Hydrogenology
Hydrogenology editorial study record

Hydrogen therapy can be used to control tumor progression and alleviate the adverse events of medications in patients with advanced non-small cell lung cancer.

Chen JB, Kong XF, Mu F, Lu TY, Lu YY, Xu KC. · Medical Gas Research. 2020;10:285560.

HumanInhaled H₂Published 2020
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Human

Reported design

Non-randomized comparative clinical study

Research topic

Cancer research

Administration classification

Inhaled H₂

Study result signal

Mixed observational signal with critical attribution limits.

Outcome type

Clinical symptoms, adverse events and time-to-event outcomes.

Reported in the source

Methods at a glance

Population or model

Patients with advanced non-small cell lung cancer receiving different treatment regimens.

Sample

58 enrolled across control, hydrogen-only and hydrogen-plus-drug groups.

Duration

Five months.

Intervention

Inhalation of 66.7% H2 and 33.3% O2 for 4 to 6 hours daily, alone or added to immunotherapy, targeted therapy or chemotherapy.

Hydrogen form

Mixed H2/O2 inhalation; Brown's-gas-style co-delivery.

H₂ specification

Maximum total flow 3,000 mL/min: H2 up to 2,001 mL/min and O2 up to 999 mL/min.

H₂ flow

Up to 2,001 mL/min.

O₂ delivered with H₂

Yes — 33.3% O2, up to 999 mL/min.

Comparator

A small sham-gas control group and non-random treatment cohorts.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Symptoms, treatment adverse events, tumor response and progression-free survival.

Reported result

The article reports symptom changes in hydrogen-treated cohorts and tumor or progression outcomes across treatment groups, but comparisons were non-random and groups differed in concurrent therapy.

Results-extraction completeness

The full article, group structure, gas specification, follow-up and reported clinical outcomes were checked.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Non-random allocation, small heterogeneous groups, baseline and co-treatment differences and no design capable of isolating hydrogen from drug effects.

Applies directly to

The studied advanced-NSCLC cohorts only; not causal evidence of cancer treatment efficacy.

Preliminary appraisal framework

Cochrane RoB 2 — preliminary

Preliminary risk-of-bias status

Some concerns

Appraisal rationale

Critical confounding by indication and concurrent cancer treatment, with small non-comparable cohorts.

Appraisal domains

Randomization reported; concealment not fully established · Deviations cannot be excluded · Available-case reporting checked · Outcome measurement varies by endpoint · No outcome-level protocol comparison completed

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 32541132 · DOI: 10.4103/2045-9912.285560

Publisher access

Free full article in PubMed Central.

Extraction basis

PubMed record and PubMed Central full text; extraction checked 9 August 2026.

Record revision

2026-08-10