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Dinesh Kumar Sinha

Researcher at Indira Gandhi Institute of Medical Sciences

Publications -  15
Citations -  244

Dinesh Kumar Sinha is an academic researcher from Indira Gandhi Institute of Medical Sciences. The author has contributed to research in topics: Bortezomib & Dexamethasone. The author has an hindex of 3, co-authored 13 publications receiving 92 citations.

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Once-per-week selinexor, bortezomib, and dexamethasone versus twice-per-week bortezomib and dexamethasone in patients with multiple myeloma (BOSTON): a randomised, open-label phase 3 trial

Sebastian Grosicki, +57 more
- 14 Nov 2020 - 
TL;DR: This phase 3, randomised, open-label trial aimed to evaluate the clinical benefit of weekly selinexor, bortezomib, and dexamethasone versus standard bortzomib and dex amethas one in patients with previously treated multiple myeloma.
Journal ArticleDOI

Effect of Age and Frailty on the Efficacy and Tolerability of Once-Weekly Selinexor, Bortezomib, and Dexamethasone in Previously Treated Multiple Myeloma

TL;DR: The phase 3 Boston trial as mentioned in this paper showed that once-weekly selinexor and bortezomib with low-dose dexamethasone (XVd) improved PFS and ORR compared with standard twice-weekly borteasomib and moderate-dose DDA in patients with previously treated multiple myeloma.
Journal ArticleDOI

Selinexor, bortezomib, and dexamethasone versus bortezomib and dexamethasone in previously treated multiple myeloma: Outcomes by cytogenetic risk.

TL;DR: In the phase 3 Boston study, patients with multiple myeloma (MM) after 1-3 prior regimens were randomized to once-weekly selinexor (an oral inhibitor of exportin 1 [XPO1]) plus bortezomib-dexamethasone (XVd) or twice-weekly borthemib-drug examethase (Vd), and XVd was associated with significant improvements in median progression-free survival (PFS), overall response rate (ORR), and lower rates of peripheral neuropathy,
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Assessment of tumor markers CA 19-9, CEA, CA 125, and CA 242 for the early diagnosis and prognosis prediction of gallbladder cancer

TL;DR: In this paper , the authors compared tumor marker levels between GBC and benign GB diseases (GBDs) and assessed the combined use of tumor markers to increase the diagnostic accuracy for GBC.