimated), completion 2016-12-01 (estimated), first posted 2013-08-02, last updated 2015-01-01
Locations1 site in China

Related Papers Related Patents Related Grants Related Experts
All trials for Effects of Chemotherapy All trials for Stage IVC Nasopharyngeal Carcinoma All trials of Recombinant Human Endostatin plus gemcitabine and cisplatin All trials of Gemcitabine and cisplatin

-Summary

The investigators designed this study to evaluate the efficiency and the acute toxicities of recombinant human endostatin (endostar) combined with chemotherapy in the metastatic nasopharyngeal carcinoma (NPC).

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+Detailed description

To evaluate the progression free survival (PFS), overall survival (OS), Acute adverse reaction of recombinant human endostatin (endostar) combined with chemotherapy to the metastatic nasopharyngeal carcinoma (NPC).

+Arms and interventions

ArmTypeInterventionsDescription
EGP groupExperimentalDrug: Recombinant Human Endostatin plus gemcitabine and cisplatinthe group of participants who undergoing Recombinant Human Endostatin plus Gemcitabine and cisplatin chemotherapy
GP groupActive comparatorDrug: Gemcitabine and cisplatinthe group of participants who undergoing only Gemcitabine and cisplatin chemotherapy
  • Recombinant Human Endostatin plus gemcitabine and cisplatin (Drug), also known as Experimental: EGP group: target therapy plus chemotherapy:4-6 cycles of Recombinant Human Endostatin plus gemcitabine and cisplatin:Endostatin:7.5mg/m2/d,d1-14,concomitant with chemotherapy for 4-6 cycles.Gemcitabine and cisplatin:4-6 cycles of GP chemotherapy with gemcitabine 1000mg/m2,d1,8,cisplatin80mg/m2,d1.Chemotherapy will be given once every three weeks.
  • Gemcitabine and cisplatin (Drug), also known as No Intervention: GP group: only chemotherapy:Gemcitabine and cisplatin:4-6 cycles of GP chemotherapy with gemcitabine 1000mg/m2,d1,8,cisplatin80mg/m2,d1.Chemotherapy will be given once every three weeks.

+Outcome measures

Primary outcomes

  • progress free survival(PFS) [2years after the inception assignment]: PFS means assignment to the date of any local or distant progress of the disease using Kaplan-Meier calculate the progress free survival rates,and find out is there significant difference between these two groups.

Secondary outcomes

  • overall survival(OS) [1 year ,2 years and 3 years after the inception of the assignment]: the overall survival denote to assignment to date of death from any cause. Using Kaplan-Meier to calculate the 2-year ,3-year,5-year overall survival rate,and find is there any significant difference between these two groups.
  • Adverse events [participants will be followed for the duration of hospital stay,an expected average of 100 days and every 3 months thereafter for 3 years]: observe and record the toxicity profile(including but not limit to mucositis,liver and kidney function,et al.)according NCI-CTCAE(3rd edition) during the neoadjuvant chemotherapy ,chemoradiation and follow-up.

Other outcomes

  • The quality of life assessment [participants will be followed for the duration of hospital stay,an expected average of 100 days and every 6 months thereafter for 3 years]: According to the most commonly used questionnaire EORTC QLQ C30 and H\&N35 35 for evaluation

+Eligibility

Sex: All, ages: 18 Years to 65 Years

Inclusion Criteria:

* metastatic nasopharyngeal carcinoma 6 months after first treatment,never receive any anticancer treatment except local radiotherapy to the bone metastasis,at least one measurable metastatic lesions,ECOG PS 0-1,Electrocardiogram (ecg) no special abnormal,comply with the test requirements, cooperate with regular follow-up.

Exclusion Criteria:

* To give local treatment,clinical severe infection(>grade 2),with the central nervous system metastases,ECOG PS≥2,patients with pregnancy or breastfeeding,has a history of peripheral nerve disease,concomitant with other serious diseases,ever or concomitant with other serious diseases except for Cervical carcinoma in situ,cure of basal cell carcinoma,bladder surface tumor,any cancer 3 years after curation.

+Locations (1)

FacilityCityCountryStatus
Zhejiang Cancer HospitalHangzhou, ZhejiangChinaRecruiting

+Investigators

  • Xiaozhong Chen, Principal investigator, Zhejiang Cancer Hospital
  • Xiaozhong Chen, Principal investigator, Zhejiang Cancer Hospital Hangzhou, Zhejiang, China 310022