Evidence map›Paper›PMID 27982423›Full record

ArticleBritish journal of haematology2017

Outcomes of primary refractory diffuse large B-cell lymphoma (DLBCL) treated with salvage chemotherapy and intention to transplant in the rituximab era.

Santosha A Vardhana, Craig S Sauter, Matthew J Matasar, Andrew D Zelenetz, Natasha Galasso, Kaitlin M Woo, Zhigang Zhang, Craig H Moskowitz

Open access · bronzeAbstract read
In one paragraph

Article in British journal of haematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 54 citations in OpenAlex.

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  20. A new therapeutic approach in very refractory diffuse large B-cell lymphoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
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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

8 authors at 1 institution in 1 country.

Santosha A VardhanaDeparment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-3100-1298
Craig S SauterDeparment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Matthew J MatasarDeparment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Andrew D ZelenetzDeparment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Natasha GalassoDepartment of Epidemiology and Biostatistics, Sloan Kettering Cancer Center, New York, NY, USA.
Kaitlin M WooDepartment of Epidemiology and Biostatistics, Sloan Kettering Cancer Center, New York, NY, USA.
Zhigang ZhangDepartment of Epidemiology and Biostatistics, Sloan Kettering Cancer Center, New York, NY, USA.
Craig H MoskowitzDeparment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Investigational Cancer Therapeutics Training Program (ICTTP)T32CA009207 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Omar Abdel-Wahab, Alexander Drilon · 1985 to 2026
$13.7M
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA009207
6 · The paper itself

Abstract

Rituximab-containing salvage chemotherapy followed by high-dose therapy and autologous stem cell transplant (ASCT) in chemosensitive patients remains the standard of care for patients with relapsed and refractory diffuse large B-cell lymphoma (DLBCL). However, its role in those patients achieving less than a complete response to first-line therapy (primary refractory disease) in the rituximab era is not well defined. We reviewed the outcomes of 82 transplant-eligible patients with primary refractory DLBCL who underwent salvage therapy with the intent of administering high-dose therapy and ASCT to patients achieving chemosensitive remission. The estimated 3-year overall and progression-free survival for all patients was 38% and 29%, respectively, and 65% and 60% respectively for patients proceeding to stem cell transplant. Long-term remission was achieved in 45% of patients achieving a partial response (PR) to initial induction therapy and <20% of patients with stable or progression of disease following initial therapy. These results suggest that salvage chemotherapy with the intent of subsequent high-dose therapy and ASCT remains a feasible strategy in certain patients with primary refractory DLBCL, particularly for those achieving a PR to frontline therapy. The primary barrier to curative therapy in patients with primary refractory disease is resistance to salvage therapy, and future studies should be aimed towards increasing the response rate in this population.

Indexed as

AdultAgedDisease-Free SurvivalFemaleHematopoietic Stem Cell TransplantationHumansIntentionLymphoma, Large B-Cell, DiffuseMaleMiddle AgedRemission InductionRituximabSalvage TherapySurvival AnalysisRituximabDLBCLlymphomarefractoryrituximabtransplant

Identifiers

PMID27982423
PMCPMC5556376
OpenAlexW2563160427

What OpenQuestion holds

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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.