Evidence map›Paper›PMID 42453145›Full record

ArticleThe Lancet regional health. Southeast Asia2026

Toxicity during induction of pulsed versus continuous prednisolone in children with acute lymphoblastic leukaemia: a multi-centre, open label, randomised, phase 3 trial from India (2016-2022).

Parag Das, Nandana Das, Gaurav Narula, Amita Trehan, Sameer Bakhshi, Venkatraman Radhakrishnan, Rachna Seth, Prashant Tembhare, Man Updesh Singh Sachdeva, Anita Chopra and 8 more

Abstract read
In one paragraph

Article in The Lancet regional health. Southeast Asia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

18 authors.

Parag DasClinical Research Unit, Tata Translational Cancer Research Centre, Tata Medical Center, Kolkata, West Bengal, 700160, India.
Nandana DasClinical Research Unit, Tata Translational Cancer Research Centre, Tata Medical Center, Kolkata, West Bengal, 700160, India.
Gaurav NarulaDepartment of Pediatric Oncology, Tata Memorial Centre, Tata Memorial Hospital, Mumbai, Maharashtra 400012, India.
Amita TrehanPediatric Hematology-Oncology Unit, Department of Pediatrics, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Sameer BakhshiDepartment of Medical Oncology, BR Ambedkar Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi, 110029, India.
Venkatraman RadhakrishnanDepartment of Medical Oncology, Cancer Institute (WIA), Adyar, Chennai, Tamil Nadu 600020, India.
Rachna SethOncology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Prashant TembhareHematopathology Laboratory, ACTREC, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, 410210, India.
Man Updesh Singh SachdevaDepartment of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Anita ChopraLaboratory Oncology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Shirley SundersinghDepartment of Oncopathology, Cancer Institute (WIA), Adyar, Chennai, Tamil Nadu 600020, India.
Soumyadeep DasDepartment of Statistics, Bidhannagar College, Kolkata 700064, India.
Manash Pratim GogoiClinical Research Unit, Tata Translational Cancer Research Centre, Tata Medical Center, Kolkata, West Bengal, 700160, India.
Mayur PariharCytogenetics Department, Tata Medical Center Kolkata, West Bengal, 700160, India.
Rahul BhattacharyaDepartment of Statistics, University of Calcutta, Kolkata 700019, India.
Shripad BanavaliDepartment of Pediatric Oncology, Tata Memorial Centre, Tata Memorial Hospital, Mumbai, Maharashtra 400012, India.
Vaskar SahaClinical Research Unit, Tata Translational Cancer Research Centre, Tata Medical Center, Kolkata, West Bengal, 700160, India.
Shekhar KrishnanClinical Research Unit, Tata Translational Cancer Research Centre, Tata Medical Center, Kolkata, West Bengal, 700160, India.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Despite the use of similar treatment protocols, induction treatment-related mortality (TRM) in children with ALL in India is 5%, compared to <1% in high income countries. This study evaluated pulsed prednisolone during induction to reduce toxicity. Methods: ICiCLe-ALL-14 (CTRI/2015/12/006434), an open-label, randomised, multicentre trial. Children ≤ 10-years with newly diagnosed B-cell precursor ALL, risk-stratified to standard- or intermediate-risk, were randomised (1:1) to receive prednisolone 60 mg/m Findings: Of 3315 patients screened at 6 centres, 2505 were eligible and 1246 randomised (623 per group). Thirty (2.4%) patients died during induction: 22/623 (3.5%) and 8/623 (1.3%) in R1A and R1B respectively (absolute risk difference 2.3%, 95% CI 0.54-4.1; p = 0.0149). Relative risk of induction death was 2.75 (95% CI 1.2-6.1) for R1A versus R1B. Grade 3-5 toxicities occurred in 46.4% (289/623) and 45.4% (283/623) of patients (p = 0.7762). CR rates were 98.8% (581/588) and 98.0% (594/606); MRD ≥ 0.01% at EoI was 26.2% and 27.9%; 3-year EFS 72.7% (95% CI 68.2-76.7) and 72.2% (67.6-76.3); OS 85.0% (81.5-87.8) and 87.0% (83.6-89.3) in R1A and R1B respectively. Multivariable analysis confirmed higher risk of induction death with continuous prednisolone (HR 3.06, 95% CI 1.4-6.9, p = 0.0069) and anthracycline use (HR 5.44, 95% CI 1.6-18.9 p = 0.0077). Interpretation: Pulsed prednisolone (R1B) during induction significantly reduced treatment-related deaths, particularly early deaths from infections compared to continuous dosing (R1A), without compromising CR rates, MRD clearance, EFS, or OS. Anthracycline use was an independent risk factor for induction mortality. Higher white cell count and anthracycline use independently predicted grade 3-4 toxicity. Funding: This study was funded partly by the Indian Council of Medical Research (Reference 79/159/2015/NCD-III), the National Cancer Grid (Reference 2016/001), DBT-Wellcome India Alliance (Margdarshi IA/M/12/1/500261) and a centre grant from the Tata Consultancy Services Foundation to the trial centre.

Indexed as

Acute lymphoblastic leukaemiaChildRandomised clinical trialSteroid

Identifiers

PMID42453145
PMCPMC13366301

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