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Giovanni Scambia

Giovanni Scambia is a gynaecologic oncologist who leads research at the Gemelli hospital.

Giovanni Scambia directs gynaecologic oncology and serves as scientific director of the Gemelli hospital, with a large surgical and trial programme in ovarian and cervical cancer.

Role
Scientific Director, Fondazione Policlinico Universitario A. Gemelli IRCCS; Professor of Gynaecology
Specialisms
Gynaecological oncologyOvarian cancer surgeryCervical cancer
Profiles

Key papers

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rctThe Lancet 2024changed practice
KEYNOTE-A18: pembrolizumab with chemoradiotherapy for locally advanced cervical cancer

Women with locally advanced cervical cancer that is node-positive or stage III-IVA should now be offered pembrolizumab alongside and after chemoradiotherapy, which improves the chance of cure. The result matters most in countries where cervical cancer is common but immunotherapy access is poorest, so its global impact depends on pricing and health-system capacity. It does not apply to early-stage disease treated with surgery or to lower-risk locally advanced disease without nodal involvement.

rctNew England Journal of Medicine 2019changed practice
PAOLA-1: olaparib added to bevacizumab maintenance in newly diagnosed ovarian cancer, with benefit confined to HRD-positive tumours

Women with newly diagnosed advanced ovarian cancer should have their tumour tested for BRCA mutations and homologous recombination deficiency, because those who are HRD-positive gain years of additional disease control and better survival from adding olaparib to bevacizumab maintenance. Those who are HRD-negative gain nothing from olaparib in this combination and should not be exposed to its toxicity and cost. HRD testing has become a routine part of ovarian cancer care as a result.

rctNew England Journal of Medicine 2018changed practice
SOLO-1: two years of olaparib maintenance after first-line chemotherapy for BRCA-mutated ovarian cancer

Every woman diagnosed with advanced high-grade ovarian cancer should be tested for BRCA mutations at diagnosis, because those who carry one should receive two years of olaparib after chemotherapy, which greatly extends the time in remission and improves long-term survival. The plateau in the survival curves suggests some patients are cured by this approach. Toxicity is mostly anaemia, fatigue and nausea, and the two-year limit appears sufficient.

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