The efficacy and safety profile of third-line treatment in patients with metastatic pancreatic adenocarcinoma.

Chi-Chen Lan, Tai-Jan Chiu, Chia-Yen Hung, Kun-Yun Yeh, Chang-Hsien Lu, Yen-Yang Chen, Jen-Shi Chen, Yu-Shin Hung, Wen-Chi Chou
Author Information
  1. Chi-Chen Lan: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Linkou Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  2. Tai-Jan Chiu: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Kaohsiung Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  3. Chia-Yen Hung: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Linkou Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan; Division of Hematology and Oncology, Department of Internal Medicine, Mackay Memorial Hospital, Taipei, Taiwan.
  4. Kun-Yun Yeh: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Keelung Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  5. Chang-Hsien Lu: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Chiayi Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  6. Yen-Yang Chen: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Kaohsiung Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  7. Jen-Shi Chen: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Linkou Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  8. Yu-Shin Hung: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Linkou Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan.
  9. Wen-Chi Chou: Department of Hematology and Oncology, Chang Gung Memorial Hospital at Linkou Branch, Chang Gung University College of Medicine, Taoyaun, Taiwan. Electronic address: wenchi3992@yahoo.com.tw.

Abstract

BACKGROUND: For metastatic pancreatic ductal adenocarcinoma (mPDAC), there are no established third-line chemotherapy options. We examined the efficacy and safety of third-line chemotherapy in patients with mPDAC in real-world practice.
METHODS: We retrospectively analyzed 257 patients with mPDAC and progressive disease after first-line treatment with gemcitabine-based regimens and second-line treatment with liposomal irinotecan plus 5-fluorouracil and leucovorin at five Taiwanese medical centers from 2018 to 2022. Treatment efficacy and toxicity were analyzed in 77 of 257 patients receiving third-line treatment subsequently. We performed univariate and multivariate analyses to identify prognostic factors for overall survival (OS) in patients receiving third-line treatment.
RESULTS: Patients receiving third-line treatment had a median OS of 4.5 months (95 % confidence interval [CI], 3.6-5.4), compared to 1.6 months (95 % CI, 1.3-1.9) for those who did not. Independent poor prognostic factors for OS included the absence of previous pancreatectomy (adjusted hazard ratio [aHR] 3.03, 95 % CI, 1.30-7.14, P = 0.001), an ECOG score of ���2 ((aHR 9.81, 95 % CI 4.34-22.1, P < 0.001), and progressive disease response during second-line treatment (aHR 1.90, 95 % CI 1.21-8.91, P = 0.020, P = 0.020). Median OS for patients with none, one, two, and three poor prognostic factors were 15.9 (95 % CI, 12.3-19.6), 7.0 (2.6-13.3), 4.4 (3.5-5.2), and 2.0 (1.7-2.2) months, respectively. 43 of 77 patients (56 %) experienced at least one grade 3 or 4 toxicity.
CONCLUSION: In real-world settings, patients with mPDAC receiving third-line chemotherapy may have a moderate survival advantage, although clinicians should carefully select patients owing to high incidence of grade 3/4 toxicities.

Keywords

MeSH Term

Humans
Pancreatic Neoplasms
Male
Female
Middle Aged
Aged
Retrospective Studies
Antineoplastic Combined Chemotherapy Protocols
Fluorouracil
Leucovorin
Treatment Outcome
Adenocarcinoma
Irinotecan
Adult
Carcinoma, Pancreatic Ductal
Gemcitabine
Deoxycytidine
Neoplasm Metastasis
Prognosis
Aged, 80 and over

Chemicals

Fluorouracil
Leucovorin
Irinotecan
Gemcitabine
Deoxycytidine

Word Cloud

Created with Highcharts 10.0.0patientsthird-linetreatment1495 %3CImPDACreceivingOS2chemotherapyefficacyprognosticfactorsmonths9P = 0metastaticpancreaticadenocarcinomasafetyreal-worldanalyzed257progressivediseasesecond-linetoxicity77survival6poor001aHR020one0gradeBACKGROUND:ductalestablishedoptionsexaminedpracticeMETHODS:retrospectivelyfirst-linegemcitabine-basedregimensliposomalirinotecanplus5-fluorouracilleucovorinfiveTaiwanesemedicalcenters20182022TreatmentsubsequentlyperformedunivariatemultivariateanalysesidentifyoverallRESULTS:Patientsmedian5confidenceinterval[CI]6-5compared3-1Independentincludedabsencepreviouspancreatectomyadjustedhazardratio[aHR]0330-714ECOGscore���28134-22P < 0response9021-891Mediannonetwothree15123-1976-135-57-2respectively4356 %experiencedleastCONCLUSION:settingsmaymoderateadvantagealthoughclinicianscarefullyselectowinghighincidence3/4toxicitiesprofileEfficacyPancreaticcancerPrognosticfactorReal-worldevidenceSafety

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