摘要:
The present invention concerns prognostic markers associated with EGFR positive cancer. In particular, the invention concerns prognostic methods based on the molecular characterization of gene expression in paraffin-embedded, fixed tissue samples of EGFR-expressing cancer, which allow a physician to predict whether a patient is likely to respond well to treatment with an EGFR inhibitor.
摘要:
The present invention relates to a method of diagnosis and therapy of cancers expressing the HER2 receptor.The invention provides antibodies or fragments thereof that recognizes an epitope of a HER2 receptor truncated form, said epitope being defined by a sequence included in SEQ ID NO: 2.The invention also provides a method of cancer diagnosis, which comprises the detection of the presence of the HER2 receptor truncated form consisting of the amino acid sequence SEQ ID NO: 1 in a patient sample.
摘要翻译:本发明涉及一种诊断和治疗表达HER2受体的癌症的方法。 本发明提供识别HER2受体截短形式的表位的抗体或其片段,所述表位由SEQ ID NO:2所包含的序列定义。本发明还提供了一种癌症诊断方法,其包括检测存在 的由病人样品中的氨基酸序列SEQ ID NO:1组成的HER2受体截短形式。
摘要:
The present invention concerns prognostic markers associated with EGFR positive cancer. In particular, the invention concerns prognostic methods based on the molecular characterization of gene expression in paraffin-embedded, fixed tissue samples of EGFR-expressing cancer, which allow a physician to predict whether a patient is likely to respond well to treatment with an EGFR inhibitor.
摘要:
The present invention relates to a method of diagnosis and therapy of cancers expressing the HER2 receptor.The invention provides antibodies or fragments thereof that recognise an epitope of the HER2 receptor truncated form CTF-611, said epitope being defined by a sequence included in SEQ ID NO: 2, and that are capable of discriminating between CTF-611 and CTF-616 (represented by SEQ ID NO:7), preferably additionally capable of discriminating between CTF-611 and CTF-613 (represented by SEQ ID NO:6).The invention also provides a method of cancer diagnosis using the disclosed antibodies, which comprises the detection of the presence of the HER2 receptor truncated form consisting of the amino acid sequence SEQ ID NO: 1 in a patient sample.
摘要翻译:本发明涉及一种诊断和治疗表达HER2受体的癌症的方法。 本发明提供识别CTF-611截断的HER2受体的表位的抗体或其片段,所述表位由SEQ ID NO:2所包含的序列定义,并且能够区分CTF-611和CTF-616 (由SEQ ID NO:7表示),优选另外能够区分CTF-611和CTF-613(由SEQ ID NO:6表示)。 本发明还提供使用所公开抗体的癌症诊断方法,其包括检测患者样品中由氨基酸序列SEQ ID NO:1组成的HER2受体截短形式的存在。
摘要:
The present invention relates to a method of diagnosis and therapy of cancers expressing the HER2 receptor.The invention provides antibodies or fragments thereof that recognises an epitope of a HER2 receptor truncated form, said epitope being defined by a sequence included in SEQ ID NO: 2.The invention also provides a method of cancer diagnosis, which comprises the detection of the presence of the HER2 receptor truncated form consisting of the amino acid sequence SEQ ID NO: 1 in a patient sample.
摘要翻译:本发明涉及一种诊断和治疗表达HER2受体的癌症的方法。 本发明提供识别HER2受体截短形式的表位的抗体或其片段,所述表位由SEQ ID NO:2所包含的序列定义。本发明还提供了一种癌症诊断方法,其包括检测存在 的由病人样品中的氨基酸序列SEQ ID NO:1组成的HER2受体截短形式。
摘要:
The present invention relates to a method of diagnosis and therapy of cancers expressing the HER2 receptor.The invention provides antibodies or fragments thereof that recognise an epitope of the HER2 receptor truncated form CTF-611, said epitope being defined by a sequence included in SEQ ID NO: 2, and that are capable of discriminating between CTF-611 and CTF-616 (represented by SEQ ID NO:7), preferably additionally capable of discriminating between CTF-611 and CTF-613 (represented by SEQ ID NO:6).The invention also provides a method of cancer diagnosis using the disclosed antibodies, which comprises the detection of the presence of the HER2 receptor truncated form consisting of the amino acid sequence SEQ ID NO: 1 in a patient sample.
摘要翻译:本发明涉及一种诊断和治疗表达HER2受体的癌症的方法。 本发明提供识别CTF-611截断的HER2受体的表位的抗体或其片段,所述表位由SEQ ID NO:2所包含的序列定义,并且能够区分CTF-611和CTF-616 (由SEQ ID NO:7表示),优选另外能够区分CTF-611和CTF-613(由SEQ ID NO:6表示)。 本发明还提供使用所公开抗体的癌症诊断方法,其包括检测患者样品中由氨基酸序列SEQ ID NO:1组成的HER2受体截短形式的存在。
摘要:
The present invention concerns prognostic markers associated with EGFR positive cancer. In particular, the invention concerns prognostic methods based on the molecular characterization of gene expression in paraffin-embedded, fixed tissue samples of EGFR-expressing cancer, which allow a physician to predict whether a patient is likely to respond well to treatment with an EGFR inhibitor.
摘要:
The present invention concerns prognostic markers associated with EGFR positive cancer. In particular, the invention concerns prognostic methods based on the molecular characterization of gene expression in paraffin-embedded, fixed tissue samples of EGFR-expressing cancer, which allow a physician to predict whether a patient is likely to respond well to treatment with an EGFR inhibitor.
摘要:
The invention relates to a pharmaceutical combination which comprises (a) a phosphoinositide 3-kinase inhibitor compound and (b) an insulin sensitivity enhancer compound for the treatment of a proliferative disease, especially a solid tumor disease; a pharmaceutical composition comprising such a combination; the use of such a combination for the preparation of a medicament for the treatment of a proliferative disease; a commercial package or product comprising such a combination as a combined preparation for simultaneous, separate or sequential use; and to a method of treatment of a warm-blooded animal, especially a human.
摘要:
The present invention concerns prognostic markers associated with EGFR positive cancer. In particular, the invention concerns prognostic methods based on the molecular characterization of gene expression in paraffin-embedded, fixed tissue samples of EGFR-expressing cancer, which allow a physician to predict whether a patient is likely to respond well to treatment with an EGFR inhibitor.