Participants are being recruited from the Hualien Tzu Chi Hospital. Recruitment began on September 12, 2021, and is expected to continue until December 2024. We expect to complete the study in the middle of 2024.

This study was approved by the research ethics committee of Hualien Tzu Chi Hospital (IRB 110-168-A), and informed consent will be collected from all study participants. The information of patients will be deidentified, and each visit will be compensated for US $16. This study was registered on the International Traditional Medicine Clinical Trial Registry website (ITMCTR2023000054).

The sample size calculation was based on the mean and SD of the amount of CD4+ between control and treatment groups based on the published literature [19]. By setting the effect size as 0.5, the sample size of each group was estimated as 64 to achieve a power of 0.80 at a significance level of .05 using G*Power software (version 3.1; Heinrich-Heine-Universität Düsseldorf). After accounting for an anticipated dropout rate of 10%, the final sample size was determined to be 70 in each group.

Patients aged 20 years and older, with a histologically confirmed diagnosis of breast cancer before the initiation of chemotherapy, are considered eligible for this study.

Patients who will not be able to complete the chemotherapy and follow-up procedures based on oncologists’ experience before grouping, those who receive other medication, and those with an Eastern Cooperative Oncology Group score of 3-4 will be excluded from the study.

This study is a real-world pragmatic clinical trial conducted at the Hualien Tzu Chi Hospital in Taiwan. Patients with breast cancer scheduled to receive chemotherapy for their cancer treatment will be recruited as per the flowchart shown in Figure 1. Patients willing to receive CHM during chemotherapy are allocated to the CHM group, whereas those in the non-CHM group will not receive CHM.

To evaluate the effectiveness of CHM, the number of WBCs, the ANC, and the use of G-CSF in patients will be measured. The following questionnaires in Taiwanese will be used: (1) the Brief Fatigue Inventory—Taiwanese Version, (2) the World Health Organization Quality of Life-BREF, (3) the National Cancer Institute-Common Terminology Criteria for Adverse Events & Patient Reported Outcomes, and (4) the body constitution questionnaire. In addition, blood samples will be collected and analyzed for immune profiles and programmed cell death protein 1 (PD-1) expression. Generally, visit 1 represents the first collection of questionnaires and blood samples before the first chemotherapy session. Following the chemotherapy regimen, the first 4 rounds of chemotherapy will be performed every 3 weeks with 3 visits (visits 2-4). Subsequently, 12 rounds of chemotherapy will be performed once per week with another 4 visits (visits 5-8, 3 weeks per visit). Patients will be followed up within 1 month of undergoing chemotherapy. Patients in the CHM group will receive complementary CHM treatment after the first chemotherapy session.

The clinical data will be extracted from the medical history system. The questionnaires will be coded and transformed into numerical values (eg, 5=very satisfied or none, 4=satisfied or light, 3=no change or intermediate, 2=unsatisfied or severe, and 1=very unsatisfied or none) to facilitate statistical analysis. Immune profiles will be analyzed using flow cytometry. The data monitoring committee, clinical trial center of Hualien Tzu Chi Hospital, is independent from the funder and competing interests. The SPIRIT (Standard Protocol Items: Recommendation for Interventional Trials) 2013 checklist is provided in Multimedia Appendix 1 [20].

Upon the diagnosis of breast cancer in a patient, a clinical nurse manages the case. The questionnaire and blood collection before chemotherapy are represented by visit 1 (red arrow in Figure 2). The first 4 rounds of chemotherapy will be performed every 3 weeks, and visits 2-4 will be located in the second, third, and fifth rounds, respectively, 1 day before chemotherapy treatment. The following 12 rounds of chemotherapy will be performed every week, and visits 5-8 will be located in the first, fourth, seventh, and tenth rounds, respectively, 1 day before chemotherapy treatment. The patients will be followed up within 1 month after chemotherapy (Figure 2 and Table 2). Patients receiving CHM 3 times per day started the first round of chemotherapy.

The primary outcome used in this study is the number of immune cells, including CD4+ and CD8+ T cells (under CD45+ and CD3+ population), CD56+ NK cells (under CD45+ population), CD19+ B cells (under CD45+ population), CD14+ monocytes (under CD45+ population), and CD11c dendritic cells (under CD45+ population), as well as PD-1 expression levels in these cells. For NK cells, the expression of NKG2D will be also confirmed. The analytic panels used are listed in Table 3.

Secondary outcomes include the number of WBCs, the ANC, evaluation of the Brief Fatigue Inventory—Taiwanese Version, World Health Organization Quality of Life-BREF, National Cancer Institute-Common Terminology Criteria for Adverse Events & Patient Reported Outcomes, body constitution questionnaire, and frequency of G-CSF inoculation.

All adverse events (AEs) will be recorded throughout the study. In cases where AEs are caused by chemotherapy or CHM intervention, prompt measures will be taken to address those AEs. If needed, participants will be withdrawn from the study. Continuous monitoring of the participant’s blood, liver, and kidney functions, body weight, and vital signs will be performed throughout the study. The possible side effects associated with CHM are listed in Table 1.

Peripheral blood (10 mL) will be collected in ethylenediaminetetraacetic acid–coated tubes and processed within 24 hours of collection. Whole blood (100 µL) will be mixed directly with the fluorescence-conjugated antibodies, including CD45, CD3, CD4, CD8, CD19, CD56, NKG2D, CD14, CD11c, and PD-1 (Table 3), protected from the light, and incubated for 20 minutes at 4 ℃. Blood cells will be washed twice with 2 mL staining buffer (phosphate buffered saline+2% fetal bovine serum), centrifuged at 300×g for 5 minutes at room temperature, and further incubated with Red Blood Cell Lysis Buffer (Thermo Fisher Scientific) for lysing the erythrocytes for 10 minutes at room temperature. This step may repeat until the red blood cell is completely lyzed. The cells will be further fixed in 2% paraformaldehyde for 10 minutes at room temperature. Subsequently, the cells will be subjected to 2 additional washes with 2 mL staining buffer and centrifuged 300×g for 5 minutes at room temperature. Then, the cells will be preserved at 4 ℃ and analyzed using flow cytometry (Lyric, BD) within 3 days.

All statistical analyses will be performed using the SPSS software (version 13.0; IBM Corp) or SAS software (version 9.4; SAS Institute Inc). Continuous variables will be reported as mean and SD, whereas categorical variables will be reported as frequencies and percentages. The Shapiro-Wilk test will be used to analyze the normality of baseline characteristics and outcome variables. The Mann-Whitney U test will be used to compare nonnormally distributed continuous data, and the 2-tailed t test will be used to compare normally distributed continuous data. The chi-square test will be used to compare categorical data between the groups. Both primary and secondary outcomes involve repeated measurement data. The Friedman test and repeated measures ANOVA will be used to compare the differences between every visit in each group in nonparametric and parametric data, respectively. In addition, we will use generalized estimating equations or repeated measures ANOVA to compare the differences between the 2 groups. We will evaluate the risks of each clinical characteristic by the multivariate logistic regression analysis and adjust the age and other factors or characteristics that may have bias in the analysis. We set P<.05 as a significant difference. All data will be recorded in a case report form.

Traditional Chinese medicine is the most commonly used drug in Taiwan and shows significant potential in alleviating side effects related to anticancer treatments, such as chemotherapy. Even with sourcing from traditional Chinese medicine pharmaceutical factories in Taiwan certified under the Good Manufacturing Practices guidelines, our rigorous approach involves continuous toxicity monitoring throughout the study to minimize AEs.

Astragalus polysaccharide (APs), a bioactive extract of Astragalus membranaceus, has many biological activities, including anti-inflammatory, antioxidant, and immunoregulatory properties [21,22]. APs may modulate immunity by activating the toll-like receptor 4 (TLR4)–mediated myeloid differentiation primary response 88 (MyD88)–dependent signaling pathway [22] and induce apoptosis in human hepatocellular carcinoma cells by decreasing the expression of Notch1 [23]. Furthermore, APs inhibit TNBC cell invasion and proliferation and induce apoptosis through the PIK3CG/AKT/BCL2 pathway [24]. APs could activate macrophages to release nitric oxide and tumor necrosis factor alpha, directly blocking breast cancer cell growth [25]. A membranaceus extract has also been reported to inhibit breast cancer cell proliferation via the PI3K/AKT/mTOR signaling pathway [26].

Polysaccharides of Angelica sinensis (Oliv) Diels promote apoptosis in breast cancer cells via cyclic adenosine monophosphate response–binding protein (CREB)–regulated caspase-3 activation [27]. In a population-based case-control study in Taiwan, the use of A sinensis showed a significant protective effect on breast cancer (adjusted odds ratio 0.95, 95% CI 0.93-0.98) [28].

Baicalin, a flavonoid compound isolated from the roots of Scutellaria lateriflora Georgi, enhanced the chemosensitivity of breast cancer cells to doxorubicin via the upregulation of oxidative stress–mediated mitochondria-dependent apoptosis [29] and inhibited the metastasis and epithelial-to-mesenchymal transition of highly aggressive breast cancer cells by targeting β-catenin signaling [30].

Atractylenolide-I, a major bioactive component from Atractylodes macrocephala, suppressed tumorigenesis of breast cancer by inhibiting TLR4-mediated NF-κB signaling pathway [31] and sensitized TNBC cells to paclitaxel by blocking connective tissue growth factor expression [32].

Fructus ligustri lucidi could enhance chemosensitivity and induce apoptosis via Tbx3 suppression in human colorectal carcinoma cells [33]. Besides, it has been reported to induce apoptosis in glioma cells in vitro and in vivo through the regulation of the AKT/mTOR pathway [34]. In addition, it induces senescence and apoptosis in hepatocellular carcinoma cells by upregulating p21 [35].

While these CHMs have mostly exhibited antitumor effects, their effects on immune cells have not been fully elucidated. Hence, we aimed to investigate the effects of these CHMs as a complementary treatment on neutropenia, a common chemotherapy side effect known to damage qi and aggravate its depletion. Notably, these CHMs not only regulate qi but also modulate immune cells and their functions. Thus, this study may provide additional insights into therapeutic strategies for breast cancer, including immunotherapy.

The strength of this study lies in its pragmatic trial design conducted in a clinical setting. Compared with randomized controlled trials, this study design has higher generalizability and provides evidence of its effectiveness in daily practice. This study has some limitations that may have affected the results. First, the internal validity was compromised. A pragmatic clinical trial design could achieve greater generalizability of the effectiveness of CHM as a complementary treatment. To improve internal validity, the statistician analyzing the data was blinded to the group assignment and adjusted for all confounding variables during data analysis. Second, there was a lack of important clinical characteristics, such as dietary and exercise habits. Although dietary intake and moderate-intensity aerobic exercise are crucial for patients with cancer during chemotherapy [36], we could not control daily diet and exercise intensity in this real-world clinical trial. In our clinical setting, oncology nurses educate all participants about the importance of healthy dietary intake and exercise habits during chemotherapy. Third, due to financial considerations, the observation time was not long enough to detect the change in the lymphocyte levels after completing chemotherapy, and further long-term and large-scale studies are needed to evaluate the variation in the number of WBCs and the ANC during the recovery phase after chemotherapy.

In conclusion, we have proposed an open-label, single-center, pragmatic clinical trial and a real-world study to evaluate the effectiveness and safety of CHMs for treating CIN in patients with breast cancer. Using this study platform, we will analyze the effects of CHM on the regulation of QoL by evaluating the complications of chemotherapy and immune cell profiles. The findings of this study may contribute to developing an effective intervention for chemotherapy-related neutropenia in patients with breast cancer in clinical practice.