Evidence map›Paper›PMID 39043707›Full record

ArticleScientific reports2024

Nanoliposomal irinotecan with fluorouracil and folinic acid, FOLFIRINOX, and S-1 as second-line treatment for unresectable pancreatic cancer after gemcitabine/nab-paclitaxel.

Taro Shibuki, Taiga Otsuka, Mototsugu Shimokawa, Junichi Nakazawa, Shiho Arima, Masaru Fukahori, Keisuke Miwa, Yoshinobu Okabe, Futa Koga, Yujiro Ueda and 24 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

34 authors.

Taro ShibukiDivision of Drug and Diagnostic Development Promotion, Department for the Promotion of Drug and Diagnostic Development, Translational Research Support Office, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa-shi, Chiba, 277-8577, Japan.
Taiga OtsukaDepartment of Medical Oncology, Saga-Ken Medical Center Koseikan, 400 Kase-machi, Saga-shi, Saga, 840-8571, Japan. otsuka.ta222@gmail.com.
Mototsugu ShimokawaClinical Research Institute, National Kyushu Cancer Center, 3-1-1 Notame, Minami-ku, Fukuoka-shi, Fukuoka, 811-1395, Japan.
Junichi NakazawaDepartment of Gastroenterology, Kagoshima City Hospital, 37-1 Uearata-cho, Kagoshima-shi, Kagoshima, 890-8760, Japan.
Shiho ArimaDigestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima-shi, Kagoshima, 890-8520, Japan.
Masaru FukahoriDivision of Gastroenterology, Department of Medicine, Kurume University School of Medicine, 67 Asahi-machi, Kurume-shi, Fukuoka, 830-0011, Japan. fukahori_masaru@med.kurume-u.ac.jp.
Keisuke MiwaMultidisciplinary Treatment Cancer Center, Kurume University Hospital, 67 Asahi-machi, Kurume-shi, Fukuoka, 830-0011, Japan.
Yoshinobu OkabeDivision of Gastroenterology, Department of Medicine, Kurume University School of Medicine, 67 Asahi-machi, Kurume-shi, Fukuoka, 830-0011, Japan.
Futa KogaDepartment of Hepatobiliary and Pancreatology, Saga Medical Center Koseikan, 400 Kase-machi, Saga-shi, Saga, 840-8571, Japan.
Yujiro UedaDepartment of Hematology and Oncology, Japanese Red Cross Kumamoto Hospital, 2-1-1 Nagamine-Minami, Higashi-ku, Kumamoto-shi, Kumamoto, 861-8520, Japan.
Yoshihito KubotsuDepartment of Internal Medicine, Karatsu Red Cross Hospital, 2430 Watada,Karatsu-shi, Saga, 847-8588, Japan.
Akitaka MakiyamaDepartment of Hematology Oncology, Japan Community Healthcare Organization Kyushu Hospital, 1-8-1 Kishinoura, Yahatanishi-ku, Kitakyushu-shi, Fukuoka, 806-8501, Japan.
Hozumi ShimokawaDepartment of Hematology Oncology, Japan Community Healthcare Organization Kyushu Hospital, 1-8-1 Kishinoura, Yahatanishi-ku, Kitakyushu-shi, Fukuoka, 806-8501, Japan.
Shigeyuki TakeshitaDepartment of Gastroenterology, Japanese Red Cross Nagasaki Genbaku Hospital, 3-15, Morimachi, Nagasaki-shi, Nagasaki, 852-8511, Japan.
Kazuo NishikawaDepartment of Medical Oncology and Hematology, Oita University Faculty of Medicine, 1-1 Idaigaoka, Hasama-machi, Yufu-shi, Oita, 879-5593, Japan.
Azusa KomoriDepartment of Medical Oncology and Hematology, Oita University Faculty of Medicine, 1-1 Idaigaoka, Hasama-machi, Yufu-shi, Oita, 879-5593, Japan.
Satoshi OtsuDepartment of Medical Oncology and Hematology, Oita University Faculty of Medicine, 1-1 Idaigaoka, Hasama-machi, Yufu-shi, Oita, 879-5593, Japan.
Ayumu HosokawaDepartment of Clinical Oncology, University of Miyazaki Hospital, 5200, Kiyotakechoukihara, Miyazaki-shi, Miyazaki, 889-1692, Japan.
Tatsunori SakaiDepartment of Medical Oncology, National Hospital Organization Kumamoto Medical Center, 1-5, Ninomaru, Chuo-ku, Kumamoto-shi, Kumamoto, 860-0008, Japan.
Hisanobu OdaDivision of Integrative Medical Oncology, Saiseikai Kumamoto Hospital, 5-3-1,Oumi, Minami-ku, Kmamoto-shi, Kumamoto, 861-4193, Japan.
Machiko KawahiraDepartment of Gastroenterology, Kagoshima Kouseiren Hospital, 1-13-1, Yojirou,Kagoshima-shi, Kagoshima, 890-0062, Japan.
Shuji AritaDepartment of Chemotherapy, Miyazaki Prefectural Miyazaki Hospital, Miyazaki, Japan.
Takuya HondaDepartment of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki-shi, Nagasaki, 852-8501, Japan.
Hiroki TaguchiDepartment of Gastroenterology, Kagoshima City Hospital, 37-1 Uearata-cho, Kagoshima-shi, Kagoshima, 890-8760, Japan.
Kengo TsuneyoshiDepartment of Gastroenterology, Izumi General Medical Center, 520, Myoujin-cho, Izumi-shi, Kagoshima, 899-0131, Japan.
Yasunori KawaguchiDepartment of Gastroenterology, Asakura Medical Association Hospital, 422-1, Raiha, Asakura-shi, Fukuoka, 838-0069, Japan.
Toshihiro FujitaDepartment of Gastroenterology, Saiseikai Sendai Hospital, 2-46 Harada-cho, Satsumasendai-shi, Kagoshima, 895-0074, Japan.
Takahiro SakaeDepartment of Gastroenterology, Saiseikai Sendai Hospital, 2-46 Harada-cho, Satsumasendai-shi, Kagoshima, 895-0074, Japan.
Kenta NioDepartment of Medical Oncology, Sasebo Kyosai Hospital, 10-17 Shimanji-cho, Sasebo-shi, Nagasaki, 857-8575, Japan.
Yasushi IdeDepartment of Internal Medicine, Karatsu Red Cross Hospital, 2430 Watada,Karatsu-shi, Saga, 847-8588, Japan.
Norio UreshinoDepartment of Medical Oncology, Saga-Ken Medical Center Koseikan, 400 Kase-machi, Saga-shi, Saga, 840-8571, Japan.
Tsuyoshi ShirakawaEikoh Hospital, 3-8-15 Befu-nishi, Shime-machi, Kasuya-gun, Fukuoka, 811-2232, Japan.
Toshihiko MizutaDepartment of Internal Medicine, Fujikawa Hospital, 1-2-6 Matsubara, Saga-shi, Saga, 840-0831, Japan.
Kenji MitsugiDepartment of Medical Oncology, Sasebo Kyosai Hospital, 10-17 Shimanji-cho, Sasebo-shi, Nagasaki, 857-8575, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to compare second-line treatment outcomes for patients with unresectable pancreatic cancer previously treated with gemcitabine plus nab-paclitaxel (GnP) therapy. We conducted an integrated analysis of two retrospective studies included 318 patients receiving nanoliposomal irinotecan + 5-fluorouracil/folinic acid (NFF) (n = 102), S-1 (n = 57), or FOLFIRINOX (n = 14) as second-line treatment. Median overall survival (OS) in the NFF group was 9.08 months, significantly better than S-1 (4.90 months, P = 0.002). FOLFIRINOX had a median OS of 4.77 months, not statistically different from NFF. Subgroup analyses of OS indicated NFF was generally superior, however, a statistical interaction was observed between the treatment regimen in serum Alb < 3.5 g/dL (P = 0.042) and serum CRP ≥ 0.3 mg/dL (P = 0.006). Median progression-free survival (PFS) was 2.93 months for NFF, significantly better than S-1 (2.53 months, P = 0.024), while FOLFIRINOX had a comparable PFS (3.04 months, P = 0.948). Multivariate analysis identified the serum CRP, serum CA19-9, duration of first-line GnP therapy, and use (yes/no) of S-1 for second-line treatment as independent predictors for OS. This study concludes that second-line NFF therapy demonstrated a more favorable OS compared to S-1 therapy, however, it is still important to consider the patient background characteristics while selecting the most appropriate treatment.

Indexed as

AlbuminsAntineoplastic Combined Chemotherapy ProtocolsDeoxycytidineDrug CombinationsFluorouracilGemcitabineIrinotecanLeucovorinOxaliplatinPaclitaxelPancreatic NeoplasmsAdultAgedAged, 80 and overFemaleHumans130-nm albumin-bound paclitaxelAlbuminsDeoxycytidineDrug CombinationsFluorouracilfolfirinoxGemcitabineIrinotecanLeucovorinLiposomesOxaliplatinOxonic AcidPaclitaxelS 1 (combination)TegafurFOLFIRINOXNanoliposomal irinotecanPancreatic cancerS-1Second line

Identifiers

PMID39043707
PMCPMC11266600

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