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BMC Cancer. 2021;21(1):537.

Comparison between FOLFIRINOX and gemcitabine plus nab-paclitaxel including sequential treatment for metastatic pancreatic cancer: a propensity score matching approach.

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제1저자 전중원 · 교신저자 이상협

소속 (3)
  1. Center for Liver and Pancreatobiliary Cancer, Research Institute and Hospital, National Cancer Center, Goyang, South Korea.
  2. Department of Internal Medicine and Liver Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea. gidoctor@korea.com.
  3. Department of Internal Medicine and Liver Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.

Abstract

BACKGROUND FOLFIRINOX (FFX) and Gemcitabine plus nab-paclitaxel (GnP) have been recommended as the first-line chemotherapy for metastatic pancreatic cancer (mPC). However, the evidence is lacking comparing not only two regimens, but also sequential treatment (FFX-GnP vs. GnP-FFX).

METHODS Data of 528 patients (FFX, n = 371; GnP, n = 157) with mPC were collected retrospectively. Propensity score matching was conducted to alleviate imbalance of the two groups. Overall survival (OS), progression free survival (PFS), and toxicity of patients were analyzed.

RESULTS In the whole population, OS (12.5 months vs. 10.3 months, P = 0.05) and PFS (7.1 months vs. 5.8 months, P = 0.02) were longer in the FFX group before matching and after matching (OS: 11.8 months vs. 10.3 months, P = 0.02; PFS: 7.2 months vs. 5.8 months, P < 0.01). For sequential treatment, OS and PFS showed no significant difference. Interruptions of chemotherapy due to toxicities were more frequent (6.8 vs. 29.3%, P < 0.001) in the GnP group, and cessation of chemotherapy showed a significant association with mortality (z = - 1.94, P = 0.03).

CONCLUSIONS FFX achieved a longer overall survival than GnP in mPC, but not in the comparison for sequential treatment. More frequent adverse events followed by treatment interruptions during GnP might lead to a poor survival outcome. Therefore, FFX would be a better first-line treatment option than GnP for mPC.

Keywords

Albumin-bound paclitaxelFolfirinoxPancreatic neoplasmsSurvival

Figures

Fig. 1
Fig. 1 Progression free survival a before and b after propensity score matching
Fig. 2
Fig. 2 Overall survival a before and b after propensity score matching
Fig. 3
Fig. 3 Progression free survival of sequential treatment in the a whole and b matched populations
Fig. 4
Fig. 4 Overall survival of sequential treatment in the a whole and b matched populations

그림 출처: PubMed Central 공개 논문 (PMC8114681)

Conflict of interest statement

The authors declare no competing interests.

그 밖의 정보
출판 형태
Comparative Study, Journal Article
저널
BMC cancer · eISSN 1471-2407
전자 출판
2021-05-11
MeSH
Aged · Albumins / administration & dosage / adverse effects · Antineoplastic Combined Chemotherapy Protocols / adverse effects / therapeutic use · Deoxycytidine / administration & dosage / adverse effects / analogs & derivatives · Female · Fluorouracil / adverse effects / therapeutic use · Humans · Irinotecan / adverse effects / therapeutic use · Leucovorin / adverse effects / therapeutic use · Male · Middle Aged · Neoplasm Metastasis · Oxaliplatin / adverse effects / therapeutic use · Paclitaxel / administration & dosage / adverse effects · Pancreatic Neoplasms / drug therapy / mortality / pathology · Propensity Score · Gemcitabine
Substances
130-nm albumin-bound paclitaxel · Albumins · folfirinox · Oxaliplatin · Deoxycytidine · Irinotecan · Paclitaxel · Leucovorin · Fluorouracil · Gemcitabine
참고문헌
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