Evidence map›Paper›PMID 35127505›Full record

ArticleFrontiers in oncology2021

Relapsed Refractory Hodgkin Lymphoma and Brentuximab Vedotin-Bendamustine Combination Therapy as a Bridge to Transplantation: Real-World Evidence From a Middle-Income Setting and Literature Review.

Vivek S Radhakrishnan, Rajat Bajaj, Vasundhara Raina, Jeevan Kumar, Saurabh J Bhave, Reghu K Sukumaran Nair, Arijit Nag, Indu Arun, Lateef Zameer, Debdeep Dey and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Outcomes of Brentuximab Vedotin Monotherapy in Refractory/Relapsed Classical Hodgkin's Lymphoma: A Multi-Center Retrospective Study on Survival and Safety.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2026
    Article
  2. Article
  3. Review
  4. Antibody-drug conjugates come of age in oncology.Nature reviews. Drug discovery · 2023
    Review
  5. Review
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

17 authors at 1 institution in 1 country.

Vivek S RadhakrishnanClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Rajat BajajClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Vasundhara RainaClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Jeevan KumarClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Saurabh J BhaveClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Reghu K Sukumaran NairPaediatric Haematology Oncology, Tata Medical Center, Kolkata, India.
Arijit NagClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Indu ArunHistopathology, Tata Medical Center, Kolkata, India.
Lateef ZameerHistopathology, Tata Medical Center, Kolkata, India.
Debdeep DeyHistopathology, Tata Medical Center, Kolkata, India.
Neeraj AroraLaboratory Haematology Cytogenetics and Molecular Pathology, Tata Medical Center, Kolkata, India.
Mayur PariharLaboratory Haematology Cytogenetics and Molecular Pathology, Tata Medical Center, Kolkata, India.
Jayanta DasNuclear Medicine, Tata Medical Center, Kolkata, India.
Rimpa B AchariRadiation Oncology, Tata Medical Center, Kolkata, India.
Deepak K MishraLaboratory Haematology Cytogenetics and Molecular Pathology, Tata Medical Center, Kolkata, India.
Mammen ChandyClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Reena NairClinical Haematology Oncology and Haematopoietic Cell Transplantation (HCT), Tata Medical Center, Kolkata, India.
Tata Medical Center · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite high cure rates with standard treatment, 30% patients with Hodgkin lymphoma develop relapsed or refractory (R/R) disease. Salvage therapy followed by autologous hematopoietic cell transplantation (HCT) is considered standard of care. Brentuximab Vedotin (Bv) in combination with Bendamustine (B) has been tested in the salvage setting with promising results. MATERIALS AND METHODOLOGY: We conducted a single centre retrospective chart review of patients who received BBv salvage therapy to determine its activity and safety in patients with R/R classical Hodgkin lymphoma (HL). Between May 2011- December 2019, 179 patients were diagnosed with R/R HL.

resultsThirty patients received BBv [median age: 30 (15-59) years, females (n=15)]. Primary refractory disease in 19 patients (63%), and 26 patients (87%) had advanced stage at treatment. Most patients received BBv after 2 prior lines of therapy [n=16 (53%)]. The median number of cycles of BBv were 3 (1-6). The number of BBv cycles delivered as outpatient was 63%. The most common Grade III/IV hematological adverse event was neutropenia [n=21, (70%)], while grade III/IV non-hematological toxicities included infections in 4 (13%), neuropathy in 4(13%), skin rash in 2 (7%), GI toxicities in 3 (10%) and liver dysfunction in 2 (7%) patients. The ORR and CR rates were 79% and 62%, respectively. Seventeen patients (57%) underwent an autologous HCT and 8 (26%) underwent an Allogeneic HCT (all haploidentical). The median follow up time from BBv administration was 12 months. Six patients died: 2 = disease progression, and 4 = non-relapse causes (Infection and sepsis = 2, GVHD=2). In addition to this, one patient progressed soon after HCT and another patient relapsed 22 months post HCT. Three year Overall survival (OS) and Event free survival (EFS) probability post-BBv treatment was 75% and 58%, respectively. OS and EFS analysis based on response (viz., CMR) to BBv demonstrated that patients in CMR had better survival probability [93% (p=0.0022) 3yr-OS and 72% (p=0.038) 3yr-EFS probability].

conclusionsBBv is an active and well-tolerated salvage treatment for patients with R/R HL, even in refractory and advanced settings. In middle-income settings, cost constraints and access determine patient uptake of this regimen.

Indexed as

bendamustineBrentuximab vedotin (Adcetris) ®Hodgkin lymphomareal world data (RWD)relapsed/refractorytransplantation

Identifiers

PMID35127505
PMCPMC8814627
OpenAlexW4207079498

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.