Effect of hydroxychloroquine on COVID-19 prevention in cancer patients undergoing treatment: a structured summary of a study protocol for a randomised controlled trial

Abstract

Objectives

In this study, we investigate the effect of hydroxychloroquine on the prevention of Novel Coronavirus Disease (COVID-19) in cancer patients being treated.

Trial design

This is a multi-centre, two-arm, parallel-group, triple-blind, phase 2-3 randomised controlled trial.

Participants

All patients over the age of 15 from 5 types of cancer are included in the study. Patients with acute lymphoid and myeloid leukemias in the first line treated with curative intent, patients with high-grade non-Hodgkin's lymphoma treated with leukemia protocols and patients with non-metastatic breast and colon cancer in the first line of treatment will enter the study. The exclusion criteria will include known sensitivity to Hydroxychloroquine, weight below 35 kilograms, history of retinopathy, history of any cardiac disease, acute respiratory tract infection in the last 2 months, having COVID-19 in the first two weeks of entering the trial, having Diabetes Mellitus, having an immuno-suppressive disease other than cancer, having chronic pulmonary disease and taking immuno-suppressant drug other than chemotherapeutic agents for current cancer. This study is performed in five academic centres affiliated to Mashhad University of Medical Sciences, Mashhad, Iran.

Intervention and comparator

Patients are randomly assigned to two groups; one being given hydroxychloroquine and the other is given placebo. During two months of treatment, the two groups are treated with either hydroxychloroquine (Amin® Pharmaceutical Company, Isfahan, Iran) or placebo (identical in terms of shape, colour, smell) as a single 200 mg tablet every other day. Patients will be monitored for COVID-19 symptoms during the follow-up period. If signs or symptoms occur (fever, cough, shortness of breath), they will be examined and investigated with a high-resolution computed tomography (CT) scan of the lungs, COVID-19 specific IgM, IgG antibody assay and a nucleic acid amplification test (NAT) for the SARS-CoV-2 virus.

Main outcomes

The primary end point of this study is to investigate the incidence of COVID-19 in patients being treated for their cancer over a 2-month period.

Randomisation

Randomisation will be performed using randomly permuted blocks. By using an online website (www.randomization.com) the randomization sequence will be produced by quadruple blocks. The allocation ratio in intervention and control groups is 1:1.

Blinding (masking)

Participants and caregivers do not know whether the patient is in the intervention or the control group. The outcome assessor and the data analyst are also blinded to group assignment.

Numbers to be randomised (sample size)

The calculated total sample size is 60 patients, with 30 patients in each group.

Trial Status

The trial began on April 14, 2020 and recruitment is ongoing. Recruitment is anticipated to be completed by June 14, 2020 There has been no change in study protocol since approval, protocol version 1 was approved April 12, 2020.

Trial registration

This trial has been registered by the title of “Effect of Hydroxychloroquine on Novel Coronavirus Disease (COVID-19) prevention in cancer patients under treatment” in Iranian Registry of Clinical Trials (IRCT) with code “IRCT20200405046958N1”, https://www.irct.ir/trial/46946. Registration date is April 14, 2020.

Full protocol

The full protocol is attached as an additional file, accessible from the Trials website (Additional file 1). In the interest in expediting dissemination of this material, the familiar formatting has been eliminated; this Letter serves as a summary of the key elements of the full protocol.

Authors’ contributions

Study design: MMN, AA, MKR, AB, SAA, MK, ZM, MSS, SE. Data gathering: MMN, AA, HR, SSS, AN, HR, SK, AJI, HM. Statistical Analysis: MKR, MMN, SE. Drafting the manuscript: MMN, AA, MKR, HR, AB, SAA, MK, ZM, MSS, HR. Final approval: All authors will approve the final version of manuscript and take direct responsibility for it.

Funding

All the financial resources required for this project have been provided by the Vice-Chancellor for Research of Mashhad University of Medical Sciences (code:990046). The funding body has no role in the design of this study, collection, analysis, and interpretation of data and in writing the manuscript.

Availability of data and materials

The final dataset of the trial will be available upon request from the primary investigator via e-mail at moeininm@mums.ac.ir, after obtaining the permission of the Regional Ethics Committee.

Ethics approval and consent to participate

The trial has been approved by the Ethical Committee of Mashhad University of Medical Sciences, Iran. Ethics committee reference number is IR.MUMS.REC.1399.078 which was registered on April 12, 2020. (Publicly available at this link)

Hereby we certify that this trial has received ethical approval from the aforementioned ethical committee as described above.

An informed consent is obtained from all participants or their legal guardians prior to recruitment.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Supplementary information

Supplementary information accompanies this paper at 10.1186/s13063-020-04485-x.