98%
921
2 minutes
20
Purpose: Modified FOLFIRINOX (mFOLFIRINOX) and nab-paclitaxel + gemcitabine are recommended as first-line treatments for metastatic pancreatic cancer. S-1, irinotecan, and oxaliplatin (S-IROX) demonstrated activity in a phase Ib trial in this population. Therefore, these three regimens were directly compared.
Methods: This randomized phase II/III trial was performed at 45 centers in Japan. Eligible patients age 20-75 years with an Eastern Cooperative Oncology Group performance status of 0 or 1 and pathologically confirmed metastatic or recurrent pancreatic cancer were randomly assigned (1:1:1) to receive mFOLFIRINOX (oxaliplatin 85 mg/m over 2 hours, irinotecan 150 mg/m over 90 minutes, l-leucovorin 200 mg/m over 2 hours, each once daily on day 1, and fluorouracil 2,400 mg/m over 46 hours on days 1-3, every 2 weeks), S-IROX (oxaliplatin 85 mg/m over 2 hours, irinotecan 150 mg/m over 90 minutes on day 1, and S-1 80 mg/m/day administered orally twice daily on days 1-7, every 2 weeks), or nab-paclitaxel (125 mg/m) + gemcitabine (1,000 mg/m) on days 1, 8, and 15 every 4 weeks. The primary end point was overall survival (OS).
Results: A total of 527 patients were enrolled, with 426 included in the planned interim analysis. The median OS was 14.0 months (hazard ratio [HR], 1.31 [95% CI, 0.97 to 1.77]) and 13.6 months (HR, 1.35 [95% CI, 1.00 to 1.82]) in the mFOLFIRINOX and S-IROX groups, respectively, as compared with 17.1 months in the nab-paclitaxel + gemcitabine group. The predictive probability of achieving superiority in the final analysis was <1% in both groups. Thus, the trial was terminated owing to its futility. Grade 3 to 4 anorexia was more frequent in the mFOLFIRINOX (23.3%) and S-IROX (27.5%) groups than in the nab-paclitaxel + gemcitabine group (5.0%).
Conclusion: Neither mFOLFIRINOX nor S-IROX appeared to be superior compared with nab-paclitaxel + gemcitabine as the first-line treatment for metastatic or recurrent pancreatic cancer.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1200/JCO.24.00936 | DOI Listing |
J Clin Oncol
July 2025
Department of Gastroenterology, Kanagawa Cancer Center, Yokohama, Japan.
Sci Rep
July 2025
Medical Center for Neck and Low Back Pain, Xijing Hospital, Fourth Military Medical University, Xi'an, 710000, China.
Research on the impact of changes in air pollutant concentrations during peak traffic hours on hospital admissions for respiratory diseases (RD) is limited. This study utilized a distributed lag nonlinear model (DLNM) to investigate this effect. Between 2014 and 2019, a total of 109,419 RD patients were hospitalized across seven hospitals in Lanzhou, China.
View Article and Find Full Text PDFNEJM Evid
July 2025
Department of Hematology, Hôpital Saint-Louis, AP-HP, Institut Hospitalo-Universitaire (IHU) Thema Saint-Louis, Institut de Recherche Saint-Louis (IRSL), Université Paris Cité, Paris.
Background: We conducted a randomized controlled trial to compare intermediate doses (IDAC) with high doses of cytarabine (HDAC) as postinduction therapy in patients 18 to 60 years of age with newly diagnosed acute myeloid leukemia (AML). The main objectives were to evaluate noninferiority in overall survival (OS) after IDAC and safety.
Methods: Patients 18 to 60 years of age with newly diagnosed AML, except those with core-binding factor, acute promyelocytic, Philadelphia chromosome-positive, or post-myeloproliferative neoplasm AML, were eligible.
Blood Neoplasia
February 2025
Hematology and Bone Marrow Transplantation, Yale School of Medicine, New Haven, CT.
Pralatrexate (Folotyn) is an antifolate indicated for the treatment of relapsed/refractory peripheral T-cell lymphoma (PTCL), and although durable clinical benefit has been demonstrated, oral and gastrointestinal mucositis and/or skin reactions are frequent toxicity complications associated with pralatrexate treatment. Leucovorin (d,l-folinic acid) administration has been used as a standard rescue for patients receiving high-dose methotrexate therapy and has recently been studied in patients with PTCL and cutaneous T-cell lymphoma receiving pralatrexate. We describe results from a multicenter, phase 2, single-arm, open-label trial, conducted with the primary objective of evaluating the effect of leucovorin in preventing or reducing the incidence of grade 2 or higher oral mucositis associated with pralatrexate treatment in cycle 1.
View Article and Find Full Text PDFJ Clin Oncol
July 2025
The University of Melbourne, Melbourne, Australia.
Purpose: This study evaluated DB-020, a formulation of thiosulfate for intratympanic (IT) injection, in patients receiving high-dose cisplatin chemotherapy.
Methods: This randomized phase Ib clinical trial enrolled patients older than 18 years from five centers in Australia and the United States scheduled for at least three cycles of cisplatin and total cumulative exposure of ≥280 mg/m. Patients received IT DB-020 (at a dose level of either 12% or 25%) in one ear and placebo in the other, once every 3 or 4 weeks, within 3 hours before receiving cisplatin.