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1.
Gan To Kagaku Ryoho ; 51(5): 529-533, 2024 May.
Article in Japanese | MEDLINE | ID: mdl-38881063

ABSTRACT

Cancer cachexia causes anorexia and metabolic disorders, eventually leading to sarcopenia, which in turn contributes to the development of functional disabilities. Although anamorelin hydrochloride tablets are marketed to treat cancer cachexia, their efficacy varies significantly among patients. Here, we investigated the efficacy of anamorelin and the factors associated with weight gain. The factors that contributed to weight gain in patients before starting anamorelin were as follows: the patients' disease stage had not progressed to refractory cachexia based on the cancer cachexia classification of the European Palliative Care Research Collaborative; the patients had received fewer lines of anticancer treatment at the start of oral administration of anamorelin; and the patients had not met all the criteria for starting treatment with anamorelin, namely, C-reactive protein level >0.5 mg/dL, hemoglobin level <12 g/dL, and albumin level <3.2 g/dL. These results suggest that early administration of anamorelin hydrochloride tablets may increase the response rate when cancer cachexia is diagnosed.


Subject(s)
Cachexia , Neoplasms , Weight Gain , Humans , Cachexia/drug therapy , Cachexia/etiology , Neoplasms/complications , Male , Female , Aged , Middle Aged , Weight Gain/drug effects , Aged, 80 and over , Glycine/analogs & derivatives , Glycine/therapeutic use , Glycine/administration & dosage , Hydrazines/therapeutic use , Hydrazines/administration & dosage , Oligopeptides
2.
Gan To Kagaku Ryoho ; 49(9): 963-967, 2022 Sep.
Article in Japanese | MEDLINE | ID: mdl-36156015

ABSTRACT

Capecitabine plus oxaliplatin(CapeOX)is widely used as postoperative adjuvant chemotherapy for gastric cancer. The CapeOX regimen often causes digestive symptoms, such as nausea and vomiting under postoperative conditions, and oxaliplatin- induced neurological symptoms, for which supportive intervention is needed. The pharmaceutical outpatient clinic of Jichi Medical University provides pharmaceutical intervention for cancer patients. This study evaluated the usefulness of the pharmaceutical outpatient clinic for gastric cancer patients receiving postoperative adjuvant chemotherapy. The primary endpoint was defined as the effect of the number of outpatient pharmacist interventions on the relative dose intensity of the CapeOX regimen. The secondary endpoint was the correlation between the number of outpatient pharmacist interventions and the worst grade of each side effect. It was observed that patients who received at least 5 outpatient pharmacist interventions had significantly higher dose intensities(p=0.019). Outpatient pharmaceutical interventions were associated with the reduction of side effect symptoms that could be managed with preventive and supportive care. These results showed that continuous intervention by outpatient pharmacists contribute to the optimization of dose intensity and reduction of side effects in gastric cancer patients receiving CapeOX as postoperative adjuvant chemotherapy.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols , Stomach Neoplasms , Ambulatory Care Facilities , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Capecitabine , Chemotherapy, Adjuvant , Fluorouracil , Humans , Oxaliplatin/therapeutic use , Stomach Neoplasms/drug therapy , Stomach Neoplasms/surgery
3.
Gan To Kagaku Ryoho ; 47(9): 1341-1344, 2020 Sep.
Article in Japanese | MEDLINE | ID: mdl-33130696

ABSTRACT

The postmarketing assessment of biosimilars is important because posttranslational modification by glycosylation is altered by the manufacturing process. A retrospective study of 15 patients with gastric cancer receiving a combination anticancer therapy with trastuzumab was performed. The most common concurrent regimen was the S-1 and oxaliplatin combination; efficacy and adverse events were assessed in this group. There was no statistically significant difference in progression-free survival between patients receiving the reference formulation and patients receiving its biosimilar. The adverse events detected were similar in both groups. In the 6 patients who switched from the reference trastuzumab to its biosimilar, adverse events did not differ before and after the switch. This small-scale retrospective study found no differences in efficacy or adverse events between the reference trastuzumab and its biosimilar.


Subject(s)
Biosimilar Pharmaceuticals , Breast Neoplasms , Stomach Neoplasms , Biosimilar Pharmaceuticals/adverse effects , Humans , Receptor, ErbB-2 , Retrospective Studies , Stomach Neoplasms/drug therapy , Trastuzumab/adverse effects
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