Pharmacokinetics, safety, tolerability, and feasibility of apatinib in combination with gefitinib in stage IIIB-IV EGFR-mutated non-squamous NSCLC : a drug-drug interaction study
© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature..
PURPOSE: Apatinib combined with gefitinib was proven to benefit advanced EGFR-mutant NSCLC patients in first-line treatment. This study aimed to evaluate the drug-drug interaction of gefitinib and apatinib when coadministered in EGFR-mutated NSCLC patients.
METHODS: In this phase 1b, multi-center, open-label, fixed-sequence study, the drug-drug interaction of gefitinib and apatinib was evaluated when coadministered in EGFR-mutated NSCLC patients. Patients received single-agent apatinib 500 mg QD on days 1-4. Gefitinib 250 mg QD was given on days 5-15 and combined with apatinib 500 mg QD on days 12-15. Serial blood samples were drawn on days 4 and 15. The plasma concentrations and other pharmacokinetics parameters were measured for apatinib with and without gefitinib.
RESULTS: The study enrolled 22 patients and 20 were analyzed for pharmacokinetics. There were no distinct differences in apatinib Cmax and AUC0-τ with versus without gefitinib (geometric LSM ratio, 0.96 [90% CI 0.84-1.10] for Cmax and 1.12 [90% CI 0.96-1.30] for AUC0-τ). Similar PFS and grade of treatment-emergent adverse events (TEAEs) were found between different Cmax and AUC0-τ of apatinib and gefitinib at 500 mg apatinib and 250 mg gefitinib dose levels.
CONCLUSIONS: Apatinib pharmacokinetics parameters were not significantly changed when coadministered with gefitinib. All TEAEs were manageable, and there was no need to change the dose level when combining apatinib and gefitinib (ClinicalTrials.gov identifier: NCT04390984, May 18, 2020).
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:92 |
---|---|
Enthalten in: |
Cancer chemotherapy and pharmacology - 92(2023), 5 vom: 30. Nov., Seite 411-418 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Ma, Yuxiang [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 18.09.2023 Date Revised 22.09.2023 published: Print-Electronic ClinicalTrials.gov: NCT04390984 Citation Status MEDLINE |
---|
doi: |
10.1007/s00280-023-04563-2 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM360179185 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM360179185 | ||
003 | DE-627 | ||
005 | 20231226082448.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1007/s00280-023-04563-2 |2 doi | |
028 | 5 | 2 | |a pubmed24n1200.xml |
035 | |a (DE-627)NLM360179185 | ||
035 | |a (NLM)37518060 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Ma, Yuxiang |e verfasserin |4 aut | |
245 | 1 | 0 | |a Pharmacokinetics, safety, tolerability, and feasibility of apatinib in combination with gefitinib in stage IIIB-IV EGFR-mutated non-squamous NSCLC |b a drug-drug interaction study |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 18.09.2023 | ||
500 | |a Date Revised 22.09.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a ClinicalTrials.gov: NCT04390984 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. | ||
520 | |a PURPOSE: Apatinib combined with gefitinib was proven to benefit advanced EGFR-mutant NSCLC patients in first-line treatment. This study aimed to evaluate the drug-drug interaction of gefitinib and apatinib when coadministered in EGFR-mutated NSCLC patients | ||
520 | |a METHODS: In this phase 1b, multi-center, open-label, fixed-sequence study, the drug-drug interaction of gefitinib and apatinib was evaluated when coadministered in EGFR-mutated NSCLC patients. Patients received single-agent apatinib 500 mg QD on days 1-4. Gefitinib 250 mg QD was given on days 5-15 and combined with apatinib 500 mg QD on days 12-15. Serial blood samples were drawn on days 4 and 15. The plasma concentrations and other pharmacokinetics parameters were measured for apatinib with and without gefitinib | ||
520 | |a RESULTS: The study enrolled 22 patients and 20 were analyzed for pharmacokinetics. There were no distinct differences in apatinib Cmax and AUC0-τ with versus without gefitinib (geometric LSM ratio, 0.96 [90% CI 0.84-1.10] for Cmax and 1.12 [90% CI 0.96-1.30] for AUC0-τ). Similar PFS and grade of treatment-emergent adverse events (TEAEs) were found between different Cmax and AUC0-τ of apatinib and gefitinib at 500 mg apatinib and 250 mg gefitinib dose levels | ||
520 | |a CONCLUSIONS: Apatinib pharmacokinetics parameters were not significantly changed when coadministered with gefitinib. All TEAEs were manageable, and there was no need to change the dose level when combining apatinib and gefitinib (ClinicalTrials.gov identifier: NCT04390984, May 18, 2020) | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Apatinib | |
650 | 4 | |a Drug–drug interaction | |
650 | 4 | |a Gefitinib | |
650 | 4 | |a Non-small cell lung cancer (NSCLC) | |
650 | 4 | |a Pharmacokinetics | |
650 | 7 | |a Gefitinib |2 NLM | |
650 | 7 | |a S65743JHBS |2 NLM | |
650 | 7 | |a apatinib |2 NLM | |
650 | 7 | |a 5S371K6132 |2 NLM | |
650 | 7 | |a Protein Kinase Inhibitors |2 NLM | |
650 | 7 | |a ErbB Receptors |2 NLM | |
650 | 7 | |a EC 2.7.10.1 |2 NLM | |
650 | 7 | |a EGFR protein, human |2 NLM | |
650 | 7 | |a EC 2.7.10.1 |2 NLM | |
700 | 1 | |a Chen, Qun |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Yang |e verfasserin |4 aut | |
700 | 1 | |a Xue, Jinhui |e verfasserin |4 aut | |
700 | 1 | |a Liu, Qianwen |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Yuanyuan |e verfasserin |4 aut | |
700 | 1 | |a Yang, Yunpeng |e verfasserin |4 aut | |
700 | 1 | |a Huang, Yan |e verfasserin |4 aut | |
700 | 1 | |a Fang, Wenfeng |e verfasserin |4 aut | |
700 | 1 | |a Hou, Zhiguo |e verfasserin |4 aut | |
700 | 1 | |a Li, Shaorong |e verfasserin |4 aut | |
700 | 1 | |a Wang, Jing |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Li |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Hongyun |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Cancer chemotherapy and pharmacology |d 1990 |g 92(2023), 5 vom: 30. Nov., Seite 411-418 |w (DE-627)NLM00036438X |x 1432-0843 |7 nnns |
773 | 1 | 8 | |g volume:92 |g year:2023 |g number:5 |g day:30 |g month:11 |g pages:411-418 |
856 | 4 | 0 | |u http://dx.doi.org/10.1007/s00280-023-04563-2 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 92 |j 2023 |e 5 |b 30 |c 11 |h 411-418 |