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A randomized phase 3 trial comparing nimotuzumab plus cisplatin chemoradiotherapy versus cisplatin chemoradiotherapy alone in locally advanced head and neck cancer.
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.
Afiliação
  • Patil VM; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Noronha V; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Joshi A; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Agarwal J; Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Ghosh-Laskar S; Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Budrukkar A; Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Murthy V; Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Gupta T; Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Mahimkar M; Mahimkar Laboratory, Advanced Center for Treatment, Research, and Education in Cancer, Navi Mumbai, India.
  • Juvekar S; Department of Radiology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Arya S; Department of Radiology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Mahajan A; Department of Radiology, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Agarwal A; Department of Nuclear Medicine, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Purandare N; Department of Nuclear Medicine, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Rangarajan V; Department of Nuclear Medicine, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Balaji A; Department of Speech and Therapy, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Chaudhari SV; Biocon Ltd, Bengaluru, India.
  • Banavali S; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Kannan S; Department of Biostatistics, Advanced Center for Treatment, Research, and Education in Cancer, Navi Mumbai, India.
  • Bhattacharjee A; Department of Epidemiology, Advanced Center for Treatment, Research, and Education in Cancer, Navi Mumbai, India.
  • D'Cruz AK; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Chaturvedi P; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Pai PS; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Chaukar D; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Pantvaidya G; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Nair D; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Nair S; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Deshmukh A; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Thiagarajan S; Department of Head and Neck Surgery, Tata Memorial Hospital, HBNI, Mumbai, India.
  • Mathrudev V; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Manjrekar A; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Dhumal S; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Maske K; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Bhelekar AS; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Nawale K; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Chandrasekharan A; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Pande N; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Goel A; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Talreja V; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Simha V; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Srinivas S; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Swami R; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Vallathol DH; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Dsouza H; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Shrirangwar S; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Turkar S; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Abraham G; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Thanky AH; Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
  • Patel U; Mahimkar Laboratory, Advanced Center for Treatment, Research, and Education in Cancer, Navi Mumbai, India.
  • Pandey MK; Mahimkar Laboratory, Advanced Center for Treatment, Research, and Education in Cancer, Navi Mumbai, India.
Cancer ; 125(18): 3184-3197, 2019 09 15.
Article em En | MEDLINE | ID: mdl-31150120
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 11 to receive either radical radiotherapy (66-70 grays) with concurrent weekly cisplatin (30 mg/m2 ) (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/m2 cisplatin in patients with locally advanced head and neck cancer who are treated with radical-intent CRT.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cisplatino / Anticorpos Monoclonais Humanizados / Quimiorradioterapia / Antineoplásicos Imunológicos / Carcinoma de Células Escamosas de Cabeça e Pescoço / Neoplasias de Cabeça e Pescoço / Antineoplásicos Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cisplatino / Anticorpos Monoclonais Humanizados / Quimiorradioterapia / Antineoplásicos Imunológicos / Carcinoma de Células Escamosas de Cabeça e Pescoço / Neoplasias de Cabeça e Pescoço / Antineoplásicos Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Índia