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FOLFIRINOX or Gemcitabine-based Chemotherapy for Borderline Resectable and Locally Advanced Pancreatic Cancer: A Multi-institutional, Patient-Level, Meta-analysis and Systematic Review

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dc.contributor.author박정엽-
dc.date.accessioned2023-07-12T03:13:15Z-
dc.date.available2023-07-12T03:13:15Z-
dc.date.issued2023-07-
dc.identifier.issn1068-9265-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/195539-
dc.description.abstractBackground: Pancreatic cancer often presents as locally advanced (LAPC) or borderline resectable (BRPC). Neoadjuvant systemic therapy is recommended as initial treatment. It is currently unclear what chemotherapy should be preferred for patients with BRPC or LAPC. Methods: We performed a systematic review and multi-institutional meta-analysis of patient-level data regarding the use of initial systemic therapy for BRPC and LAPC. Outcomes were reported separately for tumor entity and by chemotherapy regimen including FOLFIRINOX (FIO) or gemcitabine-based. Results: A total of 23 studies comprising 2930 patients were analyzed for overall survival (OS) calculated from the beginning of systemic treatment. OS for patients with BRPC was 22.0 months with FIO, 16.9 months with gemcitabine/nab-paclitaxel (Gem/nab), 21.6 months with gemcitabine/cisplatin or oxaliplatin or docetaxel or capecitabine (GemX), and 10 months with gemcitabine monotherapy (Gem-mono) (p < 0.0001). In patients with LAPC, OS also was higher with FIO (17.1 months) compared with Gem/nab (12.5 months), GemX (12.3 months), and Gem-mono (9.4 months; p < 0.0001). This difference was driven by the patients who did not undergo surgery, where FIO was superior to other regimens. The resection rates for patients with BRPC were 0.55 for gemcitabine-based chemotherapy and 0.53 with FIO. In patients with LAPC, resection rates were 0.19 with Gemcitabine and 0.28 with FIO. In resected patients, OS for patients with BRPC was 32.9 months with FIO and not different compared to Gem/nab, (28.6 months, p = 0.285), GemX (38.8 months, p = 0.1), or Gem-mono (23.1 months, p = 0.083). A similar trend was observed in resected patients converted from LAPC. Conclusions: In patients with BRPC or LAPC, primary treatment with FOLFIRINOX compared with Gemcitabine-based chemotherapy appears to provide a survival benefit for patients that are ultimately unresectable. For patients that undergo surgical resection, outcomes are similar between GEM+ and FOLFIRINOX when delivered in the neoadjuvant setting.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherSpringer-
dc.relation.isPartOfANNALS OF SURGICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols / therapeutic use-
dc.subject.MESHFluorouracil-
dc.subject.MESHGemcitabine*-
dc.subject.MESHHumans-
dc.subject.MESHLeucovorin / therapeutic use-
dc.subject.MESHMulticenter Studies as Topic-
dc.subject.MESHNeoadjuvant Therapy / adverse effects-
dc.subject.MESHOxaliplatin / therapeutic use-
dc.subject.MESHPaclitaxel-
dc.subject.MESHPancreatic Neoplasms* / drug therapy-
dc.subject.MESHPancreatic Neoplasms* / pathology-
dc.subject.MESHPancreatic Neoplasms* / surgery-
dc.titleFOLFIRINOX or Gemcitabine-based Chemotherapy for Borderline Resectable and Locally Advanced Pancreatic Cancer: A Multi-institutional, Patient-Level, Meta-analysis and Systematic Review-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorDilmurodjon Eshmuminov-
dc.contributor.googleauthorBotirjon Aminjonov-
dc.contributor.googleauthorRussell F Palm-
dc.contributor.googleauthorGiuseppe Malleo-
dc.contributor.googleauthorRyan K Schmocker-
dc.contributor.googleauthorRaëf Abdallah-
dc.contributor.googleauthorChanghoon Yoo-
dc.contributor.googleauthorWalid L Shaib-
dc.contributor.googleauthorMarcel André Schneider-
dc.contributor.googleauthorElena Rangelova-
dc.contributor.googleauthorYoo Jin Choi-
dc.contributor.googleauthorHongbeom Kim-
dc.contributor.googleauthorJ Bart Rose-
dc.contributor.googleauthorSameer Patel-
dc.contributor.googleauthorGregory C Wilson-
dc.contributor.googleauthorSarah Maloney-
dc.contributor.googleauthorLea Timmermann-
dc.contributor.googleauthorKlaus Sahora-
dc.contributor.googleauthorFabian Rössler-
dc.contributor.googleauthorVíctor Lopez-Lopez-
dc.contributor.googleauthorEmanuel Boyer-
dc.contributor.googleauthorLaura Maggino-
dc.contributor.googleauthorThomas Malinka-
dc.contributor.googleauthorJeong Youp Park-
dc.contributor.googleauthorMatthew H G Katz-
dc.contributor.googleauthorLaura Prakash-
dc.contributor.googleauthorSyed A Ahmad-
dc.contributor.googleauthorScott Helton-
dc.contributor.googleauthorJin-Young Jang-
dc.contributor.googleauthorSarah E Hoffe-
dc.contributor.googleauthorRoberto Salvia-
dc.contributor.googleauthorJulien Taieb-
dc.contributor.googleauthorJin He-
dc.contributor.googleauthorPierre-Alain Clavien-
dc.contributor.googleauthorUlrike Held-
dc.contributor.googleauthorKuno Lehmann-
dc.identifier.doi10.1245/s10434-023-13353-2-
dc.contributor.localIdA01647-
dc.relation.journalcodeJ00179-
dc.identifier.eissn1534-4681-
dc.identifier.pmid37020094-
dc.contributor.alternativeNamePark, Jeong Youp-
dc.contributor.affiliatedAuthor박정엽-
dc.citation.volume30-
dc.citation.number7-
dc.citation.startPage4417-
dc.citation.endPage4428-
dc.identifier.bibliographicCitationANNALS OF SURGICAL ONCOLOGY, Vol.30(7) : 4417-4428, 2023-07-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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