TY - JOUR
T1 - Correction to
T2 - Selinexor in combination with carboplatin and paclitaxel in patients with advanced solid tumors: Results of a single-center, multi-arm phase Ib study (Investigational New Drugs, (2022), 40, 2, (290-299), 10.1007/s10637-021-01188-1)
AU - Thein, Kyaw Z.
AU - Karp, Daniel D.
AU - Tsimberidou, Apostolia
AU - Gong, Jing
AU - Sulovic, Selma
AU - Shah, Jatin
AU - Milton, Denái R.
AU - Hong, David S.
AU - Janku, Filip
AU - McQuinn, Lacey
AU - Stephen, Bettzy A.
AU - Colen, Rivka
AU - Carter, Brett W.
AU - Yap, Timothy A.
AU - Piha-Paul, Sarina A.
AU - Fu, Siqing
AU - Meric-Bernstam, Funda
AU - Naing, Aung
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/4
Y1 - 2025/4
N2 - In the original published version of the paper, “Selinexor in combination with carboplatin and paclitaxel in patients with advanced solid tumors: Results of a single-center, multi-arm phase Ib study”, 3 patients with unconfirmed partial response (uPR) were considered to have partial response as their best response. However, as PR could not be confirmed in the subsequent scan, best response has now been corrected per RECIST criteria v1.1. for these 3 patients. Two patients are now reported to have stable disease and 1 patient is now reported to have clinical progression of disease as their best response. As a result of these changes, the objective response rate and disease control rate are corrected to be 8% and 17%, respectively. The median progression-free survival (PFS) is 3.5 months (95% confidence interval [CI]: 1.6 – 4.7 months), while the median overall survival (OS) is 10.3 months (95% CI: 4.2 – 18.7 months). To align with protocol-defined endpoints, time to treatment failure (TTF) has been deleted. Figure 1 has been revised accordingly. The authors apologize for the mistake. (Figure presented.) a Waterfall plot of maximum change in tumor measurements (per RECIST v1.1) for evaluable patients.
AB - In the original published version of the paper, “Selinexor in combination with carboplatin and paclitaxel in patients with advanced solid tumors: Results of a single-center, multi-arm phase Ib study”, 3 patients with unconfirmed partial response (uPR) were considered to have partial response as their best response. However, as PR could not be confirmed in the subsequent scan, best response has now been corrected per RECIST criteria v1.1. for these 3 patients. Two patients are now reported to have stable disease and 1 patient is now reported to have clinical progression of disease as their best response. As a result of these changes, the objective response rate and disease control rate are corrected to be 8% and 17%, respectively. The median progression-free survival (PFS) is 3.5 months (95% confidence interval [CI]: 1.6 – 4.7 months), while the median overall survival (OS) is 10.3 months (95% CI: 4.2 – 18.7 months). To align with protocol-defined endpoints, time to treatment failure (TTF) has been deleted. Figure 1 has been revised accordingly. The authors apologize for the mistake. (Figure presented.) a Waterfall plot of maximum change in tumor measurements (per RECIST v1.1) for evaluable patients.
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U2 - 10.1007/s10637-024-01493-5
DO - 10.1007/s10637-024-01493-5
M3 - Comment/debate
C2 - 39976873
AN - SCOPUS:85218674989
SN - 0167-6997
VL - 43
SP - 446
EP - 447
JO - Investigational New Drugs
JF - Investigational New Drugs
IS - 2
ER -