Demographics, Pattern of Care, and Outcome Analysis of Malignant Melanomas - Experience From a Tertiary Cancer Centre in India.

BRAF LMICs Paclitaxel-carboplatin-LD interferon regimen chemotherapy immune checkpoint inhibitors malignant melanoma oral metronomic therapy

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 16 05 2021
accepted: 30 07 2021
entrez: 27 9 2021
pubmed: 28 9 2021
medline: 28 9 2021
Statut: epublish

Résumé

Treatment of malignant melanoma has undergone a paradigm shift with the advent of immune checkpoint inhibitors (ICI) and targeted therapies. However, access to ICI is limited in low-middle income countries (LMICs). Histologically confirmed malignant melanoma cases registered from 2013 to 2019 were analysed for pattern of care, safety, and efficacy of systemic therapies (ST). There were 659 patients with a median age of 53 (range 44-63) years; 58.9% were males; 55.2% were mucosal melanomas. Most common primary sites were extremities (36.6%) and anorectum (31.4%). Nearly 10.8% of the metastatic cohort were BRAF mutated. Among 368 non-metastatic patients (172 prior treated, 185 de novo, and 11 unresectable), with a median follow-up of 26 months (0-83 months), median EFS and OS were 29.5 (95% CI: 22-40) and 33.3 (95% CI: 29.5-41.2) months, respectively. In the metastatic cohort, with a median follow up of 24 (0-85) months, the median EFS for BSC was 3.1 (95% CI 1.9-4.8) months versus 3.98 (95% CI 3.2-4.7) months with any ST (HR: 0.69, 95% CI: 0.52-0.92; P = 0.011). The median OS was 3.9 (95% CI 3.3-6.4) months for BSC alone versus 12.0 (95% CI 10.5-15.1) months in any ST (HR: 0.38, 95% CI: 0.28-0.50; P < 0.001). The disease control rate was 51.55%. Commonest grade 3-4 toxicity was anemia with chemotherapy (9.5%) and ICI (8.8%). In multivariate analysis, any ST received had a better prognostic impact in the metastatic cohort. Large real-world data reflects the treatment patterns adopted in LMIC for melanomas and poor access to expensive, standard of care therapies. Other systemic therapies provide meaningful clinical benefit and are worth exploring especially when the standard therapies are challenging to administer.

Sections du résumé

BACKGROUND BACKGROUND
Treatment of malignant melanoma has undergone a paradigm shift with the advent of immune checkpoint inhibitors (ICI) and targeted therapies. However, access to ICI is limited in low-middle income countries (LMICs).
PATIENTS AND METHODS METHODS
Histologically confirmed malignant melanoma cases registered from 2013 to 2019 were analysed for pattern of care, safety, and efficacy of systemic therapies (ST).
RESULTS RESULTS
There were 659 patients with a median age of 53 (range 44-63) years; 58.9% were males; 55.2% were mucosal melanomas. Most common primary sites were extremities (36.6%) and anorectum (31.4%). Nearly 10.8% of the metastatic cohort were BRAF mutated. Among 368 non-metastatic patients (172 prior treated, 185 de novo, and 11 unresectable), with a median follow-up of 26 months (0-83 months), median EFS and OS were 29.5 (95% CI: 22-40) and 33.3 (95% CI: 29.5-41.2) months, respectively. In the metastatic cohort, with a median follow up of 24 (0-85) months, the median EFS for BSC was 3.1 (95% CI 1.9-4.8) months versus 3.98 (95% CI 3.2-4.7) months with any ST (HR: 0.69, 95% CI: 0.52-0.92; P = 0.011). The median OS was 3.9 (95% CI 3.3-6.4) months for BSC alone versus 12.0 (95% CI 10.5-15.1) months in any ST (HR: 0.38, 95% CI: 0.28-0.50; P < 0.001). The disease control rate was 51.55%. Commonest grade 3-4 toxicity was anemia with chemotherapy (9.5%) and ICI (8.8%). In multivariate analysis, any ST received had a better prognostic impact in the metastatic cohort.
CONCLUSIONS CONCLUSIONS
Large real-world data reflects the treatment patterns adopted in LMIC for melanomas and poor access to expensive, standard of care therapies. Other systemic therapies provide meaningful clinical benefit and are worth exploring especially when the standard therapies are challenging to administer.

Identifiants

pubmed: 34568037
doi: 10.3389/fonc.2021.710585
pmc: PMC8456006
doi:

Types de publication

Journal Article

Langues

eng

Pagination

710585

Informations de copyright

Copyright © 2021 Bajpai, Abraham, Saklani, Agarwal, Das, Chatterjee, Kapoor, Eaga, Mondal, Chandrasekharan, Bhargava, Srinivas, Turkar, Rekhi, Khanna, Janu, Bal, Ostwal, Ramaswamy, Rohila, Desouza, Guha, Kumar, Menon, Rath, Patil, Noronha, Joshi, Laskar, Rangarajan, Prabhash, Gupta and Banavali.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jyoti Bajpai (J)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

George Abraham (G)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Avanish P Saklani (AP)

Department of Surgical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Anshul Agarwal (A)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Sashanka Das (S)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Ambarish Chatterjee (A)

Department of Surgical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Akhil Kapoor (A)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Prathyusha Eaga (P)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Pradip Kumar Mondal (PK)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Arun Chandrasekharan (A)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Prabhat Ghanshyam Bhargava (PG)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Sujay Srinivas (S)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Siddharth Turkar (S)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Bharat Rekhi (B)

Department of Surgical Pathology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Nehal Khanna (N)

Department of Radiation Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Amit Kumar Janu (AK)

Department of Radiodiagnosis, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Munita Bal (M)

Department of Surgical Pathology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Vikas Sureshchand Ostwal (VS)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Anant Ramaswamy (A)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Jitender Rohila (J)

Department of Surgical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Ashwin L Desouza (AL)

Department of Surgical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Amrita Guha (A)

Department of Radiodiagnosis, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Rajiv Kumar (R)

Department of Surgical Pathology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Nandini Sharrel Menon (NS)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Sushmita Rath (S)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Vijay Maruti Patil (VM)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Vanita Maria Noronha (VM)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Amit Prakashchandra Joshi (AP)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Siddhartha Laskar (S)

Department of Radiation Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Venkatesh Rangarajan (V)

Department of Nuclear Medicine, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Kumar Prabhash (K)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Sudeep Gupta (S)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Shripad Banavali (S)

Department of Medical Oncology, Tata Memorial Hospital, Homibhabha National Institute, Mumbai, India.

Classifications MeSH