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  • decodeMR Team

Real-World Data and Real-World Evidence: Current status in the APAC region

(Focus-India)


This interview was originally published in www.oncofocus.com on 08th August 2019


In the third interview of our Real-World Data series, our analyst Shilna Kunnath connected with Dr. Randeep Singh, Director Medical Oncologist, Narayana Hospitals and Oncomed Clinic, Delhi/NCR to discuss the current status of Real-world Data usage in India.




Dr. Randeep Singh

Medical Oncologist

MD, DM, ECMO, FCCP

​Director, Narayana Hospitals and Oncomed clinic, Delhi/NCR





... real-world data is helpful in the clinical evaluation of rare diseases where conducting regular controlled trials is not feasible.

Considering the rapidly transforming healthcare space, what are your overall views on the usage of Real-World Data (RWD) in healthcare decision-making?


Dr. Singh: The usage entirely depends upon the quality of the acquired data. But usually, we don’t get good-quality data from the real world. In fact, real-world data is the exact reflection of what happens in the clinic. On the contrary, the data from the clinical trial is accurate data where a controlled situation with a well-defined patient selection criterion is considered. These sort of ideal patients we usually don’t see in the clinical practice.


Some things cannot happen with real-world data. For example, if you must compare a new modality versus an existing standard modality, it cannot happen with real-world data. On the other hand, real-world data is helpful in the clinical evaluation of rare diseases where conducting regularly controlled trials is not feasible.


We know that with the introduction of the 21st Century Cures Act in 2016, USFDA has an additional focus on using RWE in regulatory decision-making. Coming to India, how is the regulatory landscape evolving in terms of usage of RWD?


Dr. Singh: In India, there is no regulatory landscape for real-world data. There are no such laws or any other initiative by government or private authority to start accumulating real-world data. There might be some work in progress, but I don’t think so we have reached that stage yet.


In the U.S., draft guidance on the appropriate use of RWD in regulatory decision-making is expected to be published by 2021. Are there any such measures in the pipeline for India as well?


Dr. Singh: In India, there is no regulatory rule no draft guidance, or guidelines to include the real-world data in decision making or at least to start working on real-world data on a larger scale. On a smaller scale, some institutes may be working on this line.


How are the key stakeholders of the healthcare value chain responding to the use of real-world evidence in decision-making?


Dr. Singh: Real-world data gives you the feel of real situations. It is the reflection of the actual practice and is simple to accumulate as compared to clinical trial data. For example, if there is a clinical trial that has already proven a drug to be of value in the western population, and you want to use it in the Indian population, real-world data can be used to compare with the data from landmark trials.


Also being an oncologist, I see much value in real-world data. In molecular oncology, real-world data will be useful in gaining insights about patient sub-groups with a specific genetic aberration.


What are the common sources of RWD? Are there any specific indications or areas in which RWD is utilized more in India?


Dr. Singh: Insurance databases, hospital-based, and population-based registries are good sources. Also, we have EMR data, where cloud-based software is used to merge data from multiple users.


What are the key barriers to the increased use of RWD?


Dr. Singh: As already discussed, the first barrier is the quality of the data. The second barrier is the limited utility of the real-world data in specific situations, such as while comparing a new modality with an existing standard modality.


Privacy is not an issue as we do not disclose a patient’s identity while analyzing it. At present, accessibility is an issue in India. There are issues related to data generation and the willingness of the involved party in sharing the generated data. It remains to be seen, if, in the coming days, data generated across the multiple institutes will be made available.


Looking forward, what is the outlook for the usage of Real-World Data (RWD) in the future?


Dr. Singh: I feel that, at least in Oncology, real-world data will make sense and if you collect the data properly with all the parameters, it can at least cover 50 – 60% of the situations where you need clinical trials.


It was an insightful discussion. Thank you for your time!


Dr. Singh: Thank you!

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