Evidence map›Paper›PMID 29866170›Full record

Trial reportCancer communications (London, England)2018

Attenuated FOLFIRINOX in the salvage treatment of gemcitabine-refractory advanced pancreatic cancer: a phase II study.

Jung Hoon Kim, Sang-Cheol Lee, Sung Yong Oh, Seo-Young Song, Namsu Lee, Eun Mi Nam, Soonil Lee, In Gyu Hwang, Hyo Rak Lee, Kyu Taek Lee and 7 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Cancer communications (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Symptom Management in Pancreatic Cancer.Current treatment options in oncology · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Immune Checkpoint Blockade in Combination with Stereotactic Body Radiotherapy in Patients with Metastatic Pancreatic Ductal Adenocarcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Jung Hoon KimDepartment of Internal Medicine, Institute of Health Sciences, Gyeongsang National University, 15 Jinju-daero 816beon-gil, Jinju, 52727, Republic of Korea.
Sang-Cheol LeeDivsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Cheonan, Cheonan, 31151, Republic of Korea.
Sung Yong OhDepartment of Internal Medicine, Dong-A University Hospital, Busan, 49201, Republic of Korea.
Seo-Young SongDepartment of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, 24289, Republic of Korea.
Namsu LeeDivsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Seoul, Seoul, 04401, Republic of Korea.
Eun Mi NamDepartment of Internal Medicine, Ewha Womans University, College of Medicine, Seoul, 07985, Republic of Korea.
Soonil LeeDepartment of Internal Medicine, Dankook University Hospital, Cheonan, 31116, Republic of Korea.
In Gyu HwangDepartment of Internal Medicine, Chung-Ang University, College of Medicine, Seoul, 06973, Republic of Korea.
Hyo Rak LeeDivision of Hematology and Medical Oncology, Department of Internal Medicine, Korea Cancer Hospital, Seoul, 01812, Republic of Korea.
Kyu Taek LeeDivsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Cheonan, Cheonan, 31151, Republic of Korea.
Sang-Byung BaeDivsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Cheonan, Cheonan, 31151, Republic of Korea.
Han Jo KimDivsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Cheonan, Cheonan, 31151, Republic of Korea.
Joung Soon JangDepartment of Internal Medicine, Chung-Ang University, College of Medicine, Seoul, 06973, Republic of Korea.
Do Hyoung LimDepartment of Internal Medicine, Dankook University Hospital, Cheonan, 31116, Republic of Korea.
Hyun Woo LeeDepartment of Hematology-Oncology, Ajou University Hospital, Suwon, 16499, Republic of Korea.
Seok Yun KangDepartment of Hematology-Oncology, Ajou University Hospital, Suwon, 16499, Republic of Korea.
Jung Hun KangDepartment of Internal Medicine, Institute of Health Sciences, Gyeongsang National University, 15 Jinju-daero 816beon-gil, Jinju, 52727, Republic of Korea. newatp@naver.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCombination therapy with oxaliplatin, irinotecan, fluorouracil, and leucovorin (FOLFIRINOX) chemotherapy drastically improves survival of advanced pancreatic cancer patients. However, the efficacy of FOLFIRINOX as a second-line treatment after gemcitabine failure has not been tested prospectively. We investigated the feasibility and safety of attenuated FOLFIRINOX in patients with gemcitabine-refractory advanced pancreatic cancer.

methodsA multicenter phase II prospective open-label, single-arm study was conducted at 14 hospitals. Patients with histologically proven invasive ductal pancreatic adenocarcinoma, a measurable or evaluable lesion, Eastern Cooperative Oncology Group performance status 0 or 1, adequate organ function, and aged 19 years or older were eligible. Attenuated FOLFIRINOX consisted of oxaliplatin 65 mg/m

resultsWe enrolled 39 patients from 14 institutions. The objective response rate was 10.3%, while the disease control rate was 64.1%. The 6-month and 1-year overall survival rates were 59.0% and 15.4%, respectively. Median progression-free survival and overall survival were 3.8 months (95% confidence interval [CI] 1.5-6.0 months) and 8.5 months (95% CI 5.6-11.4 months), respectively. Grade 3 or 4 adverse events were neutropenia (41.0%), nausea (10.3%), anorexia (10.3%), anemia (7.7%), mucositis (7.7%), pneumonia/pleural effusion (5.1%), and fatigue (5.1%). One treatment-related death attributable to septic shock occurred.

conclusionAttenuated FOLFIRINOX may be promising as a second-line therapy for gemcitabine-refractory pancreatic cancer.

Indexed as

AdenocarcinomaAdultAgedAntineoplastic Combined Chemotherapy ProtocolsDeoxycytidineDrug CombinationsDrug Resistance, NeoplasmFemaleFluorouracilGemcitabineHumansIrinotecanKaplan-Meier EstimateLeucovorinMaleMiddle AgedDeoxycytidineDrug CombinationsFluorouracilfolfirinoxGemcitabineIrinotecanLeucovorinOrganometallic CompoundsOxaliplatinAttenuated FOLFIRINOXGemcitabinePancreatic cancerSecond-line

Identifiers

PMID29866170
PMCPMC5993129

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.