Evidence map›Paper›PMID 42332845›Full record

ArticleCancer medicine2026

Safety and Tolerability of Different Total Neoadjuvant Therapies in Patients With Locally Advanced Rectal Cancer.

Shohei Udagawa, Hiroki Osumi, Senzo Taguchi, Tatsuki Noguchi, Takashi Sakamoto, Shimpei Matsui, Toshiki Mukai, Tomohiro Yamaguchi, Shota Fukuoka, Koichiro Yoshino and 8 more

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Shohei UdagawaDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Hiroki OsumiDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Senzo TaguchiDepartment of Radiation Oncology, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3932-8084
Tatsuki NoguchiDepartment of Colorectal Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Takashi SakamotoDepartment of Colorectal Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Shimpei MatsuiDepartment of Colorectal Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Toshiki MukaiDepartment of Colorectal Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3553-3590
Tomohiro YamaguchiDepartment of Colorectal Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Shota FukuokaDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Koichiro YoshinoDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Keitaro ShimozakiDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Takeru WakatsukiDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Mariko OguraDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Akira OokiDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Keisho ChinDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Kensei YamaguchiDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Takashi AkiyoshiDepartment of Colorectal Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Eiji ShinozakiDepartment of Gastroenterological Chemotherapy, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTotal neoadjuvant therapy (TNT) is the standard treatment for locally advanced rectal cancer (LARC). Few studies have focused on the toxicity of TNT. Moreover, the differences in safety and tolerability between radiotherapy-first and chemotherapy-first strategies remain unclear. This study aimed to evaluate the differences in treatment-related toxicities between radiotherapy-first and chemotherapy-first strategies for TNT in patients with LARC.

methodsPatients with LARC who were treated with TNT at a single cancer center between June 2020 and July 2023 were retrospectively included. TNT consisted of induction chemotherapy followed by long-course chemoradiotherapy (INCT-LC-CRT) or long-course chemoradiotherapy/short-course radiotherapy followed by consolidation chemotherapy (LC-CRT-CNCT/SC-RT-CNCT). Adverse events (AEs) and treatment exposure were compared between the groups.

resultsOverall, 93 patients were included. Patients in the INCT-LC-CRT and LC-CRT-CNCT/SC-RT-CNCT groups were 28 (30.1%) and 45 (48.4%) / 20 (21.5%), respectively. Chemotherapy-related grade 3 or 4 AEs were significantly more frequent in the LC-CRT-CNCT/SC-RT-CNCT group than in the INCT-LC-CRT group (50.8% vs. 17.9%, p < 0.01) but were not significantly different between the LC-CRT-CNCT and SC-RT-CNCT groups (53.3% vs. 40.0%, p = 0.42). The proportion of patients who received a full dose of chemotherapy was higher in the INCT-LC-CRT group than in the LC-CRT-CNCT/SC-RT-CNCT group (53.6% vs. 24.6%; p < 0.01). One (3.6%) and six (9.2%) patients discontinued chemotherapy owing to AEs in the INCT-LC-CRT and LC-CRT-CNCT/SC-RT-CNCT groups, respectively.

conclusionsGrade 3 or 4 AEs during chemotherapy were more frequent and required dose modification in the LC-CRT-CNCT/SC-RT-CNCT group than in the INCT-LC-CRT group.

Indexed as

ChemoradiotherapyNeoadjuvant TherapyRectal NeoplasmsAdultAgedAntineoplastic Combined Chemotherapy ProtocolsConsolidation ChemotherapyFemaleHumansInduction ChemotherapyMaleMiddle AgedNeoplasm StagingRetrospective Studiesconsolidation chemotherapyinduction chemotherapylocally advanced rectal cancertotal neoadjuvant therapy

Identifiers

PMID42332845
PMCPMC13287088

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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.