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1.
In Vivo ; 38(2): 864-872, 2024.
Article in English | MEDLINE | ID: mdl-38418111

ABSTRACT

BACKGROUND/AIM: Recent lung cancer treatments include an immune checkpoint inhibitor (ICI) pembrolizumab, platinum-based agents, plus an additional cytotoxic anticancer agent. Nutritional indices, such as the geriatric nutritional risk index (GNRI) and the prognostic nutritional index (PNI), are known to correlate with the prognosis of cancer chemotherapy. Several previous studies have investigated the relationship between PNI and treatment response in non-small cell lung cancer patients, reporting significantly increased OS and PFS in the high PNI group before treatment. However, the relationship between the three-drug combination and GNRI/PNI is unclear. The current study aimed to investigate the association of nutritional indices with duration of treatment success and occurrence of side effects in triple therapy. PATIENTS AND METHODS: Seventy-two patients with non-small cell lung cancer, treated with combination of carboplatin, pemetrexed, and pembrolizumab from November 2019 to September 30, 2022, were classified into two groups (High and Low) for GNRI and PNI, and a retrospective study was performed. RESULTS: In terms of time-to-treatment-failure (TTF), univariate and multivariate Cox proportional hazards regression analysis showed the Low-PNI group to have significantly shorter TTF than the High-PNI group (p=0.006); multivariate analysis results also showed PNI as a factor affecting TTF (HR=2.791, 95%CI=1.362-5.721, p=0.005). On the other hand, GNRI was not shown to be a factor affecting TTF. CONCLUSION: PNI at the start of treatment was an independent prognostic factor affecting treatment success time (TTF) in non-small cell lung cancer patients receiving triple therapy. However, PNI was not shown to be a prognostic predictor of irAE development.


Subject(s)
Antineoplastic Agents , Carcinoma, Non-Small-Cell Lung , Lung Neoplasms , Humans , Aged , Lung Neoplasms/drug therapy , Nutrition Assessment , Carcinoma, Non-Small-Cell Lung/drug therapy , Retrospective Studies , Prognosis , Antineoplastic Agents/therapeutic use
2.
In Vivo ; 38(1): 453-459, 2024.
Article in English | MEDLINE | ID: mdl-38148079

ABSTRACT

BACKGROUND/AIM: In recent years, the Geriatric Nutritional Risk Index (GNRI) has been reported as a predictor of prognosis in many patients with cancer. This study investigated the association of preoperative GNRI with the occurrence of adverse events and duration of treatment with capecitabine plus oxaliplatin (CAPOX), a postoperative adjuvant chemotherapy, in 59 patients with colorectal cancer from September 2019 to April 2022. PATIENTS AND METHODS: A cut-off value of 100.9 was used to categorize patients into high and low GNRI groups. RESULTS: The incidence of grade ≥2 leukopenia (p=0.03), and all grades peripheral neuropathy (p=0.04) were significantly more frequent in the low GNRI group. Analysis of factors influencing treatment duration by univariate and multivariate Cox regression proportional hazards models showed a significant difference in GNRI (p=0.0097). CONCLUSION: GNRI, a nutritional indicator assessed before the start of treatment, influences the occurrence of adverse events and duration of treatment with CAPOX as adjuvant chemotherapy. To complete CAPOX therapy, preoperatively, it is important to assess the patients' nutritional status using the GNRI and to actively intervene in nutritional therapy.


Subject(s)
Colorectal Neoplasms , Duration of Therapy , Humans , Aged , Nutritional Status , Prognosis , Oxaliplatin/adverse effects , Colorectal Neoplasms/drug therapy , Chemotherapy, Adjuvant/adverse effects , Nutrition Assessment , Risk Factors , Retrospective Studies
3.
In Vivo ; 38(1): 418-424, 2024.
Article in English | MEDLINE | ID: mdl-38148096

ABSTRACT

BACKGROUND/AIM: Compared to conventional cytotoxic anticancer agent-based therapy, treatment with immune checkpoint inhibitors (ICI) significantly prolongs overall survival. The Geriatric Nutritional Risk Index (GNRI) has been used as a new prognostic indicator in cancer. As nutritional status is associated with prognosis and indicates treatment response, we investigated the effect of the pretreatment GNRI on the (1) occurrence of ICI-induced immune-related adverse events (ir-AE) and (2) association with time to treatment failure (TTF) in ICI monotherapy for lung cancer. PATIENTS AND METHODS: In this study, 127 patients with lung cancer who were treated with ICI monotherapy were retrospectively enrolled. Based on a cutoff value of 92 for the GNRI, we investigated intergroup differences in the occurrence of adverse events and their association with TTF in the High-GNRI (≥92) and Low-GNRI (<92) groups. For intergroup comparisons, we used the Student's t-test, Welch's t-test, Fisher's direct probability test, and Mann-Whitney's U-test, and factors with p<0.05 in the intergroup comparison were extracted as explanatory variables. RESULTS: Based on the pretreatment GNRI, the median TTF was 5.1 months (95%CI=2.4-7.9 months) in the High-GNRI group and 2.3 months (95%CI=1.6-3.1 months) in the Low-GNRI group, with the High-GNRI group having a significantly longer TTF (p<0.01). The incidence of skin rash (p=0.0129) and pruritus (p<0.01) was significantly higher in the High-GNRI group. CONCLUSION: Pretreatment GNRI influences the continuation of ICI monotherapy. The High-GNRI group demonstrated a significantly higher frequency of skin lesions, which may have influenced the prolongation of TTF.


Subject(s)
Lung Neoplasms , Humans , Aged , Lung Neoplasms/drug therapy , Immune Checkpoint Inhibitors/adverse effects , Nutrition Assessment , Retrospective Studies , Duration of Therapy , Risk Factors , Geriatric Assessment , Prognosis
4.
Gan To Kagaku Ryoho ; 50(6): 701-705, 2023 Jun.
Article in Japanese | MEDLINE | ID: mdl-37317604

ABSTRACT

To date, there are no reports that examine the relationship between geriatric nutritional risk index(GNRI)at the start of chemotherapy for malignant lymphoma and adverse effects. In this study, we investigated the relationship between GNRI at the start of chemotherapy and the incidence of side effects and time to treatment failure(TTF)in(R-)EPOCH-treated patients with relapsed or refractory malignant lymphoma. A significant difference in the incidence of Grade 3 or higher thrombocytopenia was observed between high and low GNRI groups(p=0.043). The GNRI may be an indicator of hematologic toxicity in malignant lymphoma patients treated with(R-)EPOCH. There was a statistically significant difference in TTF between the high and low GNRI groups(p=0.025), suggesting that nutritional status at the start of(R-)EPOCH may affect treatment continuation.


Subject(s)
Lymphoma , Thrombocytopenia , Humans , Aged , Time-to-Treatment , Treatment Failure , Lymphoma/drug therapy , Nutritional Status
5.
In Vivo ; 37(3): 1297-1303, 2023.
Article in English | MEDLINE | ID: mdl-37103079

ABSTRACT

BACKGROUND/AIM: No studies have examined the association between the Geriatric Nutritional Risk Index (GNRI) at the initiation of chemotherapy for malignant lymphoma and the occurrence of adverse events. Therefore, we investigated the impact of GNRI at treatment initiation on the occurrence of side effects and time to treatment failure (TTF) in patients with malignant lymphoma undergoing initial rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) therapy. PATIENTS AND METHODS: This study included 131 patients who underwent initial R-CHOP therapy between March 2016 and October 2021. Patients were stratified into those with high (GNRI ≥92; n=56) or low (GNRI <92; n=75) GNRI status. RESULTS: Comparing the High GNRI group and Low GNRI group, the incidence of febrile neutropenia (FN) and Grade ≥3 creatinine increase, alkaline phosphatase (ALP) increase, albumin decrease, hemoglobin decrease, neutropenia, and thrombocytopenia were significantly higher in the Low GNRI group. TTF in the High GNRI group was significantly longer than that in the Low GNRI group (p=0.045). Multivariate analysis showed that the factors influencing the duration of treatment were PS (≥2) at the start of treatment, serum albumin level, and GNRI. CONCLUSION: In patients undergoing R-CHOP therapy, GNRI <92 at regimen initiation increased the risks of developing FN and hematologic toxicity. Multivariate analysis revealed that performance status, albumin levels, and GNRI at regimen initiation were the factors influencing treatment duration. Nutritional status at treatment initiation may influence the development of hematologic toxicity and TTF.


Subject(s)
Duration of Therapy , Lymphoma, Large B-Cell, Diffuse , Humans , Aged , Antibodies, Monoclonal, Murine-Derived/adverse effects , Rituximab/adverse effects , Vincristine/adverse effects , Prednisone/adverse effects , Cyclophosphamide/adverse effects , Doxorubicin/adverse effects , Lymphoma, Large B-Cell, Diffuse/drug therapy , Antineoplastic Combined Chemotherapy Protocols/adverse effects
6.
Nihon Shokakibyo Gakkai Zasshi ; 118(11): 1063-1070, 2021.
Article in Japanese | MEDLINE | ID: mdl-34759103

ABSTRACT

An advanced small bowel mucinous adenocarcinoma with Peutz-Jeghers syndrome was resected, and we started capecitabine plus oxaliplatin (CapeOX) as adjuvant therapy. However, local recurrence was noted, and the tumor increased even after CapeOX plus bevacizumab and fluorouracil plus leucovorin plus irinotecan plus panitumumab (FOLFIRI plus panitumumab). Pembrolizumab was administered after confirming high-frequency microsatellite instability, and the tumor shrank markedly and remained shrunk for 20 months.


Subject(s)
Adenocarcinoma, Mucinous , Colorectal Neoplasms , Peutz-Jeghers Syndrome , Adenocarcinoma, Mucinous/drug therapy , Antibodies, Monoclonal, Humanized , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bevacizumab/therapeutic use , Camptothecin/therapeutic use , Fluorouracil/therapeutic use , Humans , Leucovorin/therapeutic use , Neoplasm Recurrence, Local , Peutz-Jeghers Syndrome/drug therapy
7.
J Vasc Interv Radiol ; 24(3): 432-8, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23433417

ABSTRACT

PURPOSE: To investigate the feasibility, efficacy, and safety of transcatheter arterial embolization with N-butyl cyanoacrylate (NBCA) for gastroduodenal nonvariceal bleeding uncontrolled by endoscopic hemostasis. MATERIALS AND METHODS: Between January 2006 and December 2011, a total of 317 patients underwent emergent endoscopic therapy for nonvariceal gastroduodenal bleeding, but hemostasis was not achieved in 20 cases. Emergent surgery was performed immediately following endoscopy in two patients. Arteriography was performed in the remaining 18 patients, and embolization with NBCA was performed in 15 patients (mean age, 71.3 y) in whom the bleeding site was detected on arteriography. For embolization, NBCA was mixed with iodized oil at a ratio of 1:1.5-1:4, and no other embolic material was used in the procedure. Technical and clinical success rates, recurrent bleeding, procedural time, complications, and clinical outcomes were determined for each procedure. RESULTS: Embolization with NBCA was technically and clinically successful in all procedures, without major complications. No patient receiving embolization with NBCA experienced recurrent bleeding or required further treatment after the one-session procedure. All patients were discharged after clinical improvement. The time between puncture of the femoral artery and completion of embolization ranged from 25 to 240 minutes (mean, 66 min), and the time between the microcatheter reaching the ultimate catheter location selected for embolization and hemostasis ranged from 142 to 550 seconds (mean, 322s). CONCLUSIONS: In this limited series, embolization with NBCA was found to be a safe, feasible, and effective treatment for gastroduodenal arterial bleeding when endoscopic hemostasis had failed.


Subject(s)
Embolization, Therapeutic/methods , Enbucrilate/administration & dosage , Gastrointestinal Hemorrhage/therapy , Hemostasis, Endoscopic , Hemostatics/administration & dosage , Acute Disease , Aged , Aged, 80 and over , Embolization, Therapeutic/adverse effects , Enbucrilate/adverse effects , Ethiodized Oil/administration & dosage , Feasibility Studies , Female , Gastrointestinal Hemorrhage/diagnosis , Gastrointestinal Hemorrhage/etiology , Hemostatics/adverse effects , Humans , Male , Middle Aged , Radiography, Interventional , Recurrence , Retrospective Studies , Time Factors , Treatment Outcome
8.
Cardiovasc Intervent Radiol ; 35(4): 932-7, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22037708

ABSTRACT

Although n-butyl-2-cyanoacrylate (NBCA) has been used as an effective liquid embolization material, its indication for pseudoaneurysms has seemingly been limited because of the technical difficulties of using NBCA, such as reflux to the parent artery and causing significant infarction. Thus, considerable skill in using NBCA or a device to control blood flow during its polymerization is required to achieve embolization without severe complications. We report our new technique for controlling blood flow using diluted epinephrine in transcatheter arterial NBCA embolization of five pseudoaneurysms in four cases secondary to hemosuccus pancreaticus.


Subject(s)
Aneurysm, False/therapy , Duodenum/blood supply , Embolization, Therapeutic/methods , Enbucrilate/administration & dosage , Epinephrine/administration & dosage , Ethiodized Oil/administration & dosage , Pancreas/blood supply , Pancreatitis/therapy , Splenic Artery , Vasoconstrictor Agents/administration & dosage , Fluoroscopy , Humans , Male , Middle Aged , Tomography, X-Ray Computed , Treatment Outcome
9.
Bioorg Med Chem ; 19(16): 4721-9, 2011 Aug 15.
Article in English | MEDLINE | ID: mdl-21795053

ABSTRACT

Novel vitamin D(3) analogs with carboxylic acid were explored, focusing on a nonsecosteroidal analog, LG190178, with a bisphenyl skeleton. From X-ray analysis of these analogs with vitamin D receptor (VDR), the carboxyl groups had very unique hydrogen bonding interactions in VDR and mimicked 1α-hydroxy group and/or 3ß-hydroxy group of 1α,25-dihydroxyvitamin D(3). A highly potent analog, 6a, with good in vitro activity and pharmacokinetic profiles was identified from an SAR study. Compound 6a showed significant prevention of bone loss in a rat osteoporosis model by oral administration.


Subject(s)
Bone Density Conservation Agents/chemical synthesis , Cholecalciferol/analogs & derivatives , Osteoporosis/drug therapy , Animals , Bone Density/drug effects , Bone Density Conservation Agents/chemistry , Bone Density Conservation Agents/pharmacology , Calcitriol/analogs & derivatives , Calcitriol/chemistry , Calcitriol/pharmacology , Calcium/blood , Cell Line , Cholecalciferol/pharmacology , Cholecalciferol/therapeutic use , Drug Evaluation, Preclinical , Female , Humans , Mice , Osteocalcin/analysis , Osteocalcin/physiology , Osteoporosis/physiopathology , Rats , Rats, Sprague-Dawley , Receptors, Calcitriol/agonists , Receptors, Calcitriol/drug effects , Receptors, Calcitriol/genetics , Steroids/chemistry , Structure-Activity Relationship
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