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Phase 3 RCT comparing docetaxel-platinum with docetaxel-platinum-5FU as neoadjuvant chemotherapy in borderline resectable oral cancer.
Noronha, Vanita; Patil, Vijay; Chaturvedi, Pankaj; Mathrudev, Vijayalakshmi; Menon, Nandini; Bhattacharjee, Atanu; Singh, Ajay; Peelay, Zoya; Chakraborty, Shatabdi; Jadhav, Monica; Alone, Mitali; Bhagyavant, Priyanka; Kolkur, Manali; Srinivas, Sujay; Das, Sudeep; Roy, Somnath; Mandal, Tanmoy; Dsouza, Hollis; Saha, Saswata; Rai, Rahul; Srikanth, Anne; Shah, Darshit; Khan, Arif; Muthuluri, Hemanth; Kumar, Amit; Agarwal, Amit; Rajpurohit, Anu; Goli, Vasu Babu; Sekar, Anbarasan; Mantri, Anoop; Kanteti, Aditya Pavan Kumar; Majumdar, Swaratika; Khaddar, Satvik; Shenoy, Ramnath; Elamarthi, Prahlad; Rathnasamy, Narmadha; Kashyap, Lakhan; Abraham, George; Booma, Naveen; Simha, Vijay; Chaukar, Devendra; Pai, Prathamesh; Nair, Sudhir; Laskar, Sarbani; Nawale, Kavita; Naidu, Priyanka; Salian, Sushmita; Shelar, Priyanka; Raulo, Ravinarayan; Dhumal, Sachin Babanrao.
Afiliação
  • Noronha V; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Patil V; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Chaturvedi P; Department of Head and Neck Surgery, Tata Memorial Centre, HBNI, Mumbai, India.
  • Mathrudev V; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Menon N; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Bhattacharjee A; Section of Biostatistics, Centre for Cancer Epidemiology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Singh A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Peelay Z; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Chakraborty S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Jadhav M; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Alone M; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Bhagyavant P; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Kolkur M; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Srinivas S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Das S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Roy S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Mandal T; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Dsouza H; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Saha S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Rai R; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Srikanth A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Shah D; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Khan A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Muthuluri H; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Kumar A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Agarwal A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Rajpurohit A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Goli VB; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Sekar A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Mantri A; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Kanteti APK; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Majumdar S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Khaddar S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Shenoy R; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Elamarthi P; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Rathnasamy N; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Kashyap L; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Abraham G; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Booma N; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Simha V; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Chaukar D; Department of Head and Neck Surgery, Tata Memorial Centre, HBNI, Mumbai, India.
  • Pai P; Department of Head and Neck Surgery, Tata Memorial Centre, HBNI, Mumbai, India.
  • Nair S; Department of Head and Neck Surgery, Tata Memorial Centre, HBNI, Mumbai, India.
  • Laskar S; Department of Radiation Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Nawale K; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Naidu P; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Salian S; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Shelar P; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Raulo R; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
  • Dhumal SB; Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai, India.
Eur J Cancer ; 200: 113560, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38306841
ABSTRACT

BACKGROUND:

Neoadjuvant chemotherapy (NACT) with TPF (docetaxel, cisplatin, and 5FU) is one of the treatment options in very locally advanced oral cancer with a survival advantage over PF (cisplatin and 5FU). TP (docetaxel and cisplatin) has shown promising results with a lower rate of adverse events but has never been compared to TPF.

METHODS:

In this phase 3 randomized superiority study, adult patients with borderline resectable locally advanced oral cancers were randomized in a 11 fashion to either TP or TPF. After the administration of 2 cycles, patients were evaluated in a multidisciplinary clinic and further treatment was planned. The primary endpoint was overall survival (OS) and secondary endpoints were progression-free survival (PFS) and adverse events.

RESULTS:

495 patients were randomized in this study, 248 patients in TP arm and 247 in TPF arm. The 5-year OS was 18.5% (95% CI 13.8-23.7) and 23.9% (95% CI 18.1-30.1) in TP and TPF arms, respectively (Hazard ratio 0.778; 95% CI 0.637-0.952; P = 0.015). Following NACT, 43.8% were deemed resectable, but 34.5% underwent surgery. The 5-year OS was 50.7% (95% CI 41.5-59.1) and 5% (95%CI 2.9-8.1), respectively, in the surgically resected versus unresected cohort post NACT (P < 0.0001). Grade 3 or above adverse events were seen in 97 (39.1%) and 179 (72.5%) patients in the TP and TPF arms, respectively (P < 0.0001).

CONCLUSION:

NACT with TPF has a survival benefit over TP in borderline resectable oral cancers, with an increase in toxicity which is manageable. Patients who undergo surgery achieve a relatively good, sustained survival.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Neoplasias de Cabeça e Pescoço Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Revista: Eur J Cancer Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Neoplasias de Cabeça e Pescoço Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Revista: Eur J Cancer Ano de publicação: 2024 Tipo de documento: Article