Medical Oncology 1
Milano
Via Giacomo Venezian, 1, 20133 Milano MI
The Complex Structure of Medical Oncology 1 ensures that patients suffering from various types of cancer are cared for by a dedicated team of doctors and nurses with specific professional expertise. It comprises specialist outpatient clinics and an inpatient ward with 20 beds, staffed by senior consultants supported by junior doctors.
Our mission is to offer patients personalised diagnostic and therapeutic pathways based on multidisciplinary discussion of each individual case, adherence to internal disease-specific clinical pathways (PDTAs), and national and international guidelines.
As part of the care pathway, we always consider the opportunity to treat patients within clinical trials using innovative and experimental drugs, such as molecularly targeted drugs or new-generation immunotherapies.
The facility also benefits from:
- A team of experts in conducting Phase I-II clinical trials (Early Clinical Drug Development)
- A laboratory dedicated to the processing of biological samples for research.
Outpatient appointments, whether under the National Health Service (NHS) or as private consultations, can be booked via the Institute’s General Outpatient Booking Centre (CUP), either by visiting the reception desks on the ground floor of Block C or by calling +39 02 23901 during the following hours: 7.30am–4.30pm Monday to Friday, and 8.30am–12.30pm on Saturdays.
For NHS bookings, you must have your NHS card.
For private practice appointments, you can also book online via this link:
The Complex Unit of Medical Oncology 1 specialises in the treatment of the following cancers:
- Breast cancer;
- Cancers of the gastrointestinal tract, pancreas and biliary tract (oesophagus, stomach, small and large intestine, pancreas and biliary tract);
- Neoplasms of the thoracic region;
- Neoplasms of neuroendocrine origin;
- Melanoma and other skin cancers.
- Solid neoplasms of unknown primary origin (CUP)
- Mail: segreteria.oncologiamedica@istitutotumori.mi.it
- Tel: 0223903066
Note: dal lunedì al venerdì dalle 9.00 alle 16.00
Orari di accesso visite ai degenti:
- Un visitatore per paziente per massimo 45 minuti nella fascia dalle 13.00 alle 15.00 e dalle 17.00 alle 18.00.
Colloquio con i Medici di Reparto: dal lunedì al venerdì dalle ore 16.00 alle ore 17.30
Orari di accesso informatori scientifici:
- Previ accordi con la Segreteria di Oncologia Medica, possono essere richiesti il martedi dalle 10 alle 14, il mercoledi’ dalle 16 alle 18, il giovedi’ dalle 16 alle 18.
Prof. De Braud Filippo
Direttore di struttura complessa
Dott.ssa Ambrosini Margherita
Medical Director
Dott.ssa Armani Giovanna
Medical Director
Dott.ssa Beninato Teresa
Medical Director
Dott.ssa Bianchi Giulia Valeria
Medical Director
Dott.ssa Brambilla Marta
Medical Director
Dott.ssa Corrao Giulia
Specialist – Medical Oncology – Consultant Contract
Dott.ssa Cresta Sara
Medical Director
Dott.ssa Damian Silvia
Medical Director
Dott. Del Vecchio Michele
Medical Director
Dott.ssa Di Guardo Lorenza
Medical Director
Dott. Di Nicola Massimo
Medical Director
Dott. Duca Matteo
Medical Director
Dott.ssa Fazio Roberta
Specialist – Medical Oncology – Consultant Contract
Dott. Fotia Giuseppe
Medical Director
Dott.ssa Indini Alice
Medical Director
Dott.ssa Jacobs Flavia
Specialist – Medical Oncology – Consultant Contract
Dott. Leone Alberto Giovanni
Medical Director
Dott.ssa Ligorio Francesca
Medical Director
Dott. Lo Russo Giuseppe
Medical Director
Dott. Manca Paolo
Specialist – Medical Oncology – Consultant Contract
Dott.ssa Mazzeo Laura
Medical Director
Dott.ssa Morano Federica
Medical Director
Dott.ssa Niger Monica
Medical Director
Dott. Occhipinti Mario
Medical Director
Dott.ssa Prelaj Arsela
Medical Director
Dott.ssa Pircher Chiara Carlotta
Medical Director
Dott. Prisciandaro Michele
Medical Director
Dott.ssa Proto Claudia
Medical Director
Dott. Provenzano Leonardo
Specialist – Medical Oncology – Consultant Contract
Dott.ssa Pusceddu Sara
Medical Director
Dott. Spagnoletti Andrea
Medical Director
Dott.ssa Raimondi Alessandra
Medical Director
Dott. Rametta Alessandro
Medical Director
Dott. Randon Giovanni
Medical Director
Dott.ssa Romanò Rebecca
Medical Director
Prof. Vernieri Claudio
Medical Director
Laboratorio di ricerca OM1:
- Martinetti Antonia ( Dir. Biologo)
- Fiducioso Martina
- Garoldini Giorgia
- Selvaggio Tamara Angela
- Sottotetti Elisa
Coordinatore infermieristico:
- Lavecchia Filomena
Personale amministrativo:
- Melocchi Michela
- Radu Nadina Oana
- Zanetti Federico
- Baggio Fabrizio
- Fink Miriam Monica
- Milone Paola
- Spallone Renata
- Spanò Sestina
COLLABORATORI PROF. IN PROGETTI DI RICERCA:
- Longo Sara
- Miskovic Vanjia
- Villa Andrea
Thoracic Oncology Unit
Breast Medical Oncology
Clinical Immunotherapy for Cancer and Innovative Therapies
Medical Oncology: Melanomas
Unità Studi Clinici di Fase 1 (Early clinical Drug Development Team-ECDD)
A first-in-human study to evaluate the safety, tolerability and pharmacokinetics, pharmacodynamics and preliminary clinical activity of BAY 3713372, a novel 2nd generation PRMT5 inhibitor, in participants with MTAP-delet
A Phase 1b/2 Open-label Study Evaluating different MK-6070 and Ifinatamab Deruxtecan (MK-2400)-based regimens in First-line Extensive Stage Small Cell Lung Cancer n. MK6070-003
A Phase 1b/2, Multicenter, Open-Label Study of Anti-CEACAM5 Antibody-Drug Conjugate Precemtabart Tocentecan (M9140) in Participants With Advanced Solid Tumors (Master Protocol)
A Phase 2 Open-Label, Multi-Center Study of BMS-986504 as Monotherapy and in Combination with Other Agents in Participants with Advanced and/or Metastatic Solid Tumors with Homozygous MTAP Deletion
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of V940 in Combination with Pembrolizumab and Chemotherapy as First-Line Treatment for Participants with Metastatic Squamous NSCLC (INTerpath-013)
A Phase 3, Open-Label, Multicenter, Randomized Study of Subcutaneous vs Intravenous Tarlatamab in Participants with Relapsed Extensive-Stage Small Cell Lung Cancer After Platinum-based First-line chemotherapy (DeLLphi-31
A Phase 3, Randomized, Open-label Study to Evaluate the Efficacy and Safety of sac-TMT (Sacituzumab Tirumotecan, MK-2870) Followed by Carboplatin/Paclitaxel vs Chemotherapy, Both in Combination With Pembrolizumab as Neoa
A Phase 3, Randomized, Open-label, Study to Compare the Efficacy and Safety of Adjuvant MK-2870 in Combination with Pembrolizumab (MK-3475) Versus Treatment of Physician’s Choice (TPC) in Participants With Triple-Negativ
A Phase 3, Randomized, Placebo-Controlled Study of Adjuvant Intismeran Autogene Plus Subcutaneous Pembrolizumab and Berahyaluronidase Alfa (MK-3475A) or Intismeran Autogene Monotherapy Versus Placebo in Participants With
A Phase I/II, open-label, adaptive two-part trial to evaluate the safety, efficacy, optimal dose and pharmacokinetics of BNT326 as monotherapy and in combination with cancer immunotherapies in participants with advanced
A Phase I/II, Open-Label, Multicenter Study of ALE.P02 (Claudin-1 Targeted Antibody-Drug Conjugate) as a Monotherapy in Adult Patients with Selected Advanced or Metastatic CLDN1+ Squamous Solid Tumors
A Phase I/II, Open-label, Multicenter Study of ALE.P03 (Claudin-1 Targeted Antibody-drug Conjugate) as a Monotherapy in Adult Patients with Selected Advanced or Metastatic CLDN1+ Solid Tumors
A PHASE II, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY AND SAFETY OF INAVOLISIB PLUS RIBOCICLIB PLUS FULVESTRANT VERSUS PLACEBO PLUS RIBOCICLIB PLUS FULVESTRANT IN PATIENTS WI
A phase III, multicenter, randomized, double-blind, placebo-controlled study evaluating the efficacy and safety of inavolisib in combination with phesgo versus placebo in combination with phesgo as maintenance therapy af
A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF INAVOLISIB COMBINED WITH A CDK4/6 INHIBITOR AND LETROZOLE VERSUS PLACEBO COMBINED WITH A CDK4/6 INHIBITO
A phase III, randomized, open-label study evaluating efficacy and safety of giredestrant compared with fulvestrant, both combined with a cdk4/6 inhibitor, in patients with estrogen receptor-positive, her2-negative advanc
A TWO-PART, SEAMLESS, MULTICENTER, RANDOMIZED, OPEN LABEL, ADAPTIVE PHASE II/III STUDY OF THE BLOOD-BRAIN BARRIER PENETRANT RO7771950 VERSUS TUCATINIB, BOTH IN COMBINATION WITH TRASTUZUMAB AND CAPECITABINE, IN PATIENTSIT
An Open-label, Randomized Phase 3 Study of MK-2870 as a Single Agent and in Combination with Pembrolizumab Versus Treatment of Physician’s Choice in Participants with HR+/HER2- Unresectable Locally Advanced or Metastatic
An Open-label, Randomized, Phase 3 Study to Evaluate Patritumab
Deruxtecan Monotherapy versus Treatment of Physician’s Choice in
Hormone Receptorpositive, HER2-negative Unresectable Locally Advanced or
Metastatic Br
Basket of Baskets: A Modular, Open-label, Phase II, Multicentre Study To Evaluate Targeted Agents in Molecularly Selected Populations With Advanced Solid Tumours.
FASTing-like approach to improve the efficacy of maintenance IMMunotherapy in Extensive-stage small cell lung cancer patients not progressing on chemoimmunotherapy induction: the FASTIMMUNE trial.
First-in-Human Study of STX-478, a Mutant-Selective PI3Kα Inhibitor as
Monotherapy and in Combination With Other Antineoplastic Agents in
Participants With Advanced Solid Tumors
Targeting triple negative BREAst cancer metabolism with a combination of chemoimmunotherapy and a FASTing-like approach in the preoperative setting: the BREAKFAST 2 trial.
APOLLO 11: consortium in advanced lung cancer patients treated with innovative therapies; integration of real world data and translational research
I3LUNG - Integrative science, Intelligent data platform for Individualized Lung cancer care with Immunotherapy
SHAIPED
Understanding and addressing LATE-effects of treatment of AYA cancer survivors with AI-based digital phenotyping and non-invasive holistic approach (Late-AYA)
Building Data Rich Clinical Trials (CCE-DART)
DWH 2.0
Identification of quantitative factors and support tools to reduce the risk of adverse events after oncological treatments
SENESCENCE AS BIOMARKER OF CANCER-RELATED FATIGUE IN BREAST CANCER PATIENTS RECEIVING ADJUVANT CHEMOTHERAPY
TYME: TYmic Malignancies nEtwork per l’integrazione di dati real world e per la caratterizzazione biologica dei tumori epiteliali del timo
Last update: 23/04/2026