| CPC A61B 5/029 (2013.01) [A61B 5/021 (2013.01); A61B 5/0265 (2013.01); A61B 5/352 (2021.01); A61N 1/403 (2013.01); A61N 5/025 (2013.01); A61B 5/02007 (2013.01); A61B 5/02108 (2013.01); A61B 5/02141 (2013.01); A61B 5/0245 (2013.01); A61B 5/0255 (2013.01); A61N 5/022 (2013.01)] | 7 Claims |

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1. A system for diagnosing a cancer type in a patient, comprising:
a hemodynamic parameter (Hdp) monitor that measures Hdp values exhibited by the patient during (i) a non-exposure period and (ii) during an exposure period during which the patient is exposed to amplitude-modulated radio-frequency electromagnetic field (EMF) output signals, wherein the Hdp values comprise a pressure component, a flow component and a beat component;
an electrically-powered generator to generate the amplitude-modulated radio-frequency EMF output signals for exposing to the patient during the exposure period, comprising an amplitude modulation controller for controlling the amplitude of the amplitude-modulated radio-frequency EMF output signals;
a probe connected to the electrically powered generator through which the patient is exposed to the amplitude-modulated radio-frequency EMF output signals during the exposure period; and
a storage system comprising predetermined Hdp values comprising the pressure component, flow component and beat component from one or a plurality of surrogate patients pre-diagnosed with the cancer type, wherein the Hdp values were exhibited by the surrogate patient during (i) a non-exposure period and (ii) during an exposure period during which the surrogate patient was exposed to the amplitude-modulated radio-frequency EMF output signals, and which storage system is adapted to allow for comparison of the Hdp values of the patient and the surrogate patient(s).
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