European Journal of Cancer and Clinical Oncology最新文献

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Bone marrow micrometastases in primary breast cancer: Prognostic significance after 6 years' follow-up 原发性乳腺癌骨髓微转移:6年随访后的预后意义
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90413-8
J.L. Mansi , D. Easton , U. Berger , J.-C. Gazet , H.T. Ford , D. Dearnaley , R.C. Coombes
{"title":"Bone marrow micrometastases in primary breast cancer: Prognostic significance after 6 years' follow-up","authors":"J.L. Mansi ,&nbsp;D. Easton ,&nbsp;U. Berger ,&nbsp;J.-C. Gazet ,&nbsp;H.T. Ford ,&nbsp;D. Dearnaley ,&nbsp;R.C. Coombes","doi":"10.1016/0277-5379(91)90413-8","DOIUrl":"10.1016/0277-5379(91)90413-8","url":null,"abstract":"<div><p>Using an antiserum to epithelial membrane antigen we have screened multiple bone marrow aspirates from 350 patients with primary breast cancer taken at the time of initial surgery. 89 (25%) patients were found to have micrometastases and their presence was related to pathological size (<em>P</em> &lt; 0.01), the presence of peritumoral vascular invasion (<em>P</em> &lt; 0.001), and positive lymph nodes (<em>P</em> &lt; 0.005) but not menopausal status. At a median follow-up of 76 months (range 34–108) 107 patients had relapsed with distant metastases. 48% (43 of 89) of these patients had micrometastases initially compared with 25% (64 of 261) who did not (<em>P</em> &lt; 0.005). The test predicts for relapse in bone (<em>P</em> &lt; 0.01) and other distant sites excluding bone (<em>P</em> &lt; 0.001) and is associated with a shorter overall survival (<em>P</em> &lt; 0.005). We conclude that the detection of micrometastases signals a high likelihood of early relapse and decreased survival in breast cancer.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90413-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12943912","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 201
Left handedness is uncommon in breast cancer patients 左撇子在乳腺癌患者中并不常见
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90448-M
H. Olsson , C. Ingvar
{"title":"Left handedness is uncommon in breast cancer patients","authors":"H. Olsson ,&nbsp;C. Ingvar","doi":"10.1016/0277-5379(91)90448-M","DOIUrl":"10.1016/0277-5379(91)90448-M","url":null,"abstract":"<div><p>Left handedness was found to be significantly less common among patients with breast cancer in southern Sweden (1.5%) than among a female referent population (5%) (<em>P</em>&lt;0.0025). The findings lend support to theories suggesting that hormonal factors in early life are of importance both for handedness and for the risk of breast cancer.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90448-M","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12944349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 30
Low-grade follicular lymphomas: Analysis of prognosis in a series of 281 patients 低级别滤泡性淋巴瘤:281例患者预后分析
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90425-D
Pierre Soubeyran , Houchingue Eghbali , Françoise Bonichon , Monique Trojani , Pierre Richaud , Bernard Hœrni
{"title":"Low-grade follicular lymphomas: Analysis of prognosis in a series of 281 patients","authors":"Pierre Soubeyran ,&nbsp;Houchingue Eghbali ,&nbsp;Françoise Bonichon ,&nbsp;Monique Trojani ,&nbsp;Pierre Richaud ,&nbsp;Bernard Hœrni","doi":"10.1016/0277-5379(91)90425-D","DOIUrl":"10.1016/0277-5379(91)90425-D","url":null,"abstract":"<div><p>From 1963 to 1988, 281 patients with newly diagnosed follicular lymphomas were treated and followed at the Foundation Bergonié. Distribution of stages was: 72 I, 61 II, 83 III and 65 IV. Within stage III, two subgroups were retrospectively defined: stages III<sub>1</sub> (32 cases) included patients with less than 8 involved sites, only 1 or 2 above diaphragm, and no spleen or mediastinal enlargement. Stage III<sub>2</sub> (51 cases) included the remaining stage III cases. Median follow-up was 9 years. Complete remission (CR) rate was 82%. 10-year overall survival (OS) and time to treatment failure (TTF) rates were, respectively 38% and 29.5%. 10-year time to relapse (TTR) rate was 36%. Statistical analyses showed concordant results with two main prognostic factors: age (<span><math><mtext>&lt;60</mtext><mtext>&gt;60</mtext></math></span>) and stage (I to III<sub>1</sub>/III<sub>2</sub> and IV). Age was the most important factor for OS analysis and stage for CR and TTR analysis. This leads to only three prognostic groups with different outcome. The first includes younger patients (&lt;60 years) with limited stages (≤III<sub>1</sub>); the second, patients either older than 60 or with advanced stages; the last, elderly patients with advanced stages. CR rates of these three groups were, respectively 97%, 75% and 57%. 10-year OS were, respectively 73.5%, 27% and 0%; 10-year TTR were 54%, 22% and 0%. These results have lead to data which are easy to handle and which can help to establish a rationale for further prospective trials.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90425-D","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12945226","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 58
Mitoxantrone in malignant pleural mesothelioma: A study by the EORTC lung cancer cooperative group 米托蒽醌治疗恶性胸膜间皮瘤:EORTC肺癌合作组的研究
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90430-L
Frans J.M. van Breukelen , Karin Mattson , Giuseppe Giaccone , Nico van Zandwijk , Hans T. Planteydt , Anne Kirkpatrick , Otilia Dalesio
{"title":"Mitoxantrone in malignant pleural mesothelioma: A study by the EORTC lung cancer cooperative group","authors":"Frans J.M. van Breukelen ,&nbsp;Karin Mattson ,&nbsp;Giuseppe Giaccone ,&nbsp;Nico van Zandwijk ,&nbsp;Hans T. Planteydt ,&nbsp;Anne Kirkpatrick ,&nbsp;Otilia Dalesio","doi":"10.1016/0277-5379(91)90430-L","DOIUrl":"10.1016/0277-5379(91)90430-L","url":null,"abstract":"<div><p>46 patients with malignant pleural mesothelioma were entered in a phase II study of mitoxantrone 14 mg/m<sup>2</sup> every 3 weeks. Histology was confirmed by a pathology panel. None of the patients had received previous chemotherapy. Toxicity was mainly mild gastrointestinal and haematological side-effects. Out of 34 patients evaluated for response, only 1 partial response was recorded. Mitoxantrone at this dose and schedule has marginal activity in malignant mesothelioma.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90430-L","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12945228","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 46
The use of interferon in renal cell carcinoma 干扰素在肾细胞癌中的应用
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90585-2
Hyman B. Muss
{"title":"The use of interferon in renal cell carcinoma","authors":"Hyman B. Muss","doi":"10.1016/0277-5379(91)90585-2","DOIUrl":"10.1016/0277-5379(91)90585-2","url":null,"abstract":"<div><p>Metastatic renal cell carcinoma remains an incurable disease and current modalities can only offer major palliation to a small percentage of patients. Since treatment is palliative, choice and type of therapy must be carefully considered and reconciled with patient desires. When possible, patients should be offered participation in a clinical trial. For patients choosing progestin therapy, treatment with interferon (IFN) or other biological response modifiers can be instituted at the time of progestin failure. Those patients who have slow tumour progression and maintain a high quality of life can be observed without continued progestin therapy. Although pretreatment characteristics predict response to biologicals, no pretreatment characteristic should preclude an individual patient from a trial of IFN therapy. Whether high-dose interleukin-2 (IL-2), IL-2/lymphocyte-activated killer cells, or IL-2/IFN are superior to IFN alone is uncertain, but clinical trials currently underway should help resolve these issues.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90585-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12888266","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Resistance modification by PSC-833, a novel non-immunosuppressive cyclosporin A 新型非免疫抑制性环孢素a PSC-833的耐药修饰
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90435-G
Peter R. Twentyman, Norman M. Bleehen
{"title":"Resistance modification by PSC-833, a novel non-immunosuppressive cyclosporin A","authors":"Peter R. Twentyman,&nbsp;Norman M. Bleehen","doi":"10.1016/0277-5379(91)90435-G","DOIUrl":"10.1016/0277-5379(91)90435-G","url":null,"abstract":"<div><p>A novel non-immunosuppressive cyclosporin A, PSC-833, has been tested for its ability to circumvent resistance to doxorubicin, vincristine and colchicine in human and murine multidrug resistantant (MDR) cell lines. This compound is shown to be a highly potent resistance modifier, being 7–10-fold more potent than the parent compound, cyclosporin A, whilst approximately equal to cyclosporin A in the growth inhibitory effects of compound alone. Reversal of the P-glycoprotein-associated MDR drug accumulation defect is a major component of resistance reversal for PSC-833, as it is for cyclosporin A.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90435-G","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12978748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 117
Treatment of Ph1-positive chronic myelogenous leukaemia with recombinant interferon alfa-2b: A case report of complete cytogenetic response 重组干扰素α -2b治疗ph1阳性慢性髓性白血病:完全细胞遗传学应答一例报告
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90565-U
Shigeru Shirakawa , Tohru Kobayashi , Kazuhiro Nishii , Kenkichi Kita
{"title":"Treatment of Ph1-positive chronic myelogenous leukaemia with recombinant interferon alfa-2b: A case report of complete cytogenetic response","authors":"Shigeru Shirakawa ,&nbsp;Tohru Kobayashi ,&nbsp;Kazuhiro Nishii ,&nbsp;Kenkichi Kita","doi":"10.1016/0277-5379(91)90565-U","DOIUrl":"10.1016/0277-5379(91)90565-U","url":null,"abstract":"<div><p>A STUDY was undertaken in which eight patients aged 22 to 80 years with Ph<sup>1</sup>-positive chronic myelogenous leukaemia (CML) were treated with interferon alfa-2b at an initial dose of 4 million units (MU)/m<sup>2</sup> per day.</p><p>One patient in accelerated phase was pretreated with vindesine and prednisone, and showed an increase in white blood cell count during interferon treatment. In addition, one of the seven patients in chronic phase, who was previously untreated, dropped out because of skin eruption. According to the response criteria of Alimena <em>et al.</em> [1], three of the other six patients in chronic phase achieved haematological response (two complete, one partial) and two had cytogenetic improvements (one complete, one minor).</p><p>Adverse effects included fever (six patients), malaise (two), anorexia (one), delirium (one), liver disorder (two) and skin eruption (one).</p><p>We present here the pre-treatment features and clinical course of a patient who achieved complete cytogenetic response (CCR). A 32-year-old female patient, admitted to hospital because of marked hepatosplenomegaly (spleen 11 cm under the navel) and anaemia, was diagnosed as having Ph<sup>1</sup>-positive CML and treated with interferon alfa-2b 6 MU/body daily for 4 months and twice weekly thereafter. Her pretreatment blood cell counts were as follows: red blood cells 2.17 × 10<sup>6</sup>/μL; haemoglobin 6.6 g/dL; white blood cells (WBC) 206,700/μL; and platelets 610 × 10<sup>3</sup>/μL.</p><p>The patient achieved complete haematological response [1] at the 32nd week of interferon administration, together with resolution of hepatosplenomegaly.</p><p>Cytogenetic and molecular biological analyses revealed partial suppression of the Ph<sup>1</sup> chromosome at the 38th week (75% Ph<sup>1</sup>-positive) and complete cytogenetic response (CCR, 0% Ph<sup>1</sup>-positive) at the 140th week of interferon treatment.</p><p>In conclusion, long-term administration of interferon alfa-2b alone induced complete suppression of the Ph<sup>1</sup> chromosome in one patient with Ph<sup>1</sup>-positive CML, and the duration of this CCR is more than 4 months. The combination of alpha interferon with other treatments in order to enhance cytogenetic improvement should be investigated.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90565-U","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76824858","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Low-power laserthermia for the treatment of small hepatocellular carcinoma 小肝细胞癌的低功率激光治疗
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90429-H
Guan-Tarn Huang , Teh-Hong Wang , Jin-Chuan Sheu , Norio Daikuzono , Juei-Low Sung , Mu-Zong Wu , Ding-Shinn Chen
{"title":"Low-power laserthermia for the treatment of small hepatocellular carcinoma","authors":"Guan-Tarn Huang ,&nbsp;Teh-Hong Wang ,&nbsp;Jin-Chuan Sheu ,&nbsp;Norio Daikuzono ,&nbsp;Juei-Low Sung ,&nbsp;Mu-Zong Wu ,&nbsp;Ding-Shinn Chen","doi":"10.1016/0277-5379(91)90429-H","DOIUrl":"10.1016/0277-5379(91)90429-H","url":null,"abstract":"<div><p>Laserthermia by a novel interstitial probe adapted to low power Nd-YAG laser machine was used to treat small hepatocellular carcinoma (HCC). The set condition was 43–45°C in thermocouple with power of 2–3 W and the duration 20–30 min. In the 5 cases studied, 1 had a good result with total necrosis of the tumour without recurrence in 16 months. 1 died of liver failure 2.5 months later although death was not related to the procedure. 1 patient died of progressive disease 18 months later. The remaining 2 had recurrent tumours 5 and 12 months later, although the treated small tumours showed good response. Histological examination showed cell degeneration and necrosis. It is concluded that laserthermia is potentially useful in the treatment of the patients with small HCC.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90429-H","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12829435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 57
Lung cancer therapy in the elderly 老年人肺癌的治疗
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90410-F
J. Festen
{"title":"Lung cancer therapy in the elderly","authors":"J. Festen","doi":"10.1016/0277-5379(91)90410-F","DOIUrl":"10.1016/0277-5379(91)90410-F","url":null,"abstract":"","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90410-F","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12829458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
A meta-analysis of reported correlations between prognostic factors in breast cancer: Does axillary lymph node metastasis represent biology or chronology? 乳腺癌预后因素相关性的荟萃分析:腋窝淋巴结转移代表生物学还是年代学?
European Journal of Cancer and Clinical Oncology Pub Date : 1991-12-01 DOI: 10.1016/0277-5379(91)90418-D
Indraneel Mittra , Kenneth D. MacRae
{"title":"A meta-analysis of reported correlations between prognostic factors in breast cancer: Does axillary lymph node metastasis represent biology or chronology?","authors":"Indraneel Mittra ,&nbsp;Kenneth D. MacRae","doi":"10.1016/0277-5379(91)90418-D","DOIUrl":"10.1016/0277-5379(91)90418-D","url":null,"abstract":"<div><p>A statistical overview of published results on correlations between various prognostic factors in breast cancer was undertaken. A distinction was made between clinical (or anatomical) prognostic factors—namely, axillary lymph node status and tumour size—and eight different biological prognostic factors. The latter included: tumour grade, oestrogen and progesterone receptor status, thymidine labelling index, DNA ploidy, S-phase fraction, epidermal growth factor receptor expression and c-<em>erb</em>B-2 gene amplification (or overexpression). 139 articles were eligible for review which reported a total of 432 individual correlations. A simple form of meta-analysis was employed: the counting method, in which the number of studies achieving a statistically significant correlation or not were counted. For each possible correlation examined, the proportion of studies showing a statistically significant correlation was calculated and an exact binomial 99% confidence interval determined for that proportion. If the 99% confidence interval included 5% (the proportion of correlations that would be expected to be statistically significant if the null hypothesis was true), it was taken as failing to exclude the null hypothesis of a zero correlation, while if it excluded 5% it was taken as rejecting the null hypothesis of a zero correlation. A broad agreement was found among published reports on the existence of a statistically significant correlation between the various biological prognostic factors in breast cancer. Of the 20 correlation examined, 18 had a 99% confidence interval excluding 5%, thus rejecting the null hypothesis of a zero correlation. On the other hand, a completely different result was obtained when reports on possible correlations between lymph node status and tumour size on the one hand and the eight biological prognostic factors on the other were analysed. Of the 16 correlations examined, 13 had a 99% confidence interval including 5%, failing to reject the null hypothesis of a zero correlation. These observations suggest the hypothesis that the prognostic influence of node status and tumour size cannot be explained by an analysis of the biology of breast cancer; and is compatible with the contention that axillary node status is merely a reflection of the relative chronological age of breast cancer.</p></div>","PeriodicalId":11925,"journal":{"name":"European Journal of Cancer and Clinical Oncology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1991-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0277-5379(91)90418-D","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12998574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 59
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