» Articles » PMID: 38833249

Treatment of Locally Advanced Rectal Cancer in the Era of Total Neoadjuvant Therapy: A Systematic Review and Network Meta-Analysis

Overview
Journal JAMA Netw Open
Specialty General Medicine
Date 2024 Jun 4
PMID 38833249
Authors
Affiliations
Soon will be listed here.
Abstract

Importance: Treatment of locally advanced rectal cancer (LARC) involves neoadjuvant chemoradiotherapy plus total mesorectal excision and adjuvant chemotherapy. However, total neoadjuvant therapy (TNT) protocols (ie, preoperative chemotherapy in addition to radiotherapy) may allow better adherence and early treatment of distant micrometastases and may increase pathological complete response (pCR) rates.

Objective: To assess the efficacy and tolerability of TNT protocols for LARC.

Data Sources: MEDLINE, Embase, Cochrane Central Register of Controlled Trials (CENTRAL), and Web of Science Core Collection electronic databases and ClinicalTrials.gov for unpublished studies were searched from inception to March 2, 2024.

Study Selection: Randomized clinical trials including adults with LARC who underwent rectal resection as a final treatment were included. Studies including nonoperative treatment (watch-and-wait strategy), treatments other than rectal resection, immunotherapy, or antiangiogenic agents were excluded. Among the initially identified studies, 2.9% met the selection criteria.

Data Extraction And Synthesis: Two authors independently screened the records and extracted data. Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA)-compliant pairwise and network meta-analyses with a random-effects model were performed in a frequentist framework, and the certainty of evidence was assessed according to the confidence in network meta-analysis approach.

Main Outcomes And Measures: The primary outcome was pCR, defined as the absence of residual tumor at pathological assessment after surgery. Secondary outcomes included tolerability, toxic effects, perioperative outcomes, and long-term survival.

Results: Of 925 records identified, 27 randomized clinical trials, including 13 413 adults aged 18 years or older (median age, 60.0 years [range, 42.0-63.5 years]; 67.2% male) contributed to the primary network meta-analysis. With regard to pCR, long-course chemoradiotherapy (L-CRT) plus consolidation chemotherapy (relative risk [RR], 1.96; 95% CI, 1.25-3.06), short-course radiotherapy (S-RT) plus consolidation chemotherapy (RR, 1.76; 95% CI, 1.34-2.30), and induction chemotherapy plus L-CRT (RR, 1.57; 95% CI, 1.09-2.25) outperformed standard L-CRT with single-agent fluoropyrimidine-based chemotherapy. Considering 3-year disease-free survival, S-RT plus consolidation chemotherapy (RR, 1.08; 95% CI, 1.01-1.14) and induction chemotherapy plus L-CRT (RR, 1.12; 95% CI, 1.01-1.24) outperformed L-CRT, in spite of an increased 5-year locoregional recurrence rate of S-RT plus consolidation chemotherapy (RR, 1.65; 95% CI, 1.03-2.63).

Conclusions And Relevance: In this systematic review and network meta-analysis, 3 TNT protocols were identified to outperform the current standard of care in terms of pCR rates, with good tolerability and optimal postoperative outcomes, suggesting they should be recognized as first-line treatments.

Citing Articles

Therapeutic Management of Locally Advanced Rectal Cancer: Existing and Prospective Approaches.

Liscu H, Verga N, Atasiei D, Ilie A, Vrabie M, Rosu L J Clin Med. 2025; 14(3).

PMID: 39941583 PMC: 11818342. DOI: 10.3390/jcm14030912.


Impact of Sarcopenia on Treatment Outcomes and Toxicity in Locally Advanced Rectal Cancer.

Curcean S, Gherman A, Tipcu A, Fekete Z, Muntean A, Curcean A Medicina (Kaunas). 2024; 60(10).

PMID: 39459393 PMC: 11509686. DOI: 10.3390/medicina60101606.


Total Neoadjuvant Therapy in Locally Advanced Rectal Cancer: Insights from the Western Australian Context.

Oey O, Lin C, Khattak M, Ferguson T, Theophilus M, Tiong S Diseases. 2024; 12(10).

PMID: 39452500 PMC: 11507632. DOI: 10.3390/diseases12100257.


Achieving a Pathologic Complete Response for Locally Advanced Esophageal Adenocarcinoma Using Cone-Beam Computed Tomography-Based Online Adaptive Radiotherapy.

Bachmann N, Schmidhalter D, Corminboeuf F, Ermis E, Aebersold D, Manser P Cureus. 2024; 16(9):e68753.

PMID: 39371804 PMC: 11456338. DOI: 10.7759/cureus.68753.


Impact of radiotherapy on quality of life in patients with rectal cancer.

Tejedor P, Denost Q BJS Open. 2024; 8(5).

PMID: 39258489 PMC: 11387962. DOI: 10.1093/bjsopen/zrae105.


References
1.
Mohiuddin M, Winter K, Mitchell E, Hanna N, Yuen A, Nichols C . Randomized phase II study of neoadjuvant combined-modality chemoradiation for distal rectal cancer: Radiation Therapy Oncology Group Trial 0012. J Clin Oncol. 2006; 24(4):650-5. DOI: 10.1200/JCO.2005.03.6095. View

2.
Bujko K, Nasierowska-Guttmejer A, Wyrwicz L, Malinowska M, Krynski J, Kosakowska E . Neoadjuvant treatment for unresectable rectal cancer: an interim analysis of a multicentre randomized study. Radiother Oncol. 2013; 107(2):171-7. DOI: 10.1016/j.radonc.2013.03.001. View

3.
Bosset J, Calais G, Mineur L, Maingon P, Stojanovic-Rundic S, Bensadoun R . Fluorouracil-based adjuvant chemotherapy after preoperative chemoradiotherapy in rectal cancer: long-term results of the EORTC 22921 randomised study. Lancet Oncol. 2014; 15(2):184-90. DOI: 10.1016/S1470-2045(13)70599-0. View

4.
Petrelli F, Trevisan F, Cabiddu M, Sgroi G, Bruschieri L, Rausa E . Total Neoadjuvant Therapy in Rectal Cancer: A Systematic Review and Meta-analysis of Treatment Outcomes. Ann Surg. 2019; 271(3):440-448. DOI: 10.1097/SLA.0000000000003471. View

5.
Chakrabarti D, Rajan S, Akhtar N, Qayoom S, Gupta S, Verma M . Short-course radiotherapy with consolidation chemotherapy versus conventionally fractionated long-course chemoradiotherapy for locally advanced rectal cancer: randomized clinical trial. Br J Surg. 2021; 108(5):511-520. DOI: 10.1093/bjs/znab020. View