Evidence map›Paper›PMID 29860713›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2018

Infectious complications in adults undergoing intensive chemotherapy for acute myeloid leukemia in 2001-2005 using the Japan Adult Leukemia Study Group AML201 protocols.

Hideaki Kato, Hiroyuki Fujita, Nobu Akiyama, Shun-Ichi Kimura, Nobuhiro Hiramoto, Naoko Hosono, Tsutomu Takahashi, Kazuyuki Shigeno, Hitoshi Minamiguchi, Junichi Miyatake and 10 more

Abstract readHistorical Article
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In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 23% of its field
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

10 citing papers in PubMed, 19 citations in OpenAlex.

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  7. Medicinal Plants with Anti-Leukemic Effects: A Review.Molecules (Basel, Switzerland) · 2021
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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

20 authors at 12 institutions in 1 country.

Hideaki KatoDepartment of Hematology and Clinical Immunology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Hiroyuki FujitaDepartment of Hematology, Saiseikai Yokohama Nanbu Hospital, Yokohama, Japan. fujitah@nanbu.saiseikai.or.jp.ORCID http://orcid.org/0000-0002-6084-6863
Nobu AkiyamaDepartment of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
Shun-Ichi KimuraDivision of Hematology, Saitama Medical Center, Jichi Medical University, Shimotsuke, Japan.
Nobuhiro HiramotoDepartment of Hematology, Kobe City Medical Center General Hospital, Kobe, Japan.
Naoko HosonoDepartment of Hematology and Oncology, University of Fukui, Fukui, Japan.
Tsutomu TakahashiDepartment of Oncology/Hematology, Shimane University Hospital, Izumo, Japan.
Kazuyuki ShigenoDepartment of Hematology, Hamamatsu Medical Center, Hamamatsu, Japan.
Hitoshi MinamiguchiDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, Japan.
Junichi MiyatakeDepartment of Hematology, Sakai Hospital Kinki University Faculty of Medicine, Sakai, Japan.
Hiroshi HandaDepartment of Hematology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Yoshinobu KandaDivision of Hematology, Saitama Medical Center, Jichi Medical University, Shimotsuke, Japan.
Minoru YoshidaFourth Department of Internal Medicine, Mizonokuchi Hospital, Teikyo University School of Medicine, Tokyo, Japan.
Shuichi MiyawakiDepartment of Transfusion, Tokyo Metropolitan Ohtsuka Hospital, Tokyo, Japan.
Shigeki OhtakeKanazawa University, Kanazawa, Japan.
Tomoki NaoeNational Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Hitoshi KiyoiDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Itaru MatsumuraDepartment of Hematology and Rheumatology, Kindai University Faculty of Medicine, Higashiosaka, Japan.
Yasushi MiyazakiDepartment of Hematology and Molecular Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Japan Adult Leukemia Study Group
Jichi Medical University · JPKanazawa University · JPNagasaki University · JPSaiseikai Ibaraki Hospital · JPShiga University of Medical Science · JPUniversity of Fukui · JPGunma University · JPNagoya University · JPNational Hospital Organization · JPShimane University Hospital · JPTokyo Metropolitan Ohtsuka Hospital · JPYokohama City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe Japan Adult Leukemia Study Group (JALSG) AML201 protocols are regimens for remission induction and consolidation chemotherapy of acute myeloid leukemia (AML) and have been widely accepted in Japan since 2001. Management of infectious complications during chemotherapy has a key role in the supportive care of AML patients.

methodsBy using case report forms collected in December 2001 and December 2005, we retrospectively analyzed the infectious complications in adult patients treated by using the JALSG AML201 protocols against AML (excluding promyelocytic leukemia).

resultsOf 980 patients, 80.2% experienced febrile neutropenia (FN), 8.3% bacteremia/fungemia, and 10.3% pulmonary infection at least once during remission-induction chemotherapy. Gram-positive bacteremia accounted for 65.1% of bacteremia/fungemia in 2001-2005, compared with 38.2% in 1987-1991 and 45.9% in 1992-1995. Of 750 patients, 81.9% experienced FN, 21.9% bacteremia/fungemia, and 9.1% pulmonary infection at least once during consolidation chemotherapy. During consolidation chemotherapy, bacteremia/fungemia and pulmonary infection were significantly more frequent in the high-dose cytarabine (HDAC) arm than in the conventional multiagent arm (25.9 vs. 17.9% and 12.7 vs. 7.7%, respectively). Invasive pulmonary aspergillosis accounted for 15.8% of pulmonary infections during remission induction and 19.7% during consolidation chemotherapy.

conclusionsOur data suggest that patterns of infectious complications have changed between 1987 and 2005, possibly because of chemoprophylaxis with oral fluoroquinolones and improved diagnosis of invasive pulmonary aspergillosis by serum antigen analysis.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBacteremiaFemaleHistory, 21st CenturyHumansJapanLeukemia, Myeloid, AcuteMaleMiddle AgedRetrospective StudiesAcute myeloid leukemiaBacteremiaFebrile neutropeniaInfectious complicationJapan Adult Leukemia Study Group (JALSG)

Identifiers

PMID29860713
OpenAlexW2805807181

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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.