Westphalen, C. Benedikt, Kukiolka, Tobias, Garlipp, Benjamin, Hahn, Lars, Fuchs, Martin, Malfertheiner, Peter, Reiser, Marcel, Kuetting, Fabian, Heinemann, Volker, Beringer, Andreas and Waldschmidt, Dirk T. (2020). Correlation of skin rash and overall survival in patients with pancreatic cancer treated with gemcitabine and erlotinib - results from a non-interventional multi-center study. BMC Cancer, 20 (1). LONDON: BMC. ISSN 1471-2407

Full text not available from this repository.

Abstract

BackgroundGemcitabine/erlotinib treatment offers limited benefit in unselected patients with pancreatic ductal adenocarcinoma (PDAC). Development of skin rash has been associated with favorable outcomes in patients treated with gemcitabine/erlotinib. This study aimed to extend knowledge on the effectiveness of gemcitabine/erlotinib in metastatic PDAC in the context of clinical practice and with focus on skin rash.MethodsThis multicenter, non-interventional study enrolled 376 patients with metastatic PDAC receiving gemcitabine/erlotinib. The primary endpoint was overall survival (OS) in patients with skin rash versus no skin rash. Secondary endpoints included progression-free survival (PFS), treatment satisfaction and safety. All data were analyzed using descriptive statistics. Survival time and time to disease progression were estimated using the Kaplan-Meier method. Effectiveness endpoints were analyzed for subgroups by skin rash grade (no rash, rash grade 1, rash grade >= 2), duration of erlotinib treatment (<= 8weeks, >8weeks), Eastern Cooperative Oncology Group (ECOG) performance status at baseline (0-1, 2) and age (<= 65years, >65years).ResultsWithin the full analysis set (FAS; N=270), 48 patients (17.8%) developed grade 1 rash, 51 patients (18.9%) grade >= 2 rash, while 171 patients (63.3%) did not develop a rash. Median OS of all patients was 9.11months with an OS of 9.93months in rash-positive and 8.68months in rash-negative patients. Median PFS was 5.06months for rash-positive and 4.11months for rash-negative patients. PFS was longer in patients with rash grade >= 2 and in older patients (>65years). Examination using a multivariate Cox proportional model revealed that an age>65years was associated with longer OS (hazard ratio 0.640; p=0.0327) and PFS (hazard ratio 0.642; p=0.0026). Out of the 338 patients in the SAF, 310 patients (91.7%) experienced at least one AE, and 176 patients (52.1%) experienced skin-related side effects, all of which were CTC grade 1 to 3.ConclusionsComparing rash-positive with rash-negative patients showed no significant difference in survival. While patients with rash grade >= 2 and older patients (independent of skin reactions) showed longer PFS, this did not translate into prolonged OS. The study did not reveal new safety signals.Trial registrationClinicalTrials.gov Identifier: NCT01782690, retrospectively registered on 4 February 2013.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Westphalen, C. BenediktUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kukiolka, TobiasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Garlipp, BenjaminUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hahn, LarsUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fuchs, MartinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Malfertheiner, PeterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Reiser, MarcelUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kuetting, FabianUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Heinemann, VolkerUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Beringer, AndreasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Waldschmidt, Dirk T.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-344114
DOI: 10.1186/s12885-020-6636-7
Journal or Publication Title: BMC Cancer
Volume: 20
Number: 1
Date: 2020
Publisher: BMC
Place of Publication: LONDON
ISSN: 1471-2407
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
PHASE-III TRIAL; FOLFIRINOX; EFFICACY; OUTCOMES; DEATHS; SAFETYMultiple languages
OncologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/34411

Downloads

Downloads per month over past year

Altmetric

Export

Actions (login required)

View Item View Item