Pancreatic Cancer

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TTFields/Chemotherapy Improves Survival in Advanced Pancreatic Cancer
TTFields/Chemotherapy Improves Survival in Advanced Pancreatic Cancer

December 3rd 2024

Tumor treating fields with chemotherapy improved overall survival for patients with unresectable, locally advanced pancreatic adenocarcinoma.

Shubham Pant, MD, MBBS, highlights how pan-RAS inhibitors, RAS-directed vaccines, and biomarker testing can improve outcomes in pancreatic cancer.
Biomarker Testing, Targeted Agents May Impact RAS+ Pancreatic Cancer Care

November 30th 2024

The incorporation of palliative care specific to mental health services and therapy remains underutilized in the care of patients with pancreatic cancer.
Palliative Care May Improve Mental Health in Pancreatic Cancer Diagnoses

November 19th 2024

Managing Pancreatic Cancer Through Risk Factors, Diagnosis, and AEs
Managing Pancreatic Cancer Through Risk Factors, Diagnosis, and AEs

November 18th 2024

The 18-month overall survival rate with the mitazalimab combination in OPTIMIZE-1 exceeds a historical rate achieved with FOLFIRINOX alone.
Mitazalimab Combo Yields Meaningful Survival Benefit in Metastatic PDAC

November 7th 2024

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Pemetrexed in Pancreatic Cancer

November 2nd 2004

Single-agent gemcitabine (Gemzar) is the standard of chemotherapyfor advanced pancreatic cancer, with no phase III trials to date havingshown significantly improved survival with gemcitabine-based combinationsvs single-agent treatment. The multitargeted antifolate agentpemetrexed (Alimta) shows synergistic effects in vitro in combinationwith gemcitabine, and activity and good tolerability when used as singleagenttreatment in advanced pancreatic cancer. In a phase II trial inpatients with advanced pancreatic cancer, the combination ofgemcitabine at 1,250 mg/m2 on days 1 and 8 plus pemetrexed at 500mg/m2 on day 8 after gemcitabine every 21 days resulted in a mediansurvival of 6.5 months and a 1-year survival rate of 29%. Neutropeniawas the primary toxicity, with grade 4 toxicity in 51% of patients. Thepromising results of this trial prompted the initiation of a phase IIItrial comparing gemcitabine at 1,000 mg/m2 on days 1, 8, and 15 every28 days vs the 21-day gemcitabine/pemetrexed regimen given with vitaminsupplementation in patients with pancreatic cancer. The primaryoutcome measure was overall survival, with secondary measures includingresponse rate, progression-free survival, and quality of life.While an increase in response and time to progression was reported forthe gemcitabine/pemetrexed combination, there were no significantdifferences in survival between treatment arms.