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Robustness of evidence from randomized controlled trials (RCTs) is crucial for guiding clinical decisions in rectal cancer. We evaluated the reliability of RCTs cited by the National Comprehensive Cancer Network (NCCN) guidelines for rectal cancer using the Fragility Index (FI) that quantifies the stability of trial outcomes. RCTs referenced in the latest NCCN guidelines for rectal cancer were reviewed. Data from eligible trials were extracted. FI was calculated to assess the robustness of evidence across different treatment modalities. Sixty-seven RCTs (published: 1987-2022) involving 16,990 patients were analyzed. Most studies (58.2%) were conducted in Europe. Common treatment areas included metastatic liver disease (28.9%) and neoadjuvant chemotherapy (14.9%). Primary outcomes were disease-free survival and overall survival (OS) in 15 studies each (22.4%), local recurrence rates in 6 (9%), and tumor response in 5 (7.5%). The median FI was 9 (interquartile range [IQR] 2-20). Studies on surgical interventions had the highest median FI (21 [IQR 7-27]) followed by studies on neoadjuvant radiotherapy (19 [IQR 14-25]). Neoadjuvant immunotherapy studies had the lowest median FI of 0, indicating less robust evidence. Notably, surgical intervention studies showed the largest gap between FI and patients lost to follow-up (21 vs. 13.5), while neoadjuvant immunotherapy studies showed more patients lost to follow-up than the median FI (0 vs. 5), highlighting the need for stronger evidence. In conclusion, evidence supporting most treatments for rectal cancer in the NCCN guidelines is robust, although neoadjuvant immunotherapy requires further scrutiny due to its low FI. FI offers a nuanced perspective on the reliability of trial outcomes.
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http://dx.doi.org/10.1002/ijc.35521 | DOI Listing |
Breast Cancer Res
September 2025
Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Background: Polygenic risk scores (PRS) are not yet standard in clinical risk assessments for familial breast cancer in Sweden. This study evaluated the distribution and impact of an established PRS (PRS) in women undergoing clinical sequencing for hereditary breast cancer.
Findings: We integrated PRS into a hereditary breast cancer gene panel used in clinical practice and calculated scores for 262 women.
Can J Urol
August 2025
Department of Radiation Oncology, Baskent University Faculty of Medicine, Ankara, 06490, Turkiye.
Background: Intermediate-risk prostate cancer (IR-PC) represents a heterogeneous group requiring nuanced treatment approaches, and recent advancements in radiotherapy (RT), androgen deprivation therapy (ADT), and prostate-specific membrane antigen positron emission tomography (PSMA-PET/CT) imaging have prompted growing interest in personalized, risk-adapted management strategies. This study by the Turkish Society for Radiation Oncology aims to examine radiation oncologists' practices in managing IR-PC, focusing on RT and imaging modalities to identify trends for personalized treatments.
Methods: A cross-sectional survey was conducted among Turkish radiation oncologists treating at least 50 prostate cancer (PC) cases annually.
Cancer Rep (Hoboken)
September 2025
Department of Oncology, Eastern Health, Melbourne, Australia.
Background: Enteric-type thymic adenocarcinomas are an extremely rare and distinct subtype of thymic malignancies, as classified by the 2021 World Health Organization classification of thymic tumors. These tumors exhibit close molecular and morphologic similarity to primary gastrointestinal malignancies. To date, there are no tailored treatment guidelines for enteric-type thymic adenocarcinoma.
View Article and Find Full Text PDFJAMA
September 2025
Department of Health Policy, London School of Economics and Political Science, London, United Kingdom.
J Manag Care Spec Pharm
September 2025
Division of Medical Oncology, Department of Medicine, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles.
Background: Alectinib, brigatinib, and lorlatinib are all preferred first-line (1L) therapies for anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC) in National Comprehensive Cancer Network (NCCN) guidelines. Although clinical trials have demonstrated their efficacy, real-world evidence on treatment patterns, costs, and outcomes may help differentiate these therapies and inform optimal 1L treatment selection in the absence of head-to-head comparisons.
Objective: To evaluate real-world outcomes for patients with ALK+ NSCLC receiving 1L ALK tyrosine kinase inhibitors (TKIs), focusing on drug acquisition costs, health care utilization, and clinical outcomes.