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      A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811)

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          Abstract

          Safety and efficacy of intrapericardial (ipc) instillation of bleomycin (BLM) following pericardial drainage in patients with malignant pericardial effusion (MPE) remain unclear. Patients with pathologically documented lung cancer, who had undergone pericardial drainage for MPE within 72 h of enrolment, were randomised to either arm A (observation alone after drainage) or arm B (ipc BLM at 15 mg, followed by additional ipc BLM 10 mg every 48 h). The drainage tube was removed when daily drainage was 20 ml or less. The primary end point was survival with MPE control (effusion failure-free survival, EFFS) at 2 months. Eighty patients were enrolled, and 79 were eligible. Effusion failure-free survival at 2 months was 29% in arm A and 46% in arm B (one-sided P=0.086 by Fisher's exact test). Arm B tended to favour EFFS, with a hazard ratio of 0.64 (95% confidence interval: 0.40–1.03, one-sided P=0.030 by log-rank test). No significant differences in the acute toxicities or complications were observed. The median survival was 79 days and 119 days in arm A and arm B, respectively. This medium-sized trial failed to show statistical significance in the primary end point. Although ipc BLM appeared safe and effective in the management of MPE, the therapeutic advantage seems modest.

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          Most cited references30

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          Abnormal cytology predicts poor prognosis in cancer patients with pericardial effusion.

          Pericardial tamponade is a life-threatening disorder caused by varying medical conditions. Malignancy and complications of its treatment are a common cause of pericardial effusion. The natural history of pericardial effusion remains largely unknown. We investigated the association of malignancy with adverse outcomes after pericardiocentesis. Consecutive patients undergoing pericardiocentesis at a single institution between January 1, 1999, and January 31, 2003, were included. Death was confirmed with the Social Security Death Index. Survival estimates were obtained by the Kaplan-Meier method. Cox regression was performed to determine the clinical characteristics associated with death. Two hundred nineteen patients underwent pericardiocentesis during the study period. The effusion was cancer-related in 43.8% of cases. Median survival was 59.6 weeks (95% CI, 24.3 to 94.8 weeks). During the follow-up period, 47.9% of patients died. Cancer-related pericardial effusion was associated with decreased survival (median, 15.1 weeks). Abnormal fluid cytology was further associated with poor prognosis among patients with malignancy (median survival, 7.3 v 29.7 weeks; P = .022). Patients with cancer-related pericardial effusion were more likely to require repeat pericardiocentesis (OR = 6.0; P = .001) and pericardial surgery (odds ratio [OR] OR = 5.7; P < .001). Cancer-related effusion and abnormal cytology were independent predictors of death in a multivariate model. Malignancy is the most common cause of pericardial effusion in a tertiary care center. Cancer-related pericardial effusion is associated with adverse outcomes, and abnormal cytology further worsens prognosis. The poor survival among cancer patients with pericardial effusion and abnormal fluid cytology may have important implications for management.
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            Neoplasms metastatic to the heart: review of 3314 consecutive autopsies.

            Cardiac involvement by metastatic neoplasms is relatively uncommon and usually occurs with widely disseminated disease. Ninety-five cases with cardiac metastases from autopsies performed over a 14-year period (1974-1987) at Loyola University Medical Center are reviewed. During this period, 3314 autopsies were performed with an average annual autopsy rate of 35%. In 806 (24.3%), a malignant disease was found, and in 95 (11.8%), there was cardiac involvement by tumor. The most common malignancies encountered in order of decreasing frequency were lung, lymphoma, breast, leukemia, stomach, melanoma, liver, and colon. Although the percentage of cardiac metastasis compares favorably with previous reports in the literature, an identical rate was present during both halves of the 14-year period studied. Improved diagnostic capabilities and treatment protocols in recent years have apparently not significantly affected the incidence, distribution, or patterns of metastatic spread to the heart.
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              Cardiac metastases.

              The authors found metastases to the heart in 10.7% of 1029 autopsy cases in which a malignant neoplasm was diagnosed. The lung was the commonest primary site (36.4%) and adenocarcinoma was the most frequent cell type (36.4%) of neoplasms metastatic to heart. Nonepithelial tumors accounted for 22.7% of cardiac metastases. Epicardium was involved in 75.5% of metastatic lesions and a pericardial effusion was present with 33.7% of epicardial metastases. Although hemorrhagic effusions occurred in only 12 cases with metastases to heart, these represented 76.4% of all such effusions. Lymphomas associated with the acquired immune deficiency syndrome showed the most extensive cardiac involvement. Primary sites and cell types of cardiac metastases have evolved over time and have been modified by chemotherapy, increased survival of cancer patients, increasing incidence of lung carcinoma, and recently by the acquired immune deficiency syndrome epidemic.
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                Author and article information

                Journal
                Br J Cancer
                British Journal of Cancer
                Nature Publishing Group
                0007-0920
                1532-1827
                20 January 2009
                03 February 2009
                10 February 2009
                : 100
                : 3
                : 464-469
                Affiliations
                [1 ]Department of Medical Oncology, National Cancer Center Hospital 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan
                [2 ]JCOG Data Center, Center for Cancer Control and Information Services, National Cancer Center 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan
                [3 ]Department of Thoracic Oncology, National Cancer Center Hospital East 6-5-1 Kashiwanohara, Kashiwashi, Chiba 277-8577, Japan
                [4 ]Department of Medical Oncology, Cancer Institute Hospital 3-10-6 Ariake, Koto-ku, Tokyo 135-8550, Japan
                [5 ]Department of Medical Oncology, Niigata Cancer Center 2-15-3, Kawagishi-cho, Niigata-shi, Niigata 951-8566, Japan
                [6 ]Department of Respiratory Medicine, Yokohama Municipal Citizen's Hospital 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa 240-8555, Japan
                [7 ]Division of Thoracic Oncology, Kanagawa Cancer Center 1-1-2 Nakao, Asahi-ku, Yokohama, Kanagawa 241-0815, Japan
                [8 ]National Cancer Center Hospital East 6-5-1 Kashiwanohara, Kashiwashi, Chiba 277-8577, Japan
                Author notes
                [* ]Author for correspondence: hkkunito@ 123456ncc.go.jp
                Article
                6604866
                10.1038/sj.bjc.6604866
                2658533
                19156149
                f94cf830-20f0-4c87-85ee-7211c549f551
                Copyright 2009, Cancer Research UK
                History
                : 11 September 2008
                : 19 November 2008
                : 05 December 2008
                Categories
                Clinical Studies

                Oncology & Radiotherapy
                malignant pericardial effusion,drainage,intrapericardial instillation,lung cancer,bleomycin,sclerosis

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