Objective. To investigate the clinical value of lentinan combined with (125)I brachytherapy in the treatment of recurrent ovarian cancer. Methods. A total of 160 patients with recurrent ovarian cancer admitted at Jiaozhou Central Hospital from June 2009 to October 2015 were enrolled in this study and randomly divided into observation group (80 cases) and control group (80 cases). The control group received chemotherapy. Observation group (80 cases) was treated with lentinan combined with (125)I brachytherapy on the basis of control group, and the efficacy, adverse reactions, and Karnofsky Performance Scale (KPS) and quality of life scale (QOL) scores of the two groups were analyzed and compared. Results. After treatment, the levels of CA125, CA199, and CA724 in the 2 groups were markedly lower than those before treatment, and the observation group was lower than the control group (P < 0.05). After treatment, the proportion of CD4⁺/CD8⁺ cells and helper T cells and NK cells in the control group remarkably depleted, while the proportion of CD4⁺/CD8⁺ cells, NK cells, and B cells in the observation group increased significantly compared to that before treatment, and the level of IgA, IgG, and IgM in the control group decreased, while that in the observation group showed no conspicuous difference compared with that before chemotherapy (P > 0.05). The effective rate of observation group (85%) was higher than that of control group (75%) (P < 0.05). The overall survival of patients in the control group was (16.2 ± 2.04) months and that of the observation group was (24.8 ± 1.8) months. KPS and QOL scores in both groups were enormously higher than those before treatment, and the observation group was higher than the control group (P < 0.05). The incidence of hemoglobin reduction, leukopenia, aglobulia, granulocytopenia, nausea and vomiting, hepatorenal toxicity, and neurovirulence in the observation group was significantly lower than that in the control group. Conclusion. Lentinan combined with (125)I brachytherapy is effective in treating recurrent ovarian cancer, with mild adverse reactions and good tolerance.

1. Introduction

Ovarian cancer (OC) accounts for 5% of cancer deaths in women [1]. Recurrent ovarian cancer refers to the signs of tumor recurrence in patients who have reached complete remission after optimal cytoreduction and adjuvant platinum-based chemotherapy and have to suspend the drug for half a year [2]. After relapse, first-line chemotherapy drugs such as topotecan and doxorubicin alone have no effect on prognosis, which triggers many adverse reactions, and most patients with relapse have a poor quality of life. Therefore, additional and alternative therapeutic strategies to improve outcomes are necessary.

In the last decade, percutaneous image-guided (125)I implantation has been regarded as a useful and minimally invasive treatment for various malignancies owing to its curative effects, such as head and neck tumors and pancreatic, lung, and hepatic cancer [3–6]. At the same time, its successful application in OC is still limited. Meanwhile, (125)I particle implantation can also cause a series of adverse reactions, such as pneumothorax, pulmonary hemorrhage, and sputum blood. New drugs are urgently needed to alleviate its side effects. Lentinus edodes (Shiitake) is the world’s second-largest cultivated medicinal, edible fungus and has a long history in the oriental folklore of treating tumors [7]. Lentinan is the active ingredient extracted from the natural product Lentinus edodes mycelium, mainly composed of B1-3, B1-6 dextran [8]. Previous studies suggest that lentinan exerts its antitumor effects by activating the host’s immune response instead of directly attacking cancer cells [9]. The antitumor activity of lentinan was believed to be mediated through a thymus-dependent immune mechanism.

In this study, the clinical study of lentinan combined with (125)I brachytherapy in patients with recurrent ovarian cancer was conducted to explore the application value of this therapeutic approach in such patients.

2. Methods

2.1. Patients

A total of 160 patients with recurrent ovarian cancer after surgery from June 2009 to October 2015 at the Jiaozhou Central Hospital, Qingdao, Shandong, China, were enrolled in this study. Biopsy pathology showed 70 cases of poorly differentiated serous papillary cystadenocarcinoma, 60 cases of moderately differentiated serous papillary cystadenocarcinoma, 14 cases of highly differentiated serous papillary cystadenocarcinoma, and 16 cases of poorly differentiated mucinous papillary cystadenocarcinoma, all of which were confirmed as recurrent oocyte carcinoma by imaging and histopathological examination. All patients underwent surgical treatment in the early stage, and the preoperative TNM staging was stage III-IV. The tumor was confirmed to be recurrent by ultrasound biopsy after surgery, and the time between the first operation and the current recurrence was 24.2 ± 2.3 months. Karnofsky Performance Scale (KPS) was >60, and estimated survival time was >6 months. According to the principle of randomness, 160 cases subjects were divided into 80 cases in the observation group and 80 cases in the control group. All patients signed informed consent before participation, and this study was approved by the Ethics Committee of the Jiaozhou Central Hospital, Qingdao, Shandong, China.

2.2. Study Design

The control group was intravenously injected with Taxol liposome (135 mg/m²). Before chemotherapy, dexamethasone and diphenhydramine were routinely pretreated. Then arterial infusion chemotherapy was performed the next day. The catheter was introduced through femoral artery puncture by the Seldinger method; under the monitoring of DSA, the catheter was selected to the inferior mesenteric artery or internal iliac artery for angiography to observe the blood supply status of the tumor. Carboplatin (200 mg/m²) was diluted and slowly injected into the tumor supplying artery through the catheter. Routine symptomatic treatment such as liver protection and antiemetic and gastric protection was given, repeated once every 21 days.

The observation group was treated with (125)I particle implantation and Lentinus edodes polysaccharide tablets. The number of (125)I seeds and the planning target volume (PTV) were determined using a treatment planning system. PTV was defined as tumor target area expansion of 5–10 mm, and matched peripheral dose (MPD) was 110–160 Gy. During the operation, CT scanning was used to locate the puncture direction and puncture point. After disinfection and anesthesia, (125)I seeds were implanted percutaneously under the guidance of CT with an interval of 0.5 cm. A postoperative CT review was performed to understand the particle distribution. When lesions were present in both ovaries, the interval of particle implantation in the other lesion should be more than 3 days. Lentinus edodes polysaccharide tablets (Kaifeng Pharmaceutical Co., Ltd., Chinese drug approval number H41025015) were orally administered with 1 tablet per time and 2 times per day for 2 months. Within 3 days after (125)I seed implantation, the same chemotherapy treatment was performed as the control group.

2.3. Testing Index

Venous blood was collected before and after treatment to separate the serum. Then the level of IgG, IgM, and IgA in serum was determined by immunoturbidimetry. The kit was provided by Changchun Huili Biotechnology Co., Ltd.

Total 3 mL of fasting peripheral blood was collected from all patients before and after treatment. Flow cytometry was performed to evaluate the immune function of patients in both groups within 1 week after treatment. Total T cells (CD3⁺), helper T cells (CD3⁺ CD4⁺), killer T cells (CD3⁺CD8⁺), CD4⁺/CD8⁺, and NK cells (CD3⁻CD56⁺), CIK cells (CD3⁺CD56⁺), regulatory T cells (CD4⁺ CD25high⁺ FOXP3⁺), CD 14⁺, and CD 19⁺ B cells were detected.

Laboratory tests including hemoglobin (HGB), white blood cells (WBC), platelets (PLT), neutrophils (NEU), red blood cells (RBC), aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatinine (CREA), urea nitrogen (BUN), and electrocardiograph also were recorded before and after treatment. Chemotherapy side effects were graded according to WHO acute and subacute toxicity criteria, which were divided into 0, I, II, III, and IV. Blood toxicity, gastrointestinal reaction, liver and kidney function, cardiotoxicity, and peripheral neurotoxicity were assessed and compared between the two groups.

2.4. Evaluation Criteria for Short-Term Efficacy

Efficacy was evaluated according to RECIST criteria. Complete remission (CR) means complete disappearance of all target lesions. Partial response (PR) means reduction of the sum of the maximum diameters of target lesions ≥30%. Stable disease (SD) is the sum of the maximum diameter of the target lesions decreases without reaching PR or increases without reaching PD. Disease progression (PD) is an increase of ≥20% in the sum of the maximum diameters of the target lesions or the appearance of new lesions. The efficiency (RR) was calculated by CR + PR, while disease control rate (DCR) was calculated by CR + PR + SD.

The patient′s functional status was assessed with a KPS score, and the higher the score, the better the patients’ functional status. Quality of life scale (QOL) (SF-36) was performed to evaluate patients’ quality of life, and the higher the score, the better the quality of life.

All objects were followed up for 5–46 months, and the overall survival of patients in the two groups was statistically compared.

2.5. Statistical Method

SPSS 21.0 statistical software was performed for data analysis. The data were expressed by ± s. χ² test or t test was applied for comparison between groups, Kaplan–Meier survival analysis and log-rank test univariate analysis were used to compare the difference in survival rates between the two groups. P < 0.05 indicates that the difference is statistically significant.

3. Results

3.1. Pathological Characteristics

There were 160 patients with recurrent ovarian cancer, including 80 cases in the control group and 80 cases in the observation group. Table 1 shows that there were no significant differences in age, TNM stage, pathological type, differentiated status, and CA125 level at recurrence between the two groups, as shown in Table 1.

Table 1. Comparison of pathological characteristics between the two groups.

	Control group	Observation group	P value
Age	49 ± 5.3	48 ± 4.6	0.945
TNM stage			0.564
III	44 (55%)	47 (59%)
IV	36 (45%)	33 (41%)
Pathological type			0.215
Serous papillary cystadenocarcinoma	69 (86%)	75 (94%)
Mucinous papillary cystadenocarcinoma	11 (14%)	5 (6%)
Differentiated			0.341
Poorly differentiated	46 (58%)	40 (50%)
Moderately differentiated	28 (35%)	32 (40%)
Highly differentiated	6 (7%)	8 (10%)
CA125			0.645
≤35 U/ml	21 (26)	25 (31)
>35 U/ml	59 (74)	55 (69)

3.2. Blood-Related Indexes

The HGB, WBC, PLT, NEU, and RBC levels in two groups before treatment showed no statistically significant difference (P > 0.05). After treatment, the level of HGB, WBC, NEU, and RBC in control group decreased enormously, and the level of WBC and NEU in observation group attenuated tremendously, while the level of HGB, WBC, NEU, and RBC in observation group was obviously higher than that of control group, as shown in Table 2.

Table 2. Comparison of blood-related indexes between two groups (

± s).

	Control group		P value	Observation group		P value
	Before treatment	After treatment	P value	Before treatment	After treatment	P value
WBC (×10⁹L)	7.02 ± 0.56	1.84 ± 0.24	<0.001	7.09 ± 0.48	4.05 ± 0.16 ^∗∗	0.032
NEU (×10⁹L)	5.02 ± 0.45	1.45 ± 0.26	0.015	4.97 ± 0.78	2.68 ± 0.45 ^∗	0.045
HGB (g/L)	115.84 ± 13.65	71.26 ± 10.23	0.002	116 ± 14.62	110.25 ± 12.15 ^∗∗	0.315
PLT (×10⁹L)	251.23 ± 32.15	227.16 ± 26.12	0.124	249.13 ± 14.26	239.45 ± 32.16	0.421
RBC (×10¹²L)	4.87 ± 0.15	1.38 ± 0.24	0.026	4.97 ± 0.12	3.15 ± 0.21 ^∗	0.051

Versus control group, ^∗P < 0.05, ^∗∗P < 0.01.

3.3. Immunologic Function

In order to further analyze the effect of Lentinus edodes polysaccharide combined with (125)I particle and chemotherapy treatment on the immune status of patients, the proportion of each immune cell in peripheral blood of patients before and after treatment was compared, as shown in Table 3. After chemotherapy treatment, the proportion of helper T cells, CD4⁺/CD8⁺ cells, and NK cells in the control group remarkably depleted, while after Lentinus edodes polysaccharide combined with (125)I particle and chemotherapy treatment, the proportion of CD4⁺/CD8⁺ cells, NK cells, and B cells in the observation group aggrandized enormously compared to that before treatment.

Table 3. Proportion of peripheral blood immune cells in the two groups before and after treatment (median (P25, P75)).

	Control group (%)		P value	Observation group (%)		P value
	Before treatment	After treatment	P value	Before treatment	After treatment	P value
CD3⁺	75.76 (47.78, 87.79)	75.18 (52.36, 82.31)	0.915	74.54 (51.23, 80.31)	73.61 (50.31, 81.24)	0.769
CD3⁺ CD4⁺	48.89 (18.97, 65.12)	39.6 (19.02, 78.68)	0.034	45.36 (17.65, 71.62)	49.75 (13.64, 74.16)	0.054
CD3⁺CD8⁺	33.89 (17.84, 45.26)	35.62 (20.69, 49.74)	0.549	36.16 (21.36, 48.37)	34.15 (19.65, 47.59)	0.512
CD4⁺/CD8⁺	1.65 (0.61, 2.89)	1.09 (0.48, 2.84)	0.048	1.69 (0.69, 2.79)	2.43 (0.64, 3.86) ^∗	0.019
CD3⁻CD56⁺	9.65 (5.24, 41.26)	8.25 (5.81, 37.64)	0.031	9.26 (6.31, 42.36)	14.26 (5.96, 36.16) ^∗	0.023
CD3⁺CD56⁺	3.68 (0.42, 10.29)	3.45 (0.59, 9.78)	0.794	3.78 (0.39, 11.29)	4.22 (0.57, 9.78)	0.145
CD 14⁺	4.78 (0.23, 32.04)	5.21 (0.02, 24.17)	0.359	5.61 (0.29, 36.19)	6.26 (0.16, 30.26)	0.278
CD 19⁺	8.41 (2.71, 17.41)	8.14 (5.78, 37.26)	0.571	7.89 (2.61, 26.45)	11.45 (5.14, 33.15) ^∗	0.036
CD4⁺ CD25high⁺ FOXP3⁺	4.74 (0.04, 11.68)	3.36 (0.15, 12.27)	0.401	4.16 (0.12, 12.31)	5.48 (0.34, 16.45)	0.141

Versus control group, ^∗P < 0.05, ^∗∗P < 0.01.

The level of immunoglobulin (IgA, IgG, and IgM) in the control group decreased immensely after chemotherapy compared with before chemotherapy. In contrast, the level of IgA, IgG, and IgM in the observation group showed no apparent difference after treatment compared with before chemotherapy (P > 0.05), as shown in Table 4.

Table 4. Comparison of immunoglobulin levels between the two groups (

± s, g/L).

	Control group		P value	Observation group		P value
	Before treatment	After treatment	P value	Before treatment	After treatment	P value
IgG	12.94 ± 1.02	10.84 ± 0.24	0.025	12.77 ± 0.93	12.65 ± 1.02 ^∗	0.082
IgM	1.76 ± 0.21	1.20 ± 0.12	0.004	1.75 ± 0.36	1.88 ± 0.36 ^∗∗	0.056
IgA	2.39 ± 0.23	1.87 ± 0.36	0.016	2.31 ± 1.01	2.44 ± 0.95 ^∗	0.054

Versus control group, ^∗P < 0.05, ^∗∗P < 0.01.

3.4. Tumor Markers

There was no difference in the level of CA125, CA199, and CA724 between the two groups after treatment compared with before treatment (P > 0.05). After treatment, the levels of CA125, CA199, and CA724 in both groups alleviated broadly, while the levels of CA125, CA199, and CA724 in the observation group diminished prominently than the control group (P < 0.05), as shown in Table 5.

Table 5. Comparison of tumor markers in blood between the two groups before and after treatment (

± s).

Group	CA125 (U/ml)		P value	CA199 (IU/ml)		P value	CA724 (IU/ml)		P value
Group	Before treatment	After treatment	P value	Before treatment	After treatment	P value	Before treatment	After treatment	P value
Control group	48.32 ± 12.32	25.64 ± 6.15	0.012	81.23 ± 7.36	53.21 ± 3.64	0.004	34.68 ± 4.61	14.56 ± 4.8	0.006
Observation group	49.12 ± 11.13	18.45 ± 3.14	0.003	80.64 ± 6.45	41.54 ± 4.65	<0.001	35.48 ± 6.48	9.12 ± 4.71	<0.001
P value	0.821	0.027		0.754	0.018		0.634	0.035

3.5. Therapeutic Effect

According to the evaluation of the therapeutic effect of solid tumor, the DCR of the two groups was 60/80 (75%) and 68/80 (85%), respectively, while the efficacy of Lentinus edodes polysaccharide combined with (125)I particle and chemotherapy treatment was superior to that of chemotherapy alone (P < 0.05) (Table 6). A total of 160 subjects were followed up for 5–46 months (median time: 26 months). The overall survival of patients in the control group was (16.2 ± 2.04) months and that of the observation group was (24.8 ± 1.8) months (Figure 1). Log-rank test was applied to compare the survival of the two groups, and the observation group was significantly higher than the control group.

Table 6. Comparison of short-term efficacy between the two groups, n (%).

Group	n	CR	PR	SD	PD	RR	DCR
Control group	80	13 (16%)	45 (56%)	2 (3%)	20 (25%)	58 (73%)	60 (75%)
Observation group	80	16 (20%)	48 (60%)	4 (5%)	12 (15%)	64 (80%)	68 (85%)
χ²	4.312
P value	0.026

Details are in the caption following the image — **Figure 1**
Open in figure viewer PowerPoint

The overall survival of the two groups.

3.6. KPS and QOL Score

There was no significant difference in KPS score and QOL score between the two groups before treatment. The scores of KPS and QOL in both groups were significantly improved after treatment, and the observation group was significantly higher than the control group (P < 0.05), as shown in Table 7.

Table 7. Comparison of KPS and QOL scores between the two groups (

± s).

Group	KPS score		P value	QOL score		P value
Group	Before treatment	After treatment	P value	Before treatment	After treatment	P value
Control group	71.43 ± 5.31	80.12 ± 6.32	0.034	24.61 ± 6.21	37.65 ± 5.87	0.041
Observation group	70.65 ± 5.87	93.12 ± 5.87	0.005	25.65 ± 6.48	50.21 ± 4.87	0.002
P value	0.742	0.025		0.674	0.035

3.7. Incidence of Adverse Reactions

The incidence of nausea and vomiting, neurotoxicity, and hepatorenal toxicity in the observation group was lower than that in the control group (P < 0.05), as shown in Table 8.

Table 8. Comparison of the incidence of adverse reactions between the two groups (n).

Adverse reactions	Control group				Observation group				P value	χ²
Adverse reactions	I	II	III	IV	I	II	III	IV	P value	χ²
Nausea and vomiting	16	8	2	0	7	2	0	0	0.005	5.123
Renal injury	5	0	0	0	1	0	0	0	0.041	2.654
Liver injury	6	1	0	0	2	0	0	0	0.036	4.659
Neurovirulence	4	0	0	0	3	0	0	0	0.157	1.054

4. Discussion

Ovarian cancer is a gynecological malignant tumor with high incidence, and most patients are accompanied by ascites, which is difficult to treat and results in a poor prognosis. At present, chemotherapy is still the preferred treatment for recurrent ovarian cancer, but it is difficult to achieve the desired outcomes by chemotherapy or radiotherapy because of the large tumor load in patients with recurrent ovarian cancer [10]. Therefore, looking for adjuvant treatment options has become the focus of clinical research.

(125)I radioactive particles can have a continuous effect on tumor cells, block cells in G₂/M phase, prolong cell cycle, and lead to the loss of proliferation ability of tumor cells [11, 12]. (125)I radioactive particles are implanted within the range of radiation therapy, and the dose of radiation dose decreases with the increase of distance. Therefore, (125)I particle implantation can produce a high dose at the site, while the radiation dose of surrounding normal tissues is low, with highly conformal radiation [13–15]. Zhao et al. found that (125)I seed implantation based on CT-guided 3D template-assisted technique can effectively alleviate the tumor and improve the survival rate in patients with refractory malignant tumors [16]. Despite the significant effect of (125)I seed implantation in the treatment of cancer, the adverse reactions caused by it cannot be ignored [17]. Zhang et al. reported that (125)I brachytherapy triggers a higher relative risk of pneumothorax, pneumorrhagia, and bloody sputum compared with chemotherapy alone [18]. Martinez-Monge et al. reported that the complication rate of 125I radiotherapy with short-range and high dose rate was 20% [19]. Therefore, it is equally important to kill tumor cells and protect immune function in tumor treatment.

Lentinan has significant inhibitory effects on the transplanted tumor, allogeneic tumor, and primary tumor, preventing carcinogenic effects caused by chemical factors or viruses, inhibiting and preventing postoperative micrometastasis of gastric cancer, lung cancer, liver cancer, rectal cancer, and breast cancer [20–24]. Kimura et al. used lentinan in combination with chemotherapy to treat recurrent gastric cancer and found that lentinan can reduce adverse reactions to chemotherapy and improve the immune and nutritional status of patients [25]. The mechanism of lentinan’s action does not involve the direct attack on the pathogenic source, but to improve the balance of the host body by stimulating the maturation, differentiation and proliferation of immune cells, to restore and improve the responsiveness of host cells to lymphokines, hormones, and other physiologically active factors [26]. In this study, lentinan tablets combined with (125)I particle implantation were applied to observe the effects in antitumor and immune function.

In this study, we used lentinan combined with (125)I particle implantation to treat patients with recurrent ovarian cancer, and we found that the complete remission rate was 20% and partial remission rate was 60% after treatment, significantly higher than the control group, and the overall survival in the observation group was significantly higher than that in the control group, suggesting that (125)I particle implantation was effective in the treatment of recurrent ovarian cancer patients. After treatment, the proportion of CD4⁺/CD8⁺ cells, helper T cells, and NK cells in the control group remarkably depleted, while the proportion of CD4⁺/CD8⁺ cells, NK cells, and B cells in the observation group aggrandized enormously, and the level of IgA, IgG, and IgM in the control group decreased immensely, while that in the observation group did not change significantly, suggesting that lentinan can substantially improve the immunosuppression induced by radiotherapy and chemotherapy. The observation of toxicity in this study suggested that hematological toxicity in the control group mainly manifested as hemoglobin reduction, leukopenia, aglobulia, and granulocytopenia. At the same time, the above reactions were alleviated in the observation group after taking lentinan, indicating that lentinan can promote bone marrow hyperplasia. The main toxic reactions of the digestive system were nausea and vomiting; these reactions in this study mainly occurred 2–8 days after intravenous infusion, while these symptoms were relieved after lentinan treatment. Concurrently, the incidence of hepatorenal toxicity and neurovirulence could be alleviated by lentinan treatment.

In this comparative evaluation, we observed that the lentinan combined (125)I particles implantation treatment of recurrent ovarian cancer could improve the recent curative effect of recurrent ovarian cancer, strengthen the immune function of the patients, and reduce the treatment of gastrointestinal reaction and bone marrow suppression. It could lessen other side effects and improve the quality of life of patients, suggesting that lentinan combined (125)I brachytherapy may be an effective therapeutic approach for recurrent ovarian cancer.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Qin Jiang and Shuai Pang contributed equally to this work.

Open Research

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

References

1 Siegel R. L., Miller K. D., and Jemal A., Cancer statistics, 2020, CA: A Cancer Journal for Clinicians. (2020) 70, no. 1, 7–30, https://doi.org/10.3322/caac.21590.
10.3322/caac.21590
PubMed Web of Science® Google Scholar
2 Classe J. M., Jaffre I., Frenel J. S., Bordes V., Dejode M., Dravet F., Ferron G., Marchal F., Berton Rigaud D., Loussouarn D., and Campion L., Prognostic factors for patients treated for a recurrent FIGO stage III ovarian cancer: a retrospective study of 108 cases, European Journal of Surgical Oncology. (2011) 37, no. 11, 971–977, https://doi.org/10.1016/j.ejso.2011.08.138, 2-s2.0-80053623186.
10.1016/j.ejso.2011.08.138
CAS PubMed Web of Science® Google Scholar
3 Chen Y., Jiang Y., Ji Z., Jiang P., Xu F., Zhang Y., Guo F., Peng R., Li X., Sun H., Lei R., Fan J., Li W., and Wang J., Efficacy and safety of CT-guided 125I seed implantation as a salvage treatment for locally recurrent head and neck soft tissue sarcoma after surgery and external beam radiotherapy: a 12-year study at a single institution, Brachytherapy. (2020) 19, no. 1, 81–89, https://doi.org/10.1016/j.brachy.2019.09.006, 2-s2.0-85073945689.
10.1016/j.brachy.2019.09.006
PubMed Web of Science® Google Scholar
4 Li C.-G., Zhou Z.-P., Jia Y.-Z., Tan X.-L., and Song Y.-Y., Radioactive 125I seed implantation for locally advanced pancreatic cancer: a retrospective analysis of 50 cases, World journal of clinical cases. (2020) 8, no. 17, 3743–3750, https://doi.org/10.12998/wjcc.v8.i17.3743.
10.12998/wjcc.v8.i17.3743
PubMed Web of Science® Google Scholar
5 Dai F., Wang J., An H., Lei T, Tang K, Ma X, Duo P, Ren P, and Chai W, Therapy of 125I particles implantation inhibited the local growth of advanced non-small cell lung cancer: a retrospective clinical study, American Journal of Tourism Research. (2019) 11, no. 6, 3737–3749.
CAS Google Scholar
6 Ying X. H., Zhang D. K., and Chen L., Differential population screening and efficacy analysis of (125)I implantation after radiofrequency ablation of primary liver cancer, Zhonghua Yi Xue Za Zhi. (2020) 100, no. 17, 1310–1314.
CAS PubMed Google Scholar
7 Bisen P. S., Baghel R. K., Sanodiya B. S., Thakur G. S., and Prasad G. B. K. S., Lentinus edodes: a macrofungus with pharmacological activities, Current Medicinal Chemistry. (2010) 17, no. 22, 2419–2430, https://doi.org/10.2174/092986710791698495, 2-s2.0-77955635127.
10.2174/092986710791698495
CAS PubMed Web of Science® Google Scholar
8 Wasser S., Medicinal mushrooms as a source of antitumor and immunomodulating polysaccharides, Applied Microbiology and Biotechnology. (2002) 60, no. 3, 258–274, https://doi.org/10.1007/s00253-002-1076-7, 2-s2.0-0037210695.
10.1007/s00253-002-1076-7
CAS PubMed Web of Science® Google Scholar
9 Ina K., Kataoka T., and Ando T., The use of lentinan for treating gastric cancer, Anti-Cancer Agents in Medicinal Chemistry. (2013) 13, no. 5, 681–688, https://doi.org/10.2174/1871520611313050002, 2-s2.0-84880171040.
10.2174/1871520611313050002
CAS PubMed Web of Science® Google Scholar
10 Yang C., Xia B.-R., Zhang Z.-C., Zhang Y.-J., Lou G., and Jin W.-L., Immunotherapy for ovarian cancer: adjuvant, combination, and neoadjuvant, Frontiers in Immunology. (2020) 11, 577869, https://doi.org/10.3389/fimmu.2020.577869.
10.3389/fimmu.2020.577869
CAS PubMed Web of Science® Google Scholar
11 Wang Z.-M., Lu J., and Zhang L. Y., Biological effects of low-dose-rate irradiation of pancreatic carcinoma cellsin vitrousing125I seeds, World Journal of Gastroenterology. (2015) 21, no. 8, 2336–2342, https://doi.org/10.3748/wjg.v21.i8.2336, 2-s2.0-84923807835.
10.3748/wjg.v21.i8.2336
CAS PubMed Web of Science® Google Scholar
12 Li C., Yao L., Gong J., Pang H., Shan Q., Wang Z., Lu J., and Wang Z., Efficacy of gefitinib combined with 125I radioactive particles in the treatment of transplanted lung cancer tumors in nude mice, CardioVascular and Interventional Radiology. (2020) 43, no. 9, 1364–1370, https://doi.org/10.1007/s00270-020-02550-1.
10.1007/s00270-020-02550-1
Web of Science® Google Scholar
13 Sánchez Sánchez R., González Jiménez A. D., Rebollo Aguirre A. C., Mendoza Arnau I., Menjón Beltrán S., Vergara Alcaide M. E., Osorio Ceballos J. L., and Llamas Elvira J. M., 125I radioactive seed localization for non-palpable lesions in breast cancer, Revista Española de Medicina Nuclear e Imagen Molecular. (2019) 38, no. 6, 343–347, https://doi.org/10.1016/j.remnie.2019.07.001.
10.1016/j.remnie.2019.07.001
CAS PubMed Web of Science® Google Scholar
14 Yang Y., Chen A., Ma J., Wu A, and Xu F, Effects of radioactive 125I on apoptosis of HGC-27 gastric cancer cells, Oncology letters. (2019) 18, no. 5, 4916–4922, https://doi.org/10.3892/ol.2019.10832, 2-s2.0-85073755956.
10.3892/ol.2019.10832
CAS PubMed Web of Science® Google Scholar
15 Chen X., Zhu F., Wang B., Zhou Y., Fan T., and Kee W., Clinical effect of iodine-125 seed implantation in patients with primary liver cancer and its effect on Th1/Th2 cells in peripheral blood, Journal of Oncology. (2021) 2021, 6, 6199732, https://doi.org/10.1155/2021/6199732.
10.1155/2021/6199732
PubMed Web of Science® Google Scholar
16 Zhao G. S., Liu S., Yang L., Li C., Wang R. Y., Zhou J., and Zhang Y. W., Evaluation of radioactive 125I seed implantation for the treatment of refractory malignant tumours based on a CT-guided 3D template-assisted technique: efficacy and safety, BMC Cancer. (2020) 20, no. 1, https://doi.org/10.1186/s12885-020-07223-3.
10.1186/s12885-020-07223-3
Web of Science® Google Scholar
17 Li W. W., Dai Z. Y., and Wan H. G., Endovascular implantation of iodine-125 seeds strand and portal vein stenting followed by transcatheter arterial chemoembolization combined therapy with sorafenib for hepatocellular carcinoma with main portal vein tumor thrombus, Zhonghua Yi Xue Za Zhi. (2016) 96, no. 23, 1838–1842.
CAS PubMed Google Scholar
18 Zhang W., Li J., Li R., Zhang Y., Han M., and Ma W., Efficacy and safety of iodine-125 radioactive seeds brachytherapy for advanced non-small cell lung cancer-A meta-analysis, Brachytherapy. (2018) 17, no. 2, 439–448, https://doi.org/10.1016/j.brachy.2017.11.015, 2-s2.0-85038923594.
10.1016/j.brachy.2017.11.015
PubMed Web of Science® Google Scholar
19 Martínez-Monge R., Nag S., and Martin E. W., Three different intraoperative radiation modalities (electron beam, high-dose-rate brachytherapy, and iodine-125 brachytherapy) in the adjuvant treatment of patients with recurrent colorectal adenocarcinoma, Cancer. (1999) 86, no. 2, 236–247.
10.1002/(SICI)1097-0142(19990715)86:2<236::AID-CNCR7>3.0.CO;2-9
CAS PubMed Web of Science® Google Scholar
20 Sano B., Sugiyama Y., Kunieda K., Sano J., and Saji S., Antitumor effects induced by the combination of TNP-470 as an angiogenesis inhibitor and lentinan as a biological response modifier in a rabbit spontaneous liver metastasis model, Surgery Today. (2002) 32, no. 6, 503–509, https://doi.org/10.1007/s005950200085, 2-s2.0-0035989922.
10.1007/s005950200085
CAS PubMed Web of Science® Google Scholar
21 Ina K., Furuta R., Kataoka T., Kayukawa S., Ina H., and Yoneda M., Chemo-immunotherapy using lentinan for the treatment of gastric cancer with liver metastases, Medical sciences (Basel, Switzerland). (2016) 4, no. 2, https://doi.org/10.3390/medsci4020008.
10.3390/medsci4020008
PubMed Google Scholar
22 Shiio T., Kitamura K., Ohishi K., and Yugari Y., Suppressive effect of lentinan on pulmonary metastases in murine tumors, Gan No Rinsho. (1987) 33, no. 12, 1427–1430.
CAS PubMed Google Scholar
23 Yasutomi M., Surgery and adjuvant therapy of cancer of the large intestine, Gan To. Kagaku Ryoho. (1986) 13, no. 7, 2307–2317.
CAS PubMed Google Scholar
24 Chihara G., Recent progress in immunopharmacology and therapeutic effects of polysaccharides, Developments in Biological Standardization. (1992) 77, 191–197.
CAS PubMed Web of Science® Google Scholar
25 Kimura Y., Iijima S., and Kato T., TS-1 and lentinan combination immunochemotherapy for advanced or recurrent gastric cancer: a preliminary report, Gan To. Kagaku Ryoho. (2003) 30, no. 11, 1791–1793.
PubMed Google Scholar
26 Wang J., Li W., Huang X., Liu Y., Li Q., Zheng Z., and Wang K., A polysaccharide from Lentinus edodes inhibits human colon cancer cell proliferation and suppresses tumor growth in athymic nude mice, Oncotarget. (2017) 8, no. 1, 610–623, https://doi.org/10.18632/oncotarget.13481, 2-s2.0-85009818965.
10.18632/oncotarget.13481
PubMed Google Scholar

Citing Literature

All articles

Lentinan Combined with (125)I Brachytherapy for Recurrent Ovarian Cancer

Abstract

1. Introduction

2. Methods

2.1. Patients

2.2. Study Design

2.3. Testing Index

2.4. Evaluation Criteria for Short-Term Efficacy

2.5. Statistical Method

3. Results

3.1. Pathological Characteristics

3.2. Blood-Related Indexes

3.3. Immunologic Function

3.4. Tumor Markers

3.5. Therapeutic Effect

3.6. KPS and QOL Score

3.7. Incidence of Adverse Reactions

4. Discussion

Conflicts of Interest

Authors’ Contributions

Open Research

Data Availability

References

Citing Literature

Figures

References

Information

About Wiley Online Library

Help & Support

Opportunities

Connect with Wiley