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1.
Eur J Cancer Care (Engl) ; 21(5): 650-60, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22339814

ABSTRACT

This study explored the perceived effects of an aesthetic care/wig programme for Italian women suffering from chemotherapy-induced alopecia. Despite advances in the treatment of many side effects of chemotherapy, alopecia remains difficult to resolve. Literature suggests that patients' reactions to alopecia and camouflaging strategies depend on their gender, individual characteristics, social context, and culture. A qualitative study was designed involving 20 patients from Sicily (Italy), who participated in an aesthetic care programme. Data were collected through semi-structured interviews, and an Interpretative Phenomenological Analysis was conducted on transcriptions. Our findings showed that, even if expected, alopecia is experienced as a traumatic event that challenges a woman's femininity, as reported by many other enquiries. Diverging from other studies, the wig is perceived as very helpful, since it camouflages baldness and reduces the 'sick aspect' related to alopecia. Patients consider their wig to be a 'friend', and it appears that through the aesthetic care programme they received support they otherwise would not have sought. We conclude that aesthetic care/wig programmes can help women affected by alopecia to cope with cancer 'stigma', especially in those rural contexts where psychosocial programmes are not frequently embraced by patients due to environmental and cultural barriers.


Subject(s)
Alopecia/psychology , Alopecia/rehabilitation , Hair , Adaptation, Psychological , Adult , Aged , Alopecia/chemically induced , Antineoplastic Agents/adverse effects , Esthetics , Female , Humans , Italy , Middle Aged , Neoplasms/drug therapy , Neoplasms/psychology , Qualitative Research , Stress, Psychological/prevention & control , Surveys and Questionnaires
2.
Clin Ter ; 157(3): 283-99, 2006.
Article in Italian | MEDLINE | ID: mdl-16900856

ABSTRACT

Treatment of gastrointestinal stromal tumors (GIST) has been revolutioned by the recently discovered molecular mechanism responsible for the oncogenesis of this disease. In addition, due to the rapid progress at molecular and clinical level observed in the last few years, there is a need to review the current state of the art in order to delineate appropriate guidelines for the optimal management of these tumors. A panel of experts from several specialities, including medical oncology, surgery, pathology, molecular biology and imaging, were invited to participate in a meeting to present and discuss a number of pre-selected questions, and to achieve a consensus according to the categories of the National Comprehensive Cancer Network (NCCN) and the Standard Options Recommandations (SOR) of the French Federation of Cancer Centers. Generally, consensus points were from categories 2A of the NCCN and B2 of the SOR. Conventional histologic examination with immunohistochemistry for CD117, CD34, SMA, S-100 and desmin is considered standard. Molecular analysis for the identification of KIT and PDGFRA mutation may be indicated in CD117-negative GIST. Complete tumor resection with negative margins is the optimal surgical treatment. Adjuvant imatinib should be considered an experimental approach. Neoadjuvant imatinib is also experimental, although its use may be justified in unresectable or marginally resectable GIST. Imatinib should be started in metastatic or recurrent disease, and should be continued until progressive disease or drug intolerance. In these cases, sunitinib can be used. The optimal criteria for the assessment and monitoring of GIST undergoing imatinib therapy are not well known, but they should include reduction in tumor size and disease stabilization, as well as reduction of tumor density on CT scan and metabolic activity on PET scan.


Subject(s)
Gastrointestinal Stromal Tumors/diagnosis , Gastrointestinal Stromal Tumors/therapy , Antineoplastic Agents/therapeutic use , Benzamides , Combined Modality Therapy , Decision Trees , Disease Progression , Humans , Imatinib Mesylate , Neoplasm Recurrence, Local , Piperazines/therapeutic use , Practice Guidelines as Topic , Pyrimidines/therapeutic use
3.
J Chemother ; 15(4): 323-8, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12962359

ABSTRACT

Surgical sepsis is still too frequent (the thirteenth cause of death in the U.S.) with an estimated cost of 5-10 billion dollars. Since the early 1990s antibiotic resistance has become a serious public health problem, with a relevant increase in nosocomial gram-positive infections. The oxazolidinones, a new class of antibiotics acting on bacterial synthesis at a very early stage, were first commercialized in 1987, and linezolid was the first antibiotic in this class registered for clinical use. This new molecule has been shown to be effective in a variety of aerobic and anaerobic infections (both nosocomial and community-acquired), especially those due to gram-positive agents. Linezolid has complete bioavailability in parenteral and oral administration, is well tolerated and shows little toxicity, thus favoring a shortened hospital stay, improving the patient's quality of life and reducing social costs. Oxazolidinones may be considered the first choice in the treatment of resistant gram-positive infections.


Subject(s)
Anti-Bacterial Agents/pharmacology , Gram-Positive Bacterial Infections/drug therapy , Oxazolidinones/pharmacology , Postoperative Complications/drug therapy , Sepsis/drug therapy , Acetamides/pharmacology , Administration, Oral , Anti-Bacterial Agents/therapeutic use , Biological Availability , Drug Resistance, Microbial , Humans , Infusions, Intravenous , Linezolid , Oxazolidinones/therapeutic use , Postoperative Complications/microbiology , Sepsis/microbiology
5.
Cytometry ; 42(1): 27-34, 2000 Feb 15.
Article in English | MEDLINE | ID: mdl-10679740

ABSTRACT

In order to determine retrospectively the impact of some cytometric and immunohistochemical parameters on the overall survival of gastric cancer patients treated with surgery alone, paraffin-embedded tumor samples from 137 gastric carcinoma patients undergoing curative resection from 1987-1993 were analyzed by flow cytometry (FCM) and immunohistochemistry (p53, c-erbB-2, and PCNA expression). FCM-derived parameters were DNA ploidy and fraction of S-phase cells (SPF). Multiple regression analysis was applied to determine the prognostic significance of the conventional clinicopathologic findings together with the flow cytometric and immunohistochemical parameters on overall survival. When all parameters were entered simultaneously into the Cox regression model, stage and DNA ploidy (DNA index >1.35) clearly emerged as the only independent prognostic factors. When the stages were analysed separately, the independent prognostic factors resulted DNA ploidy in early stages (I-II) and grading in stage IIIA tumors. For stage IIIB tumors, no independent prognostic factor was found. These results indicate that the DNA ploidy pattern is a valuable predictor of survival in curatively resected gastric cancer patients, especially when less advanced tumors are taken into consideration.


Subject(s)
Carcinoma/surgery , Stomach Neoplasms/surgery , Adult , Aged , Aged, 80 and over , Carcinoma/metabolism , Carcinoma/pathology , DNA/analysis , Female , Flow Cytometry , Follow-Up Studies , Humans , Immunohistochemistry , Male , Middle Aged , Neoplasm Staging , Ploidies , Proliferating Cell Nuclear Antigen/analysis , Receptor, ErbB-2/analysis , Regression Analysis , Retrospective Studies , Stomach Neoplasms/metabolism , Stomach Neoplasms/pathology , Survival Analysis , Tumor Suppressor Protein p53/analysis
6.
J Exp Clin Cancer Res ; 19(4): 467-9, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11277324

ABSTRACT

Treatment with 5-fluorouracil (5-FU) or recombinant interferon-gamma (IFN), alone or in combination, was found to increase carcinoembryonic antigen (CEA) expression in several carcinoma cell lines. In this study we examined the in vitro effect of these agents on CEA expression of tumor cells, obtained from a patient operated for rectal cancer. The results showed that exposure of cancer cells to 5-FU or to IFN resulted in increased CEA levels in terms of percentage of CEA-positive cells and mean fluorescence values, as indicated by FACS analysis. However, drug combination did not induce CEA expression higher than that provided by single agents alone. Treatment with 5-FU or with IFN produced a reduction of the total number of viable cells. Moreover, Western blot analysis revealed that exposure of cancer cells to each drug was followed by a substantial increase of the total cellular CEA content. On the contrary, 5-FU in combination with IFN did not increase the expression of the antigen more than that obtained by single agents. Noteworthy, exposure of CEA-negative cells from adjacent normal rectal tissue to both agents alone or in combination, did not result in CEA induction. In conclusion, the present results suggest new approaches aimed at (a) increasing the sensitivity of diagnostic procedures based on detection of CEA-positive tumor cells; (b) facilitating the recognition of CEA-positive cancer cells by immune responses induced by anti-CEA peptide vaccines.


Subject(s)
Carcinoembryonic Antigen/metabolism , Fluorouracil/pharmacology , Interferon-gamma/pharmacology , Rectal Neoplasms/metabolism , Adult , Carcinoembryonic Antigen/blood , Female , Flow Cytometry , Humans , Recombinant Proteins , Rectal Neoplasms/pathology , Rectal Neoplasms/surgery , Tumor Cells, Cultured
7.
J Chemother ; 11(6): 573-6, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10678802

ABSTRACT

The incidence of infections in general surgery is related to different factors. Cost-benefit analysis of antimicrobic prophylaxis is positive, even though incorrect use may be even dangerous (development of resistance and/or superinfections, for instance). The authors report data on a study concerning a total of 316 patients divided into two series, who had antimicrobic prophylaxis before a surgical operation. 274 patients out of 316 (or 86.7%) had an ultra-short (one-shot-only) or short (<24 hours) prophylaxis, 42 (13.3%) standard (>24 hours). The operations performed were classified following class of contamination, i.e. I (clean), II (potentially contaminated), III (contaminated). Antibiotics used were ceftizoxime, cefepime, ceftriaxone, piperacillin and gentamicin in combination. A total of 16 postoperative infections was observed (5%); 11 of these 16 belonged to class III operations. Escherichia coli and Staphylococcus aureus were isolated in most of the infected wounds. The data confirm what is reported in the literature. The authors conclude that a preoperative single-shot 3rd or 4th generation cephalosporin reduces the incidence of wound infections in clean and clean-contaminated surgery.


Subject(s)
Antibiotic Prophylaxis , Cephalosporins/administration & dosage , Surgical Wound Infection/classification , Surgical Wound Infection/prevention & control , Cost-Benefit Analysis , Humans , Incidence , Prognosis , Risk Assessment , Surgical Procedures, Operative/adverse effects , Surgical Wound Infection/microbiology
9.
J Surg Oncol Suppl ; 3: 154-7, 1993.
Article in English | MEDLINE | ID: mdl-7684913

ABSTRACT

Extrahepatic bile duct (EHBD) tumors often become symptomatic in an advanced stage when curative resection is seldom possible. In a group of 111 patients, 7 (6.3%) received no treatment, 32 (28.8%) underwent non-operative biliary drainage (NOD), and 72 (64.8%) underwent surgical exploration. Radical resection was possible in only 25 cases (34.7%); 14 patients (19.4%) underwent a biliary digestive bypass (BDB), 15 (20.8%) received a transtumoral biliary prosthesis (TBP), and 18 (25.0%) an external biliary drainage (EBD). Average survival rates were: 6.5 months after BDB, 4.0 months after TBP, and 2.8 months after EBD. In a second group of 2,066 patients with primary and secondary malignant obstruction of the upper EHBD, treated with the insertion of a Carey-Coons transhepatic transtumoral biliary prosthesis, the average survival was 4.3 months. The early morbidity rate was 0.6%. Obstruction of the prosthesis occurred in 91 patients (4.4%), and the late morbidity rate was 3.6%. Although EHBD tumor treatment results are generally poor, surgical exploration should be performed in all patients with acceptable surgical risk, and without evidence of disseminated disease. When resection of the tumor is not feasible, we favor the use of a BDB or of a biliary prosthesis over that of an external drainage. In poor risk cases or cases with evidence of disseminated disease, we prefer the placement of an internal prosthesis (PTBD or endoscopic.


Subject(s)
Bile Duct Neoplasms/surgery , Cholestasis, Extrahepatic/surgery , Palliative Care , Adult , Aged , Aged, 80 and over , Anastomosis, Surgical , Bile Duct Neoplasms/complications , Bile Ducts/surgery , Catheterization/adverse effects , Catheterization/instrumentation , Cholestasis, Extrahepatic/etiology , Drainage , Equipment Failure , Female , Humans , Jejunum/surgery , Male , Middle Aged , Prostheses and Implants/adverse effects , Prosthesis Failure , Survival Rate
10.
Ann Oncol ; 2(10): 759-64, 1991.
Article in English | MEDLINE | ID: mdl-1801883

ABSTRACT

Twelve patients with metastatic colorectal cancer received alternating cycles of low immunomodulating doses of alpha-IFN + 5-Fluorouracil (5-FU) or 5-FU alone. Hematological, biochemical and physical evaluation showed that both treatment cycles were well tolerated. However, transient fever and moderate flu-like symptoms were observed following alpha-IFN administration. Treatment with 5-FU alone produced long-lasting inhibition of CD8+ T lymphocytes, but did not depress NK activity (NKA). Combined treatment with alpha-IFN produced a short-term increase of NKA and antagonized the effect of 5-FU on CD8+ cells on day 5 of the cycle. Parallel studies on in vitro models showed antiproliferative effects of 5-FU on PHA-stimulated MNC and confirmed the preferential inhibition of CD8+ cells. Pretreatment with alpha-IFN did not reverse the effect of 5-FU on CD8+ lymphocytes, but partially protected MNC from the toxic effects of the drug. This was presumably due to the cytostatic effects induced by alpha-IFN on MNC before exposure to the cycle-specific antineoplastic agent. This investigation suggests that alpha-IFN could play a positive role in immuno-chemotherapy of colorectal cancer through multiple mechanisms not entirely related to direct antitumor effects of the agent.


Subject(s)
Colorectal Neoplasms/therapy , Fluorouracil/therapeutic use , Interferon-alpha/therapeutic use , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cell Division/drug effects , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/immunology , Dose-Response Relationship, Drug , Drug Administration Schedule , Fluorouracil/administration & dosage , Fluorouracil/adverse effects , Humans , Immunity, Innate/immunology , Immunotherapy , Interferon alpha-2 , Interferon-alpha/administration & dosage , Killer Cells, Natural/drug effects , Killer Cells, Natural/immunology , Leukocytes, Mononuclear/drug effects , Recombinant Proteins , Tumor Cells, Cultured
12.
Minerva Chir ; 44(20): 2143-8, 1989 Oct 31.
Article in Italian | MEDLINE | ID: mdl-2622551

ABSTRACT

The authors dealt with 37 patients suffering from advanced liver cirrhosis with ascites. Eighteen patients out of them underwent Denver peritoneum-jugular shunt as a first choice procedure, the other 19 patients underwent lymphovenous anastomosis. The extremely advanced hepatic damage and the general conditions of these patients discouraged us to perform a portocaval shunt. In the 19 patients who underwent lymphovenous anastomosis we had no mortality rate. Two patients showed post-operative complications: 1 patient complained which hoarseness regressed in 5 months and the other patient suffered from a spleno-mesenteric-portal thrombosis with digestive hemorrhage from gastro-esophageal varices. In 6 patients out of 19 who underwent lymphovenous anastomosis, we did not obtain any immediate positive effects on ascites. In 4 patients, after 3 months, the ascites came back ingravescent and in the other 9 patients the positive effects on ascites were still evident after 1 year. Despite failure to obtain very comforting results, they suggest to employ this technique at any rate, as the first procedure, to make ascites more "manageable", because of its safety.


Subject(s)
Ascites/surgery , Jugular Veins/surgery , Thoracic Duct/surgery , Anastomosis, Surgical , Ascites/physiopathology , Female , Humans , Male , Middle Aged
13.
J Chemother ; 1(2): 128-35, 1989 Apr.
Article in English | MEDLINE | ID: mdl-2732781

ABSTRACT

Twelve patients with advanced colorectal cancer were subjected to alternating cycles of treatment with low immunomodulating doses of recombinant alpha-interferon (alpha IFN) + 5-fluorouracil (5FU) or with 5FU alone. Hematological, biochemical and physical evaluation of the patients showed that alpha IFN + 5FU cycles were well tolerated like 5FU alone, except for modest and transient fever following alpha IFN administration. At hematological nadir (day 15-18 of each cycle) lymphocytopenia and granulocytopenia were more pronounced during alpha IFN + 5FU than 5FU cycles. No difference was found for platelet nadir. At the beginning of each cycle complete leukocyte recovery was observed in all cases. Platelet recovery was also complete, although counts were higher after alpha IFN + 5FU than after 5FU alone. Clinical results showed 1 complete remission, 1 partial remission, 5 stable disease and 5 progressive disease. These data point out that low doses of alpha IFN can be safely associated with 5FU. However further studies are required to establish the possible therapeutic value of alpha IFN-mediated immunomodulation for immunochemotherapy of colorectal cancer.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Colonic Neoplasms/drug therapy , Fluorouracil/adverse effects , Interferon Type I/adverse effects , Leukopenia/chemically induced , Rectal Neoplasms/drug therapy , Adult , Aged , Female , Humans , Male , Middle Aged
14.
Minerva Med ; 80(4): 363-6, 1989 Apr.
Article in Italian | MEDLINE | ID: mdl-2725937

ABSTRACT

Personal experience of 31 patients suffering from intractable ascites due to advanced liver cirrhosis between 1978 and 1987 is reported. Seventeen patients were selected for a peritoneojugular shunt: in 3 patients the Le Veen shunt was performed and in 14 the Denver shunt was preferred. The high postoperative morbidity and mortality due to liver failure, DIC, hepatorenal syndrome, bleeding, sepsis and cerebral thrombosis is pointed out. Careful selection of patients to be submitted to this surgical procedure is essential because of the high morbidity due to ascites reinfusion. DIC has to be diagnosed as soon as possible and, when severe, the prompt interruption of the peritoneojugular shunt is mandatory.


Subject(s)
Peritoneovenous Shunt/methods , Adult , Aged , Ascites/complications , Ascites/mortality , Ascites/surgery , Female , Humans , Liver Cirrhosis/complications , Liver Cirrhosis/mortality , Liver Cirrhosis/surgery , Male , Middle Aged , Peritoneovenous Shunt/adverse effects , Peritoneovenous Shunt/instrumentation , Postoperative Complications/etiology , Postoperative Complications/mortality , Postoperative Complications/prevention & control
16.
J Surg Oncol ; 35(4): 266-8, 1987 Aug.
Article in English | MEDLINE | ID: mdl-3302542

ABSTRACT

A controlled study of short-term prophylaxis with cefuroxime was performed on a group of 52 patients with colorectal neoplasms who underwent elective surgery. The patients were divided into two groups, A and B. Group A received the antibiotic immediately before surgery, intraincisionally and immediately after the end of operation; group B was treated only postoperatively. Each patient received a total of 5,250 mg of cefuroxime. Wound sepsis was demonstrated in 11.5% of cases of group A and 23.0% of group B (P less than 0.01); another type of sepsis was observed in 34% of group A and 11.5% of group B (P less than 0.001). There was no difference in the operative mortality in the two groups.


Subject(s)
Cefuroxime/therapeutic use , Cephalosporins/therapeutic use , Colonic Neoplasms/drug therapy , Premedication , Rectal Neoplasms/drug therapy , Clinical Trials as Topic , Colonic Neoplasms/complications , Colonic Neoplasms/surgery , Humans , Intraoperative Care , Middle Aged , Postoperative Care , Rectal Neoplasms/complications , Rectal Neoplasms/surgery , Surgical Wound Infection/epidemiology , Surgical Wound Infection/prevention & control , Time Factors
17.
J Int Med Res ; 15(4): 245-50, 1987.
Article in English | MEDLINE | ID: mdl-3653502

ABSTRACT

The antibiotic erythromycin lactobionate given intravenously acts almost exclusively on Gram-positive bacteria. Even at high plasma and tissue concentrations there is an almost total absence of side-effects. It could be considered, therefore, as first choice in the treatment of patients with infectious respiratory diseases. Most of the 40 patients admitted to the present study were elderly and all had either acute or chronic and becoming acute respiratory disease. Their clinical symptoms and levels of phlogosis improved on treatment with erythromycin lactobionate without any interruption of therapy due to side-effects and toxicity. The absence of unfavourable pharmacological interactions further enhances the usefulness of the drug. In view of the excellent response to monotherapy with erythromycin lactobionate and the few groups of resistant bacteria found in those cases when it was possible to check, it was not considered necessary to investigate any synergistic association with other antibiotics. It can be concluded, therefore, that therapy with erythromycin lactobionate in patients with infective respiratory disease is favourable and patients show excellent tolerability.


Subject(s)
Erythromycin/analogs & derivatives , Respiratory Tract Infections/drug therapy , Adult , Aged , Bacteria/isolation & purification , Erythromycin/administration & dosage , Erythromycin/adverse effects , Erythromycin/therapeutic use , Female , Humans , Infusions, Intravenous , Male , Middle Aged
18.
Ital J Surg Sci ; 17(1): 21-6, 1987.
Article in English | MEDLINE | ID: mdl-2884197

ABSTRACT

A multicenter double-blind clinical trial was undertaken to evaluate the efficacy of a short-term somatostatin treatment versus a short-term vasopressin treatment on acute hemorrhage from esophageal varices in patients with liver cirrhosis and portal hypertension. Forty-nine patients with massive hemorrhage and endoscopic diagnosis of bleeding esophageal varices completed the study. Patients were randomly assigned to somatostatin treatment (24 patients: 250 micrograms/hr i.v. for 48 hrs) or vasopressin treatment (25 patients: 0.1 U/min i.v. for 48 hrs). The Sengstaken-Blakemore tube was utilized, when needed, for a six hour period. In case of failure the patients were crossed-over to the other treatment. Patients in whom the bleeding stopped at 48 hrs, were randomly assigned to somatostatin (250 micrograms/hr i.v.) or placebo for seven days. Bleeding stopped in 68% of patients treated with somatostatin and in 28% of patients treated with vasopressin (p less than 0.0013). Mortality rate was lower, but not significantly so, in the somatostatin group compared to the vasopressin group. No differences were noted between somatostatin and placebo in preventing bleeding recurrences. These data suggest that somatostatin, when combined if necessary with a 6 hour period of balloon tamponade, is more effective than vasopressin at low doses in controlling severe hemorrhage from esophageal varices in patients with liver cirrhosis and portal hypertension. A clinical use of somatostatin seems to be indicated in these patients.


Subject(s)
Esophageal and Gastric Varices/drug therapy , Gastrointestinal Hemorrhage/drug therapy , Somatostatin/therapeutic use , Clinical Trials as Topic , Double-Blind Method , Humans , Random Allocation , Time Factors , Vasopressins/therapeutic use
19.
Arch Surg ; 121(7): 833-5, 1986 Jul.
Article in English | MEDLINE | ID: mdl-2872874

ABSTRACT

In a randomized, double-blind placebo-controlled clinical trial, the effect of ranitidine was compared with the effect of somatostatin in the control of massive gastrointestinal tract bleeding. Ninety-six patients completed the study. Rates of continuing bleeding and death, incidence of surgery, and blood transfusion requirements were not significantly different in the three treatment groups. Eighteen of the 96 patients presented with a visible vessel at endoscopy. In this group the percent of patients with continuing bleeding, mean transfusion requirements, and mortality were significantly higher than in patients without a visible vessel. Seven patients with a visible vessel underwent surgery and six survived; 11 patients underwent conservative measures and eight died. Ranitidine and somatostatin do not seem to alter the clinical course of patients with upper gastrointestinal tract hemorrhage.


Subject(s)
Gastrointestinal Hemorrhage/drug therapy , Ranitidine/therapeutic use , Somatostatin/therapeutic use , Adult , Aged , Blood Transfusion , Clinical Trials as Topic , Double-Blind Method , Endoscopy , Female , Gastrointestinal Hemorrhage/surgery , Gastrointestinal Hemorrhage/therapy , Humans , Infusions, Parenteral , Male , Middle Aged , Random Allocation , Ranitidine/administration & dosage , Recurrence , Somatostatin/administration & dosage
20.
J Surg Oncol ; 30(2): 113-5, 1985 Oct.
Article in English | MEDLINE | ID: mdl-4079424

ABSTRACT

A consecutive series of 100 patients affected by breast cancer and referred for surgical treatment were studied for the eventual spread of the tumour to the liver (echography, carcinoembryonic antigen [CEA], hepatic enzymes). Hepatic echography was positive in five cases: two also had bone and skin metastases at the time of diagnosis, and one was a case of remastectomy (these three patients died rather quickly of the disease); the remaining two patients are free of the disease 24 months after surgery and thus should be considered false-positive cases. Hepatic enzymes were not significant. The same was true for CEA except in nine cases with levels much greater than 20 ng/ml (six of these had early local and/or distant metastases). It is concluded that the usefulness of routine hepatic echography before locoregional treatment of breast cancer is rather limited. CEA much greater than 20 ng/ml may be useful prognostically.


Subject(s)
Liver Neoplasms/pathology , Alanine Transaminase/analysis , Aspartate Aminotransferases/analysis , Breast Neoplasms/surgery , Carcinoembryonic Antigen/analysis , Humans , Liver Neoplasms/enzymology , Liver Neoplasms/secondary , Prospective Studies
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