AbstractAbstract
[en]
Background
Clinical efficacy of aggressive end-of-life (EOL) chemotherapy remains unclear.Method
Medical records of patients with advanced cancer between August 2011 and August 2016 were retrospectively analyzed. The primary endpoint was to identify prognostic factors at the last administration of chemotherapy. The secondary endpoint was to analyze the relationship between EOL symptoms and EOL treatment details.Results
Among 300 evaluated patients, the number of patients who died within 14 and 30 days from the last administration of chemotherapy were 16 (5.3%) and 50 (16.7%), respectively. Multivariate analysis revealed that ECOG-PS (OR 3.698, p < 0.001) and GPS2 (OR 3.791, p = 0.028) were significant prognostic factors. The MST of patients with both PS 2–4 and GPS2 (+) was 38 days, while that in patients with both PS 0–1 and GPS2 (−) was 134.5 days. The prevalence rate of nausea and vomiting (25.0%) and the mean hydration volume (0.50 L/day) in patients who died within 30 days from the chemotherapy was significantly higher than others (7.4%) (0.20 L/day).Conclusion
ECOG-PS and GPS were significant prognostic factors for aggressive EOL chemotherapy. Information on these factors may aid clinical decision-making in terms of risk–benefit balance, particularly in patients with poor prognosis.Primary Subject
Source
Copyright (c) 2019 Japan Society of Clinical Oncology; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
Journal
International Journal of Clinical Oncology; ISSN 1341-9625; ; v. 24(4); p. 454-459
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Iwase, Toshiaki; Sangai, Takafumi; Fujimoto, Hiroshi; Sawabe, Yuji; Matsushita, Kazuyuki; Nagashima, Kengo; Sato, Yasunori; Nakagawa, Ayako; Masuda, Takahito; Nagashima, Takeshi; Ohtsuka, Masayuki, E-mail: tiwase@mdanderson.org2020
AbstractAbstract
[en]
Purpose
: Recent studies suggest that the quality and quantity of visceral adipose tissue (VAT) play significant roles in adipocyte function, and are related to insulin resistance. We tested the hypothesis that high amounts of upper VAT (aVAT) and low-quality VAT worsen treatment outcomes via altered insulin metabolism.Methods
: Cohort 1 included 106 women with breast cancer who were undergoing surgery. Homeostasis model assessment of insulin resistance (HOMA-R), insulin-like growth factor (IGF)-1, and IGF-binding protein 3 (IGFBP3) were measured before the initiation of treatment. aVAT was measured via computed tomography (CT). VAT quality was assessed using CT-determined Hounsfield units (VAT-HU). Associations between the variables investigated and VAT quality and quantity were analyzed. Cohort 2 included 271 patients who underwent chemotherapy. Associations between the variables investigated and survival outcomes after chemotherapy were analyzed via retrospective chart review.Results
: In cohort 1, aVAT was significantly correlated with insulin and HOMA-R levels. As body mass index (BMI) class increased, mean IGF-1 increased and mean IGFBP3 decreased, but these trends were not statistically significant. In cohort 2, aVAT was significantly positively correlated with BMI. The patients in the third aVAT tertiles had significantly shorter distant disease-free survival (dDFS) after neoadjuvant chemotherapy setting. In multivariate analysis, aVAT and VAT-HU were significantly associated with shorter dDFS.Conclusions
: High aVAT and low-quality VAT were associated with poor survival outcome, increased insulin levels, and insulin resistance. The present study suggests the importance of evaluating the quality and quantity of VAT when estimating insulin resistance and treatment outcomes.Primary Subject
Source
Copyright (c) 2019 © Springer Science+Business Media, LLC, part of Springer Nature 2019; Indexer: nadia, v0.3.6; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
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Hashimoto, Jun; Kato, Ken; Ito, Yoshinori; Kojima, Takashi; Akimoto, Tetsuo; Daiko, Hiroyuki; Hamamoto, Yasuo; Matsushita, Hisayuki; Katano, Susumu; Hara, Hiroki; Tanaka, Yoichi; Saito, Yoshihiro; Nagashima, Kengo; Igaki, Hiroyasu, E-mail: kenkato@ncc.go.jp2019
AbstractAbstract
[en]
Background
Preoperative chemoradiotherapy (CRT) is a standard treatment for stage II/III esophageal cancer. Preoperative chemotherapy is also considered a standard treatment for stage II/III esophageal squamous cell carcinoma (ESCC) in patients who undergo radical lymph node dissection. We conducted a feasibility study of preoperative CRT with cisplatin plus 5-fluorouracil (CF) and elective lymph node irradiation followed by esophagectomy with radical lymph node dissection in patients with stage II/III ESCC.Methods
Patients with clinical stage II/III, excluding T4, ESCC (International Union Against Cancer TNM classification system, 6th edition) were eligible. Chemotherapy comprised two courses of CF infusion repeated after 4-weeks. Radiation therapy was concurrently administered to the primary tumor, metastatic lymph nodes, and regional lymph nodes at a dose of 41.4 Gy. After the completion of CRT, transthoracic esophagectomy with 2–3 fields lymphadenectomy was performed. The primary endpoint was the completion rate of protocol treatment with R0 resection.Results
Thirty-one eligible patients were enrolled. During CRT, the most common grade 3 or 4 toxicities were leukopenia (65%), neutropenia (65%), anemia (13%), thrombocytopenia (13%), febrile neutropenia (13%), anorexia (16%), esophagitis (16%) and hyponatremia (16%). Thirty patients (96.8%) underwent surgery. One patient received palliative chemotherapy because of appearance of lung metastasis during CRT. The completion rate of protocol treatment was 93.5% (29/31). There was one treatment-related death after surgery. Pathological complete response was achieved in 42% (13/30).Conclusion
Preoperative CRT with CF and elective lymph node irradiation showed an acceptable toxicity and promising activity especially in ESCC.Primary Subject
Source
Copyright (c) 2019 Japan Society of Clinical Oncology; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
International Journal of Clinical Oncology; ISSN 1341-9625; ; v. 24(1); p. 60-67
Country of publication
ANTIMETABOLITES, AZINES, BODY, DIGESTIVE SYSTEM, DISEASES, DRUGS, HEMIC DISEASES, HETEROCYCLIC COMPOUNDS, HYDROXY COMPOUNDS, IMMUNE SYSTEM DISEASES, INTAKE, LYMPHATIC SYSTEM, MEDICINE, NEOPLASMS, NUCLEAR MEDICINE, ORGANIC COMPOUNDS, ORGANIC FLUORINE COMPOUNDS, ORGANIC HALOGEN COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, ORGANS, PYRIMIDINES, RADIOLOGY, RESPIRATORY SYSTEM, SYMPTOMS, TESTING, THERAPY, URACILS
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