Progetti

A seguire i progetti nati dalla cooperazione tra Oncotech e gruppi di ricerca GIM (Gruppo Italiano Mammella), GIR (Gruppo Italiano Rene) e il CRPO (Centro Regione Prevenzione Oncologico):

GRUPPO GIM (Gruppo Italiano Mammella)

Il Gruppo GIM può essere considerato uno dei gruppi di ricerca indipendenti in campo oncologico con maggiori potenzialità a livello internazionale, sia per la capacità di arruolare pazienti e proporre nuovi studi clinici sia per le innovative tecnologie di cui si avvale.
  • centri aderenti: 158
  • sperimentatori coinvolti: 500
GIM1
(N-1)
A phase III randomized study of Sequential Epidoxorubicin plus Cyclophospamide Followed By Docetaaxel (EC->D) versus the Combination of 5-fluorouracil, Epidoxorubicin and Cyclophospamide (FEC) as Adjuvant Treatment of Node-Negative Early Breast Cancer Patients.
GIM2
A phase III randomized study of EC followed by Paclitaxel versus FEC followed by Paclitaxel, all given either every 3 or 2 weeks supported by Pegfilgrastim for node positive breast cancer patients.
GIM3
(FATA)
A phase III study comparing anastrozole, letrozole and exemestane, upfront (for 5 years) or sequentially (for 3 years after 2 years of tamoxifen), as adjuvant treatment of postmenopausal patients with endocrine-responsive breast cancer.
GIM4
(LEAD)
LEtrozole Adjuvant therapy Duration (LEAD) study: standard versus long treatment. A phase III trial in post-menopausal women with early breast cancer.
GIM5
(CYPLEC)
Letrozole adjuvant therapy after Tamoxifen. Study of gene CYP19 correlation with letrozole efficacy in postmenopausal early breast cancer patients.
GIM6
(PROMISE)
Prevention of chemotherapy-induced menopause by temporary ovarian suppression with Triptorelin versus control in young breast cancer patients. A randomized phase III multicenter study.
GIM7
(DOT)
Dose Optimization of Trastuzumab. Studio di fase III volto a valutare l'efficacia e la tossicità di Trastuzumab alla dose di mantenimento di 1mg/kg/settimana verso la dose standard di 2mg/kg/settimana in combinazione con chemioterapia nelle pazienti con carcinoma mammario metastatico.
GIM8
(OVER)
A Randomized Trial with factorial Design comparing Fulvestrant ± Lapatinib ± Aromatase Inhibitor in metastatic breast cancer progressing after Aromatase Inhibitor therapy.
GIM9
(NEO-ADIXERN)
A feasibility study of dose-dense FEC with G-CSF support followed by dose-dense Ixabepilone with G-CSF support as neoadjuvant chemotherapy in ER-negative breast cancer.
GIM10
(CONSENT)
A phase III study comparing the concurrent versus the sequential administration of chemotherapy and aromatase inhibitors, as adjuvant treatment of post-menopausal patients with endocrine-responsive early breast cancer.
GIM11
(BERGI)
A Phase II Single Arm Trial Evaluating the Efficacy and Safety of Eribulin in Combination With Bevacizumab for Second-Line Treatment of Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer Progressing after First-Line Therapy With Bevacizumab and Paclitaxel.
GIM12
(TYPHER)
A randomised, multicentre, open-label Phase II trial investigating activity of chemotherapy and lapatinib and trastuzumab in patients with HER2-positive metastatic breast cancer (MBC) refractory to anti HER2 therapies.
GIM13
(AMBRA)
Observation of Medical Treatments in MBC HER2-negative Patients (Advanced Metastatic BReAst Cancer).
GIM14
(BIO-META)
Evaluation of medical treatments (chemotherapy, hormonal therapy and biological therapies) in metastatic breast cancer patients according to biologic subtype and line of treatment.
GIM15
(NEPA)
One day antiemetic prophylaxis of NEPA (netupitant plus palonosetron) and dexamethasone to prevent chemotherapy-induced nausea and vomiting (CINV) in breast cancer patients receiving a combination chemotherapy of doxorubicin or epirubicin with cyclophosphamide (AC-based regimen).
GIM16
(FEVEX)
Fulvestrant followed by everolimus plus exemestane vs examestane and everolimus followed by fulvestrant in postmenopausal women with hormone receptor positive (HR+) and human epidermal growth factor receptor type 2 negative (HER2-) locally advanced (LABC) or metastatic breast cancer (MBC) previously treated with non steroidal aromatase inhibitors (NSAI): a multicentre, phase III trial.
GIM18
(FUMANCE)
Randomized phase III study of fulvestrant as maintenance therapy after first-line chemotherapy in HER2 negative postmenopausal metastatic breast cancer patients.
GIM19
(STAR)
Observational study on evaluation of compliance to aromatase inhibitors treatment in patients with hormone positive breast cancer.
GIM20
(CITOHER2)
A prospective, exploratory, multi-site, observational study evaluating the cytokinome profile in patients with her2 positive metastatic breast cancer candidate to receive Trastuzumab Emtansine.
GIM21
(LiqERBcept)
Liquid Biopsy: intercepting mutational trajectories of HER2 breast cancer in patients under T-DM1 treatment
GIM22
(ERICA)
Second line ERIbulin followed by CApecitabine or the reverse sequence in HER2-negative Metastatic Breast Cancer (MBC) patients: a randomized phase II study - ERICA trial
GIM23
(POSTER)
Prospective observational study of adjuvant hormone treatment in estrogen-receptor positive premenopausal early breast cancer patients
GIM24
(PALBO-BP)
Palbociclib plus fulvestrant in women with hormone receptor positive and human epidermal growth factor receptor type 2 negative locally advanced or metastatic breast cancer previously treated with a CDK4/6 inhibitor in combination with hormonal therapy: a multicenter, phase II trial - Palbo-BP
GIM25
(CAPT)
A Phase II trial of atezolizumab plus CArboplatin plus Paclitaxel as first-line Therapy in metastatic triple-negative PD-L1 positive breast cancer patients
GIM26
(TRASTHER)
Observational study of effectiveness and safety of trastuzumab emtansine (T-DM1)
GIM27
(THERAPY)
Non-interventional, multicentric, prospective, observational study to describe the effectiveness of tucatinib in combination with capecitabine and trastuzumab in the treatment of metastatic HER-2 positive breast cancer patients in real world setting
GIM28
(ELMER)
EvoLution of Neoadjuvant TreatMent in 'triple-negative' or 'HER-2-positive' breast cancer diagnosed in the EaRly phase: retrospective multicentre study on the therapeutic approach most commonly adopted in the Italian oncology centres
GIM30
(RAPID)
An observational, multicenter study evaluating the safety of ReAl-lifePertuzumab and Trastuzumab Fixed Dose combination: the RAPID study
LUNG-NEPA A standard regimen of dexamethasone in comparison to two dex-sparing regimens in addition to NEPA in preventing CINV in naïve NSCLC patients to be treated with cisplatin based chemotherapy: a three-arm, open-label, randomized study.
CABACARE CABAzitaxel with or without prednisone in patients with metastatic CAstration REsistant prostate cancer (mCRPC) progressed during or after a previous docetaxel-based chemotherapy: a multi-center, prospective, two-arm, open label, non inferiority phase II study.
ARIES
ARIES Avelumab as single agent in metastatic or locally advanced urothelial cancer in patients unfit for cisplatin. The ARIES study
LANZA Circulating tumor cells count in patients with prostate cancer receiving enzalutamide: the LANZA trial.
PRO-BONO Prospective observational study on the impact of the Oncotype DX® Breast Cancer Assay ontreatment decisions and resources optimization in hormone receptor-positive/HER2-negativeearly breast cancer patients.
DURWIN A prospective, multi-center, open-label, single-arm, two- step phase II study of DURvalumab (MEDI4736) in patients WIth poor performance status as first-liNe treatment for advanced urothelial cancer.
Tide-A Phase II study of avelumab plus intermittent axitinib in previously untreated patients with metastatic renal cell carcinoma.
AxIn Phase II study of axitinib intensification plus nivolumab compared to nivolumab alone after induction with nivolumab plus ipilimumab in mRCC patients without previous complete response.
PE-PE Efficacy of PErioperative PEmbrolizumab treatment in patients with resectable metastases from kidney cancer.
XELOX-TARAV Studio di fase I-II Con la combinazione di Bevacizumab (rhuMAb VEGF) e Erlotinib (EGFR TKI) più Oxaliplatino e Capecitabina (XELOX) in pazienti con carcinoma del colon-retto metastatico: studio XELOX-TARAV

GRUPPO GIR (Gruppo Italiano Rene)

il Gruppo GIR, nonostante sia di recente costituzione, può vantare già un considerevole numero di Centri aderenti e si appresta a diventare uno dei maggiori poli di attrazione non solo per la quantità dei progetti presentati ma anche per la loro qualità ed attualità scientifica in campo oncologico.
  • centri aderenti: 90
  • sperimentatori coinvolti: 240
GIR1 Sunitinib either before or after cytoreductive nephrectomy a phase ii trial in patients with metastatic renal cell carcinoma.
GIR2 (MOTOR) Medical optimization of TORisel (MoTOR): Multicenter, phase II evaluation of Torisel as II-line treatment for metastatic RCC patients progressing after cytokine therapy, tyrosine kinase, or angiogenesis inhibitors.
Screening senologico (donne di età 50 - 69 anni), della cervice uterina (donne di età 24 - 64 anni) e del colon retto (donne e uomini di età 50 - 74 anni)
di tutte le persone residenti nella regione
Campania.