Evidence map›Paper›PMID 38577858›Full record

ArticleThe Indian journal of medical research2024

Long-term clinical outcomes of combined modality therapy for advanced-stage Hodgkin lymphoma in the PET era: A retrospective study.

Swati Chugh, Goutam Panda, Smruti Mokal, Hasmukh Jain, Bhausaheb Bagal, Nehal Khanna, Sridhar Epari, Sachin Punatar, Lingaraj Nayak, Anant Gokarn and 4 more

Open access · diamondAbstract read
In one paragraph

Article in The Indian journal of medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 92% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Article
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

14 authors at 2 institutions in 1 country.

Swati ChughDepartment of Radiation Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Goutam PandaDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Smruti MokalDepartment of Pathology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Hasmukh JainDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Bhausaheb BagalDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Nehal KhannaDepartment of Radiation Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Sridhar EpariDepartment of Clinical Research Secretariat, Tata Memorial Centre, BARC Training School Complex, Mumbai, Maharashtra, India.
Sachin PunatarDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Lingaraj NayakDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Anant GokarnDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Naveen KhattryDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Manju SengarDepartment of Medical Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Siddhartha LaskarDepartment of Radiation Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Jayant S GodaDepartment of Radiation Oncology, Hematolymphoid Disease Management Group, Tata Memorial Center, BARC Training School Complex, Mumbai, Maharashtra, India.
Homi Bhabha National Institute · INTata Memorial Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND

objectivesThe role of consolidation radiation therapy (CRT) after complete metabolic response to chemotherapy in advanced-stage (stage III and IV) Hodgkin lymphoma (HL) is controversial. This study was undertaken to assess the clinical outcomes in terms of event free survival, local failure free survival and overall survival in individuals with advanced HL treated with chemotherapy and CRT.

methodsA retrospective review was conducted to study the long-term clinical outcomes in individuals diagnosed with HL and treated with chemotherapy and CRT from 2012 to 2016 at a tertiary cancer care hospital in India.

resultsData from 203 study participants with advanced-stage HL were analyzed. Positron emission tomography-computed tomography (PET-CT) was done at baseline and after 2 cycles for response assessment. The median age at presentation was 32 yr [interquartile range (IQR): 26-46]. Early metabolic response (after 2 cycles) and delayed metabolic response (after 4 or 6 cycles) were observed in 74.4 and 25.6 per cent of individuals, respectively. With a median follow up of 52 months (IQR: 40-67), the five-year event-free survival (EFS), local failure-free survival (LFFS) and overall survival (OS) were 83.2, 95.1 and 94.6 per cent, respectively. On univariate analysis, extranodal disease was associated with inferior EFS (P=0.043). Haemoglobin <10.5 g/dl (P=0.002) and Hasenclever index >3 (P=0.00047) were associated with poorer OS. Relapses were observed in 28/203 (13.8%) study participants with predominance at central nodal stations. The median time to relapse was 19.4 months (IQR: 13-33). Local relapse alone (at the irradiated site) was observed in 5/28 study participants, systemic (distant) relapse in 14/28 individuals, while both systemic and local relapse was observed in 9/28 participants. Extranodal disease (P=0.05), bulky disease (P=0.005) and haemoglobin concentration ≤10.5 g/dl (P=0.036) were significant predictors for disease relapse. INTERPRETATION

conclusionsIndividuals with advanced-stage HL treated with anthracycline-based chemotherapy (anthracycline-based chemotherapy with doxorubicin, bleomycin, vinblastine and dacarbazine regimen) and CRT had excellent long-term outcomes. As isolated infield failures are uncommon, selective consolidation with conformal RT to high-risk sites improves final disease outcomes.

Indexed as

Hodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyDacarbazineDoxorubicinHemoglobinsHumansNeoplasm Recurrence, LocalNeoplasm StagingPositron Emission Tomography Computed TomographyRecurrenceRetrospective StudiesTreatment OutcomeDacarbazineDoxorubicinHemoglobins

Identifiers

PMID38577858
PMCPMC11050758
OpenAlexW4394608043

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.