Oncotarget, ISSN 1949-2553, 04/2018, Volume 9, Issue 27, pp. 18997 - 19005
Metastatic melanoma carrying BRAF mutations represent a still unmet medical need as success of BRAF inhibitors is limited by development of resistance....
Tumor marker | Metastatic melanoma | Prognosis | Resistance to therapy | NAMPT
Tumor marker | Metastatic melanoma | Prognosis | Resistance to therapy | NAMPT
Journal Article
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 474 - 474
Journal Article
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 45, pp. 79809 - 79815
As diverse therapeutic options are now available for advanced melanoma patients, predictive markers that may assist treatment decision are needed. A model...
Biomarker | Ipilimumab | Eosinophil | Melanoma | Predictive | SURVIVAL | TRIAL | METASTATIC MELANOMA | PEMBROLIZUMAB | ipilimumab | predictive | melanoma | TO-LYMPHOCYTE RATIO | eosinophil | biomarker | CELL BIOLOGY
Biomarker | Ipilimumab | Eosinophil | Melanoma | Predictive | SURVIVAL | TRIAL | METASTATIC MELANOMA | PEMBROLIZUMAB | ipilimumab | predictive | melanoma | TO-LYMPHOCYTE RATIO | eosinophil | biomarker | CELL BIOLOGY
Journal Article
Supportive Care in Cancer, ISSN 0941-4355, 2/2013, Volume 21, Issue 2, pp. 643 - 647
Patients’ care has been associated with a high burden of psychological symptoms in caregivers. This study identifies characteristics associated with mood...
Pain Medicine | Nursing | Rehabilitation Medicine | Medicine & Public Health | Coping and adaptation | Psychological distress | Caregiver | Mood disorders | Oncology | Families’ burden | Nursing Management/Nursing Research | Cancer | Families' burden | DEPRESSION SCALE | HOSPITAL ANXIETY | PARTNERS | ONCOLOGY | FAMILIES | HEALTH CARE SCIENCES & SERVICES | REHABILITATION | PSYCHOLOGICAL IMPACT | COPING STRATEGIES | Caregivers - statistics & numerical data | Caregivers - psychology | Humans | Middle Aged | Risk Factors | Male | Stress, Psychological - psychology | Forecasting | Neoplasms | Mood Disorders - epidemiology | Mood Disorders - etiology | Young Adult | Mood Disorders - diagnosis | Stress, Psychological - epidemiology | Adult | Female | Italy | Aged | Stress, Psychological - complications | Caregivers | Family | Cancer patients | Care and treatment | Stress (Psychology) | Depression, Mental | Families & family life | Emotional disorders
Pain Medicine | Nursing | Rehabilitation Medicine | Medicine & Public Health | Coping and adaptation | Psychological distress | Caregiver | Mood disorders | Oncology | Families’ burden | Nursing Management/Nursing Research | Cancer | Families' burden | DEPRESSION SCALE | HOSPITAL ANXIETY | PARTNERS | ONCOLOGY | FAMILIES | HEALTH CARE SCIENCES & SERVICES | REHABILITATION | PSYCHOLOGICAL IMPACT | COPING STRATEGIES | Caregivers - statistics & numerical data | Caregivers - psychology | Humans | Middle Aged | Risk Factors | Male | Stress, Psychological - psychology | Forecasting | Neoplasms | Mood Disorders - epidemiology | Mood Disorders - etiology | Young Adult | Mood Disorders - diagnosis | Stress, Psychological - epidemiology | Adult | Female | Italy | Aged | Stress, Psychological - complications | Caregivers | Family | Cancer patients | Care and treatment | Stress (Psychology) | Depression, Mental | Families & family life | Emotional disorders
Journal Article
International Journal of Oncology, ISSN 1019-6439, 09/2016, Volume 49, Issue 3, pp. 1164 - 1174
BRAF inhibitors (BRAFi) have proven clinical benefits in patients with BRAF-mutant melanoma. However, acquired resistance eventually arises. The effects of...
GSK2126458A | Melanoma | Dabrafenib | BRAF | Drug resistance | Invasion | Bevacizumab | MUTANT MELANOMA | melanoma | IMPROVED SURVIVAL | VEMURAFENIB RESISTANCE | RANDOMIZED CONTROLLED-TRIAL | MUTATED MELANOMA | MATRIX METALLOPROTEINASES | METASTATIC MELANOMA | PROMOTES INVASIVENESS | invasion | MEK INHIBITION | ONCOLOGY | bevacizumab | drug resistance | dabrafenib | ENDOTHELIAL GROWTH-FACTOR
GSK2126458A | Melanoma | Dabrafenib | BRAF | Drug resistance | Invasion | Bevacizumab | MUTANT MELANOMA | melanoma | IMPROVED SURVIVAL | VEMURAFENIB RESISTANCE | RANDOMIZED CONTROLLED-TRIAL | MUTATED MELANOMA | MATRIX METALLOPROTEINASES | METASTATIC MELANOMA | PROMOTES INVASIVENESS | invasion | MEK INHIBITION | ONCOLOGY | bevacizumab | drug resistance | dabrafenib | ENDOTHELIAL GROWTH-FACTOR
Journal Article
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 69, pp. 113472 - 113493
The pituitary tumor transforming gene 1 (PTTG1) is implicated in tumor growth, metastasis and drug resistance. Here, we investigated the involvement of PTTG1...
Dabrafenib | Proliferation | PTTG1 | Invasion | Melanoma | CANCER-CELLS | proliferation | SOLID TUMORS | INDUCED APOPTOSIS | melanoma | MALIGNANT-MELANOMA | DEPENDENT KINASE INHIBITOR | MESENCHYMAL TRANSITION | CELL BIOLOGY | invasion | PROMOTES MIGRATION | MUTATED METASTATIC MELANOMA | dabrafenib | TUMOR-TRANSFORMING GENE-1 | ENDOTHELIAL GROWTH-FACTOR
Dabrafenib | Proliferation | PTTG1 | Invasion | Melanoma | CANCER-CELLS | proliferation | SOLID TUMORS | INDUCED APOPTOSIS | melanoma | MALIGNANT-MELANOMA | DEPENDENT KINASE INHIBITOR | MESENCHYMAL TRANSITION | CELL BIOLOGY | invasion | PROMOTES MIGRATION | MUTATED METASTATIC MELANOMA | dabrafenib | TUMOR-TRANSFORMING GENE-1 | ENDOTHELIAL GROWTH-FACTOR
Journal Article
Cancer Investigation, ISSN 0735-7907, 5/2014, Volume 32, Issue 4, pp. 144 - 149
Of 93 patients with pretreated, BRAFV600 mutation-positive advanced melanoma who received vemurafenib or dabrafenib before (n = 45) or after (n = 48) treatment...
Treatment | Molecular biology | Cutaneous melanoma | Tumor immunology | THERAPY | ONCOLOGY | FOLLOW-UP | VEMURAFENIB | Skin Neoplasms - drug therapy | Humans | Ipilimumab | Middle Aged | Oximes - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Imidazoles - administration & dosage | Melanoma - enzymology | Male | Molecular Targeted Therapy | Indoles - administration & dosage | Young Adult | Skin Neoplasms - enzymology | Time Factors | Melanoma - genetics | Skin Neoplasms - mortality | Aged, 80 and over | Adult | Female | Retrospective Studies | Proto-Oncogene Proteins B-raf - metabolism | Skin Neoplasms - pathology | Drug Administration Schedule | Kaplan-Meier Estimate | Treatment Outcome | Disease Progression | Melanoma - secondary | Proto-Oncogene Proteins B-raf - antagonists & inhibitors | Protein Kinase Inhibitors - administration & dosage | Antibodies, Monoclonal - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Proto-Oncogene Proteins B-raf - genetics | Melanoma - drug therapy | Skin Neoplasms - genetics | Italy | Aged | Mutation | Sulfonamides - administration & dosage | Melanoma - mortality
Treatment | Molecular biology | Cutaneous melanoma | Tumor immunology | THERAPY | ONCOLOGY | FOLLOW-UP | VEMURAFENIB | Skin Neoplasms - drug therapy | Humans | Ipilimumab | Middle Aged | Oximes - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Imidazoles - administration & dosage | Melanoma - enzymology | Male | Molecular Targeted Therapy | Indoles - administration & dosage | Young Adult | Skin Neoplasms - enzymology | Time Factors | Melanoma - genetics | Skin Neoplasms - mortality | Aged, 80 and over | Adult | Female | Retrospective Studies | Proto-Oncogene Proteins B-raf - metabolism | Skin Neoplasms - pathology | Drug Administration Schedule | Kaplan-Meier Estimate | Treatment Outcome | Disease Progression | Melanoma - secondary | Proto-Oncogene Proteins B-raf - antagonists & inhibitors | Protein Kinase Inhibitors - administration & dosage | Antibodies, Monoclonal - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Proto-Oncogene Proteins B-raf - genetics | Melanoma - drug therapy | Skin Neoplasms - genetics | Italy | Aged | Mutation | Sulfonamides - administration & dosage | Melanoma - mortality
Journal Article
International Journal of Oncology, ISSN 1019-6439, 04/2016, Volume 48, Issue 4, pp. 1581 - 1589
The placenta growth factor (PlGF) is a member of the vascular endothelial growth factor (VEGF) family, which shares with VEGF-A the tyrosine kinase receptor...
bevacizumab | melanoma | vasculogenic mimicry | PlGF | neuropilin-1 | SURVIVAL | ACTIVATION | VEGF | INHIBITS GROWTH | FACTOR RECEPTOR-1 | INVASIVENESS | AGENT | BREAST-CANCER CELLS | ONCOLOGY | ENDOTHELIAL-CELLS
bevacizumab | melanoma | vasculogenic mimicry | PlGF | neuropilin-1 | SURVIVAL | ACTIVATION | VEGF | INHIBITS GROWTH | FACTOR RECEPTOR-1 | INVASIVENESS | AGENT | BREAST-CANCER CELLS | ONCOLOGY | ENDOTHELIAL-CELLS
Journal Article
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, ISSN 1756-9966, 06/2019, Volume 38, Issue 1, pp. 272 - 24
BackgroundDevelopment of resistance to inhibitors of BRAF (BRAFi) and MEK (MEKi) remains a great challenge for targeted therapy in patients with BRAF-mutant...
MIGRATION | SURVIVAL | THERAPEUTICS | MICRORNA-126 | proliferation | CANCER CELLS | BRAF inhibitors | melanoma | miR-126-3p | DRUG-RESISTANCE | acquired resistance | invasiveness | METASTATIC MELANOMA | ONCOLOGY | PATHWAY | BRAF INHIBITOR RESISTANCE | ENDOTHELIAL GROWTH-FACTOR | Cell proliferation | Prognosis | MicroRNA | Gene mutations | Melanoma | Genetic aspects | Research
MIGRATION | SURVIVAL | THERAPEUTICS | MICRORNA-126 | proliferation | CANCER CELLS | BRAF inhibitors | melanoma | miR-126-3p | DRUG-RESISTANCE | acquired resistance | invasiveness | METASTATIC MELANOMA | ONCOLOGY | PATHWAY | BRAF INHIBITOR RESISTANCE | ENDOTHELIAL GROWTH-FACTOR | Cell proliferation | Prognosis | MicroRNA | Gene mutations | Melanoma | Genetic aspects | Research
Journal Article
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. LB-115 - LB-115
Journal Article
Cancer Immunology, Immunotherapy, ISSN 0340-7004, 01/2019, Volume 68, Issue 1, pp. 97 - 107
CTLA-4 blockade by means of ipilimumab (IPI) potentiates the immune response and improves overall survival (OS) in a minority of metastatic melanoma (MM)...
Best response | Adverse events | Overall survival | Ipilimumab | Soluble CTLA-4 | NEUTROPHIL | VARIANTS | LONG-TERM SURVIVAL | POLYMORPHISM | IMMUNOLOGY | LYMPHOCYTE ANTIGEN 4 | REGULATOR | THERAPY | ONCOLOGY | RELEVANCE | ASSOCIATION | EXPRESSION | Melanoma - metabolism | Predictive Value of Tests | Humans | Middle Aged | Kaplan-Meier Estimate | Solubility | CTLA-4 Antigen - metabolism | Male | Melanoma - pathology | Biomarkers, Tumor - blood | Young Adult | Neoplasm Metastasis | Antineoplastic Agents, Immunological - therapeutic use | CTLA-4 Antigen - blood | Ipilimumab - therapeutic use | Melanoma - drug therapy | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Italy | Aged | Serum levels | CTLA-4 protein | Immune response | Melanoma | Biomarkers | Metastasis | Patients | Digestive tract | Enzyme-linked immunosorbent assay | Metastases
Best response | Adverse events | Overall survival | Ipilimumab | Soluble CTLA-4 | NEUTROPHIL | VARIANTS | LONG-TERM SURVIVAL | POLYMORPHISM | IMMUNOLOGY | LYMPHOCYTE ANTIGEN 4 | REGULATOR | THERAPY | ONCOLOGY | RELEVANCE | ASSOCIATION | EXPRESSION | Melanoma - metabolism | Predictive Value of Tests | Humans | Middle Aged | Kaplan-Meier Estimate | Solubility | CTLA-4 Antigen - metabolism | Male | Melanoma - pathology | Biomarkers, Tumor - blood | Young Adult | Neoplasm Metastasis | Antineoplastic Agents, Immunological - therapeutic use | CTLA-4 Antigen - blood | Ipilimumab - therapeutic use | Melanoma - drug therapy | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Italy | Aged | Serum levels | CTLA-4 protein | Immune response | Melanoma | Biomarkers | Metastasis | Patients | Digestive tract | Enzyme-linked immunosorbent assay | Metastases
Journal Article
Supportive Care in Cancer, ISSN 0941-4355, 10/2012, Volume 20, Issue 10, pp. 2553 - 2557
Cancer leads to a complicated pattern of change in quality of life (QoL).The aims of this study were to assess the impact of treatment-related side effects on...
Pain Medicine | Cancer patients | Rehabilitation Medicine | Nursing | Well-being | Medicine & Public Health | Treatment-related | Oncology | Nursing Management/Nursing Research | Quality of life | RECOGNITION | PSYCHIATRIC MORBIDITY | ANXIETY | SYMPTOM PREVALENCE | CHEMOTHERAPY | BREAST-CANCER | WOMEN | CLUSTERS | ONCOLOGY | HEALTH CARE SCIENCES & SERVICES | PSYCHOLOGICAL DISTRESS | REHABILITATION | ASSOCIATION | Humans | Middle Aged | Logistic Models | Male | Antineoplastic Agents - therapeutic use | Neoplasms - drug therapy | Regression Analysis | Antineoplastic Agents - adverse effects | Aged, 80 and over | Quality of Life | Adult | Female | Surveys and Questionnaires | Aged | Care and treatment | Chemotherapy | Analysis | Cancer | Cancer therapies | Side effects
Pain Medicine | Cancer patients | Rehabilitation Medicine | Nursing | Well-being | Medicine & Public Health | Treatment-related | Oncology | Nursing Management/Nursing Research | Quality of life | RECOGNITION | PSYCHIATRIC MORBIDITY | ANXIETY | SYMPTOM PREVALENCE | CHEMOTHERAPY | BREAST-CANCER | WOMEN | CLUSTERS | ONCOLOGY | HEALTH CARE SCIENCES & SERVICES | PSYCHOLOGICAL DISTRESS | REHABILITATION | ASSOCIATION | Humans | Middle Aged | Logistic Models | Male | Antineoplastic Agents - therapeutic use | Neoplasms - drug therapy | Regression Analysis | Antineoplastic Agents - adverse effects | Aged, 80 and over | Quality of Life | Adult | Female | Surveys and Questionnaires | Aged | Care and treatment | Chemotherapy | Analysis | Cancer | Cancer therapies | Side effects
Journal Article
The Oncologist, ISSN 1083-7159, 06/2019, Volume 24, Issue 6, pp. e327 - e337
Background Patients with a history of autoimmune diseases (AIDs) have not usually been included in clinical trials with immune checkpoint inhibitors. Materials...
Autoimmune disease | Immune checkpoint inhibitors | Immunotherapy | Performance status | Anti‐programmed death‐1 | Sex | Anti-programmed death-1 | CRITERIA | MANAGEMENT | EFFICACY | IMMUNE-CHECKPOINT INHIBITORS | THERAPY | ONCOLOGY | ADVANCED MELANOMA | SEX-DIFFERENCES | ELDERLY-PATIENTS | ASSOCIATION | ADVERSE EVENTS
Autoimmune disease | Immune checkpoint inhibitors | Immunotherapy | Performance status | Anti‐programmed death‐1 | Sex | Anti-programmed death-1 | CRITERIA | MANAGEMENT | EFFICACY | IMMUNE-CHECKPOINT INHIBITORS | THERAPY | ONCOLOGY | ADVANCED MELANOMA | SEX-DIFFERENCES | ELDERLY-PATIENTS | ASSOCIATION | ADVERSE EVENTS
Journal Article
European Journal of Cancer, ISSN 0959-8049, 07/2018, Volume 97, pp. 59 - 61
Journal Article
Recenti progressi in medicina, ISSN 0034-1193, 07/2010, Volume 101, Issue 7-8, p. 277
Genetic factors could alter drug metabolism and activity and could predict drug toxicity and/or efficacy. Several chemotherapy agents are administered in...
Camptothecin - toxicity | Fluorouracil - toxicity | Drug Resistance, Neoplasm | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - metabolism | Taxoids - therapeutic use | Toxicology | Time Factors | Enzyme Inhibitors - toxicity | Antimetabolites, Antineoplastic - metabolism | Camptothecin - analogs & derivatives | Fluorouracil - metabolism | Camptothecin - metabolism | Pharmacogenetics | Neoplasms - mortality | Genotype | Thymidylate Synthase - genetics | Cisplatin | Neoplasms - drug therapy | Polymorphism, Genetic | Antineoplastic Agents, Phytogenic - toxicity | Antimetabolites, Antineoplastic - therapeutic use | Animals | Antimetabolites, Antineoplastic - toxicity | Survival Analysis | Dihydrouracil Dehydrogenase (NADP)
Camptothecin - toxicity | Fluorouracil - toxicity | Drug Resistance, Neoplasm | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - metabolism | Taxoids - therapeutic use | Toxicology | Time Factors | Enzyme Inhibitors - toxicity | Antimetabolites, Antineoplastic - metabolism | Camptothecin - analogs & derivatives | Fluorouracil - metabolism | Camptothecin - metabolism | Pharmacogenetics | Neoplasms - mortality | Genotype | Thymidylate Synthase - genetics | Cisplatin | Neoplasms - drug therapy | Polymorphism, Genetic | Antineoplastic Agents, Phytogenic - toxicity | Antimetabolites, Antineoplastic - therapeutic use | Animals | Antimetabolites, Antineoplastic - toxicity | Survival Analysis | Dihydrouracil Dehydrogenase (NADP)
Journal Article
JOURNAL FOR IMMUNOTHERAPY OF CANCER, ISSN 2051-1426, 04/2019, Volume 7, Issue 1, pp. 102 - 11
Purpose: To investigate the efficacy and safety of concurrent stereotactic radiosurgery (SRS) and ipilimumab or nivolumab in patients with untreated melanoma...
SURVIVAL | SOLID TUMORS | OPEN-LABEL | IMMUNOLOGY | fractionated stereotactic radiosurgery | stereotactic radiosurgery | RADIATION-THERAPY | CELL LUNG-CANCER | RESPONSES | PEMBROLIZUMAB | ONCOLOGY | LOCAL RADIATION | immunotherapy | RADIOTHERAPY | OUTCOMES | melanoma brain metastases | checkpoint inhibitors | Usage | Care and treatment | Ipilimumab | Radiosurgery | Dosage and administration | Metastasis | Research | Cancer | Antigens | Toxicity | Brain cancer | Immunotherapy | Melanoma | Radiation therapy | Patients | Cancer therapies | Tumors
SURVIVAL | SOLID TUMORS | OPEN-LABEL | IMMUNOLOGY | fractionated stereotactic radiosurgery | stereotactic radiosurgery | RADIATION-THERAPY | CELL LUNG-CANCER | RESPONSES | PEMBROLIZUMAB | ONCOLOGY | LOCAL RADIATION | immunotherapy | RADIOTHERAPY | OUTCOMES | melanoma brain metastases | checkpoint inhibitors | Usage | Care and treatment | Ipilimumab | Radiosurgery | Dosage and administration | Metastasis | Research | Cancer | Antigens | Toxicity | Brain cancer | Immunotherapy | Melanoma | Radiation therapy | Patients | Cancer therapies | Tumors
Journal Article
American Journal of Clinical Pathology, ISSN 0002-9173, 2014, Volume 142, Issue 1, pp. 121 - 132
Objectives: The outcome of patients with primary melanoma (PM) cannot be completely explained based on currently adopted clinical-histopathologic criteria. In...
MSH6 | Survival | Mismatch repair | Melanoma | APOPTOSIS | MALIGNANT MELANOCYTIC LESIONS | METHYLATING AGENTS | METASTASIS | IMMUNOREACTIVITY | DYSPLASTIC NEVI | PATHOLOGY | G CHECKPOINT | BENIGN | CUTANEOUS MELANOMA | DNA-REPAIR | Melanoma - metabolism | MutL Protein Homolog 1 | Prognosis | Humans | Middle Aged | Adenosine Triphosphatases - metabolism | Male | Nuclear Proteins - metabolism | Survival Rate | MutS Homolog 2 Protein - metabolism | Skin Neoplasms - metabolism | DNA-Binding Proteins - metabolism | Skin Neoplasms - mortality | DNA Mismatch Repair | DNA Repair Enzymes - metabolism | Adult | Female | Aged | Mismatch Repair Endonuclease PMS2 | Adaptor Proteins, Signal Transducing - metabolism | Nevus - metabolism | Melanoma - mortality
MSH6 | Survival | Mismatch repair | Melanoma | APOPTOSIS | MALIGNANT MELANOCYTIC LESIONS | METHYLATING AGENTS | METASTASIS | IMMUNOREACTIVITY | DYSPLASTIC NEVI | PATHOLOGY | G CHECKPOINT | BENIGN | CUTANEOUS MELANOMA | DNA-REPAIR | Melanoma - metabolism | MutL Protein Homolog 1 | Prognosis | Humans | Middle Aged | Adenosine Triphosphatases - metabolism | Male | Nuclear Proteins - metabolism | Survival Rate | MutS Homolog 2 Protein - metabolism | Skin Neoplasms - metabolism | DNA-Binding Proteins - metabolism | Skin Neoplasms - mortality | DNA Mismatch Repair | DNA Repair Enzymes - metabolism | Adult | Female | Aged | Mismatch Repair Endonuclease PMS2 | Adaptor Proteins, Signal Transducing - metabolism | Nevus - metabolism | Melanoma - mortality
Journal Article
Recenti Progressi in Medicina, ISSN 0034-1193, 2010, Volume 101, Issue 7-8, pp. 277 - 282
Journal Article
Frontiers in Immunology, ISSN 1664-3224, 04/2017, Volume 8
Ipilimumab (IPI) blocks CTLA- 4 immune checkpoint resulting in T cell activation and enhanced antitumor immunity. IPI improves overall survival (OS) in 22% of...
Best overall response | CTLA-4 variants | Overall survival | Ipilimumab | Melanoma | Predictive/prognostic factor | SUSCEPTIBILITY | melanoma | ANTIBODY | IMMUNOLOGY | CANCER | predictive/prognostic factor | BIOMARKERS | POLYMORPHISMS | INHIBITION | AUTOIMMUNITY | ipilimumab | DISEASE | overall survival | BLOCKADE | CYTOTOXICITY | best overall response | Usage | Genetic variation | Physiological aspects | Genetic aspects | Drug therapy
Best overall response | CTLA-4 variants | Overall survival | Ipilimumab | Melanoma | Predictive/prognostic factor | SUSCEPTIBILITY | melanoma | ANTIBODY | IMMUNOLOGY | CANCER | predictive/prognostic factor | BIOMARKERS | POLYMORPHISMS | INHIBITION | AUTOIMMUNITY | ipilimumab | DISEASE | overall survival | BLOCKADE | CYTOTOXICITY | best overall response | Usage | Genetic variation | Physiological aspects | Genetic aspects | Drug therapy
Journal Article
Journal of Translational Medicine, ISSN 1479-5876, 01/2015, Volume 13, Issue Suppl 1, pp. 1 - 2
Journal Article