INFO & CONTACTS:  +39 02 2390 1

Medical Oncology 1

Milano
Via Giacomo Venezian, 1, 20133 Milano MI

Prof. De Braud

Prof. De Braud Filippo

Direttore di struttura complessa

Typology: Clinical Area, Complex Structure

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:

 

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)

Segreteria Oncologia medica 1

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

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)

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

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