Molecular insights from comprehensive genomic profiling data in advanced metastatic colorectal cancer in South Asian population: A retrospective observational study

Author:

Fathima Nusrath1,Verma Krithika1,Subramanyam Paridhy V.1,Mukherjee Nilesh1,Tanwar Nishtha1,Jayaraman Sharanya1,Rangan Saranya1,Mahanti Shreya1,Saha Prabir1,Javle Vyomesh1,Khuntia Satya P.1,Santani Harshi1,Ashwini P1,Peddagangannagari Sreekanth R.1,Gowda Pooja1,Varghese Linu1,Gore Adwaita2,Patel Amol3,Sainani Anjana4,Karpe Ashay5,Avinash C. B.6,Patodiya Bharat7,Biswas Ghanashyam8,Lokeshwar Nilesh9,Ranade Rohit R.10,Rajpurohit Sajjan11,Juat Necy S.12,Tagarda Federico Miguel R.13,Cornel-Ong Annielyn14,Teh Catherine15,Gangadharan V. P.16,Jain Amit17,Sumon Mostafa A.18,Deshpande Ramakant19,Patil Vijay20,Sathyanarayanan Vishwanath21,Suresh A.V.S.22,Chugh Bhuvan23,Zawar Abhinav24,Gupta Ajay25,Shah Akshay26,Punia Ankur27,Rumman Kamruzumman28,Kamath Mangesh29,Raghuram Saadvik7,Vivek Sai29,Shrestha Sudip30,Gupta Vineet G.31,Pramanik Raja32,Bhosale Bharat5,Kothari Rushabh33,Warrier Arun R.34,Guhan P.35,Lavingia Viraj36,Sarathy Vinu37,Mishra Sourav K.38,Thirumalairaj Raja39,Nayak Sandeep40,Rishi Kshitij D.1,Goswami Hitesh M.1,Veldore Vidya H.1

Affiliation:

1. 4basecare Onco Solutions Pvt. Ltd., Bengaluru, Karnataka, India

2. Max Nanavati Hospital, Mumbai, Maharashtra, India

3. TMH, Mumbai, Maharashtra, India

4. Sainani Medicare, Mumbai, Maharashtra, India

5. Sunrise Oncology Centre, Mumbai, Maharashtra, India

6. Clearmedi Radiant Hospital, Mysore, Karnataka, India

7. Dr. Lal Path Labs, Delhi, India

8. Sparsh Hospital and Critical Care (P) Ltd., Bhubaneswar, Odisha, India

9. Lilavati Hospital, Mumbai, Maharashtra, India

10. Narayana Hrudayalaya, Bengaluru, Karnataka, India

11. Jivinsha Hospital, Delhi, India

12. Makati Medical Centre, Philippines

13. St. Luke’s Medial Center, Philippines

14. Global Care Cancer Institute, Philippines

15. National Kidney and Transplant Institute, Philippines

16. Indira Gandhi Co-Operative Hospital, Kochi, Kerala, India

17. Valentis Cancer Hospital, Meerut, Uttar Pradesh, India

18. Japan Bangladesh Friendship Hospital, Dhaka, Bangladesh

19. ACI Cumballa Hill Hospital, Mumbai, Maharashtra, India

20. Hinduja Hospital, Mumbai, Maharashtra, India

21. Apollo Hospital, Bengaluru, Karnataka, India

22. Continental Hospital, Hyderabad, Telangana, India

23. Max Hospital, Delhi, India

24. Kamalnayan Bajaj Hospital, Aurangabad, Maharashtra, India

25. Indraprastha Apollo Hospitals, Delhi, India

26. Global Hospital, Mumbai, Maharashtra, India

27. Oncoquest, Delhi, India

28. Health and Hope Hospital, Dhaka, Bangladesh

29. Sri Shankara Cancer Hospital and Research Centre, Bengaluru, Karnataka, India

30. Nepal Cancer Hospital and Research Centre, Lalitpur, Nepal

31. Fortis Shalimar, Delhi, India

32. AIIMS, Delhi, India

33. Narayana Multispeciality Hospital, Ahmedabad, Gujarat, India

34. Aster Medcity, Kochi, Kerala, India

35. Sri Ramakrishna Hospital, Coimbatore, Tamil Nadu, India

36. Shalby Hospitals, Ahmedabad, Gujarat, India

37. Bangalore Baptist Hospital, Bengaluru, Karnataka, India

38. AIIMS, Bhubaneswar, Odisha, India

39. Apollo Speciality Hospital, Chennai, Tamil Nadu, India

40. Fortis Hospital, Bengaluru, Karnataka, India

Abstract

ABSTRACT Background: An increase in colorectal cancer incidence has been reported in India, often presenting in advanced stages and resulting in poor survival. However, the genomic and therapeutic landscape is not well understood. Objective: The primary objective of the study was to understand the mutational profile of metastatic colorectal cancer in the Southeast Asian cohort, and the secondary objective was to define the proportion of patients with therapeutically significant variants. Materials and Methods: This retrospective study was conducted between January 2021 and September 2023, at 4baseCare Onco Solutions Pvt. Ltd., Bengaluru, Karnataka, India. Comprehensive genomic profiling (CGP) and biomarker testing for MSI, TMB, and PD-L1 was carried out in 477 metastatic advanced (Stage III/IV) colorectal cancer patients, for the current retrospective-observational study. Results: With CGP, we identified drivers/clinically actionable variants in 78.6% of the cohort (375 patients). Although 30.8% of our cohort (147 patients) was eligible to available targeted therapy, 29.5% (141 patients) were found to harbor variants imparting therapeutic resistance. The combined mutation frequency of APC, TP53, and KRAS was >50%, while KRAS constituted >90% of all RAS mutations. The mismatch repair (MMR) genes including MLH1, MLH3, MSH3, and POLE were exclusively found in colon cancers. Genomic alterations in several genes of prognostic/therapeutic significance were seen (mutations in PIK3CA, SMAD4, BRAF, and amplifications in KRAS, EGFR, and ERBB2). Of those tested, 15.8% (41 patients) of the cohort had high tumor mutation burden (TMB-H), 14% had high microsatellite instability (MSI-H) (46 patients), and 26.8% were programmed death-ligand 1 (PD-L1) positive (30 patients). Conclusion: Our study shows that CGP is an advantageous option for identifying subsets of patients eligible for various targeted therapies, thus, improving patient outcomes.

Publisher

Medknow

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