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Of course, the cost benefits of this protocol variant are traded for PDR performance.
The benefits of this protocol are simplicity, nontoxicity, low cost, simple work-up, and an environmentally benign nature.
The major benefits of this protocol are that it incorporates a standardized tissue dissociation process that allows for uniform and consistent homogenization of tissue that is not easily achieved with manual homogenization methods.
However, whether the clinical benefits of this protocol can be provided to a majority of patients remains debatable.
The benefits of this protocol include that it is straightforward to implement, and that the molecular steps are scalable to large numbers of individuals.
Future research may provide detailed information about the economic benefits of this protocol, since the causal relation of performing the complete protocol, occurrence of medication errors and ADEs, and associated costs, was not determined.
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The main benefit of this protocol is 30 min time to results.
The most prominent benefit of this protocol is that high percentages of target cells were generated from hESCs within a short period.
While further research could evaluate the potential benefit of this protocol to any ultimate outcome, the delay in definitive treatment allowed for improved awareness and decision making on the part of the patient and his family.
Here we did a systematic review of published phase II trials of bevacizumab plus irinotecan for recurrent HGG and used the previous mathematical technology to analyze the survival and response benefit of this treatment protocol.
The potential public health benefit of the protocol may be far reaching, in terms of more rapid identification of EPTB cases even at a peripheral hospital level, where imaging modalities are scarce and most HIV and TB care will be delivered in the future.
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