1.Effect of combined gastrointestinal internal and external nutritional support in the treatment of elderly patients with lung cancer
Jianying JIN ; Qinhui DONG ; Dan JIN
Chinese Journal of Primary Medicine and Pharmacy 2017;24(23):3553-3557
Objective To explore the effect of combined gastrointestinal internal and external nutritional support in the treatment of elderly patients with lung cancer.Methods According to the random number table method,86 patients with advanced non-small cell lung cancer(NSCLC) were divided into the control group and observation group,43 cases in each group.The observation group was given nutritional intervention on the basis of treatment in the control group.The 12-month survival rate,median progression time and median survival time were evaluated.The clinical efficacy of the two groups was evaluated.The quality of life before and after treatment was evaluated by the KPS score.Results The 12-month survival rate of the observation group was 39.53%,which was significantly higher than 18.60% of the control group(x2 =4.56,P =0.03).The median survival time and median survival of the observation group were (7.85 ± 1.27) months,(9.98 ± 1.71) months,respectively,which were significantly higher than (6.07 ±0.98)months,(7.99 ± 1.38)months of the control group(t =7.27,5.93,P =0.00,0.00).The total effective rate of the observation group was 88.37%,which was significantly higher than 55.81% of the control group (x2 =11.32,P =0.00).The KPS scores of the observation group and the control group after treatment were (73.17 ± 2.75)points,(59.68 ±2.52) points,respectively,which were higher than (52.75 ± 2.02) points,(53.01 ± 1.98) points before treatment,and the KPS scores of the observation group were significantly higher than those of the control group (t =39.24,13.64,P =0.00,0.00).The incidence rate of adverse reaction in the observation group was 48.84%,which in the control group was 55.81%,the difference was not statistically significant (x2 =0.41,P =0.51).The CD4+ cells,CD4+/CD8+ and NK cells in the control group were significantly lower than those before treatment (t =6.14,8.44,7.48,P =0.00,0.00,0.00),which in the observation group were significantly higher than before treatment (t =4.89,5.17,6.33,P =0.00,0.00,0.00),the differences were statistically significant compared with the control group after treatment(t =8.11,4.26,5.88,P =0.00,0.00,0.00).The levels of hemoglobin and albumin in the observation group were significantly higher than those in the control group(t =3.88,6.39,P =0.00,0.00).Conclusion The combination of chemotherapy combined with nutritional intervention in the treatment of locally advanced NSCLC is beneficial to improve the immune function and nutritional status of patients,improve clinical efficacy and survival of patients,better improve their quality of life,and will not increase adverse reactions.
2.Evaluation of efficacy and safety of tislelizumab combined with chemotherapy in neoadjuvant treatment for resectable esophageal cancer
Qin WU ; Dong WU ; Jianlong XIE ; Qinhui LUO ; Liangling LAO ; Yubin ZENG ; Liyao LIN
Journal of International Oncology 2024;51(10):620-626
Objective:To analyze the short-term efficacy and safety of tislelizumab combined with neoadjuvant chemotherapy in the treatment of resectable esophageal squamous cell carcinoma (ESCC) .Methods:The clinical data of 56 patients with ESCC who received neoadjuvant therapy combined with surgical resection in the Department of Thoracic Surgery, Affiliated Hospital of Guangdong Medical University from April 2021 to October 2023 were collected. According to the different preoperative neoadjuvant therapy methods, the patients were divided into neoadjuvant chemotherapy combined with immunotherapy group (chemoimmunization group, n=24) and neoadjuvant chemotherapy group (chemotherapy group, n=32). The postoperative tumor regression grade, objective response rate (ORR), disease control rate (DCR), pathological complete response (pCR) rate, major pathological remssion (MPR) rate, R0 resection rate, perioperative indicators, and security were compared between the two groups. Results:In chemoimmunization group, the tumor regression grade was better than that in chemotherapy group, with a statistically significant difference ( Z=9.39, P=0.025). The ORR and the DCR were 75.00% (18/24) and 91.67% (22/24) in chemoimmunization group, and 46.88% (15/32) and 65.62% (21/32) in chemotherapy group, with statistically significant differences ( χ2=4.48, P=0.034; χ2=5.21, P=0.022). The R0 resection rate was 87.50% (21/24) in chemoimmunization group, which was higher than that of the chemotherapy group [59.38% (19/32) ], with a statistically significant difference ( χ2=5.31, P=0.021). The pCR rate and MPR rate were 29.17% (7/24) and 54.17% (13/24) in chemoimmunization group, and 6.25% (2/32) and 28.12% (9/32) in chemotherapy group, there was no statistically significant difference in pCR rate ( χ2=3.78, P=0.052), but there was a statistically significant difference in MPR rate ( χ2=3.89, P=0.048). The interval between the end of neoadjuvant treatment and the start of surgery was (42.71±8.29) days in chemoimmunization group, and (42.25±8.03) days in chemotherapy group. The intraoperative blood loss of patients was (215.54±57.85) ml in chemoimmunization group, and (229.65±57.74) ml in chemotherapy group. The operation time of patients was (293.52±37.50) minutes in chemoimmunization group, and (295.31±37.66) minutes in chemotherapy group. The postoperative hospitalization time of patients was (17.90±3.49) days in chemoimmunization group, and (18.42±3.82) days in chemotherapy group, all with no statistically significant differences ( t=0.21, P=0.835; t=0.90, P=0.370; t=0.18, P=0.861; t=0.52, P=0.603). In terms of postoperative complications, there was no statistically significant difference in the total incidence of postoperative complications between the two groups [62.50% (15/24) vs. 84.38% (27/32), χ2=0.59, P=0.440]. The main adverse drug reactions in the two groups included decreased white blood cell count, nausea and vomiting, liver dysfunction, pruritus, hypothyroidism, etc. Most of them were grade 1-2, 3 cases were grade 3, and no grade 4 adverse reactions occurred. The total incidence of adverse reactions was 62.50% (15/24) in chemoimmunization group, and 65.62% (21/32) in chemotherapy group, with no statistically significant difference ( χ2=0.06, P=0.809) . Conclusion:For the preoperative neoadjuvant therapy of resectable ESCC, the combination of tislelizumab and chemotherapy has better short-term efficacy and better safety than the single chemotherapy scheme, which can improve the surgical efficacy.