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The Radiation Therapy Oncology Group (RTOG) protocol 95-17 was a Phase I/II trial to evaluate multicatheter brachytherapy as the sole method of adjuvant breast radiotherapy for Stage I/II breast carcinoma after breast-conserving surgery.
Chemotherapy is an important method of adjuvant therapy for pancreatic cancer.
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The following methods of adjuvant therapy were proposed for the treatment of HCC patients: cellular immunotherapy [ 11], interferon (IFN) therapy [ 12], and therapy using endogenous IFN inducers [ 13].
The primary objective is to compare the overall survival at two years postoperatively between two different methods of adjuvant treatment: therapy with 5-FU, cisplatin, interferon alpha 2b combined with radiation and the standard treatment from the ESPAC-1-Trial with 5-FU plus folinic acid.
Furthermore, incorporation into lipid particles has been previously shown to be an effective delivery method of lipophilic adjuvants such as MPLA.
Using the various models of the natural history of breast cancer, researchers have then modeled the initiation time of metastatic growth; the effects of screening on metastases; the effects of surgery on recurrence; and methods of effective adjuvant chemotherapy.
According to our estimation methods, the complete cost of adjuvant chemotherapy including trastuzumab will represent between 1.3 and 2.4% of the global budget of the Health Department (MAD 9.8 billion or USD 1.274 billion).
According to our estimation methods, the complete cost of adjuvant chemotherapy including trastuzumab will range from 1.3 to 2.4% of the global budget of the Moroccan Health Department (MAD 9.8 billion or USD 1.274 billion).
A highly efficient and cost-effective method for comparison of adjuvants with a new antigen is to conduct multiple small-scale, phase 1, comparative studies in humans with a new antigen, using adjuvants previously found to be safe with other antigens in human trials.
The aim of this study was to determine a relationship between vaccine potency (amount of PD50 per dose) and fraction of clinically protected cattle following homologous challenge with infectious foot-and-mouth disease (FMD) virus, and to determine the effect of method of fractionation, serotype, type of adjuvant, valency and type of virus culture on the dose response curve.
However, little is known about the most effective method or timing of delivery of adjuvant chemotherapy.
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CEO of Professional Science Editing for Scientists @ prosciediting.com