Evidence map›Paper›PMID 36160741›Full record

ArticleWorld journal of gastrointestinal oncology2022

Duodenal-type follicular lymphoma more than 10 years after treatment intervention: A retrospective single-center analysis.

Makoto Saito, Akio Mori, Shihori Tsukamoto, Takashi Ishio, Emi Yokoyama, Koh Izumiyama, Masanobu Morioka, Takeshi Kondo, Hirokazu Sugino

Abstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2022. 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
–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

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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

Who cites it

5 citing papers in PubMed.

  1. Review
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  5. Duodenal-type follicular lymphoma inAmerican journal of nuclear medicine and molecular imaging · 2023
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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

9 authors.

Makoto SaitoBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan. ikyoku@aiiku-hp.or.jp.
Akio MoriBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Shihori TsukamotoBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Takashi IshioBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Emi YokoyamaBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Koh IzumiyamaBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Masanobu MoriokaBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Takeshi KondoBlood Disorders Center, Aiiku Hospital, Sapporo 064-0804, Japan.
Hirokazu SuginoDepartment of Cancer Pathology, Hokkaido University, Faculty of Medicine, Sapporo 060-8638, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuodenal-type follicular lymphoma (D-FL) has been recognized as a rare entity that accounts for approximately 4% of primary gastrointestinal lymphomas. D-FL follows an indolent clinical course compared with common nodal FL and is generally considered to have a better prognosis. Therefore, the "watch and wait" approach is frequently adopted as the treatment method. Alternatively, there is an option to actively intervene in D-FL. However, the long-term outcomes of such cases are poorly understood.

aimTo clarify the clinical outcomes after long-term follow-up in cases of D-FL with treatment intervention.

methodsWe retrospectively analyzed patients who met the following criteria: the lesion was confirmed by endoscopy, the diagnosis of D-FL was confirmed histopathologically, and the patient was followed-up for more than 10 years after the intervention at our center.

resultsWe identified 5 cases of D-FL. Two patients showed a small amount of bone marrow involvement (Stage IV). Rituximab was used as a treatment for remission in all 5 patients. It was also used in combination with chemotherapy in 2 Stage IV patients as well as for maintenance treatment. Radiation therapy was performed in 2 cases, which was followed by complete remission (CR). Eventually, all 5 patients achieved CR and survived for more than 10 years. However, 3 patients experienced recurrence. One patient achieved a second CR by retreatment, and in another case, the lesion showed spontaneous disappearance. The remaining patient had systemic widespread recurrence 13 years after the first CR. Biopsy results suggested that the FL lesions were transformed into diffuse large B-cell lymphoma. The patient died 4 years later despite receiving various chemotherapies.

conclusionIn this study, the treatment for patients of D-FL in Stage IV was successful. In the future, criteria for how to treat "advanced" D-FL should be established based on additional cases. This study of patients with D-FL indicates that whole-body follow-up examinations should continue for a long time due to a fatal recurrence 13 years after reaching CR.

Indexed as

ChemotherapyDuodenal-type follicular lymphomaLong-term follow-upRadiationRituximabTreatment

Identifiers

PMID36160741
PMCPMC9412938

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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.