doi : 10.1016/j.annonc.2020.10.482
Volume 32, Issue 1, January 2021, Pages 1-3
doi : 10.1016/j.annonc.2020.11.001
Volume 32, Issue 1, January 2021, Pages 4-5
B. Glimelius
doi : 10.1016/j.annonc.2020.10.598
Volume 32, Issue 1, January 2021, Pages 6-8
J. Jee, B.T. Li
doi : 10.1016/j.annonc.2020.11.010
Volume 32, Issue 1, January 2021, Pages 9-11
L. Meza, P.G. Bergerot, N. Agarwal, S.K. Pal
doi : 10.1016/j.annonc.2020.10.481
Volume 32, Issue 1, January 2021, Pages 12-14
P.G. Casali, M. Vyas, European Society for Medical Oncology (ESMO)
doi : 10.1016/j.annonc.2020.10.472
Volume 32, Issue 1, January 2021, Pages 15-19
J.C. Del Paggio, I.F. Tannock
doi : 10.1016/j.annonc.2020.10.469
Volume 32, Issue 1, January 2021, Pages 20-22
B. Eichhorst, T. Robak, E. Montserrat, P. Ghia, ... U. Mey
doi : 10.1016/j.annonc.2020.09.019
Volume 32, Issue 1, January 2021, Pages 23-33
M.-L. Schubert, M. Schmitt, L. Wang, C.A. Ramos, ... P. Dreger
doi : 10.1016/j.annonc.2020.10.478
Volume 32, Issue 1, January 2021, Pages 34-48
P.A. Fasching, T. Link, J. Hauke, F. Seither, ... S. Loibl
doi : 10.1016/j.annonc.2020.10.471
Volume 32, Issue 1, January 2021, Pages 49-57
The efficacy and toxicity of olaparib as combination therapy in early breast cancer (BC) patients with homologous recombinant deficiency (HRD) [score high and/or germline (g) or tumour (t) BRCA1/2 mutation] is not well described. GeparOLA (ClinicalTrials.gov, NCT02789332) investigated olaparib in combination with paclitaxel in HER2-negative early BC with HRD.
O. Sipos, H. Tovey, J. Quist, S. Haider, ... A. Grigoriadis
doi : 10.1016/j.annonc.2020.10.475
Volume 32, Issue 1, January 2021, Pages 58-65
In the TNT trial of triple negative breast cancer (NCT00532727), germline BRCA1/2 mutations were present in 28% of carboplatin responders. We assessed quantitative measures of structural chromosomal instability (CIN) to identify a wider patient subgroup within TNT with preferential benefit from carboplatin over docetaxel.
F. Petrelli, E. Rulli, R. Labianca, S. Lonardi, ... A. Sobrero
doi : 10.1016/j.annonc.2020.10.477
Volume 32, Issue 1, January 2021, Pages 66-76
Oxaliplatin-based adjuvant chemotherapy is the standard treatment of high-risk colon cancer (CC). A shorter duration (3 months) can achieve a similar outcome [in terms of relapse-free survival (RFS)] to a longer duration. This study reports the overall survival (OS) analysis of the three or six colon adjuvant (TOSCA) phase III study. It assessed different adjuvant chemotherapy durations in patients with resected high-risk stage II and stage III CC.
K. Yamazaki, T. Yamanaka, M. Shiozawa, D. Manaka, ... T. Yoshino
doi : 10.1016/j.annonc.2020.10.480
Volume 32, Issue 1, January 2021, Pages 77-84
Oxaliplatin-based adjuvant chemotherapy may be associated with debilitating peripheral sensory neuropathy (PSN) in patients with high-risk stage II colon cancer. This open-label, multicenter, randomized phase III trial was conducted as a prospective pooled analysis to investigate the non-inferiority of 3 versus 6 months of adjuvant oxaliplatin-based chemotherapy.
M. Shi, A. Gu, H. Tu, C. Huang, ... Y.L. Wu
doi : 10.1016/j.annonc.2020.10.479
Volume 32, Issue 1, January 2021, Pages 85-96
Polymeric micellar paclitaxel (pm-Pac) is a novel Cremophor EL-free, nanoparticle micellar formulation of paclitaxel. We aimed to compare the efficacy and safety between pm-Pac plus cisplatin and solvent-based paclitaxel (sb-Pac) plus cisplatin in advanced non-small-cell lung cancer (NSCLC).
L. Albiges, P. Barthélémy, M. Gross-Goupil, S. Negrier, ... B. Escudier
doi : 10.1016/j.annonc.2020.09.021
Volume 32, Issue 1, January 2021, Pages 97-102
Treatment with tivozanib, a highly selective and potent vascular endothelial growth factor receptor tyrosine kinase inhibitor, has demonstrated single-agent efficacy in advanced renal cell carcinoma (RCC) along with minimal off-target toxicities and a favorable adverse event (AE) profile. We report final results from TiNivo, a phase Ib/II study of tivozanib combined with nivolumab.
L. Tobalina, J. Armenia, E. Irving, M.J. O'Connor, J.V. Forment
doi : 10.1016/j.annonc.2020.10.470
Volume 32, Issue 1, January 2021, Pages 103-112
Germline mutations in the BRCA1 or BRCA2 (BRCA) genes predispose to hereditary breast and ovarian cancer and, mostly in the case of BRCA2, are also prevalent in cases of pancreatic and prostate malignancies. Tumours from these patients tend to lose both copies of the wild-type BRCA gene, which makes them exquisitely sensitive to platinum drugs and poly(ADP-ribose) polymerase inhibitors (PARPi), treatments of choice in these disease settings. Reversion secondary mutations with the capacity of restoring BRCA protein expression have been documented in the literature as bona fide mechanisms of resistance to these treatments.
A. Marra, D. Generali, P. Zagami, V. Cervoni, ... G. Curigliano
doi : 10.1016/j.annonc.2020.10.473
Volume 32, Issue 1, January 2021, Pages 113-119
Patients with cancer have high risk for severe complications and poor outcome to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-related disease [coronavirus disease 2019 (COVID-19)]. Almost all subjects with COVID-19 develop anti-SARS-CoV-2 immunoglobulin G (IgG) within 3 weeks after infection. No data are available on the seroconversion rates of cancer patients and COVID-19.
S. Hiltbrunner, C. Britschgi, P. Schuberth, L. Bankel, ... A. Curioni-Fontecedro
doi : 10.1016/j.annonc.2020.10.474
Volume 32, Issue 1, January 2021, Pages 120-121
D.S. Hersby, T.H. Do, A.O. Gang, T.H. Nielsen
doi : 10.1016/j.annonc.2020.09.020
Volume 32, Issue 1, January 2021, Pages 121-123
A. Bauer-Mehren, D. Rüttinger
doi : 10.1016/j.annonc.2020.10.467
Volume 32, Issue 1, January 2021, Pages 123-124
F. Avanzini
doi : 10.1016/j.annonc.2020.09.022
Volume 32, Issue 1, January 2021, Pages 124-125
M. Schuler
doi : 10.1016/j.annonc.2020.10.593
Volume 32, Issue 1, January 2021, Page 126
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