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Peer-reviewedCC BYClinics and Research in Hepatology and Gastroenterology

Relative dose intensity of gemcitabine-nab-paclitaxel combination as second-line or more in locally advanced or metastatic pancreatic adenocarcinoma

Abstract

• Relative dose intensity (RDI) of gemzar-nab-paclitaxel (GNP) has not been reported in second line and more in advanced pancreatic carcinoma. • The RDI is relatively low with 50 % of patients who received GNP at a RDI ≥70 % during the first months of treatment resulting of treatment schedule modification in two third of cases and a full dose in only 15 %. • There was no significant difference in prognosis between RDI <70 % and ≥70 % supporting that alternative GNP regimens may be of interest in that setting. Gemcitabine-nab-paclitaxel (GNP) is widely used in treating advanced or metastatic pancreatic adenocarcinoma (a/mPA), but no data are available regarding its relative dose intensity (RDI) beyond the first line. To assess the impact of the RDI of GNP as second-line or greater therapy (L2+) for a/mPA. Patients with a/mPA undergoing L2+ treatment were retrospectively included. The RDI was analysed from the start of GNP to the first CT scan. Overall survival (OS), progression-free survival (PFS) and toxicity were analysed according to the RDI at a predefined threshold of 70 %. A total of 116 patients were included, with a median RDI of 70 % (range, 20 %-114 %). There was no significant difference in OS or PFS between RDI<70 % and ≥70 %, with median of 7.0 and 8.1 months (adjusted HR = 1.35; CI95 % [0.89–2.05]; p = 0.2) and 3.1 vs 3.4 months (adjusted HR = 1.36; CI95 % [0.91–2.05]; p = 0.14), respectively. Grade ≥3 toxicities were more common in RDI <70 % as compared to RDI ≥70 % (56.9 % vs. 37.9 %, p = 0.04) and responsible for more GNP dose reductions (67.7 % vs. 50 %, p = 0.13) and schedule modifications (72.4 % vs. 48.2 %, p = 0.008). Our results suggest that the level of GNP exposure, at a predefined RDI threshold of 70 %, had no significant effect on survival in our patients treated in L2+ for a/mPA. Alternative GNP regimens may be evaluated in patients undergoing L2+ treatment for a/mPA.

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BibTeX
@article{grancher2026relative,
  title = {{Relative dose intensity of gemcitabine-nab-paclitaxel combination as second-line or more in locally advanced or metastatic pancreatic adenocarcinoma}},
  author = {Adrien Grancher and Leila Tagemouati and André Gillibert and Lilian Schwarz and Virginie Vernon and David Sefrioui and Pierre Michel and Marie Dutherage and Frédéric Di Fiore},
  journal = {Clinics and Research in Hepatology and Gastroenterology},
  year = {2026},
  month = sep,
  doi = {10.1016/j.clinre.2025.102583},
  url = {https://hal.science/hal-05742246v1},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Relative dose intensity of gemcitabine-nab-paclitaxel combination as second-line or more in locally advanced or metastatic pancreatic adenocarcinoma
AU  - Adrien Grancher
AU  - Leila Tagemouati
AU  - André Gillibert
AU  - Lilian Schwarz
AU  - Virginie Vernon
AU  - David Sefrioui
AU  - Pierre Michel
AU  - Marie Dutherage
AU  - Frédéric Di Fiore
PY  - 2026
DA  - 2026/09/08
JO  - Clinics and Research in Hepatology and Gastroenterology
DO  - 10.1016/j.clinre.2025.102583
UR  - https://hal.science/hal-05742246v1
AB  - • Relative dose intensity (RDI) of gemzar-nab-paclitaxel (GNP) has not been reported in second line and more in advanced pancreatic carcinoma. • The RDI is relatively low with 50 % of patients who received GNP at a RDI ≥70 % during the first months of treatment resulting of treatment schedule modification in two third of cases and a full dose in only 15 %. • There was no significant difference in prognosis between RDI <70 % and ≥70 % supporting that alternative GNP regimens may be of interest in that setting. Gemcitabine-nab-paclitaxel (GNP) is widely used in treating advanced or metastatic pancreatic adenocarcinoma (a/mPA), but no data are available regarding its relative dose intensity (RDI) beyond the first line. To assess the impact of the RDI of GNP as second-line or greater therapy (L2+) for a/mPA. Patients with a/mPA undergoing L2+ treatment were retrospectively included. The RDI was analysed from the start of GNP to the first CT scan. Overall survival (OS), progression-free survival (PFS) and toxicity were analysed according to the RDI at a predefined threshold of 70 %. A total of 116 patients were included, with a median RDI of 70 % (range, 20 %-114 %). There was no significant difference in OS or PFS between RDI<70 % and ≥70 %, with median of 7.0 and 8.1 months (adjusted HR = 1.35; CI95 % [0.89–2.05]; p = 0.2) and 3.1 vs 3.4 months (adjusted HR = 1.36; CI95 % [0.91–2.05]; p = 0.14), respectively. Grade ≥3 toxicities were more common in RDI <70 % as compared to RDI ≥70 % (56.9 % vs. 37.9 %, p = 0.04) and responsible for more GNP dose reductions (67.7 % vs. 50 %, p = 0.13) and schedule modifications (72.4 % vs. 48.2 %, p = 0.008). Our results suggest that the level of GNP exposure, at a predefined RDI threshold of 70 %, had no significant effect on survival in our patients treated in L2+ for a/mPA. Alternative GNP regimens may be evaluated in patients undergoing L2+ treatment for a/mPA.
SN  - 2210-7401
SN  - 2210-741X
ER  -