Cervical Cancer

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Results from the phase 3 KEYNOTE-826 trial show that the safety profile of pembrolizumab plus chemotherapy was manageable in cervical cancer.
Pembrolizumab Plus Chemotherapy Improves OS, PFS in Cervical Cancer

December 17th 2024

Results from the phase 3 KEYNOTE-826 trial show that the safety profile of pembrolizumab plus chemotherapy was manageable in cervical cancer.

Data from the INTERLACE trial shows induction chemotherapy followed by chemoradiotherapy prolongs overall survival in locally advanced cervical cancer.
Induction Chemotherapy Combination Boosts PFS/OS in Cervical Cancer

November 3rd 2024

Subgroup data indicate a positive efficacy trend for TG4001 plus avelumab among patients with cervical cancer.
Cancer Vaccine Combo Does Not Improve PFS in Cervical/Anogenital Tumors

October 15th 2024

Expert Commentary on the Product Profile of Tisotumab Vedotin in Cervical Cancer
Expert Commentary on the Product Profile of Tisotumab Vedotin in Cervical Cancer

September 25th 2024

Pembrolizumab/CRT Improve Survival in High-Risk Locally Advanced Cervical Cancer
Pembrolizumab/CRT Improve Survival in High-Risk Locally Advanced Cervical Cancer

September 14th 2024

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Phase II Studies of Pemetrexed in Metastatic Breast and Gynecologic Cancers

November 2nd 2004

Pemetrexed (Alimta) is active in a variety of solid tumors, includingbreast and gynecologic cancers. Phase II trials of pemetrexed at a doseof 600 mg/m2 without vitamin B12 and folic acid supplementation inlargely pretreated metastatic breast cancer patients demonstrated objectiveresponse rates of 21% and 28%, with generally manageableneutropenia constituting the primary toxicity. In phase II trials using500 mg/m2 with or without vitamin supplementation in anthracyclineandtaxane-pretreated patients, response rates were lower (approximately9%) and treatment was generally well tolerated irrespective ofvitamin supplementation status. A phase II trial is currently comparingpemetrexed doses of 600 and 900 mg/m2 with vitamin B12 supplementationin patients with previously untreated advanced breast cancer. In aphase II trial in patients with advanced cervical cancer, pemetrexed at600 mg/m2 without vitamin supplementation and 500 mg/m2 with supplementationproduced similar response rates, with the frequency of neutropeniabeing somewhat lower among patients receiving the lower doseand vitamin supplementation. Preliminary results in an ongoing phaseII trial indicate activity of the regimen of gemcitabine (Gemzar) at1,000 mg/m2 plus pemetrexed at 500 mg/m2 with vitamin supplementationin patients with ovarian cancer. Ongoing and future studies willestablish optimal dosing regimens of pemetrexed and potential benefitsof vitamin supplementation in the settings of metastatic breastcancer and gynecologic malignancies.