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folinic acid/vėžys

Nuoroda įrašoma į mainų sritį
Puslapis 1 nuo 118 rezultatus
Background - Rationale Aflibercept The addition of aflibercept to the standard FOLFIRI regimen as second-line therapy was evaluated in a large phase III study (EFC10262-VELOUR). This combination significantly improved both PFS (4.7 to 6.9 months, HR=0.76; P=<0.001) and OS (12.1 to 13.5 months,

Intermittent or Continuous Panitumumab Plus FOLFIRI for RAS/B-RAF Wild-type Metastatic Colorectal Cancer

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
This will be a multicenter open label randomized phase II study. The study population will include untreated RAS wild-type metastatic colorectal (mCRC) patients with unresectable disease. A total of 136 patients will be enrolled. All Patients will receive an induction treatment with panitumumab as 1
PRIMARY OBJECTIVES: I. To evaluate the efficacy of systemic induction of mFOLFIRINOX, followed by HAI floxuridine-dexamethasone administered concurrently with systemic mFOLFIRI. II. To assess safety of treatment with HAI floxuridine-dexamethasone delivered concurrently with systemic

FOLFIRINOX With Digoxin in Patients With Resectable Pancreatic Cancer

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
Methods: Patients with resectable pancreatic cancer will be treated with oxaliplatin 85 mg/m² IV over 2 hours, irinotecan 150 mg/m² given concurrently with folinic acid 400 mg/m² IV over 90 min, followed by a 46-hour infusion of 5-fluorouracil 2400 mg/m². Slow oral digitalization will be used

FOLFOX vs Gemcitabine in Patients With Metastatic Pancreatic Cancer Non-fit to FOLFIRINOX

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
This trial is an open label, multicenter, randomized phase III trial comparing gemcitabine vs FOLFOX in patients with metastatic pancreatic adenocarcinoma and non-fit for FOLFIRINOX. Adults fulfilling inclusion criteria and non-inclusion criteria will be randomized between a FOLFOX arm and a

Nalirinox Neo-pancreas RAS Mut ctDNA Study

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija

AREG, EREG and EGFR: Response to Anti-EGFR Agents in Colorectal Cancer

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
Background: The anti-EGFR agents, cetuximab and panitumumab are approved by NICE for the first-line treatment of patients with RAS wild-type (RAS-wt) advanced colorectal cancer (aCRC). However RAS-wt status is not sufficient to guarantee anti-EGFR benefit. Differential tumour expression of the EGFR

Safety, Tolerability and Efficacy of Regorafenib in Combination With FOLFIRINOX in Patients With Colorectal Cancer

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
Colorectal cancer (CRC) is a major cause of morbidity and mortality globally. More than 50% of patients can be expected to develop metastatic disease, and most of these patients will require palliative systemic therapy. The primary goal for patients who present with technically resectable liver
Primary objective - Main objective of phase I: To evaluate the acute toxicity of treatment with FOLFIRINOX 3 - bevacizumab - Main objective of phase II: To evaluate the efficacy of treatment with FOLFIRINOX 3 - bevacizumab in terms of objective response according to the RECIST criteria. Secondary

Alternative Neoadjuvant Chemotherapy in Resectable and Borderline Resectable Pancreatic Cancer

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
This research study is a Phase Ib clinical trial. It will assess the Safety, tolerability, and feasibility of gemcitabine-nab paclitaxel alternating with nal-IRI/5FU/leucovorin (NAPOLI) in de novo resectable and borderline resectable pancreatic cancer. Subjects must have a newly diagnosed resectable
Pancreatic cancer (PC) is the seventh cause from cancer and the fifth cause from cancer-related death in Europe. Nearly as many deaths occur from PC than the number of new cases diagnosed each year, reflecting the poor prognosis typically associated with this disease. PC is insidious in onset and is

Second-line Therapy for Patients With Progressive Poorly Differentiated Extra-pulmonary Neuroendocrine Carcinoma

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija

Nal-iri/lv5-fu Versus Paclitaxel as Second Line Therapy in Patients With Metastatic Oesophageal Squamous Cell Carcinoma

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
Principal objective: • To evaluate the survival of patients at 9 months Secondary objectives: - Progression-free survival (PFS) (clinical and/or radiological) - Overall survival (OS) - Best response rate during treatment according to RECIST 1.1 criteria (according to the investigator and the

Study of Eryaspase in Combination With Chemotherapy Versus Chemotherapy Alone as 2nd-Line Treatment in PAC

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
Patients who meet all inclusion and exclusion criteria will be randomized in a 1:1 ratio to one of the following treatment arms (see figure below): - Arm A (investigational arm): eryaspase in combination with either gemcitabine/Abraxane or irinotecan-based therapy (FOLFIRI [FOLinic

Masitinib in Combination With FOLFIRI in Third or Fourth Line of Treatment of Patients With Metastatic Colorectal Cancer

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
The objective is to compare the efficacy and safety of masitinib in combination with FOLFIRI (irinotecan, 5-fluorouracil and folinic acid) versus Best Supportive Care in third or fourth line treatment of patients with metastatic colorectal cancer.
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