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Misleading nomenclature in the IARC Monographs Programme: a straightforward solution to improve accuracy and clarity

Abstract

The International Agency for Research on Cancer (IARC) Monographs Programme plays an important role in cancer prevention by identifying potential carcinogenic hazards. However, the terminology used in IARC’s classifications and Monographs can confuse the public, health professionals, and policymakers. Terms like “carcinogenic to humans” imply causation, although classifications only indicate increased risk under certain conditions. For example, the lifetime incidence of mesothelioma among firefighters is approximately 14 in 10,000, compared to 7 in 10,000 in the general population. Despite doubling the risk, occupational exposure as a firefighter does not cause this type of cancer in 9,986 out of 10,000 firefighters. However, the IARC concludes that “occupational exposure as a firefighter causes mesothelioma” (IARC Working Group on the Identification of Carcinogenic Hazards to Humans. Occupational Exposure as a Firefighter. Lyon: IARC; 2023. pp. 1–730. PMID: 37963216). In addition, the lack of essential information about dosage and context in the IARC carcinogen lists can lead to agents with health benefits under certain conditions (e.g., solar radiation, red meat consumption, approved drugs) being perceived as universally harmful, discouraging beneficial exposures, behaviors, or treatments. Here, I propose renaming the groups of agents classified by the IARC and adding basic labels to specific agents to improve the accuracy and interpretability of the IARC classification lists. These adjustments do not interfere with the IARC’s objective of identifying potential hazards, are easy to implement, and enhance accuracy and clarity, providing stronger support to guide cancer prevention strategies.

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Misleading nomenclature in the IARC Monographs Programme: a straightforward solution to improve accuracy and clarity

Author: López Lázaro, Miguel
Publisher: Open Exploration Publishing
Year: 2025
DOI: 10.37349/emed.2025.1001280
Source: https://idus.us.es/bitstreams/8c56a3a1-7da9-4f14-b3e3-8753d11a2068/download
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Explo a ion o Medicine
Open Access Pe spec i e
Misleading nomencla u e in he IARC Monog aphs P og amme: a
s aigh o wa d solu ion o imp o e accu acy and cla i y
Miguel López-Láza o*
Depa men o Pha macology, Facul y o Pha macy, Uni e si y o Se ille, 41012 Se illa, Spain
*Co espondence: Miguel López-Láza o, Depa men o Pha macology, Facul y o Pha macy, Uni e si y o Se ille, 41012
Se illa, Spain. [email p o ec ed]
Academic Edi o : Alessand o O aiano, Is i u o Nazionale Tumo i di Napoli, IRCCS “G. Pascale”, I aly
Recei ed: No embe 12, 2024 Accep ed: Janua y 17, 2025 Published: Feb ua y 7, 2025
Ci e his a icle: López-Láza o M. Misleading nomencla u e in he IARC Monog aphs P og amme: a s aigh o wa d solu ion
o imp o e accu acy and cla i y. Explo Med. 2025;6:1001280. h ps://doi.o g/10.37349/emed.2025.1001280
Abs ac
The In e na ional Agency o Resea ch on Cance (IARC) Monog aphs P og amme plays an impo an ole
in cance p e en ion by iden i ying po en ial ca cinogenic haza ds. Howe e , he e minology used in
IARC’s classi ica ions and Monog aphs can con use he public, heal h p o essionals, and policymake s.
Te ms like “ca cinogenic o humans” imply causa ion, al hough classi ica ions only indica e inc eased isk
unde ce ain condi ions. Fo example, he li e ime incidence o meso helioma among i e igh e s is
app oxima ely 14 in 10,000, compa ed o 7 in 10,000 in he gene al popula ion. Despi e doubling he isk,
occupa ional exposu e as a i e igh e does no cause his ype o cance in 9,986 ou o 10,000 i e igh e s.
Howe e , he IARC concludes ha “occupa ional exposu e as a i e igh e causes meso helioma” (IARC
Wo king G oup on he Iden i ica ion o Ca cinogenic Haza ds o Humans. Occupa ional Exposu e as a
Fi e igh e . Lyon: IARC; 2023. pp. 1–730. PMID: 37963216). In addi ion, he lack o essen ial in o ma ion
abou dosage and con ex in he IARC ca cinogen lis s can lead o agen s wi h heal h bene i s unde ce ain
condi ions (e.g., sola adia ion, ed mea consump ion, app o ed d ugs) being pe cei ed as uni e sally
ha m ul, discou aging bene icial exposu es, beha io s, o ea men s. He e, I p opose enaming he g oups
o agen s classi ied by he IARC and adding basic labels o speci ic agen s o imp o e he accu acy and
in e p e abili y o he IARC classi ica ion lis s. These adjus men s do no in e e e wi h he IARC’s objec i e
o iden i ying po en ial haza ds, a e easy o implemen , and enhance accu acy and cla i y, p o iding
s onge suppo o guide cance p e en ion s a egies.
Keywo ds
In e na ional Agency o Resea ch on Cance , IARC classi ica ion, IARC g oups, IARC lis , ca cinogen,
ca cinogenesis
In oduc ion
The Monog aphs P og amme o he In e na ional Agency o Resea ch on Cance (IARC), a b anch o he
Wo ld Heal h O ganiza ion (WHO), plays a key ole in cance p e en ion by iden i ying po en ial
Explo Med. 2025;6:1001280 | h ps://doi.o g/10.37349/emed.2025.1001280 Page 2
ca cinogenic haza ds. Al hough IARC does no make policy ecommenda ions, i s classi ica ions ha e a
signi ican global impac , o en in luencing egula ions and policies. Go e nmen s wo ldwide ely on IARC
cance classi ica ions o de elop a wide ange o egula ions, such as communica ing cance haza ds, se ing
moni o ing and epo ing equi emen s, imposing usage es ic ions, and es ablishing exposu e limi s o
ca cinogens [1–3]. Fo example, in 2009, he IARC Monog aphs P og amme classi ied he use o UV-
emi ing anning de ices in G oup 1 (ca cinogenic o humans). A e his classi ica ion, es ic ions o bans
on hese de ices we e ecommended o implemen ed, and a me a-analysis showed ha he global use o
indoo anning signi ican ly dec eased ollowing hese es ic ions [4]. This example shows how iden i ying
haza ds can encou age ac ions o p e en cance [3].
As s a ed in i s p eamble, he IARC Monog aphs ocus on iden i ying po en ial ca cinogenic haza ds,
no on assessing he ac ual isk o cance in exposed indi iduals. A ca cinogenic haza d e e s o an agen
capable o causing cance unde speci ic condi ions, while cance isk measu es he likelihood o cance
occu ing a a speci ic le el o exposu e. The Monog aphs assess he s eng h o he e idence ha an agen
is a ca cinogenic haza d unde speci ic condi ions, p o iding he i s s ep in unde s anding po en ial isks
associa ed wi h ce ain agen s [1, 2, 5].
In isk assessmen , he e a e ou main s eps: haza d iden i ica ion, dose- esponse assessmen ,
exposu e assessmen , and isk cha ac e iza ion. The IARC Monog aphs ocus on haza d iden i ica ion. This
is an essen ial s ep bu does no o e a comple e isk assessmen . Al hough he Monog aphs ha e been
c i icized o no pe o ming all ou s eps [6], hei objec i e is o iden i y haza ds and encou age
egula o y bodies o conduc he ull isk assessmen s ha guide speci ic policies and p o ec ions, a ask
beyond he scope o he Monog aphs P og amme [7].
Howe e , ocusing on iden i ying po en ial haza ds wi hou unde aking a comple e isk assessmen
can lead o con usion and conce n i he indings a e no p esen ed accu a ely and clea ly. Fo example,
some agen s p o ide heal h bene i s a mode a e exposu es bu may become ha m ul a highe exposu es.
Since he Monog aphs iden i y agen s ha can po en ially cause cance unde ce ain, some imes
uncommon, condi ions, bene icial agen s a no mal exposu es can be classi ied as ca cinogenic o humans
unde he IARC p o ocol. I dosage and con ex a e no clea ly speci ied, labeling hese agen s as
ca cinogenic o humans can con use he public, heal h p o essionals, and policymake s [8].
The e minology used in he IARC classi ica ions is ano he sou ce o unnecessa y con usion and
conce n. The e m “ca cinogenic o humans” used o G oup 1 agen s implies an ine i abili y o cance
causa ion. E ymologically, ca cinogenic means “p oducing cance ” o “causing cance ”. Many dic iona ies
de ine ca cinogenic his way, which in luences how he gene al popula ion unde s ands he e m
“ca cinogenic o humans”. Fo ins ance, acco ding o he Ox o d English Dic iona y, ca cinogenic means
“ ha causes cance o induces he malignan ans o ma ion o cells”. Impo an ly, his li e al meaning is
also used in he inal e alua ion sec ion o all Monog aphs o agen s classi ied in G oup 1. Fo example,
acco ding o he IARC’s Monog aphs, “sola adia ion causes cu aneous malignan melanoma, squamous cell
ca cinoma o he skin and basal cell ca cinoma o he skin” [9], and “occupa ional exposu e as a i e igh e
causes meso helioma” [10]. These examples show ha he IARC Monog aphs o en use he e ms “causes
cance ” and “inc eases he isk o cance ” in e changeably.
The ollowing example may cla i y he dis inc ion be ween “causes cance ” and “inc eases he isk o
cance ”. Based on SEER Incidence Da a, 1975–2021, he li e ime incidence o meso helioma in he gene al
popula ion is app oxima ely 7 in 10,000 indi iduals. This es ima e de i es om an annual incidence a e o
abou 0.9 pe 100,000 people, which, accumula ed o e an a e age li espan o 80 yea s, yields a li e ime
isk o 0.072%. Fi e igh e s ha e abou wice he isk o meso helioma compa ed o he gene al popula ion
[11], esul ing in a li e ime incidence o app oxima ely 14 in 10,000 among i e igh e s. These da a indica e
ha , while being a i e igh e inc eases he isk o de eloping his cance , i does no cause i in 9,986 ou o
10,000 i e igh e s. Howe e , he IARC s a es ha “occupa ional exposu e as a i e igh e causes
meso helioma” [10]. I exposu e o an agen esul s in cance o 14 people bu no o 9,986 people, is i
accu a e o say ha exposu e o he agen causes cance ? Wouldn’ i be mo e p ecise o say ha exposu e
o he agen inc eases he isk o cance ?
Explo Med. 2025;6:1001280 | h ps://doi.o g/10.37349/emed.2025.1001280 Page 3
Using his inaccu a e and ala ming e minology migh help discou age exposu e o agen s ha a e
ha m ul in almos all scena ios, like obacco smoke. Howe e , he same e minology is also used o agen s
ha a e bene icial a ce ain doses o in speci ic con ex s. Fo example, excessi e exposu e o sola
adia ion inc eases he isk o skin cance , bu no mal sun exposu e is essen ial o p oducing i amin D,
which is i al o human heal h. When dose o con ex de e mines whe he an agen is bene icial o
ha m ul, labels like “ca cinogenic o humans” o “causes cance ” can mislead he public and discou age
bene icial beha io s, ul ima ely ha ming hei heal h. This misunde s anding has al eady occu ed. The ac
ha he IARC, he cance agency o he WHO, labels sola adia ion as “ca cinogenic o humans” has likely
led many people o a oid sunligh . Obse a ional s udies ha e shown ha a oiding sun exposu e is a isk
ac o o all-cause mo ali y [12]. A isk analysis o a p ospec i e s udy ound ha nonsmoke s who
a oided sun exposu e had a li e expec ancy simila o smoke s wi h high sun exposu e [13]. Compa ed o
hose wi h he highes sun exposu e, sun a oide s had a educed li e expec ancy o 0.6–2.1 yea s [13, 14].
The IARC a ely speci ies dose and con ex in i s lis o ca cinogens, e en hough hese ac o s a e
c ucial in de e mining ac ual cance isk. Fo example, while ed mea is classi ied as “p obably
ca cinogenic o humans” (G oup 2A), mode a e consump ion o e s high-quali y p o ein and essen ial
nu ien s such as B i amins, i on, and zinc. In egions wi h limi ed ood a ailabili y, ed mea may be a
di icul - o- eplace sou ce o hese nu ien s. Wi hou cla i ying he le el o consump ion a which ed mea
poses a isk, people migh a oid i en i ely, missing ou on i s heal h bene i s. Simila ly, se e al app o ed
d ugs a e classi ied as G oup 1 ca cinogens, e en hough hey a e s anda d ea men s o speci ic diseases
and o e signi ican heal h bene i s when used app op ia ely. These examples show ha imp ecise labels
ha lack dose and con ex may discou age bene icial beha io s, ea men s, o exposu es ha ha e posi i e
heal h e ec s.
The need o mo e accu a e e minology is e iden o a oid unnecessa y con usion and ensu e ha
people, heal h p o essionals, and policymake s make in o med decisions based on a clea unde s anding o
isk. The IARC ecognizes he need o imp o e communica ion o i s e alua ion esul s and has ecen ly
added use - iendly ea u es like “ equen ly asked ques ions” and in og aphics o explain i s classi ica ions
and he suppo ing e idence [7]. Howe e , he ongoing use o imp ecise e minology and he lack o
essen ial con ex , especially in he IARC’s classi ica ion lis o ca cinogens, will likely con inue o cause
con usion and conce n un il hese issues a e p ope ly add essed. This manusc ip p oposes a
s aigh o wa d solu ion o he IARC Monog aphs o enhance he accu acy and cla i y o i s
communica ions.
A s aigh o wa d solu ion o imp o e accu acy and p e en unnecessa y
con usion
The i s s ep o imp o e accu acy and p e en unnecessa y con usion is o ename he g oups o agen s
classi ied by he IARC Monog aphs. As shown in Table 1, G oup 1 (ca cinogenic o humans) could be
enamed as “agen s ha inc ease cance isk in humans”; G oup 2A (p obably ca cinogenic o humans) as
“agen s ha p obably inc ease cance isk in humans”; G oup 2B (possibly ca cinogenic o humans) as
“agen s ha possibly inc ease cance isk in humans”; and G oup 3 (no classi iable as o i s ca cinogenici y
o humans) as “agen s wi h insu icien o no e idence o cance isk in humans”.
Since IARC classi ica ions only indica e e idence o inc eased isk unde ce ain condi ions, hese new
g oup names emphasize cance isk a he han implying di ec causa ion. As shown in he i e igh e
example, he e m “inc eases cance isk” is mo e p ecise han “is ca cinogenic” o “causes cance ” and is
easie o mos people o unde s and, including heal h p o essionals and policymake s. The p oposed name
o G oup 3 e lec s IARC’s ecen me ging o wo ca ego ies: he o me G oup 3 (no classi iable as o i s
ca cinogenici y o humans) and he now-elimina ed G oup 4 (p obably no ca cinogenic o humans). This
change is impo an o cla i y ha no all agen s in his g oup a e suspec ed o inc easing cance isk.
The second s ep o imp o ing accu acy and educing unnecessa y con usion is o add concise labels o
speci ic agen s o p o ide essen ial con ex and minimize misin e p e a ion. A leas wo basic labels should
be used o speci ic agen s: “excessi e” o agen s whe e dose de e mines whe he he agen is bene icial o
Explo Med. 2025;6:1001280 | h ps://doi.o g/10.37349/emed.2025.1001280 Page 4
Table 1. P oposed classi ica ion sys em o imp o e accu acy and cla i y
Ca ego y Cu en classi ica ion sys em P oposed classi ica ion sys em
Ca cinogenic o humans Agen s ha inc ease cance isk in humansG oup 1
Tobacco smoke, plu onium, occupa ional
exposu e as a i e igh e , sola adia ion,
e oposide, e c.
Tobacco smoke, plu onium, occupa ional exposu e as a
i e igh e , excessi e sola adia ion, e oposide
(bene icial unde ce ain condi ions), e c.
P obably ca cinogenic o humans Agen s ha p obably inc ease cance isk in humansG oup 2A
Consump ion o ed mea , ac olein, mala hion,
e c.
Excessi e consump ion o ed mea , ac olein,
mala hion, e c.
Possibly ca cinogenic o humans Agen s ha possibly inc ease cance isk in humansG oup 2B
Radio equency elec omagne ic ields,
aspa ame, digoxin, e c.
Radio equency elec omagne ic ields, aspa ame,
digoxin (bene icial unde ce ain condi ions), e c.
No classi iable as o i s ca cinogenici y o
humans
Agen s wi h insu icien o no e idence o cance isk in
humans
G oup 3
Diazepam, co ee d inking, ea, e c. Diazepam, co ee d inking, ea, e c.
Cu en and p oposed classi ica ion sys em o agen s e alua ed in he In e na ional Agency o Resea ch on Cance (IARC)
Monog aphs, wi h examples p o ided in each g oup o show how speci ic agen s could be labeled
ha m ul, and “(bene icial unde ce ain condi ions)” o agen s whe e con ex de e mines whe he he
agen is bene icial o ha m ul. Fo agen s whe e dose and con ex do no o e any heal h bene i s, such as
obacco smoke o occupa ional exposu e as a i e igh e , no labels a e necessa y (Table 1).
The label “excessi e” could p ecede agen s ha a e bene icial a mode a e exposu es (e.g., sola
adia ion, ed mea consump ion) o cla i y ha mode a e exposu e can ha e heal h bene i s. In con as ,
he label “excessi e” would be unnecessa y o agen s lacking demons a ed heal h bene i s a mode a e
exposu es o ha can be easily subs i u ed, such as aspa ame. While aspa ame and o he agen s on he
IARC lis s migh pose cance isks only a high doses, enaming he g oups as shown in Table 1 would be
su icien o help p e en misleading headlines like “Aspa ame is a possible ca cinogen” [15]. The exis ence
o such headlines, e en in espec ed scien i ic jou nals, sugges s ha he cu en IARC g oup names can be
misin e p e ed e en by scien is s [15].
The label “(bene icial unde ce ain condi ions)” could apply o agen s ha , a no mal exposu e le els,
p o ide heal h bene i s in speci ic con ex s despi e po en ial cance isks a he same exposu e le els.
Examples include app o ed d ugs like e oposide o digoxin. Adding his basic con ex would help people
unde s and ha ce ain agen s o e heal h bene i s while ca ying a po en ial cance isk. Wi hou hese
cla i ica ions, he IARC lis s migh unin en ionally discou age he use o essen ial ea men s; o example,
e oposide and digoxin a e ac ually included in he WHO Model Lis o Essen ial Medicines (23 d lis , 2023)
[16].
Conclusions
In conclusion, he changes p oposed in his manusc ip o e a s aigh o wa d and e ec i e solu ion o he
IARC Monog aphs P og amme o enhance bo h he accu acy and cla i y o i s scien i ic communica ions. By
upda ing he classi ica ion language om “ca cinogenic o humans” o mo e p ecise e ms like “agen s ha
inc ease cance isk in humans”, he p oposed sys em educes he likelihood o misin e p e a ion while
p ese ing he IARC’s ocus on iden i ying po en ial haza ds wi hou conduc ing ull isk assessmen s. Since
“ca cinogenic haza ds o humans” can be de ined as “agen s ha inc ease cance isk in humans”, he
cu en i le, IARC Monog aphs on he Iden i ica ion o Ca cinogenic Haza ds o Humans, emains ully
consis en wi h he p oposed g oup names in Table 1. Addi ionally, adding con ex -sensi i e labels, such as
“excessi e” o “(bene icial unde ce ain condi ions)”, p o ides essen ial con ex o agen s ha o e heal h
bene i s a mode a e exposu e le els o in speci ic si ua ions. These adjus men s nei he al e he IARC’s
ounda ional mission no equi e signi ican changes, ye hey would imp o e cla i y, enhance accu acy,
and p o ide s onge suppo o cance p e en ion s a egies.
Explo Med. 2025;6:1001280 | h ps://doi.o g/10.37349/emed.2025.1001280 Page 5
Abb e ia ions
IARC: In e na ional Agency o Resea ch on Cance
WHO: Wo ld Heal h O ganiza ion
Decla a ions
Acknowledgmen s
The au ho acknowledges his esea ch eam o help ul discussions.
Au ho con ibu ions
MLL: Concep ualiza ion, In es iga ion, W i ing—o iginal d a , W i ing— e iew & edi ing.
Con lic s o in e es
The au ho decla es no con lic o in e es .
E hical app o al
No applicable.
Consen o pa icipa e
No applicable.
Consen o publica ion
No applicable.
A ailabili y o da a and ma e ials
No applicable.
Funding
No applicable.
Copy igh
© The Au ho (s) 2025.
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