Evidence map›Paper›PMID 39449303›Full record

ArticleHematology reports2024

Utilizing Clinical Transformation Criteria for Prognostic Stratification in Follicular Lymphoma Prior to Initial Immunochemotherapy.

Yoshikazu Hori, Hiroki Hosoi, Takayuki Hiroi, Ke Wan, Shogo Murata, Masaya Morimoto, Toshiki Mushino, Akinori Nishikawa, Takashi Sonoki

Abstract read
In one paragraph

Article in Hematology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  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

9 authors.

Yoshikazu HoriDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.ORCID 0000-0002-4754-2128
Hiroki HosoiDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.ORCID 0000-0002-8682-7476
Takayuki HiroiDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.
Ke WanClinical Study Support Center, Wakayama Medical University, Wakayama 641-8509, Japan.ORCID 0000-0002-1563-7181
Shogo MurataDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.ORCID 0000-0001-8060-6683
Masaya MorimotoDepartment of Hematology, Kinan Hospital, Wakayama 646-8588, Japan.
Toshiki MushinoDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.
Akinori NishikawaDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.ORCID 0000-0001-9286-6909
Takashi SonokiDepartment of Hematology/Oncology, Wakayama Medical University, Wakayama 641-8509, Japan.

Funding

Japan Society for the Promotion of Science KAKENHI (21K16248)Takeda Science Foundation N.A.
6 · The paper itself

Abstract

backgroundAlthough the prognosis of follicular lymphoma (FL) has improved, some patients experience early disease progression, including progression of disease within 24 months (POD24). Histological transformation is a critical event in FL. However, the heterogeneity of FL tumors makes it challenging to diagnose transformation accurately. We retrospectively applied the clinical transformation criteria used for FL transformation assessments at relapse or disease progression to conduct transformation assessments before the initial immunochemotherapy.

methodsSixty-six FL patients who first received immunochemotherapy between January 2009 and February 2023 at our institution were selected. Twenty-three were clinical-transformation-positive (CLT+).

resultsThe progression-free survival (PFS) rate of the CLT+ patients was significantly lower than that of the clinical-transformation-negative (CLT-) patients. In the POD24 assessment subgroup, the CLT+ patients had a higher incidence of POD24 than the CLT- patients. There was no significant difference in PFS between the patients treated with CHOP-like regimens and those treated with bendamustine regimens. In the CHOP-like group, the CLT+ patients exhibited significantly lower PFS than the CLT- patients. In the bendamustine group, the clinical transformation did not affect PFS.

conclusionClinical transformation criteria may be useful for the prognostic stratification of FL prior to immunochemotherapy. Additionally, they may serve as predictors of POD24.

Indexed as

early progressionfollicular lymphomaprognostic factortransformation

Identifiers

PMID39449303
PMCPMC11503408

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