This podcast reviews the International Psoriasis Council (IPC) 2025 guidance on reclassifying psoriasis severity and redefining failure of topical therapies. Clinical features such as high-impact disease sites, failure of topical treatment, or BSA >10% all factor into whether patients are candidates for systemic therapy in this new guidance. Despite broad endorsement, many clinicians remain uncertain about applying the new framework. This activity aims to raise awareness, clarify updated criteria, and align practice with current evidence supporting earlier use of IL-23 and IL-17 inhibitors in appropriate patients.
When Topicals Fail: The New IPC Consensus Every Clinician Should Know

Announcer:
Welcome to CE on ReachMD. This activity, titled “When Topicals Fail: The New International Psoriasis Council Consensus Every Clinician Should Know” is provided by Prova Education.
Prior to beginning the activity, please be sure to review the faculty and commercial support disclosure statements as well as the learning objectives.
Dr. Stein-Gold:
Today, we will discuss the 2025 International Psoriasis Council Consensus, promoting earlier evidence-based escalation to systemic therapy in psoriasis. This is CE on ReachMD, and I'm Dr. Linda Stein-Gold. I'm the Director of Dermatology Clinical Research at Henry Ford Health System in Detroit, Michigan, and I'm thrilled to be joined by my friend and colleague, Dr. Bruce Strober. Welcome, Bruce.
Dr. Strober:
Thank you, Linda. It's a pleasure to be here.
Dr. Stein-Gold:
Well, it's such an exciting time in psoriasis. We have some wonderful new topical, oral, and biologic treatment options. I feel like if somebody has very localized disease, we're pretty good at getting them under control. If somebody has very extensive disease, we're pretty good at getting them under control. But some of our patients seem to cycle on topicals and we don't tend to advance them. And I feel like there's kind of an unmet need on these patients who maybe don't have the most extensive disease, maybe have a little more localized disease, but really aren't getting better.
And I know that the IPC got together with a group of psoriasis enthusiasts and experts, and they put together new guidelines on how to figure out when to advance patients to appropriate systemic therapy. And Bruce, you were a lead author on this paper. Can you help us to understand who should advance to systemic therapy?
Dr. Strober:
Right. Well, it was all about an appropriate advancement for people who are on topical therapy or who already are severe enough to perhaps skip topical therapy. The ultimate consensus was that there's two categories of patients with psoriasis: those who are appropriate for topicals and those who are appropriate for systemic therapy or phototherapy.
Now, basically, to be appropriate for systemic therapy, you of course, need to either fail topical therapy or perhaps be inappropriate just at the get-go. You just look at the patient, you're like, they’re too severe, I need to go right to a systemic. But the other two criteria were very straightforward. You could be 10% or more of your BSA, and again, that's a person who should be on systemic therapy. Or a person who has high impact limited disease. Some people call it special site involvement; for example, the scalp, the hands, the feet, genitals, and nails. And those patients, of course,would be candidates for topical therapy right out of the gate. But on the other hand,many of them are deserving of systemic therapy, even though their BSA would be less than 10%.
So, the upshot is these are people who couldn't enroll in a clinical trial for a systemic therapy, or at least a registrational clinical trial, where you require BSA of 10% or more, or a POSI of 12. These are patients who wouldn't achieve those thresholds, but nevertheless could be on systemic therapy. And we've actually studied this in many different settings, but in particularly real world registries, a large percentage of patients in dermatology fall into those categories where they don't really have enough to be in a clinical trial but nevertheless are getting systemic therapy and/or phototherapy beyond just topical therapy.
Dr. Stein-Gold:
So, I really like that. I’m so thrilled with this new classification because people get so fixated on mild, moderate, or severe disease. But putting people in these two categories, either topical therapy or systemic-worthy, I think is great.
So, as I understand what the paper told us was, if you have 10% or more, you're systemic worthy. If you have a high impact site, as you described, or if you have failed topical therapy. So, I think that really what you're telling us is there are a lot of patients who should be advanced to systemic therapy who have really been stuck in a topical treatment regimen.
Dr. Strober:
Yeah, and the survey suggests that there's a – I want to make it clear, our specialty has gotten very good over the past two decades in terms of using systemic therapies, particularly biologics. We're very comfortable with biologics, but nevertheless, if you survey patients, there are still many by percentage who are undertreated. They're not being advanced beyond topicals. They are cycled through topical after topical, never, ever getting to a systemic. And that's what we're really addressing,the undertreatment of a certain subset of psoriasis patients. And by the way, when surveyed, express a lot of frustration with just the topical churn, as it's called, even though they know they’re severe enough to be on a systemic therapy.
Dr. Stein-Gold:
So, let's talk a little bit more about that, Bruce, and it brings me to the second publication from the IPC. And that's where we talk about this group of topical failures, the IPC has actually put out a consensus paper helping us to understand, well, what does a topical failure actually mean. Can you elaborate on this?
Dr. Strober:
Well, I would see this as sort of the sequel to the first paper I just discussed. We got pushback because we didn't really define well enough what is a topical failure. And we did that on purpose because it's somewhat of a murky concept, what is a topical failure. But there is some congealing around a concept that people should not be continuously treated with topical medications if they're not achieving certain benchmarks.
So, in this update, so to speak, we say patients should be clear, almost clear, or 1% or less on their BSA to be deemed a success on a topical. Clear, almost clear, like an IGA-01 or 1% less BSA. And to get there, they could march through two 4-week consecutive trials of topicals, meaning you could try one topical for up to 4 weeks. And if that doesn't work, you can go to a second topical up to 4 weeks, just seeing whether you're getting anywhere with these specific regimens of whether it's corticosteroids or non-steroidal topicals. We have many, as you know, some new, some old. But the idea is now you have a definition of what it means to fail a topical.
If you don't get clear, almost clear, and you don't do it within a certain specific timeframe, at that point, then you can kind of cassette that definition into the original IPC categorization. Now, you've called a person appropriately a topical failure with a real, valid measuring stick. Which we think is very practical. And there's a few extra comments within the paper about limiting the use of high-potency topical steroids, perhaps 2 weeks. But otherwise, the 4-week rule is a good one, and two consecutive 4-week intervals.
Dr. Stein-Gold:
I think this is just a wonderful guideline for us to help us to understand it. And it's important that you're not saying not to use topical therapy because as you mentioned, we do have topical steroids, but we have this wealth of new non-steroidal options that are also quite effective on their own. But I think this gives us some guidance to not do that topical churning, as you mentioned earlier. So, I appreciate this. Do you think that this is going to allow us to be a little more aggressive in our treatments?
Dr. Strober:
Well, we hope it allows the providers in the dermatology universe some specific guidance because prior to this, what could be defined as a topical failure is very open-ended. And while these are not obviously hard and fast rules, it imparts a message to you know new and seasoned therapeuticians. Listen, you can try topicals, but you know move away from them once you see there's no success being achieved. And this is ultimately because patients deserve more given all of our systemic options.
Dr. Stein-Gold:
Bruce, let's now talk a little bit more about that systemic world. We talked about the fact that we have some wonderful new topicals. We have some fantastic biologic agents that are getting the majority of our patients to clear, almost clear. But we have an oral space that actually doesn't necessarily have the trio of great efficacy, great safety, and great tolerability. And we do have some newcomers on the horizon that are in clinical trials. Can you talk to us about what you're most excited about in the oral space?
Dr. Strober:
Well, I think we're on the precipice of a new era in oral therapeutics for psoriasis, mainly because the efficacy is going to jump to another level that may not quite hit our top rung modern biologic therapies, but really nip at the heels with regard to their efficacy. We have oral IL-23 receptor antagonism in the form of a molecule called icotrokinra, and we have some TYK2 inhibitors that are in the pipeline as well, that are built on the mechanism of action first introduced by deucravacitinib. But now these will probably be more efficacious for people with psoriasis.
I'm most excited by, I think, the oral IL-23 receptor blocker, icotrokinra, that's likely to be the first of these medicines to be approved. Only because it's going to be once daily, it's going to be of a mechanism of action, specifically IL-23 pathway inhibition, that we're familiar with, and I believe it'll have the same tolerability and safety profile that our biologic IL-23 inhibitors currently possess. So, there'll be a lot of comfort with this medicine. It’s efficacy looks to be really strong. I can’t overstate the importance of they're going to launch this medicine with an approval in patients 12 years of age and up, so it'll be an adolescent approval right at launch. We've never seen that before. And I think that'll go a long way into making it a very successful option.
Dr. Stein-Gold:
I agree with you. I think this is really an exciting time for the oral therapy landscape. I have done clinical trials with all of these new drugs. I'm also excited about this new peptide, the IL-23 receptor inhibitor. And I think we all want great efficacy, but we also worry about safety and tolerability. And I think with this drug, we actually see a drug that is going to provide us with – as you mentioned, we're getting close to the biologic type efficacy – but with a safety profile that's actually really quite good, and a tolerability profile that’s quite good.
Do you see these drugs as kind of the first step towards systemic therapy, or do you see them used in potentially any type of a patient?
Dr. Strober:
Well, I think more the latter. You'll see them used in all types of psoriasis patients.
The issue will come down to whether the provider is biased towards infrequent injections, which we have, obviously, that work really well, versus a daily oral medication that also works well. And this is going to be a discussion between the provider and the patient regarding what are their expectations in a medication.
There are arguments on both sides regarding biologics versus orals, but only now will we really be able to say the orals are really close in the efficacy to the injectables, and therefore they become even a more valid choice for the patient.
Dr. Stein-Gold:
So, Bruce, we're just about out of time, but can you give us one final take-home message?
Dr. Strober:
Well, the take-home message is, and it harkens back to the disease recategorization, and systemic versus topicals. I think the important point is that you use, as a competent therapeutician, all at your fingertips. You use topicals, but increasingly use non-steroidal topicals. I'm really biased towards that. I try very hard not to prescribe topical steroids, even though they have a payer advantage in many instances.
And then, I don't make patients languish on topicals. I think you need to set that expectation early with a patient, you put on a topical that, you know we're going to try this. We may try two, but ultimately I want you to consider internal medications, whether they're oral or injectable, as really, liberating. Ultimately, oral and systemic therapies are very liberating the patients because they're free from topical applications, and generally, they do better.
And then, finally, which is not written about enough, when we treat systemically, we often treat other tissues and organs that are negatively affected by psoriasis, because psoriasis needs to be viewed as as a systemic illness with the skin as its most outward facing manifestation. We have psoriatic arthritis, of course, but we have a lot of cardiovascular comorbiditythat probably is positively impacted by the use of systemic therapies. And so, think of the patient as a holistic approach that in many instances, topicals will not address.
Dr. Stein-Gold:
Well, Bruce, that was a wonderful take home message. And I hope that all of our listeners will learn more and really try to help get our patients under control.
That's all we have time for today. So, I want to thank our audience for listening and thank you, Bruce, for joining me and sharing your valuable insights. It was great speaking with you today.
Dr. Strober:
My pleasure. Thank you.
Dr. Stein-Gold:
Thanks so much.
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Overview
Disclosure of Relevant Financial Relationships
In accordance with the ACCME Standards for Integrity and Independence, it is the policy of Global Learning Collaborative (GLC that faculty and other individuals who are in the position to control the content of this activity disclose any real or apparent financial relationships relating to the topics of this educational activity. Global Learning Collaborative (GLC has full policies in place that have identified and mitigated financial relationships and conflicts of interest to ensure independence, objectivity, balance, and scientific accuracy prior to this educational activity.
The following faculty/staff members have reported financial relationships with ineligible companies within the last 24 months.Faculty:
Linda Stein Gold, MD
Director of Clinical Research
Department of Dermatology
Henry Ford Health
Detroit, MI
Dr. Stein Gold has reported the following relevant financial relationships or relationships with ineligible companies of any amount during the past 24 months:
Advisor/Consultant: AbbVie Inc., Amgen Inc., Bristol Myers Squibb, Eli Lilly and Company, Johnson & Johnson, LEO Pharma A/S, Takeda Pharmaceutical Company
Contracted Researcher: AbbVie Inc., Amgen Inc., Bristol Myers Squibb, Eli Lilly and Company, Johnson & Johnson, LEO Pharma A/S, Takeda Pharmaceutical Company
Bruce Strober, MD, PhD
Clinical professor
Department of Dermatology
Yale University
Cromwell, CT
Dr. Strober has reported the following relevant financial relationships or relationships with ineligible companies of any amount during the past 24 months:
Advisor/Consultant: CorEvitas Psoriasis and GPP Registries, Oruka, Incyte
Contracted Researcher: AbbVie, Alumis, Almirall, Amgen, Apogee, Arcutis, Boehringer Ingelheim, Bristol-Myers-Squibb, CorEvitas, Dermavant, Dimagi, Immunovant, Incyte, Johnson & Johnson, Leo, Eli Lilly, Maruho, Neurocrine, Novartis, Oruka, Meiji Seika Pharma, Protagonist, Pfizer, UCB Pharma, Rapt, Regeneron, Sanofi-Genzyme, SelectION, Takeda
Other: Mindera Health, selectION
Reviewers/Content Planners/Authors:- Tim Person has no relevant relationships to disclose.
- Rosanne Strauss, PharmD, MBA has no relevant relationships to disclose.
- Brian P. McDonough, MD, FAAFP, has no relevant relationships to disclose.
Learning Objectives
Upon completion of this activity, learners should be better able to:
- Apply updated consensus-driven clearance targets that aim for PASI 100 vs 75 in eligible patients with moderate-to-severe plaque psoriasis, while integrating the IPC's 2025 definition of topical therapy failure as a critical determinant of treatment escalation
- Construct a revised initiation pathway for moderate-to-severe plaque psoriasis that incorporates earlier, guidance-aligned use of IL-based therapy, applying the 2025 IPC topical therapy failure definition as the escalation threshold
Target Audience
This activity has been designed to meet the educational needs of dermatologists, dermatology APPs, and PCPs as well as all other physicians, physician assistants, nurse practitioners, nurses, and healthcare providers involved in managing patients with psoriasis.
Accreditation and Credit Designation Statements
In support of improving patient care, this activity has been planned and implemented by Global Learning Collaborative (GLC) and the International Psoriasis Council. GLC is jointly accredited by the American Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC) to provide continuing education for the healthcare team.
Global Learning Collaborative (GLC) designates this audio only activity for a maximum of 0.25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Global Learning Collaborative (GLC) designates this activity for 0.25 nursing contact hour(s). Nurses should claim only the credit commensurate with the extent of their participation in the activity.
Global Learning Collaborative (GLC) has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit(s) for activities planned in accordance with AAPA CME Criteria. This activity is designated for 0.25 AAPA Category 1 CME credit(s). Approval is valid until December 31, 2026. PAs should claim only the credit commensurate with the extent of their participation in the activity. Provider(s)/Educational Partner(s)

Prova Education and International Psoriasis Council designs and executes continuing education founded on evidence-based medicine, clinical need, gap analysis, learner feedback, and more. Our mission is to serve as an inventive and relevant resource for clinical content and educational interventions across a broad spectrum of specialties. Prova Education's methodology demonstrates a commitment to continuing medical education and the innovative assessment of its effects. Our goal is clear—to develop and deliver the best education in the most impactful manner and to verify its results with progressive outcomes research.Commercial Support
This activity is supported by an independent educational grant from Johnson & Johnson.
Disclaimer
The views and opinions expressed in this educational activity are those of the faculty and do not necessarily represent the views of GLC. This presentation is not intended to define an exclusive course of patient management; the participant should use his/her clinical judgment, knowledge, experience, and diagnostic skills in applying or adopting for professional use any of the information provided herein. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patients’ conditions and contraindications or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities. Links to other sites may be provided as additional sources of information.
Reproduction Prohibited
Reproduction of this material is not permitted without written permission from the copyright owner.System Requirements
- Supported Browsers (2 most recent versions):
- Google Chrome for Windows, Mac OS, iOS, and Android
- Apple Safari for Mac OS and iOS
- Mozilla Firefox for Windows, Mac OS, iOS, and Android
- Microsoft Edge for Windows
- Recommended Internet Speed: 5Mbps+
Publication Dates
Release Date:
Expiration Date:
Overview
This podcast reviews the International Psoriasis Council (IPC) 2025 guidance on reclassifying psoriasis severity and redefining failure of topical therapies. Clinical features such as high-impact disease sites, failure of topical treatment, or BSA >10% all factor into whether patients are candidates for systemic therapy in this new guidance. Despite broad endorsement, many clinicians remain uncertain about applying the new framework. This activity aims to raise awareness, clarify updated criteria, and align practice with current evidence supporting earlier use of IL-23 and IL-17 inhibitors in appropriate patients.
Disclosure of Relevant Financial Relationships
In accordance with the ACCME Standards for Integrity and Independence, it is the policy of Global Learning Collaborative (GLC that faculty and other individuals who are in the position to control the content of this activity disclose any real or apparent financial relationships relating to the topics of this educational activity. Global Learning Collaborative (GLC has full policies in place that have identified and mitigated financial relationships and conflicts of interest to ensure independence, objectivity, balance, and scientific accuracy prior to this educational activity.
The following faculty/staff members have reported financial relationships with ineligible companies within the last 24 months.Faculty:
Linda Stein Gold, MD
Director of Clinical Research
Department of Dermatology
Henry Ford Health
Detroit, MI
Dr. Stein Gold has reported the following relevant financial relationships or relationships with ineligible companies of any amount during the past 24 months:
Advisor/Consultant: AbbVie Inc., Amgen Inc., Bristol Myers Squibb, Eli Lilly and Company, Johnson & Johnson, LEO Pharma A/S, Takeda Pharmaceutical Company
Contracted Researcher: AbbVie Inc., Amgen Inc., Bristol Myers Squibb, Eli Lilly and Company, Johnson & Johnson, LEO Pharma A/S, Takeda Pharmaceutical Company
Bruce Strober, MD, PhD
Clinical professor
Department of Dermatology
Yale University
Cromwell, CT
Dr. Strober has reported the following relevant financial relationships or relationships with ineligible companies of any amount during the past 24 months:
Advisor/Consultant: CorEvitas Psoriasis and GPP Registries, Oruka, Incyte
Contracted Researcher: AbbVie, Alumis, Almirall, Amgen, Apogee, Arcutis, Boehringer Ingelheim, Bristol-Myers-Squibb, CorEvitas, Dermavant, Dimagi, Immunovant, Incyte, Johnson & Johnson, Leo, Eli Lilly, Maruho, Neurocrine, Novartis, Oruka, Meiji Seika Pharma, Protagonist, Pfizer, UCB Pharma, Rapt, Regeneron, Sanofi-Genzyme, SelectION, Takeda
Other: Mindera Health, selectION
Reviewers/Content Planners/Authors:- Tim Person has no relevant relationships to disclose.
- Rosanne Strauss, PharmD, MBA has no relevant relationships to disclose.
- Brian P. McDonough, MD, FAAFP, has no relevant relationships to disclose.
Learning Objectives
Upon completion of this activity, learners should be better able to:
- Apply updated consensus-driven clearance targets that aim for PASI 100 vs 75 in eligible patients with moderate-to-severe plaque psoriasis, while integrating the IPC's 2025 definition of topical therapy failure as a critical determinant of treatment escalation
- Construct a revised initiation pathway for moderate-to-severe plaque psoriasis that incorporates earlier, guidance-aligned use of IL-based therapy, applying the 2025 IPC topical therapy failure definition as the escalation threshold
Target Audience
This activity has been designed to meet the educational needs of dermatologists, dermatology APPs, and PCPs as well as all other physicians, physician assistants, nurse practitioners, nurses, and healthcare providers involved in managing patients with psoriasis.
Accreditation and Credit Designation Statements
In support of improving patient care, this activity has been planned and implemented by Global Learning Collaborative (GLC) and the International Psoriasis Council. GLC is jointly accredited by the American Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC) to provide continuing education for the healthcare team.
Global Learning Collaborative (GLC) designates this audio only activity for a maximum of 0.25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Global Learning Collaborative (GLC) designates this activity for 0.25 nursing contact hour(s). Nurses should claim only the credit commensurate with the extent of their participation in the activity.
Global Learning Collaborative (GLC) has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit(s) for activities planned in accordance with AAPA CME Criteria. This activity is designated for 0.25 AAPA Category 1 CME credit(s). Approval is valid until December 31, 2026. PAs should claim only the credit commensurate with the extent of their participation in the activity. Provider(s)/Educational Partner(s)

Prova Education and International Psoriasis Council designs and executes continuing education founded on evidence-based medicine, clinical need, gap analysis, learner feedback, and more. Our mission is to serve as an inventive and relevant resource for clinical content and educational interventions across a broad spectrum of specialties. Prova Education's methodology demonstrates a commitment to continuing medical education and the innovative assessment of its effects. Our goal is clear—to develop and deliver the best education in the most impactful manner and to verify its results with progressive outcomes research.Commercial Support
This activity is supported by an independent educational grant from Johnson & Johnson.
Disclaimer
The views and opinions expressed in this educational activity are those of the faculty and do not necessarily represent the views of GLC. This presentation is not intended to define an exclusive course of patient management; the participant should use his/her clinical judgment, knowledge, experience, and diagnostic skills in applying or adopting for professional use any of the information provided herein. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patients’ conditions and contraindications or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities. Links to other sites may be provided as additional sources of information.
Reproduction Prohibited
Reproduction of this material is not permitted without written permission from the copyright owner.System Requirements
- Supported Browsers (2 most recent versions):
- Google Chrome for Windows, Mac OS, iOS, and Android
- Apple Safari for Mac OS and iOS
- Mozilla Firefox for Windows, Mac OS, iOS, and Android
- Microsoft Edge for Windows
- Recommended Internet Speed: 5Mbps+
Publication Dates
Release Date:
Expiration Date:
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