3716. Scientific advances and the end of tuberculosis: a report from the Lancet Commission on Tuberculosis.
作者: Michael Reid.;Yvan Jean Patrick Agbassi.;Nimalan Arinaminpathy.;Alyssa Bercasio.;Anurag Bhargava.;Madhavi Bhargava.;Amy Bloom.;Adithya Cattamanchi.;Richard Chaisson.;Daniel Chin.;Gavin Churchyard.;Helen Cox.;Claudia M Denkinger.;Lucica Ditiu.;David Dowdy.;Mark Dybul.;Anthony Fauci.;Endalkachew Fedaku.;Mustapha Gidado.;Mark Harrington.;Janika Hauser.;Petra Heitkamp.;Nick Herbert.;Ani Herna Sari.;Philip Hopewell.;Emily Kendall.;Aamir Khan.;Andrew Kim.;Irene Koek.;Sergiy Kondratyuk.;Nalini Krishnan.;Chu-Chang Ku.;Erica Lessem.;Erin V McConnell.;Payam Nahid.;Matt Oliver.;Madhukar Pai.;Mario Raviglione.;Theresa Ryckman.;Marco Schäferhoff.;Sachin Silva.;Peter Small.;Guy Stallworthy.;Zelalem Temesgen.;Kitty van Weezenbeek.;Anna Vassall.;Gustavo E Velásquez.;Nandita Venkatesan.;Gavin Yamey.;Armand Zimmerman.;Dean Jamison.;Soumya Swaminathan.;Eric Goosby.
来源: Lancet. 2023年402卷10411期1473-1498页 3719. NALIRIFOX versus nab-paclitaxel and gemcitabine in treatment-naive patients with metastatic pancreatic ductal adenocarcinoma (NAPOLI 3): a randomised, open-label, phase 3 trial.
作者: Zev A Wainberg.;Davide Melisi.;Teresa Macarulla.;Roberto Pazo Cid.;Sreenivasa R Chandana.;Christelle De La Fouchardière.;Andrew Dean.;Igor Kiss.;Woo Jin Lee.;Thorsten O Goetze.;Eric Van Cutsem.;A Scott Paulson.;Tanios Bekaii-Saab.;Shubham Pant.;Richard A Hubner.;Zhimin Xiao.;Huanyu Chen.;Fawzi Benzaghou.;Eileen M O'Reilly.
来源: Lancet. 2023年402卷10409期1272-1281页
Pancreatic ductal adenocarcinoma remains one of the most lethal malignancies, with few treatment options. NAPOLI 3 aimed to compare the efficacy and safety of NALIRIFOX versus nab-paclitaxel and gemcitabine as first-line therapy for metastatic pancreatic ductal adenocarcinoma (mPDAC).
3720. CFTR modulator therapy: transforming the landscape of clinical care in cystic fibrosis.
作者: Jennifer L Taylor-Cousar.;Paul D Robinson.;Michal Shteinberg.;Damian G Downey.
来源: Lancet. 2023年402卷10408期1171-1184页
Following discovery of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in 1989 and subsequent elucidation of the varied CFTR protein abnormalities that result, a new era of cystic fibrosis management has emerged-one in which scientific principles translated from the bench to the bedside have enabled us to potentially treat the basic defect in the majority of children and adults with cystic fibrosis, with a resultant burgeoning adult cystic fibrosis population. However, the long-term effects of these therapies on the multiple manifestations of cystic fibrosis are still under investigation. Understanding the effects of modulators in populations excluded from clinical trials is also crucial. Furthermore, establishing appropriate disease measures to assess efficacy in the youngest potential trial participants and in those whose post-modulator lung function is in the typical range for people without chronic lung disease is essential for continued drug development. Finally, recognising that a health outcome gap has been created for some people and widened for others who are not eligible for, cannot tolerate, or do not have access to modulators is important.
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