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Introduction: Very early recurrence in pancreatic ductal adenocarcinoma has been defined as recurrence ≤3 months after resection. Besides others, neoadjuvant treatment is delivered based on the assumption of preoperative eradication of micrometastasis as well as local downstaging. Prognostic factors of very early recurrence after neoadjuvant treatment remain largely unexplored.
Methods: All patients who underwent resection for pancreatic ductal adenocarcinoma after neoadjuvant treatment were identified from 2 institutional databases. Clinicopathologic data and demographics were extracted. Univariable and multivariable logistic regression modeling was performed. Multicollinearity was assessed with a variance inflation factor.
Results: After excluding patients who died within 90 days postresection and CA19-9 nonsecretors, 305 patients remained. A total of 178 (58.4%) patients received FOLFIRINOX, 39 (12.8%) received gemcitabine-based neoadjuvant treatment and 88 (28.9%) received various combinations. Pancreatic head resection was performed in 240 (78.7%) patients, whereas 65 (21.3%) underwent distal or total pancreatectomy. In total, 28 (9.1%) patients experienced recurrence ≤3 months. Median overall survival was 6 months (95% confidence interval: 5-32 months) in patients with very early recurrence, compared with 40 months (95% confidence interval: 32-60 months) in the remaining cohort (P < .0001). In multivariable regression analysis, positive lymph node status was associated with very early recurrence (odds ratio: 2.57, 95% confidence interval: 1.15-5.8). Notably, no association with R status, type of neoadjuvant treatment, or preoperative CA19-9 levels was detected.
Conclusion: Positive lymph node status is an independent prognostic marker for very early recurrence after neoadjuvant treatment, indicating that these patients require closer follow-up and may benefit from additional or early initiation of adjuvant therapy.
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http://dx.doi.org/10.1016/j.surg.2025.109647 | DOI Listing |
Front Endocrinol (Lausanne)
September 2025
Department of Visceral, Thoracic and Vascular Surgery, Philipps University Marburg, Marburg, Germany.
Introduction: The prognosis of anaplastic thyroid carcinoma (ATC) remains poor. Mutation-based targeted therapies and immune checkpoint inhibitors (ICI) have gained increasing importance in the treatment of advanced tumor stages. This study aimed to investigate whether mutation-based neoadjuvant therapy can convert an initially unresectable tumor into a resectable state, optimizing local tumor control and prolonging overall survival.
View Article and Find Full Text PDFOphthalmic Plast Reconstr Surg
September 2025
Orbital Oncology and Ophthalmic Plastic Surgery, Department of Plastic Surgery, The University of Texas MD Anderson Cancer Center.
Solitary fibrous tumor, formerly also referred to as hemangiopericytoma, is a fibroblastic mesenchymal neoplasm of the orbit that rarely metastasizes but has a propensity for local recurrence. We describe 5 cases of orbital solitary fibrous tumors that were treated with radiation. In 3 patients, radiation therapy was given in the neoadjuvant setting prior to surgery.
View Article and Find Full Text PDFOphthalmic Plast Reconstr Surg
September 2025
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, U.S.A.
This study aimed to report clinical outcomes of topical chemotherapy for ocular adnexal sebaceous carcinoma (OaSC) with intraepithelial spread. A retrospective chart review of patients with OaSC treated at the Bascom Palmer Eye Institute between 2000 and 2023 was conducted. Patient inclusion criteria included: (1) biopsy-proven diagnosis of OaSC, (2) intraepithelial pagetoid involvement confirmed by conjunctival map biopsy, (3) implementation of topical chemotherapy for tumor control, and (4) repeat conjunctival map biopsy following cessation of topical chemotherapy.
View Article and Find Full Text PDFJ Pediatr Hematol Oncol
September 2025
Department of Pediatric, The University of Jordan.
Background: Rhabdomyosarcoma (RMS) typically responds well to a combination of treatments with favorable prognosis in children 1 to 9 years old. However, infants may fare worse due to receiving less aggressive local therapy for concerns about long-term effects of surgery/radiation. This study investigates the clinical characteristics, treatment approach, and survival outcomes of RMS in children under 2.
View Article and Find Full Text PDFInt J Surg Pathol
September 2025
Department of Pathology, Tata Memorial Hospital & Advanced Centre for Treatment and Research, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Undifferentiated carcinomas with osteoclast-like giant cells of the pancreaticobiliary tract (UCOGCs) are rare but distinctive tumors with limited literature. To study the clinicopathologic characteristics of UCOGCs including morphology, immunohistochemistry (IHC), management, and survival outcomes. Assessment of 12 patients of UCOGC found over 10 years from a tertiary care oncology center database.
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