Daily Cosmetic Research Analysis
Analyzed 26 papers and selected 3 impactful papers.
Summary
Three studies advance cosmetic and oncologic practice: a large Taiwanese cohort refines selection for intraoperative radiation therapy in breast-conserving surgery, a randomized split-face trial shows subdermal PDLLA skin booster injections are significantly less painful than intradermal delivery, and proteomics of sensitive skin reveals barrier, metabolic, and neuro-neuroimmune pathways as actionable targets for product development.
Research Themes
- Patient selection and adjuvant strategies for IORT in breast-conserving therapy
- Pain optimization in aesthetic injectable techniques (PDLLA skin boosters)
- Proteomics-driven biomarkers and pathways in sensitive skin for cosmetic innovation
Selected Articles
1. Intraoperative radiation therapy (IORT) in Taiwanese breast cancer patients: factors influencing local relapse risk and disease-free survival.
In a 1,306-patient cohort undergoing IORT during breast-conserving surgery, local recurrence was driven by tumor biology and adherence to adjuvant therapy rather than age. Adding EBRT to high-risk patients reduced recurrence by 48.8%, aligning outcomes with low-risk groups.
Impact: Provides large-scale, real-world evidence refining IORT selection and emphasizing adjuvant therapy adherence, with direct implications for recurrence risk mitigation and aesthetic breast conservation strategies.
Clinical Implications: Do not restrict IORT eligibility by age alone; incorporate tumor biology (e.g., Ki-67) and ensure adherence to endocrine therapy and indicated EBRT, particularly for high-risk patients, to optimize oncologic and cosmetic outcomes.
Key Findings
- Three-year disease-free survival was 93.11% with overall local recurrence of 9.3% (1.78% after excluding non-adherent cases).
- Multivariable predictors of local recurrence included Ki-67 > 30%, omission of hormone therapy, and omission of indicated EBRT; age < 45 was not an independent risk factor.
- In high-risk patients, supplemental EBRT reduced recurrence by 48.8%, achieving outcomes comparable to low-risk patients.
Methodological Strengths
- Large cohort (n=1,306) with multivariable adjustment
- Clear risk stratification and analysis of adjuvant therapy effects
Limitations
- Retrospective design with potential selection and information bias
- Median follow-up of 30.5 months may underestimate late recurrences; generalizability beyond Asian populations uncertain
Future Directions: Prospective validation of refined selection criteria, longer follow-up for late events, and integration of molecular profiling to personalize IORT and adjuvant EBRT.
BACKGROUND: Intraoperative radiation therapy (IORT) delivered during breast-conserving surgery may streamline treatment and enhance cosmetic outcomes. However, optimal patient selection criteria remain uncertain, especially in Asian populations, where international guidelines may not be fully applicable. This study aimed to evaluate local recurrence rates, identify key prognostic factors, and assess the impact of supplemental external beam radiation therapy (EBRT) in Taiwanese patients receiving IORT. MATERIALS AND METHODS: This retrospective analysis included 1,306 Taiwanese patients who underwent IORT between June 2014 and December 2021. Patients were stratified into low-risk and high-risk groups based on institutional criteria. Low-risk patients were those meeting all of the following: age ≥ 45 years, tumor size ≤ 3.5 cm, negative nodal involvement, Ki-67 ≤ 30%, hormone receptor (HR) positivity, and HER2 negativity. Patients who did not meet one or more of these criteria were classified as high-risk and were recommended to receive supplemental external beam radiation therapy (EBRT) following IORT. RESULTS: In our cohort of 1,306 patients, the 3-year disease-free survival rate was 93.11% [95% confidence interval (CI): 91.6-94.4%], with 87 patients (6.89%) experiencing recurrence. The median age was 52 years, and the median follow-up duration was 30.5 months. The overall local recurrence rate was 9.3%, which declined to 1.78% after excluding patients who did not receive indicated adjuvant therapies. Multivariable analysis identified Ki-67 > 30%, omission of hormone therapy, and omission of recommended EBRT as significant predictors of local recurrence, whereas age < 45 was not independently associated with increased risk. Among high-risk patients, the addition of EBRT was associated with a 48.8% reduction in recurrence, achieving outcomes comparable to those of low-risk patients. CONCLUSIONS: Age alone should not determine IORT eligibility. A multifaceted approach, including tumour biology and adherence to recommended therapies, is essential. Supplemental EBRT improves outcomes in high-risk patients, and adapting guidelines may enhance patient selection in Asian populations.
2. Comparative Pain Assessment of Intradermal Versus Subdermal Skin Booster Injections Using PDLLA: A Randomized, Double-Blinded Split-Injection Study.
In a randomized, double-blinded split-injection study (n=21), subdermal PDLLA injections were significantly less painful than intradermal injections (VAS 3.85 vs 6.18; p<0.001). Age influenced intradermal pain (higher under 40), but not subdermal pain.
Impact: Directly informs technique choice in aesthetic practice by quantifying pain differences with a rigorous split-design, supporting subdermal delivery for better patient comfort.
Clinical Implications: Prefer subdermal PDLLA injections to reduce pain and potentially improve adherence and satisfaction without increasing downtime; consider age-related sensitivity for intradermal procedures.
Key Findings
- Subdermal PDLLA injections yielded significantly lower pain than intradermal injections (VAS 3.85 vs 6.18; p<0.001).
- No gender differences in pain; patients under 40 experienced higher pain with intradermal injections.
- Randomized, double-blinded, split-injection design enhances internal validity for technique comparison.
Methodological Strengths
- Randomized, double-blinded, within-subject split design
- Standardized injection parameters (32G needle) and immediate VAS assessment
Limitations
- Small sample size and single-center setting limit generalizability
- Focus on immediate pain without longer-term efficacy or safety outcomes
Future Directions: Larger multicenter trials integrating pain, efficacy, and safety endpoints; exploration of adjuncts (topical anesthetics, cannula use) and anatomical site variability.
BACKGROUND: Poly-D,L-lactic acid (PDLLA) skin boosters are widely used for biostimulatory skin rejuvenation, but comparative data on pain perception between injection techniques remain limited. OBJECTIVE: To compare patient-reported pain between intradermal and subdermal PDLLA injections using a randomized, double-blinded, split-injection design. METHODS: Twenty-one healthy participants (aged 27-64) each received ten facial injections: five intradermal and five subdermal, administered in randomized order using a 32G needle. Pain was assessed using a Visual Analogue Scale (VAS) immediately after each injection. The primary outcome was the difference in mean VAS scores between techniques. Secondary analyses examined the effects of age and gender on pain perception. RESULTS: The mean VAS score for intradermal injections was significantly higher than for subdermal injections (6.18 vs. 3.85, p<0.001). No significant gender-based differences were observed. Patients under 40 reported higher intradermal pain than older subjects (p=0.04), but age had no impact on subdermal pain. CONCLUSION: Subdermal PDLLA injections are significantly less painful than intradermal injections, likely due to lower nerve density and reduced dermal resistance. With equivalent efficacy and minimal downtime, subdermal injection may be preferable for patient comfort and compliance. LEVEL OF EVIDENCE V: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266.
3. A Systemic Pathophysiological View of Sensitive Skin Revealed by Proteomics: Beyond Barrier and Inflammation.
Tape-strip proteomics (30 SS vs 30 NS) delineated a sensitive-skin signature involving cytoskeletal/tight junction remodeling, heightened oxidative metabolism with redox imbalance, and MAPK/neurotrophin pathway activation. These pathways offer candidate biomarkers and targets for barrier-restoring, antioxidant, and neurosensory-modulating formulations.
Impact: Provides a systems-level, molecular map of sensitive skin directly from human stratum corneum, moving beyond barrier-only concepts and enabling mechanism-informed cosmetic development.
Clinical Implications: Informs biomarker-driven stratification of sensitive skin and supports designing products targeting tight junction support, antioxidant/redox modulation, and neurosensory pathways.
Key Findings
- Sensitive skin showed enrichment in cytoskeletal remodeling, cell-cell adhesion, and tight junction pathways, indicating dynamic but impaired barrier regulation.
- Oxidative phosphorylation and fatty acid β-oxidation were elevated, alongside glutathione-related enzymes, indicating altered redox balance and oxidative stress.
- MAPK and neurotrophin-associated pathways were upregulated, suggesting active neuro-inflammatory crosstalk driving sensitivity.
Methodological Strengths
- Noninvasive tape-stripping with 4D DIA proteomics enables high-depth profiling directly from human stratum corneum
- Case-control design with equal SS and NS groups facilitates differential pathway analysis
Limitations
- Cross-sectional design without functional validation limits causal inference
- Potential confounding from demographics, skincare routines, or batch effects not fully detailed
Future Directions: Validate candidate biomarkers in independent cohorts, link proteomic signatures to clinical severity and sensory testing, and perform interventional studies targeting identified pathways.
BACKGROUND: Sensitive skin (SS) is a common dermatological condition characterized by enhanced reactivity to environmental, chemical, and cosmetic stimuli, often accompanied by impaired barrier function and discomfort sensation such as burning or itching. Despite its high prevalence, the molecular mechanism underlying SS remains poorly understood. OBJECTIVES: This study aimed to perform a comprehensive proteomics analysis to characterize molecular alterations in SS compared with nonsensitive skin (NS), thereby uncovering key pathways involved in barrier dysfunction, oxidative stress, and neuroinflammatory responses. METHOD: Thirty subjects with SS and 30 with NS were recruited. Stratum corneum samples were collected via tape stripping and analyzed using four-dimensional data-independent acquisition (DIA) proteomics. RESULTS: Proteomic profiling revealed distinct molecular signatures between SS and NS. SS exhibited enrichment of pathways related to cytoskeletal remodeling, cell-cell adhesion, and tight junction organization, consistent with impaired but dynamically compensatory barrier regulation. Enhanced oxidative phosphorylation and fatty acid β-oxidation indicated increased metabolic activity, while elevated glutathione-related enzyme functions reflected altered redox balance and oxidative stress. Additionally, upregulation of MAPK signaling and neurotrophin-associated pathways suggested active neuro-inflammatory crosstalk, potentially contributing to heightened cutaneous sensitivity and inflammatory susceptibility. Additional alterations were observed in other cellular processes, reflecting the complex molecular landscape of SS. CONCLUSION: These findings provide new insights into the molecular basis of SS, highlighting the interplay between barrier dysfunction, oxidative stress, and neuronal activation. The identified proteins and pathways may serve as potential biomarkers for SS assessment and as targets for the development of cosmetic products or therapeutic strategies aimed at restoring skin homeostasis.