lewis-y-antigen and Rectal-Neoplasms

lewis-y-antigen has been researched along with Rectal-Neoplasms* in 2 studies

Other Studies

2 other study(ies) available for lewis-y-antigen and Rectal-Neoplasms

ArticleYear
Clinical evaluation of BR96 sFv-PE40 immunotoxin therapy in canine models of spontaneously occurring invasive carcinoma.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2005, Jan-15, Volume: 11, Issue:2 Pt 1

    The immunotoxin BR96 sFv-PE40 is an effective antitumor agent against human breast and lung carcinoma xenografts in rodents. This study was designed to (a) determine the frequency with which canine carcinoma cells express Lewis(y) (Le(y)) antigen, thereby identifying canine carcinoma types suitable for the clinical evaluation of BR96 sFv-PE40, and (b) determine the safety and efficacy of BR96 sFv-PE40 in a canine model of spontaneously occurring cancers for investigation of targeted therapy.. Carcinoma tissue samples were obtained from client-owned dogs presented for medical care. The tissues were assessed for Le(y) antigen expression using immunohistochemical methods. Dogs with tumors expressing Le(y) antigen were offered enrollment in a clinical trial to receive twice-weekly infusions of 4 to 12 mg/m(2) BR96 sFv-PE40. Clinical toxicity and response data were assessed at each treatment.. Twenty-two of 61 carcinomas evaluated were positive for Le(y) expression, including mammary, prostate, lung, and rectal carcinomas, and 12 dogs were enrolled in the clinical trial. The primary side effect was transient emesis. Partial responses or disease stabilization were noted in dogs with inflammatory mammary, bronchogenic, rectal, and tonsillar carcinoma. At least nine of the dogs developed antibodies to the immunotoxin after two to five infusions.. Although development of anti-BR96 sFv-PE40 antibodies limited the long-term effectiveness of this immunotoxin in dogs, rapid clinical responses in several aggressive canine carcinomas suggest the immunotoxin has utility for treatment of certain naturally occurring tumors and that its clinical evaluation for treatment of similar human carcinomas is warranted.

    Topics: Animals; Antibodies, Monoclonal; Dogs; Female; Immunotherapy; Immunotoxins; Lewis Blood Group Antigens; Lung Neoplasms; Male; Mammary Neoplasms, Experimental; Mice; Neoplasm Invasiveness; Prostatic Neoplasms; Recombinant Fusion Proteins; Rectal Neoplasms

2005
Expression of tumor-related antigens Lewis(a) Lewis(b), X, Y, Span-1 and CEA in relation to differentiation and prognosis in rectal adenocarcinomas.
    APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 1996, Volume: 104, Issue:11

    Expression of Le(a) (Lewis(a)), Le(b) (Lewis(b)), X (Lewis X), Y (Lewis Y), SPan-1 and CEA was detected by an immunohistochemical method using a panel of antibodies in paraffin-embedded materials from 45 rectal adenocarcinomas and the corresponding normal mucosa. The relationships between antigen expression and grade of differentiation and survival were analyzed. Compared to the expression in normal mucosa, the expression of Le(a) was decreased in tumors while the expression of Le(b), X, Y. SPan-1 and CEA was increased. The expression of Le(a) and SPan-1 was associated with the grade of differentiation (p = 0.0001 and p = 0.02, respectively). Positive expression of Le(a) and SPan-1 correlated with poor prognosis (p = 0.0001 and p = 0.002, respectively), but positive expression of Y predicated favorable prognosis (p = 0.01). Our findings indicate that some of the tumor-related antigens might provide information important for the diagnosis, determining histologic differentiation and prognosis in rectal adenocarcinomas.

    Topics: Adenocarcinoma; Antigens, Neoplasm; Carcinoembryonic Antigen; Cell Differentiation; Humans; Immunoenzyme Techniques; Intestinal Mucosa; Lewis Blood Group Antigens; Lewis X Antigen; Rectal Neoplasms

1996