Evidence map›Paper›PMID 40557347›Full record

ArticleAnnals of surgery open : perspectives of surgical history, education, and clinical approaches2025

Neoadjuvant Chemotherapy Versus Adjuvant Chemotherapy for Very Low-Lying Clinical T3 Rectal Cancer: The NAIR Phase 2/3 Randomized Clinical Trial.

Yuichiro Tsukada, Norio Saito, Yuji Nishizawa, Riki Ohno, Fumihiko Fujita, Keiji Koda, Masayuki Ohue, Eiji Shinto, Akihiko Murata, Yoshikazu Koide and 6 more

Abstract read
In one paragraph

Article in Annals of surgery open : perspectives of surgical history, education, and clinical approaches, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Observational
  2. Observational
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

16 authors.

Yuichiro TsukadaFrom the Department of Colorectal Surgery, National Cancer Center Hospital East, Kashiwa, Japan.
Norio SaitoDepartment of General Surgery, Saito Rosai Hospital, Chiba, Japan.
Yuji NishizawaFrom the Department of Colorectal Surgery, National Cancer Center Hospital East, Kashiwa, Japan.
Riki OhnoDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, Japan.
Fumihiko FujitaDepartment of Surgery, Kurume University, Kurume, Japan.
Keiji KodaDepartment of Surgery, Teikyo University Chiba Medical Center, Chiba, Japan.
Masayuki OhueDepartment of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.
Eiji ShintoDepartment of Surgery, National Defense Medical College, Saitama, Japan.
Akihiko MurataDepartment of Surgery, Aomori Prefectural Central Hospital, Aomori, Japan.
Yoshikazu KoideDepartment of Surgery, Fujita Health University Hospital, Aichi, Japan.
Koji IkedaFrom the Department of Colorectal Surgery, National Cancer Center Hospital East, Kashiwa, Japan.
Hideaki BandoDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Motoko SuzukiDepartment of Data Science, National Cancer Center Hospital East, Kashiwa, Japan.
Toshihiro MisumiDepartment of Data Science, National Cancer Center Hospital East, Kashiwa, Japan.
Takayuki YoshinoDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Masaaki ItoFrom the Department of Colorectal Surgery, National Cancer Center Hospital East, Kashiwa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine whether neoadjuvant chemotherapy (NAC) followed by total mesorectal excision (TME) and adjuvant chemotherapy (AC) is superior to TME followed by AC for very low-lying clinical (c) T3 rectal cancer. Background: Preoperative radiation is widely used for preoperative treatment of cT3 rectal cancer; however, it worsens patient-reported outcomes (PROs). Preoperative treatment without radiation is expected to preserve PROs. Methods: Patients with cT3N-anyM0 rectal cancer located within 5 cm from the anal verge were randomly assigned (1:1) to the NAC group (3 months of NAC followed by TME and 3 months of AC) or AC group (TME followed by 6 months of AC). NAC and AC comprised mFOLFOX6 (oxaliplatin, l-folinic acid, and fluorouracil) or CAPOX (oxaliplatin and capecitabine). The primary endpoint was the 3-year recurrence-free survival (RFS). PROs were analyzed. Results: Between February 2013 and March 2019, 130 patients were randomly assigned to the NAC (n = 65) or AC (n = 65) groups; of these, 127 were evaluable (NAC, n = 65; AC, n = 62). At a median follow-up of 37.4 months, the 3-year RFS was 75.5% and 70.9% in NAC and AC groups, respectively [hazard ratio (HR) = 0.67, 60% confidence interval (CI) = 0.48-0.86, 95% CI = 0.34-1.32; Conclusions: NAC for very low-lying cT3 rectal cancer improved RFS without worsening PROs although LRR remained high. Trial Registration: UMIN Clinical Trials Registry: UMIN000009510/Japan Registry of Clinical Trials: jRCTs031180278.

Indexed as

intersphincteric resectionneoadjuvant chemotherapyrandomized clinical trialrectal cancer

Identifiers

PMID40557347
PMCPMC12185085

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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.