Impact of nanorobotic drug delivery on Quality of Life in Patients with solid tumors
DOI:
https://doi.org/10.5281/zenodo.22812126Keywords:
nanorobotic drug delivery, quality of life, solid tumors, nanoparticle chemotherapy, cancer toxicityAbstract

Background: Conventional chemotherapy distributes throughout the body largely independent of tumor location, producing systemic toxicity that instruments such as the QLQ-C30 and FACT-G were built to quantify as patient-reported quality of life [1,2].
Objective: This review synthesizes evidence on how nanoparticle and early nanorobotic drug delivery reshape quality of life in solid tumors, from measurement instruments through biodistribution rationale to trial evidence.
Methods: We conducted a narrative synthesis of psychometric validation studies, randomized trials comparing nanoparticle formulations with conventional chemotherapy, a pooled toxicity meta-analysis, and mechanistic reviews of nanoparticle and nanorobotic delivery.
Findings: Pegylated liposomal doxorubicin cut cardiac toxicity to roughly 7% against roughly 26% with conventional doxorubicin at comparable efficacy [12]; nab-paclitaxel eliminated solvent-related hypersensitivity while improving response rate [16]; and a pooled analysis found lower grade 3 or higher hematologic toxicity and neuropathy with nanoparticle chemotherapy [20], while nanorobotic platforms remain largely preclinical [5,6].
Conclusions: Nanoparticle delivery improves quality of life in solid tumors chiefly by reducing or redistributing systemic toxicity rather than by uniformly improving tumor control, and emerging nanorobotic trials should build validated quality-of-life endpoints in directly [7,24].
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