Clinical Benefit of Comprehensive Genomic Profiling for Advanced Cancers in India

Author:

Mathew Aju1ORCID,Joseph Serena1,Boby Jeffrey2,Benny Steve3,Veedu Janeesh4,Rajappa Senthil5,Rohatgi Nitesh6,Sirohi Bhawna7ORCID,Jain Reetu8,Agarwala Vivek9ORCID,Shukla Deepak Kumar10ORCID,Mehta Anurag11ORCID,Pramanik Raja12ORCID,Talwar Vineet11ORCID,Maka Vinayak13,Raut Nirmal14ORCID

Affiliation:

1. MOSC Medical College, Kolenchery, Ernakulam, Ernakulam, India

2. Government Medical College, Kozhikode, India

3. Government Medical College, Thrissur, India

4. University of Kentucky, Lexington, KY

5. Indo American Cancer Hospital and Research Institute, Hyderabad, India

6. Fortis Hospital, Delhi, India

7. Apollo Proton Cancer Centre, Chennai, India

8. Jaslok Hospital, Mumbai, India

9. Narayana Superspecialty Hospital, Kolkata, India

10. Manipal Comprehensive Cancer Center, Jaipur, India

11. Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India

12. All India Institute of Medical Sciences, New Delhi, India

13. M. S. Ramaiah Medical College, Bengaluru, India

14. Bhaktivedanta Hospital and Research Centre, Mumbai, India

Abstract

PURPOSE Comprehensive genomic profiling (CGP) assay is increasingly used in low-middle–income countries to detect clinically relevant genomic alterations despite its clinical benefits not being well known. Here, we describe the proportion of patients with advanced cancer in India who received targeted therapy for an actionable genetic alteration identified on CGP assays. METHODS This was a multicenter, retrospective cohort study in adult patients with advanced nonhematologic malignancies who underwent a CGP test. If patients received a targeted therapy for ≥ 6 months, they were considered to have obtained a clinical benefit from the medication, whereas those continuing for ≥ 12 months were considered to have attained an exceptional response. Descriptive statistics were used to describe the proportion of patients with subsequent targeted therapy. RESULTS During 2019-2020, 12 medical oncologists provided CGP reports for 297 patients; 221 met the inclusion criteria. Patients received a median of two lines (range: 0-5) of prior systemic therapy. On the basis of the CGP assay, 21 patients (10%) received targeted therapy. Among them, 33% was for human epidermal growth factor receptor 2 (HER2) amplification (nonbreast cancer) and 19% for HER2 or epidermal growth factor receptor exon 20 insertion mutation (lung cancer). After excluding patients with HER2 or epidermal growth factor receptor exon 20 insertions, 8% of 217 patients received targeted therapy. In the overall cohort of 221 patients, clinical benefit was seen in nine patients (4%), of whom two were exceptional responders (1%). CONCLUSION We observed that in a low-middle–income country setting, 10% of patients received targeted therapy on the basis of CGP assay. Only 4% of patients who underwent CGP testing obtained a clinical benefit.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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