A randomized phase 3 trial comparing nimotuzumab plus cisplatin chemoradiotherapy versus cisplatin chemoradiotherapy alone in locally advanced head and neck cancer. Issue 18 (31st May 2019)
- Record Type:
- Journal Article
- Title:
- A randomized phase 3 trial comparing nimotuzumab plus cisplatin chemoradiotherapy versus cisplatin chemoradiotherapy alone in locally advanced head and neck cancer. Issue 18 (31st May 2019)
- Main Title:
- A randomized phase 3 trial comparing nimotuzumab plus cisplatin chemoradiotherapy versus cisplatin chemoradiotherapy alone in locally advanced head and neck cancer
- Authors:
- Patil, Vijay Maruti
Noronha, Vanita
Joshi, Amit
Agarwal, Jaiprakash
Ghosh‐Laskar, Sarbani
Budrukkar, Ashwini
Murthy, Vedang
Gupta, Tejpal
Mahimkar, Manoj
Juvekar, Shashikant
Arya, Supreeta
Mahajan, Abhishek
Agarwal, Archi
Purandare, Nilendu
Rangarajan, Venkatesh
Balaji, Arun
Chaudhari, Sameer Vasant
Banavali, Shripad
Kannan, Sadhana
Bhattacharjee, Atanu
D'Cruz, Anil K.
Chaturvedi, Pankaj
Pai, Prathamesh S.
Chaukar, Devendra
Pantvaidya, Gouri
Nair, Deepa
Nair, Sudhir
Deshmukh, Anuja
Thiagarajan, Shivakumar
Mathrudev, Vijayalakshmi
Manjrekar, Aparna
Dhumal, Sachin
Maske, Kamesh
Bhelekar, Arti Sanjay
Nawale, Kavita
Chandrasekharan, Arun
Pande, Nikhil
Goel, Alok
Talreja, Vikas
Simha, Vijai
Srinivas, Sujay
Swami, Rohit
Vallathol, Dilip Harindran
Dsouza, Hollis
Shrirangwar, Sameer
Turkar, Siddharth
Abraham, George
Thanky, Aditi Harsh
Patel, Usha
Pandey, Manish Kumar
Prabhash, Kumar
… (more) - Abstract:
- Abstract : Background: Because the addition of nimotuzumab to chemoradiation in patients with locally advanced head and neck cancer improved outcomes in a phase 2 study, the authors conducted a phase 3 study to confirm these findings. Methods: This open‐label, investigator‐initiated, phase 3, randomized trial was conducted from 2012 to 2018. Adult patients with locally advanced head and neck cancer who were fit for radical chemoradiation were randomized 1:1 to receive either radical radiotherapy (66‐70 grays) with concurrent weekly cisplatin (30 mg/m 2 ) (CRT) or the same schedule of CRT with weekly nimotuzumab (200 mg) (NCRT).The primary endpoint was progression‐free survival (PFS); key secondary endpoints were disease‐free survival (DFS), duration of locoregional control (LRC), and overall survival (OS). An intent‐to‐treat analysis also was performed. Results: In total, 536 patients were allocated equally to both treatment arms. The median follow‐up was 39.13 months. The addition of nimotuzumab improved PFS (hazard ratio [HR], 0.69; 95% CI, 0.53‐0.89; P = .004), LRC (HR, 0.67; 95% CI, 0.50‐0.89; P = .006), and DFS (HR, 0.71; 95% CI, 0.55‐0.92; P = .008) and had a trend toward improved OS (HR, 0.84; 95% CI, 0.65‐1.08; P = .163). Grade 3 through 5 adverse events were similar between the 2 arms, except for a higher incidence of mucositis in the NCRT arm (66.7% vs 55.8%; P = .01). Conclusions: The addition of nimotuzumab to concurrent weekly CRT improves PFS, LRC, andAbstract : Background: Because the addition of nimotuzumab to chemoradiation in patients with locally advanced head and neck cancer improved outcomes in a phase 2 study, the authors conducted a phase 3 study to confirm these findings. Methods: This open‐label, investigator‐initiated, phase 3, randomized trial was conducted from 2012 to 2018. Adult patients with locally advanced head and neck cancer who were fit for radical chemoradiation were randomized 1:1 to receive either radical radiotherapy (66‐70 grays) with concurrent weekly cisplatin (30 mg/m 2 ) (CRT) or the same schedule of CRT with weekly nimotuzumab (200 mg) (NCRT).The primary endpoint was progression‐free survival (PFS); key secondary endpoints were disease‐free survival (DFS), duration of locoregional control (LRC), and overall survival (OS). An intent‐to‐treat analysis also was performed. Results: In total, 536 patients were allocated equally to both treatment arms. The median follow‐up was 39.13 months. The addition of nimotuzumab improved PFS (hazard ratio [HR], 0.69; 95% CI, 0.53‐0.89; P = .004), LRC (HR, 0.67; 95% CI, 0.50‐0.89; P = .006), and DFS (HR, 0.71; 95% CI, 0.55‐0.92; P = .008) and had a trend toward improved OS (HR, 0.84; 95% CI, 0.65‐1.08; P = .163). Grade 3 through 5 adverse events were similar between the 2 arms, except for a higher incidence of mucositis in the NCRT arm (66.7% vs 55.8%; P = .01). Conclusions: The addition of nimotuzumab to concurrent weekly CRT improves PFS, LRC, and DFS. This combination provides a novel alternative therapeutic option to a 3‐weekly schedule of 100 mg/m 2 cisplatin in patients with locally advanced head and neck cancer who are treated with radical‐intent CRT. Abstract : The addition of nimotuzumab to concurrent weekly cisplatin and chemoradiotherapy improves outcomes. This combination provides a novel alternative therapeutic option to a 3 weekly schedule of 100 mg/m 2 cisplatin in patients with head and neck cancer. … (more)
- Is Part Of:
- Cancer. Volume 125:Issue 18(2019)
- Journal:
- Cancer
- Issue:
- Volume 125:Issue 18(2019)
- Issue Display:
- Volume 125, Issue 18 (2019)
- Year:
- 2019
- Volume:
- 125
- Issue:
- 18
- Issue Sort Value:
- 2019-0125-0018-0000
- Page Start:
- 3184
- Page End:
- 3197
- Publication Date:
- 2019-05-31
- Subjects:
- Chemoradiation -- epidermal growth factor receptor (EGFR) -- head and neck cancer -- nimotuzumab
Cancer -- Periodicals
Cancer -- Cytopathology -- Periodicals
616.99405 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0142 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cncr.32179 ↗
- Languages:
- English
- ISSNs:
- 0008-543X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.450000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11635.xml