Low-cost oral metronomic chemotherapy versus intravenous cisplatin in patients with recurrent, metastatic, inoperable head and neck carcinoma: an open-label, parallel-group, non-inferiority, randomised, phase 3 trial.


Journal

The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665

Informations de publication

Date de publication:
09 2020
Historique:
received: 18 03 2020
revised: 20 05 2020
accepted: 27 05 2020
entrez: 23 8 2020
pubmed: 23 8 2020
medline: 5 9 2020
Statut: ppublish

Résumé

Regimens for palliation in patients with head and neck cancer recommended by the US National Comprehensive Cancer Network (NCCN) have low applicability (less than 1-3%) in low-income and middle-income countries (LMICs) because of their cost. In a previous phase 2 study, patients with head and neck cancer who received metronomic chemotherapy had better outcomes when compared with those who received intravenous cisplatin, which is commonly used as the standard of care in LMICs. We aimed to do a phase 3 study to substantiate these findings. We did an open-label, parallel-group, non-inferiority, randomised, phase 3 trial at the Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India. We enrolled adult patients (aged 18-70 years) who planned to receive palliative systemic treatment for relapsed, recurrent, or newly diagnosed squamous cell carcinoma of the head and neck, and who had an Eastern Cooperative Oncology Group performance status score of 0-1 and measurable disease, as defined by the Response Evaluation Criteria In Solid Tumors. We randomly assigned (1:1) participants to receive either oral metronomic chemotherapy, consisting of 15 mg/m Between May 16, 2016, and Jan 17, 2020, 422 patients were randomly assigned: 213 to the oral metronomic chemotherapy group and 209 to the intravenous cisplatin group. All 422 patients were included in the intention-to-treat analysis, and 418 patients (211 in the oral metronomic chemotherapy group and 207 in the intravenous cisplatin group) were included in the per-protocol analysis. At a median follow-up of 15·73 months, median overall survival in the intention-to-treat analysis population was 7·5 months (IQR 4·6-12·6) in the oral metronomic chemotherapy group compared with 6·1 months (3·2-9·6) in the intravenous cisplatin group (unadjusted HR for death 0·773 [95% CI 0·615-0·97, p=0·026]). In the per-protocol analysis population, median overall survival was 7·5 months (4·7-12·8) in the oral metronomic chemotherapy group and 6·1 months (3·4-9·6) in the intravenous cisplatin group (unadjusted HR for death 0·775 [95% CI 0·616-0·974, p=0·029]). Grade 3 or higher adverse events were observed in 37 (19%) of 196 patients in the oral metronomic chemotherapy group versus 61 (30%) of 202 patients in the intravenous cisplatin group (p=0·01). Oral metronomic chemotherapy is non-inferior to intravenous cisplatin with respect to overall survival in head and neck cancer in the palliative setting, and is associated with fewer adverse events. It therefore represents a new alternative standard of care if current NCCN-approved options for palliative therapy are not feasible. Tata Memorial Center Research Administration Council. For the Hindi, Marathi, Gujarati, Kannada, Malayalam, Telugu, Oriya, Bengali, and Punjabi translations of the abstract see Supplementary Materials section.

Sections du résumé

BACKGROUND
Regimens for palliation in patients with head and neck cancer recommended by the US National Comprehensive Cancer Network (NCCN) have low applicability (less than 1-3%) in low-income and middle-income countries (LMICs) because of their cost. In a previous phase 2 study, patients with head and neck cancer who received metronomic chemotherapy had better outcomes when compared with those who received intravenous cisplatin, which is commonly used as the standard of care in LMICs. We aimed to do a phase 3 study to substantiate these findings.
METHODS
We did an open-label, parallel-group, non-inferiority, randomised, phase 3 trial at the Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India. We enrolled adult patients (aged 18-70 years) who planned to receive palliative systemic treatment for relapsed, recurrent, or newly diagnosed squamous cell carcinoma of the head and neck, and who had an Eastern Cooperative Oncology Group performance status score of 0-1 and measurable disease, as defined by the Response Evaluation Criteria In Solid Tumors. We randomly assigned (1:1) participants to receive either oral metronomic chemotherapy, consisting of 15 mg/m
FINDINGS
Between May 16, 2016, and Jan 17, 2020, 422 patients were randomly assigned: 213 to the oral metronomic chemotherapy group and 209 to the intravenous cisplatin group. All 422 patients were included in the intention-to-treat analysis, and 418 patients (211 in the oral metronomic chemotherapy group and 207 in the intravenous cisplatin group) were included in the per-protocol analysis. At a median follow-up of 15·73 months, median overall survival in the intention-to-treat analysis population was 7·5 months (IQR 4·6-12·6) in the oral metronomic chemotherapy group compared with 6·1 months (3·2-9·6) in the intravenous cisplatin group (unadjusted HR for death 0·773 [95% CI 0·615-0·97, p=0·026]). In the per-protocol analysis population, median overall survival was 7·5 months (4·7-12·8) in the oral metronomic chemotherapy group and 6·1 months (3·4-9·6) in the intravenous cisplatin group (unadjusted HR for death 0·775 [95% CI 0·616-0·974, p=0·029]). Grade 3 or higher adverse events were observed in 37 (19%) of 196 patients in the oral metronomic chemotherapy group versus 61 (30%) of 202 patients in the intravenous cisplatin group (p=0·01).
INTERPRETATION
Oral metronomic chemotherapy is non-inferior to intravenous cisplatin with respect to overall survival in head and neck cancer in the palliative setting, and is associated with fewer adverse events. It therefore represents a new alternative standard of care if current NCCN-approved options for palliative therapy are not feasible.
FUNDING
Tata Memorial Center Research Administration Council.
TRANSLATIONS
For the Hindi, Marathi, Gujarati, Kannada, Malayalam, Telugu, Oriya, Bengali, and Punjabi translations of the abstract see Supplementary Materials section.

Identifiants

pubmed: 32827483
pii: S2214-109X(20)30275-8
doi: 10.1016/S2214-109X(20)30275-8
pii:
doi:

Substances chimiques

Cisplatin Q20Q21Q62J

Banques de données

CTRI
['CTRI/2015/11/006388']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1213-e1222

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Vijay Patil (V)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Vanita Noronha (V)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Sachin Babanrao Dhumal (SB)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Amit Joshi (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Nandini Menon (N)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Atanu Bhattacharjee (A)

Section of Biostatistics, Centre for Cancer Epidemiology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Suyash Kulkarni (S)

Department of Radiodiagnosis, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Suman Kumar Ankathi (SK)

Department of Radiodiagnosis, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Abhishek Mahajan (A)

Department of Radiodiagnosis, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Nilesh Sable (N)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Kavita Nawale (K)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Arti Bhelekar (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Sadaf Mukadam (S)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Arun Chandrasekharan (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Sudeep Das (S)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Dilip Vallathol (D)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Hollis D'Souza (H)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Amit Kumar (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Amit Agrawal (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Satvik Khaddar (S)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Narmadha Rathnasamy (N)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Ramnath Shenoy (R)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Lakhan Kashyap (L)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Rahul Kumar Rai (RK)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

George Abraham (G)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Saswata Saha (S)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Swaratika Majumdar (S)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Naveen Karuvandan (N)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Vijai Simha (V)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Vasu Babu (V)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Prahalad Elamarthi (P)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Annu Rajpurohit (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Kanteti Aditya Pavan Kumar (KAP)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Anne Srikanth (A)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Rahul Ravind (R)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Shripad Banavali (S)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India.

Kumar Prabhash (K)

Department of Medical Oncology, Tata Memorial Center, Homi Bhabha National Institute, Mumbai, India. Electronic address: id-kumarprabhashtmh@gmail.com.

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