An Audit of Systemic Therapy in Medullary Carcinoma Thyroid.

Immediate Medullary thyroid cancer Sorafenib Symptomatic Tyrosine kinase inhibitor (TKI)

Journal

Indian journal of surgical oncology
ISSN: 0975-7651
Titre abrégé: Indian J Surg Oncol
Pays: India
ID NLM: 101532448

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 05 04 2021
accepted: 23 06 2021
entrez: 25 4 2022
pubmed: 26 4 2022
medline: 26 4 2022
Statut: ppublish

Résumé

There is a paucity of evidence of the impact of sorafenib on MCT and it is the preferred therapy used in India. We decided to do an audit of all patients of MCT who were referred to us for systemic therapy. The objective of this exercise was to identify the treatment pattern, outcomes, and adverse events with therapy in MCT. Baseline demographics (age, gender, ECOG PS, comorbidities, habits), tumor details (site of metastasis), previous treatment details, clinical features at metastasis (symptomatic or asymptomatic), the pattern of treatment, adverse events (CTCAE version 4.02), date of progression, date of death and status, and follow-up were extracted from the rare tumor database and electronic medical records. Out of 75 patients referred for therapy for MCT, 47 (62.7%) patients were considered for immediate tyrosine kinase inhibitors as they had symptomatic status and 28 (37.3%) patients were kept on observation due to the asymptomatic nature of the disease. Out of the 28 patients, 15 (53.6%, n = 28) patients were subsequently started on TKI while in 13 (46.4%, n = 28) patients observation was continued. In the overall cohort, the median PFS was 18.9 months (95% CI 11.9-29.9) and OS was 26.6 months (95% CI 14.4-39.0). Among variables tested, only female gender had an impact on PFS (hazard ratio = 0.364 95% CI 0.148-0.895; P = 0.028) and the absence of lung metastasis had a positive impact on OS (hazard ratio = 0.443 95% CI 0.207-0.95; P = 0.037). Most commonly used TKI was sorafenib (n = 61) and sunitinib in 1 patient. The most common adverse events with TKI were palmo-plantar dysesthesia (50, 80.6%) and oral mucositis (25, 40.2%). The strategy of treating symptomatic MCT and observing in asymptomatic MCT is associated with reasonable PFS and OS. Sorafenib is the most commonly used TKI in our setup and provides similar outcomes as globally.

Identifiants

pubmed: 35462671
doi: 10.1007/s13193-021-01381-x
pii: 1381
pmc: PMC8986934
doi:

Types de publication

Journal Article

Langues

eng

Pagination

61-67

Informations de copyright

© Indian Association of Surgical Oncology 2021.

Déclaration de conflit d'intérêts

Conflict of InterestThe authors declare no competing interests.

Références

J Clin Oncol. 2012 Jan 10;30(2):134-41
pubmed: 22025146
Exp Clin Endocrinol Diabetes. 2019 Apr;127(4):240-246
pubmed: 29506310
J Clin Oncol. 2010 May 10;28(14):2323-30
pubmed: 20368568
Thyroid. 2015 Jun;25(6):567-610
pubmed: 25810047
Drugs. 2020 Nov;80(17):1865-1870
pubmed: 33136236
N Engl J Med. 2020 Aug 27;383(9):825-835
pubmed: 32846061
Head Neck. 2019 Aug;41(8):2823-2829
pubmed: 31162772
Eur J Endocrinol. 2011 Aug;165(2):315-22
pubmed: 21566072
J Clin Oncol. 2013 Oct 10;31(29):3639-46
pubmed: 24002501
Thyroid. 2017 Sep;27(9):1142-1148
pubmed: 28635560
Thyroid. 2016 Mar;26(3):414-9
pubmed: 26701095

Auteurs

Aditya Pavan Kumar Kanteti (APK)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

George Abraham (G)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Vijay M Patil (VM)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Nandini Menon (N)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Tanmoy Mandal (T)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Sobin V Jacob (SV)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Keshav Garg (K)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Anbarasan Sekar (A)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Rup Jyoti Sarma (RJ)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Laxma Reddy Mekala (LR)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Dipti Nakti (D)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Neha Mittal (N)

Department of Pathology, Tata Memorial Hospital, Mumbai, India.

Munita Bal (M)

Department of Pathology, Tata Memorial Hospital, Mumbai, India.

Swapnil Rane (S)

Department of Pathology, Tata Memorial Hospital, Mumbai, India.

Nilendu C Purandare (NC)

Department of Nuclear Medicine, Tata Memorial Hospital, Mumbai, India.

Abhishek Mahajan (A)

Department of Radiology, Tata Memorial Hospital, Mumbai, India.

Nilesh Sable (N)

Department of Radiology, Tata Memorial Hospital, Mumbai, India.

Suman Kumar (S)

Department of Radiology, Tata Memorial Hospital, Mumbai, India.

Vanita Noronha (V)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Kumar Prabhash (K)

Department of Medical Oncology, Tata Memorial Hospital, Parel, Mumbai 400012 India.

Classifications MeSH