Evidence map›Paper›PMID 41219905›Full record

ArticleBMC cancer2025

Efficacy and safety of neoadjuvant chemoradiotherapy versus chemotherapy alone in locally advanced rectal cancer.

Chunna Zhang, Fuyu Zhang, Hujian Hong, Yanli Qu

Abstract readComparative Study
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chunna ZhangDepartment of Radiation Oncology, The Fourth Affiliated Hospital of China Medical University, Liaoning, China.
Fuyu ZhangDepartment of Radiation Oncology, The Fourth Affiliated Hospital of China Medical University, Liaoning, China.
Hujian HongDepartment of Radiotherapy, Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute, No.44 xiaoheyan Road, Dandong District, Shenyang, Liaoning, 110801, China.
Yanli QuDepartment of Radiotherapy, Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute, No.44 xiaoheyan Road, Dandong District, Shenyang, Liaoning, 110801, China. quyanli@cancerhops-In-cmu.com.ORCID http://orcid.org/0000-0002-7533-6815

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe neoadjuvant chemotherapy (nCT) could achieve outcomes comparable to neoadjuvant chemoradiotherapy (nCRT) and reduced radiation toxicity, radiotherapy is questioned. Comparing nCRT and nCT in locally advanced rectal cancer (LARC) in the real world to identify patient subgroups that may benefit most from each approach.

methodsThis retrospective study included patients with rectal cancer located within 10 cm from the anal verge and clinical staging of T2N + M0 or T3-4NanyM0. Patients were stratified into the nCRT group, which received radiotherapy (45.0 to 50.4 Gy/25 or 28 fractions) with concurrent Capecitabine chemotherapy, or the nCT group which received chemotherapy alone.

resultsIn total, 380 patients (nCRT, n = 196, nCT, n = 184) were recruited. The rate of pathologic complete response (pCR) in the nCRT and nCT group was 22.4% and 9.2%, T downstaging was 69.4% and 47.8%, and tumor regression grade (TRG) 1–2 was 59.7% and 24.5%, respectively. Similarly, The nCRT group also had a favorable pCR, T downstaging, and TRG 1–2 rate than the nCT group in the bad-risk, advanced-risk, and subgroup A (tumors located at < 8 cm from the anal verge). In contrast, outcomes were comparable for subgroup B (tumors located at ≥ 8 cm) between the two groups. Moreover, the nCRT had a better rate of 3-year locoregional relapse-free survival (LRFS) (98.1% vs. 88.0%, P = 0.031) in the bad-risk category compared with the nCT group. Conversely, the disease-free survival (DFS) and overall survival (OS) were similar. The nCRT was associated with a higher rate of grade 1–2 myelosuppression (69.9% vs. 37.0%), diarrhea (54.1% vs. 10.3%), preventive stoma (62.8% vs. 44.6%), postoperative bowel obstruction (9.2% vs. 1.1%), and postoperative anastomotic stenosis (4.1% vs. 0.5%) (all P < 0.05).

conclusionTumor location and risk category may serve as a practical index for clinical decision-making on neoadjuvant therapy strategies in LARC. Patients with bad-risk or tumors located at < 8 cm from the anal verge may be benefited from nCRT.

Indexed as

ChemoradiotherapyNeoadjuvant TherapyRectal NeoplasmsAdultAgedCapecitabineChemoradiotherapy, AdjuvantFemaleHumansMaleMiddle AgedNeoplasm StagingPathologic Complete ResponseRetrospective StudiesTreatment OutcomeCapecitabineAdverse eventLocally advanced rectal cancerNeoadjuvant therapyTumor location

Identifiers

PMID41219905
PMCPMC12607225

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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.