This information is not medical advice and is not a substitute for diagnosis or treatment by a physician.Data sources and disclaimers (data limitations, copyright, etc.)The analysis on "Effects of peginterferon alfa-2b (peg-intron): A Synthesis of Findings from 27 Studies" on this page is based on PubMed data provided by the U.S. National Library of Medicine (NLM). However, NLM does not endorse or verify these analyses.

This analysis is based on research papers included in PubMed, but medical research is constantly evolving and may not fully reflect the latest findings. There may also be biases towards certain research areas.

This information is not medical advice and is not a substitute for diagnosis or treatment by a physician. If you have concerns about "Effects of peginterferon alfa-2b (peg-intron): A Synthesis of Findings from 27 Studies", please consult your doctor.

For NLM copyright information, please see Link to NLM Copyright Page
PubMed data is obtained via Hugging Face Datasets: Link to Dataset
Please check the disclaimer.
This page's analysis is based on PubMed data provided by the U.S. National Library of Medicine (NLM).
Original Abstract of the Article

Major Research Findings

Peginterferon alfa-2b (peg-intron) has been shown to be an effective treatment for a variety of diseases, including chronic hepatitis B, chronic hepatitis C, polycythemia vera, osteosarcoma, melanoma, and renal cell carcinoma.

In the treatment of chronic hepatitis B, a study ( 12 ) found that HBcrAg is useful for predicting HBeAg seroconversion. Another study ( 18 ) found that peg-intron is an effective treatment for HBeAg-positive chronic hepatitis B patients in China. A study ( 16 ) found that intensifying treatment with peg-intron in patients coinfected with HIV and HBV genotypes H or G who are being treated with a tenofovir/emtricitabine-containing regimen may be effective.

In the treatment of chronic hepatitis C, a study ( 27 ) found that peg-intron had comparable safety and efficacy to albinterferon alfa-2b in HIV/HCV genotype 1 coinfected patients. Another study ( 19 ) found that peginterferons alfa-2a and alfa-2b had comparable efficacy in patients infected with hepatitis C virus (HCV) genotype 1. A study ( 24 ) found that daclatasvir with peg-intron alfa-2a or alfa-2b may be beneficial for the treatment of chronic HCV genotype 1 infection. A study ( 22 ) found that telaprevir with peginterferon/ribavirin was effective in treating HCV infection that aggressively recurs after orthotopic liver transplant (OLT). A study ( 14 ) found that vaniprevir with peg-intron alfa-2b and ribavirin was more effective than PR alone for the treatment of HCV genotype 1 infection in treatment-naive Japanese patients. A study ( 13 ) found that vaniprevir with peg-intron alfa-2b and ribavirin was effective for Japanese patients with HCV genotype 1 infection who had previously failed treatment with interferon-based regimens. A study ( 25 ) found that infections during peg-intron/ribavirin therapy were associated with the magnitude of decline in absolute lymphocyte count. A study ( 17 ) found that peg-intron with ribavirin was clinically effective and cost-effective for the treatment of chronic hepatitis C in children and young people. A study ( 11 ) found that peg-intron with ribavirin was effective for people with ongoing injecting drug use or receiving opioid substitution therapy (OST) with HCV genotypes 2/3 infection. A study ( 10 ) found that entecavir was a promising drug for HBV-related glomerulopathy, especially in IFN-resistant cases.

In the treatment of polycythemia vera, a study ( 5 ) found that ropeginterferon alfa-2b was effective in maintaining hematocrit on target levels in low-risk patients with polycythemia vera compared to standard phlebotomy. A study ( 7 ) compared the effectiveness of different therapeutic strategies in patients with polycythemia vera (PV) and essential thrombocythemia (ET). A study ( 2 ) found that ropeginterferon alfa-2b was promising for the treatment of adults with polycythemia vera. A study ( 3 ) found that ropeginterferon alfa-2b, a novel long-acting pegylated interferon alfa-2b, had a favorable safety profile, pharmacokinetics, and pharmacodynamics. A study ( 6 ) found that ropeginterferon alfa-2b demonstrated remarkable long-term hematological response and sustained JAK2V617F allele burden reduction.

In the treatment of osteosarcoma, a study ( 15 ) found that pegylated interferon alfa-2b maintenance therapy might improve outcomes for patients with resectable high-grade osteosarcoma who showed good histologic response to induction chemotherapy.

In the treatment of melanoma and renal cell carcinoma, a study ( 9 ) found that pembrolizumab combined with peg-intron showed promising antitumor activity in patients with advanced melanoma or renal cell carcinoma.

In the treatment of COVID-19, a study ( 4 ) found that peg-intron alfa-2b was effective and safe in subjects with moderate COVID-19 when used with the standard of care.

Benefits and Risks

Benefits Summary

Peg-intron has been shown to be an effective treatment for a variety of diseases, including chronic hepatitis B, chronic hepatitis C, polycythemia vera, osteosarcoma, melanoma, and renal cell carcinoma. In particular, it may be useful for predicting HBeAg seroconversion in chronic hepatitis B. In chronic hepatitis C, peg-intron has been shown to have comparable safety and efficacy to albinterferon alfa-2b in HIV/HCV genotype 1 coinfected patients. In polycythemia vera, it has been shown to be effective in maintaining hematocrit on target levels in low-risk patients compared to standard phlebotomy.

Risks Summary

Peg-intron can cause a number of side effects, including flu-like symptoms, fatigue, fever, headache, nausea, and vomiting. More serious side effects, such as a decrease in blood cells, inflammation of the liver, and thyroid problems, have also been reported. If you are using peg-intron, it is important to understand these risks and use the medication safely as directed by your doctor.

Comparison Between Studies

Similarities

These studies suggest that peg-intron may be an effective treatment for a variety of diseases. They also show that there are risks associated with the use of peg-intron.

Differences

It is difficult to directly compare these studies because they differ in their target diseases, treatment methods, and evaluation methods. However, many of these studies suggest that peg-intron is an effective treatment.

Consistency and Contradictions in Results

These studies suggest that peg-intron may be an effective treatment for a variety of diseases. However, there are also risks associated with its use. While these studies suggest that peg-intron is an effective treatment, the use of peg-intron should be carefully considered on a case-by-case basis.

Notes on Practical Application

Peg-intron may be an effective treatment for a variety of diseases, but its use should be carefully considered on a case-by-case basis. It is important to understand the risks and benefits of using peg-intron and to use the medication safely as directed by your doctor.

Limitations of Current Research

While these studies suggest that peg-intron may be an effective treatment for a variety of diseases, its effects may vary depending on the individual patient. These studies have not adequately investigated the long-term effects of peg-intron. Further research on the long-term effects of peg-intron is needed.

Future Research Directions

Research on the long-term effects of peg-intron is needed. Research is also needed to investigate the effects of peg-intron on a variety of diseases in more detail. Research on combination therapy involving peg-intron is particularly important.

Conclusion

Peg-intron may be an effective treatment for a variety of diseases, but its use should be carefully considered on a case-by-case basis. It is important to understand the risks and benefits of using peg-intron and to use the medication safely as directed by your doctor. Research on the long-term effects of peg-intron is needed.


Literature analysis of 27 papers
Positive Content
23
Neutral Content
2
Negative Content
2
Article Type
11
0
1
3
27

Language : English


Language : English


Language : English


Language : English


Author: BarbuiTiziano, VannucchiAlessandro Maria, De StefanoValerio, MasciulliArianna, CarobbioAlessandra, FerrariAlberto, GhirardiArianna, RossiElena, CiceriFabio, BonifacioMassimiliano, IurloAlessandra, PalandriFrancesca, BenevoloGiulia, PaneFabrizio, RiccoAlessandra, CarliGiuseppe, CaramellaMarianna, RapezziDavide, MusolinoCaterina, SiragusaSergio, RumiElisa, PatriarcaAndrea, CascavillaNicola, MoraBarbara, CacciolaEmma, MannarelliCarmela, LoscoccoGiuseppe Gaetano, GuglielmelliPaola, BettiSilvia, LunghiFrancesca, ScaffidiLuigi, BucelliCristina, VianelliNicola, BelliniMarta, FinazziMaria Chiara, TognoniGianni, RambaldiAlessandro


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Author: BielackStefan S, SmelandSigbjørn, WhelanJeremy S, MarinaNeyssa, JovicGordana, HookJane M, KrailoMark D, GebhardtMark, PápaiZsuzsanna, MeyerJames, NadelHelen, RandallR Lor, DeffenbaughClaudia, NagarajanRajaram, BrennanBernadette, LetsonG Douglas, TeotLisa A, GoorinAllen, BaumhoerDaniel, KagerLeo, WernerMathias, LauChing C, Sundby HallKirsten, GelderblomHans, MeyersPaul, GorlickRichard, WindhagerReinhard, HelmkeKnut, ErikssonMikael, HoogerbruggePeter M, SchombergPaula, TunnPer-Ulf, KühneThomas, JürgensHeribert, van den BergHenk, BöhlingTom, PictonSusan, RenardMarleen, ReichardtPeter, GerssJoachim, Butterfass-BahloulTrude, MorrisCarol, HogendoornPancras C W, SeddonBeatrice, CalaminusGabriele, MichelagnoliMaria, DhoogeCatharina, SydesMatthew R, BernsteinMark,


Language : English


Language : English


Language : English


Author: ChengJun, WangYuming, HouJinlin, LuoDuande, XieQing, NingQin, RenHong, DingHuiguo, ShengJifang, WeiLai, ChenShijun, FanXiaoling, HuangWenxiang, PanChen, GaoZhiliang, ZhangJiming, ZhouBoping, ChenGuofeng, WanMobin, TangHong, WangGuiqiang, YangYuxiu, MohamedRosmawati, GuanRichard, LeeTzong-Hsi, ChangWen-Hsiung, ZhenfeiHuang, YeZhang, XuDaozhen


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


Language : English


This site uses cookies. Visit our privacy policy page or click the link in any footer for more information and to change your preferences.