Low Dose Radiation Therapy for Covid-19 Pneumonia

August 30, 2020 updated by: Daya Nand Sharma, All India Institute of Medical Sciences, New Delhi

Low Dose Radiation Therapy for Covid-19 Pneumonia: A Pilot Study

Radiotherapy in low doses (30 to 100 cGy) was a popular treatment of viral pneumonias until 1940s. Low dose radiation therapy (LDRT) could possibly reduce the inflammation and prevent the cytokine storm thus mitigating the severity of pneumonitis. This is a single arm study designed to assess the feasibility and clinical efficacy of low dose radiation therapy (70 cGy in single fraction) in the patients with COVID-19 pneumonia. A total of 10 eligible patients (as per inclusion criteria) will be recruited and response will be assessed based on the symptomatic improvement or deterioration by using the National Early Warning Score (NEWS). The NEWS score will be recorded on baseline and then on Day 3, Day 7 and Day 14.

Study Overview

Status

Unknown

Conditions

Detailed Description

There is no specific antiviral treatment recommended for COVID-19, and no vaccine is currently available. The treatment is symptomatic, and oxygen therapy represents the major treatment intervention for patients with severe infection. Mechanical ventilation may be necessary in cases of respiratory failure refractory to oxygen therapy, whereas hemodynamic support is essential for managing septic shock. The death rate ranges from 2-15% in different group of patients.

COVID-19 pandemic is unprecedented in modern history of humankind and it has become imperative to find novel treatments to mitigate the casualties caused by infection. The clinical spectrum of COVID-19 varies from mild symptoms to critical conditions requiring ventilatory support and ICU care. According to Chinese CDC report, 81% patients had mild disease (non-pneumonia and mild pneumonia), 14% had severe disease and 5% had critical disease. Based on severity of symptoms, there are several scoring methods which can predict the outcome of disease. National early warning score (NEWS) is a popular scoring system used for non-ICU patients suffering from acute illness. This score helps in quickly determining the degree of illness and intervention required. It also provides likelihood of death or admission to an ICU. Based on this score any illness can be categorized as mild (Score <4), moderate (Score 5-6 or individual 3) and severe (Score ≥7). According to this scoring system, Covid-19 patients having a score of 5-6 will have probability of 15.7% critical events (HDU/ICU admission or 30-day mortality) and those having score ≥7 will have about 24.1% critical events.

The pathogenesis of COVID-19 pneumonitis appears to involve a cytokine storm with elevated pro- inflammatory cytokines such as IL-6 and TNFα among many others, leading to an onslaught of neutrophils and macrophages, diffuse alveolar damage and respiratory failure. This is where a potential opportunity for low-dose radiation therapy (LDRT) emerges. LDRT is a potential treatment for COVID-19 pneumonia since it has an anti-inflammatory action. Successful management of worsening pneumonia will reduce the development of ARDS and thereby preventing deaths.

Availability of megavoltage beam in modern times has improved our dosimetry in treating deep targets. Radiotherapy which can penetrate lobar and interstitial space can help in preventing both lobar as well as interstitial pneumonia. In the absence of any effective drug and, historical data suggests that low dose of 0.5 to 1 Gy radiotherapy to whole lung can possibly prevent cytokine storm and critical events (ICU admission, mechanical ventilation or death).

The initial use of X-rays to treat patients with pneumonia was reported in 1907. This report offered a new mechanistic insight founded on the dose response, proposing that low doses of X-rays would affect disease resolution. It was observed that not only did the X-ray treatment has lifesaving potential, but it was also effective when other treatments had reached their therapeutic limits as seen in cases of chronic bronchopneumonia, which could be resolved with a single administration of X-rays. Subsequent reports suggested that LDRT was successful in decreasing the mortality rate in untreated patients from about 30% to 5-10%.

Rationale for the Study: It is reasonable to try an LDRT treatment of 30 to 100 cGy to the lungs of a patient with COVID-19 pneumonia as it could reduce the inflammation and relieve the life-threatening symptoms. The recent emerging literature indicates that the efficacy of thoracic LDRT must be investigated as it would present a negligible risk to COVID-19 pneumonia patients, and have the potential to reduce the fatality rates.

Study Design: Interventional, Clinical, Single arm, Pilot study Number of patients: 10 Treatment: Patient will be treated as per COVID-19 standard management protocol of the treating institute along with intervention of Low Dose Radiotherapy (LDRT) 70cGy in single fraction.

Treatment field- Field adequately covering both the lungs. Beam energy : 6MV X-ray photons Number of beams- 2 (1 Anterior and 1 posterior field). Prescription point - Midway of anterior-posterior chest separation. Treatment Workflow: Patients will be maneuvered to lie down on treatment couch in a supine position, with hands above head. Gantry rotated to 90 degree, a lateral chest X ray portal image will be taken, which will guide in measuring dose prescription point. Gantry rotated back to 0 degree; an adequate field size will be opened. Total treatment duration will be about 20-30 minutes.

Response Assessment and statistical analysis: Response will be assessed based on the symptomatic improvement or deterioration by using the NEWS score. The NEWS score will be recorded on baseline and then on Day 3 (D-3), Day 7 (D-7) and Day 14 (D-14). To compare the NEWS score (baseline and post LDRT), student t test (paired) will be used. For statistical significance, p value of 0.1 will be considered significant. Number of patients requiring ICU admission or undergoing death following LDRT will also be recorded to assess critical events.

Study Type

Interventional

Enrollment (Actual)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Delhi
      • New Delhi, Delhi, India, 110029
        • All India Institute of Medical Sciences, New Delhi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Confirmed cases of Covid-19 (by RT-PCR).
  2. Age >18 years.
  3. Patients with National Early Warning Score (NEWS) score ≥ 5.
  4. Consent

Exclusion Criteria:

  1. Patients on mechanical ventilatory support.
  2. Hemodynamically unstable patients

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Study Arm
Patient will be treated with a dose of 70 cGy in one fraction radiation therapy in addition to standard therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Symptomatic improvement by National Early warning score (NEWS)
Time Frame: Day 3
NEWS score
Day 3
Symptomatic improvement by National Early warning score (NEWS)
Time Frame: Day 7
NEWS score
Day 7
Symptomatic improvement by National Early warning score (NEWS)
Time Frame: Day 14
NEWS score
Day 14
Length of hospital stay
Time Frame: 30 days or date of death whichever is earlier
Days
30 days or date of death whichever is earlier
Number of ICU admissions or deaths
Time Frame: 30 days
Number of patients
30 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Daya Nand Sharma, MD, AIIMS, New Delhi

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 13, 2020

Primary Completion (Actual)

August 27, 2020

Study Completion (Anticipated)

September 1, 2020

Study Registration Dates

First Submitted

May 17, 2020

First Submitted That Met QC Criteria

May 18, 2020

First Posted (Actual)

May 19, 2020

Study Record Updates

Last Update Posted (Actual)

September 1, 2020

Last Update Submitted That Met QC Criteria

August 30, 2020

Last Verified

August 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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