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Cazzaniga, Walter

https://orcid.org/0000-0002-0372-5694

Mayo Clinic

Royal Marsden NHS Foundation Trust

Citations 2

Primary retroperitoneal lymph node dissection in clinical stage 2a/b non‐seminomatous germ cell tumour
Antonelli, Luca , Heidenreich, Axel , Baky, Fady , Branger, Nicolas , Daneshmand, Siamak , Djaladat, Hooman , Eggener, Scott E. , Sexton, Wade J. , Nicol, David , Olson, Kathleen, Paffenholz, Pia , Porter, James , Qian, Zhiyu , Rocco, Nicholas R., Stroup, Sean P. , Tachibana, Isamu , Cary, Clint , Daneshmand, Siamak , Djaladat, Hooman , Ghoreifi, Alireza , Nicol, David , Nicolai, Nicola , Paffenholz, Pia , Porter, James , Stroup, Sean P , Fankhauser, Christian Daniel , Bagrodia, Aditya , Amini, Armon , Cazzaniga, Walter , Clinton, Timothy Nguyen , Ghoreifi, Alireza , Hamilton, Robert J , Ho, Matthew, Nazzani, Sebastiano , Olson, Kathleen, Yerrapragada, Anirudh , Terbuch, Angelika , Singla, Nirmish

BJU International | December 11, 2024 | Volume: 135 | Issue: 4 | Pages: 621-628

10.1111/bju.16618 Get It

Objectives To reassess the role of primary retroperitoneal lymph node dissection (RPLND) in patients with marker‐negative non‐seminomatous germ cell tumour (NSGCT) clinical stage (CS) 2a, to explore results in patients with CS 2b and to evaluate surgical methods, recurrence, and adjuvant chemotherapy indications. Materials and Methods Data from 17 institutions were collected, comprising 305 men who underwent primary RPLND for CS 2 NSGCT. Regression analyses were conducted to predict histology in the RPLND specimen and disease‐free survival (DFS). Results A larger retroperitoneal lymph node diameter was associated with pure teratoma in the RPLND specimen (odds ratio [OR] 1.02, 95% confidence interval [CI] 1.01–1.07; P = 0.03), but no association was observed with DFS. The 5‐year DFS rates in marker negative CS 2a and 2b were 79% and 76%. In men with non‐teratomatous viable cancer in the RPLND specimen, the 5‐year DFS rates for CS 2a and 2b were 95% and 87% with adjuvant chemotherapy, and 67% and 74% without adjuvant chemotherapy. We did not identify an association between the number of adjuvant chemotherapy cycles and DFS. Conclusions Our study suggests considering primary RPLND not only in marker‐negative CS 2a but also in CS 2b. Further research should determine the efficacy of primary RPLND in men with CS 2c and marker‐positive CS 2, as well as which patients may benefit from adjuvant chemotherapy and the optimal cycle number.
Risk Factors for Relapse in Nonseminomatous Testicular Cancer After Postchemotherapy Retroperitoneal Lymph Node Dissection With Viable Residual Cancer
Antonelli, Luca , Ardizzone, Davide, Tachibana, Isamu , Adra, Nabil , Cary, Clint , Sexton, Wade J. , Daneshmand, Siamak , Franza, Andrea , Heidenreich, Axel , Paffenholz, Pia , Saoud, Ragheed , Eggener, Scott E. , Oswald, Nathaniel W., Olson, Kathleen, Tryakin, A. , Javaud, Christophe, Cazzaniga, Walter , Nicol, David , Gerdtsson, Axel , Tandstad, Torgrim , Fizazi, Karim , Sexton, Wade J , Bagrodia, Aditya , Daneshmand, Siamak , Nazzani, Sebastiano , Franza, Andrea , Heidenreich, Axel , Saoud, Ragheed , Eggener, Scott , Oswald, Nathaniel, Tryakin, Alexey , Fedyanin, Mikhail , Cazzaniga, Walter , Gerdtsson, Axel , Fizazi, Karim , Fankhauser, Christian Daniel , Hugar, Lee A. , Mego, Michal , Nicolai, Nicola , Giannatempo, Patrizia , Ho, Matthew, Olson, Kathleen, Naoun, Natacha

Journal of Clinical Oncology | September 1, 2023 | Volume: 41 | Issue: 34 | Pages: 5296-5305

10.1200/jco.23.00443 Get It

What is the role of pcRPLND in men with retroperitoneal vital cancer after first-line chemotherapy? This question arises because of the potential predictive value of miR371 in identifying residual cancer even before pcRPLND! @cdfankhauser shared data within a multicenter cohort study redefining future practice in the miR371 era.