Evidence map›Paper›PMID 42323757›Full record

ArticleDiscover oncology2026

Bevacizumab added to conventional induction chemotherapy for children with high risk neuroblastoma (BRAVEN trial).

Jagdish Prasad Meena, Debasish Sahoo, Harshita Makkar, Sujata Bhattacharya, Aditya Kumar Gupta, Deepam Pushpam, Manisha Jana, Aanchal Kakkar, Bangkim Chandra Khangembam, Maroof Ahmad Khan and 16 more

Abstract read
In one paragraph

Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Jagdish Prasad MeenaDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India. drjpmeena@yahoo.com.ORCID https://orcid.org/0000-0001-6024-9762
Debasish SahooDivision of Pediatric Hematology Oncology, Department of Medical Oncology Hematology, All India Institute of Medical Sciences, Bhubaneswar, 751019, India.
Harshita MakkarDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Sujata BhattacharyaDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Aditya Kumar GuptaDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Deepam PushpamDepartment of Medical Oncology, Dr. BRA, IRCH, All India Institute of Medical Sciences, New Delhi, 110029, India.
Manisha JanaDepartment of Radiodiagnosis and Interventional Radiology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Aanchal KakkarDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Bangkim Chandra KhangembamDepartment of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India.
Maroof Ahmad KhanDepartment of Biostatistics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Narendra Kumar ChaudharyDepartment of Pediatrics, All India Institute of Medical Sciences, Bhopal, 462020, India.
Nidhi ChopraDepartment of Pediatrics, Vardhman Mahavir Medical College and attached Safdarjung Hospital, New Delhi, 110029, India.
Prashant PrabhakarDepartment of Pediatrics, Vardhman Mahavir Medical College and attached Safdarjung Hospital, New Delhi, 110029, India.
Amitabh SinghDepartment of Pediatrics, Vardhman Mahavir Medical College and attached Safdarjung Hospital, New Delhi, 110029, India.
Shilpa Khanna AroraDivision of Pediatric Hematology and Oncology, Department of Pediatrics, Atal Bihari Vajpayee Institute of Medical Sciences & attached Dr Ram Manohar Lohia Hospital, New Delhi, 110001, India.
Nishant VermaDepartment of Pediatrics, King George Medical University (KGMU), Lucknow, Uttar Pradesh, 226003, India.
Sonali MohapatraDivision of Pediatric Hematology Oncology, Department of Medical Oncology Hematology, All India Institute of Medical Sciences, Bhubaneswar, 751019, India.
Maharshi TrivediDivision of Pediatric Hematology, Oncology, and BMT, The Gujarat Cancer & Research Institute (GCRI), Ahmedabad, Gujrat, 380016, India.
Parichay SinghDepartment of Pediatric Oncology, Homi Bhabha Cancer Hospital and Mahamana Pandit Madan Mohan Malviya Cancer Centre, Varanasi, Uttar Pradesh, 133603, India.
Vineeta GuptaDivision of Pediatric Hematology Oncology and BMT, Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University (BHU), Varanasi, Uttar Pradesh, 221005, India.
Pankaj DwivediDepartment of Pediatric Oncology, National Cancer Institute (NCI), Nagpur, Maharashtra, 441108, India.
Sameer BakhshiDepartment of Medical Oncology, Dr. BRA, IRCH, All India Institute of Medical Sciences, New Delhi, 110029, India.
Imteyaz Ahmad KhanDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Lata SinghDepartment of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Piali MandalDepartment of Pediatrics, Lady Hardinge Medical College and attached Kalawati Saran Children Hospital, New Delhi, 110001, India.
Rachna SethDivision of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.

Funding

Indian Council of Medical Research (ICMR) Grant ID: IG/Dev.Res/00407/2027-2024 [215357])
6 · The paper itself

Abstract

backgroundDespite advances in multimodal therapy, high-risk neuroblastoma (HR-NB) continues to have poor outcomes. Response to induction chemotherapy is a key predictor of long-term survival, yet intensive multi-agent regimens have not substantially improved prognosis.

objectivesThis study aims to evaluate the efficacy and safety of adding bevacizumab to conventional induction chemotherapy in HR-NB.

methodsThis prospective, multicenter, randomized controlled trial will enroll newly diagnosed high-risk neuroblastoma patients, randomized to receive either conventional induction chemotherapy alone (control) or bevacizumab plus conventional induction chemotherapy (intervention). Response to induction therapy will be assessed according to standard criteria, and patients achieving a complete or good partial response will proceed to autologous stem cell transplantation (ASCT). All participants will be followed for at least 2 years to evaluate event-free survival (EFS) and overall survival (OS). The primary outcome, response rate, will be reported as a proportion, and EFS and OS will be analyzed using Kaplan-Meier plots and log-rank tests. The secondary outcomes (toxicity and minimal residual disease) will be reported as proportions. Prognostic factors will be evaluated with univariate and multivariate Cox regression analyses. EXPECTED OUTCOMES: The study aims to demonstrate that adding bevacizumab to conventional induction chemotherapy improves response rates, increases the proportion of patients eligible for autologous stem cell transplantation (ASCT), and improves survival outcomes, with manageable toxicities.

trial registrationThis study is registered with the Clinical Trials Registry of India (CTRI/2024/09/074065, dated: 19/09/2024).

Indexed as

BevacizumabInductionNeuroblastomaOutcomeRemissionTransplant

Identifiers

PMID42323757
PMCPMC13534399

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.