This invention relates to humanized antibodies that selectively bind the 31.1 epitope on the A33 protein differentially expressed in cancers including, lung cancer, ovarian cancer, pancreas cancer, breast cancer, and colon cancer, and diagnostic and therapeutic usages.

Contemplated cancer treatments comprise recursive analysis of patient-, cancer-, and location-specific neoepitopes from various biopsy sites of a patient after treatment or between successive rounds of immunotherapy and/or chemotherapy to inform further immunotherapy. Recursive analysis preferably includes various neoepitope attributes to so identify treatment relevant neoepitopes.

Provided herein are antibody molecules that bind specifically to C-MET and related nucleic acid molecules, vectors and host cells. Also provided herein are medical uses of such antibody molecules.

The invention discloses oncogenic fusion proteins. The invention provides methods for treating gene-fusion based cancers.

An agent for use in detecting, monitoring, and/or imaging cancer cells and/or cancer cell metastasis, migration, dispersal, and/or invasion, and/or for treating cancer in a subject includes a targeting peptide, at least one of a detectable moiety, therapeutic agent, or a theranostic agent, and a peptide or peptidomimetic spacer that directly or indirectly links the targeting peptide to the at least one of the detectable moiety, therapeutic agent, or theranostic agent.

The present disclosure provides methods of determining a response to at least one therapy by a subject having cancer, wherein the at least one therapy comprises the administration of at least one SMARCA4-targeting compound. The present disclosure also provides methods of treating a cancer in a subject, wherein the subject has been previously administered at least one therapeutically effective amount of at least one SMARCA4-targeting compound. The present disclosure also provides a method of identifying at least one SMARCA4-targeting compound. The present disclosure also provides a method of modulating an epithelial/mesenchymal state in at least one cell.

The invention provides an anti-CEA antibody for use in detecting CEA, treating disorders associated with CEA expression, diagnosing cancers characterized by aberrant CEA expression, and predicting effectiveness of cancer drug therapies.

The present invention provides a modified human cancer cell comprising a recombinant polynucleotide encoding an allele of a human leukocyte antigen gene. The present invention also provides methods for selecting a whole-cell cancer vaccine for a subject having cancer and methods of treating cancer using whole-cell cancer vaccines of the present invention. In addition, the present invention provides a method of determining the HER2 status of a cell. Compositions and kits are also provided herein.

The present application discloses anti-NME antibodies and their use in treating or preventing diseases.

The present invention provides therapeutic and diagnostic methods and compositions for treating a human metastatic cancer. Specifically, the invention provides methods of treatment and methods for determining whether an individual suffering from a cancer is responding to an AXL decoy protein-based therapy, predicting responsiveness of an individual suffering from a cancer to treatment comprising an AXL decoy protein, and methods of selecting a therapy for an individual suffering from cancer.