Evidence map›Paper›PMID 26790967›Full record

ArticleCancer research and treatment2016

Splenomegaly and Its Associations with Genetic Polymorphisms and Treatment Outcome in Colorectal Cancer Patients Treated with Adjuvant FOLFOX.

Mi-Jung Kim, Sae-Won Han, Dae-Won Lee, Yongjun Cha, Kyung-Hun Lee, Tae-Yong Kim, Do-Youn Oh, Se Hyung Kim, Seock-Ah Im, Yung-Jue Bang and 1 more

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Article in Cancer research and treatment, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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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

12 citing papers in PubMed.

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4 · The record

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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

11 authors.

Mi-Jung KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Sae-Won HanDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Dae-Won LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Yongjun ChaDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Kyung-Hun LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Tae-Yong KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Do-Youn OhDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Se Hyung KimDepartment of Radiology and Institute of Radiation Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Seock-Ah ImDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Yung-Jue BangDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Tae-You KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSplenomegaly is a clinical surrogate of oxaliplatin-induced sinusoidal obstruction syndrome (SOS). We investigated development of splenomegaly and its association with treatment outcome and genetic polymorphisms following adjuvant 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) in colorectal cancer (CRC) patients. MATERIALS AND

methodsSplenomegaly was determined by spleen volumetry using computed tomography images obtained before initiation of chemotherapy and after completion of adjuvant FOLFOX in CRC patients. Ten genetic polymorphisms in 4 SOS-related genes (VEGFA, MMP9, NOS3, and GSTP1) were analyzed using DNA from peripheral blood mononuclear cells.

resultsOf 124 patients included, increase in spleen size was observed in 109 (87.9%). Median change was 31% (range, -42% to 168%). Patients with splenomegaly had more severe thrombocytopenia compared to patients without splenomegaly during the chemotherapy period (p < 0.0001). The cumulative dose of oxaliplatin and the lowest platelet count during the chemotherapy period were clinical factors associated with splenomegaly. However, no significant associations were found between genetic polymorphisms and development of splenomegaly. Disease-free survival was similar regardless of the development of splenomegaly.

conclusionSplenomegaly was frequently observed in patients receiving adjuvant FOLFOX and resulted in more severe thrombocytopenia but did not influence treatment outcome. Examined genetic polymorphisms did not predict development of splenomegaly.

Indexed as

AdultAgedAge FactorsAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantColorectal NeoplasmsDisease-Free SurvivalDNAFemaleFluorouracilGenotyping TechniquesGlutathione S-Transferase piHepatectomyHepatic Veno-Occlusive DiseaseHumansLeucovorinDNAFluorouracilGlutathione S-Transferase piGSTP1 protein, humanLeucovorinMatrix Metalloproteinase 9MMP9 protein, humanNitric Oxide Synthase Type IIINOS3 protein, humanOrganoplatinum CompoundsVascular Endothelial Growth Factor AVEGFA protein, humanColorectal neoplasmsGenetic polymorphismOxaliplatinSinusoidal obstruction syndromeSplenomegaly

Identifiers

PMID26790967
PMCPMC4946369

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