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Spots Global Cancer Trial Database for Therapeutic Gain by Induction-concurrent Chemoradiotherapy and/or Accelerated Fractionation for Nasopharyngeal Carcinoma

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Trial Identification

Brief Title: Therapeutic Gain by Induction-concurrent Chemoradiotherapy and/or Accelerated Fractionation for Nasopharyngeal Carcinoma

Official Title: Randomized Trial to Evaluate Therapeutic Gain by Changing Chemoradiotherapy From Concurrent-adjuvant to Induction-concurrent Sequence, and Radiotherapy From Conventional to Accelerated Fractionation for Advanced Nasopharyngeal Carcinoma

Study ID: NCT00379262

Study Description

Brief Summary: The objectives of this clinical study are threefold: 1. To compare the benefits in cancer control and survival obtained from adding induction-concurrent chemotherapy to radiation with those from adding concurrent-adjuvant chemotherapy to radiation. 2. To test whether replacing fluorouracil with Xeloda in combining with cisplatin in the chemotherapy plan will maintain or improve further the chemotherapy benefits while reducing the duration of hospital stay. 3. To see if accelerated fractionation radiotherapy can improve the outcome of patients as compared with conventional fractionation radiotherapy.

Detailed Description: 1. primary objectives include 1. comparing induction chemotherapy with Cisplatin + 5-Fluorouracil versus adjuvant chemotherapy with Cisplatin + 5-Fluorouracil(PF-Pvs P-PF) 2. comparing induction chemotherapy with Cisplatin + Capecitabine versus adjuvant chemotherapy with Cisplatin + 5-Fluorouracil(PX-P vs P-PF) 3. comparing accelerated fractionation versus conventional fractionation (AF vs CF)radiotherapy. 2. secondary objectives include 1. comparing induction chemotherapy with Cisplatin + Capecitabine versus induction chemotherapy with Cisplatin + 5-Fluorouracil(PX-P vs PX-P) 2. Comparing concurrent-adjuvant (CA) versus induction-concurrent (IC) chemotherapy sequence.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cancer Center, Sun Yat Sen University, Guangzhou, , China

Department of Clinical Oncology, Pamela Youde Nethersole Eastern Hospital, Hong Kong, , China

Department of Clinical Oncology, Prince of Wales Hospital, Hong Kong, , China

Department of Clinical Oncology, Princess Margaret Hospital, Hong Kong, , China

Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, , China

Department of Clinical Oncology, Queen Mary Hospital, Hong Kong, , China

Department of Clinical Oncology, Tuen Mun Hospital, Hong Kong, , China

Contact Details

Name: Anne W.M. Lee, F.R.C.R.

Affiliation: Department of Clinical Oncology, Pamela Youde Nethersole Eastern Hospital, Hong Kong

Role: PRINCIPAL_INVESTIGATOR

Name: Roger K.C. Ngan, F.R.C.R

Affiliation: Department of Clinical Oncology, Quen Elizabeth Hospital, Hong Kong

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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