A Phase 2 interventional study of Pembrolizumab Injection in Squamous Cell Carcinoma, sponsored by Diwakar Davar. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-16.
Sponsored by Diwakar Davar · Phase 2, Interventional, and Treatment
This phase II single-arm two-stage neoadjuvant study of pembrolizumab in patients with PD-1 naïve high-risk resectable cutaneous squamous cell carcinoma (cSCC) will be conducted over a 52-week period. The study will include patients who have not undergone surgery to remove disease, to formally evaluate whether both biologically and clinically high-risk disease may benefit from neoadjuvant anti-PD-1 therapy. Response to neoadjuvant anti-PD-1 therapy will be evaluated for association with improved landmark Relapse-free Survival (RFS).
Patients with high-risk resectable cSCC who have yet to undergo definitive surgery will be eligible to enroll. Patients with nodal and/or in-transit relapse including those who have received prior adjuvant RT are eligible to enroll. This trial excludes patients who have received either nivolumab or pembrolizumab or other anti-PD-(L)1 therapy. Suitable patients will be identified pre-operatively. Patients will undergo a 28-day screening evaluation consisting of systemic staging scans, tumor biopsy, and blood studies to confirm suitability. Once enrolled, patients will receive pembrolizumab peri-operatively for 6 weeks (200mg Q3Wq3; 2 cycles) prior to definitive surgery (Neoadjuvant Phase). Following peri-operative therapy, patients will undergo restaging scans and surgical evaluation followed by definitive surgical resection (Surgical Phase). Post-operatively, patients will receive 15 further cycles of pembrolizumab over a 45-week period (200mg q3Q3W) (Adjuvant Phase). In the post-operative period, if patients are deemed eligible for RT, this will be administered concurrently with pembrolizumab. The total duration of pembrolizumab therapy is 1 year (52 weeks).
1. Male/female participants who are at least 18 years of age on the day of signing informed consent with histologically confirmed diagnosis of high-risk localized or locooregional cSCC as defined below may be enrolled in this study.
i. T2 and Nx and M0 (tumor >2 cm and ≤4 cm in greatest dimension) OR;
ii. T3 and Nx and M0 (tumor >4 cm or minor bone erosion or perineural invasion or deep invasion) OR;
Perineural invasion is defined as tumor cells within the nerve sheath of a nerve lying deeper than the dermis or measuring 0.1 mm or larger in caliber, or presenting with clinical or radiographic involvement of named nerves without skull base invasion or transgression.
iii. T4 and Nx and M0 (tumor with gross cortical bone/marrow, skull base invasion and/or skull base foramen invasion if deemed surgically resectable) OR;
iv. Tx and N1-3 and M0 (if deemed surgically resectable) OR;
b. NOTE:
i. If T2, tumors must possess ≥2 NCCN/BWH clinical or pathologic risk factor(s) as stated below.
ii. NCCN/BWH clinical risk factors:
1. Tumors ≥20 mm on trunk or extremities (excluding pretibia, hands, feet, nail units, and ankles).
2. Tumors ≥10 mm on cheeks, forehead, scalp, neck, or pretibial areas.
iii. NCCN/BWH pathologic risk factors:
Histopathologically documented perineural, lymphatic, or vascular involvement (as stated in the pathology report or written documentation by Mohs surgeon).
c. NOTE: Tumors of any size on the "mask areas" of the face [central face, eyelids, eyebrows, periorbital nose, lips (cutaneous and vermilion) are not eligible.
d. NOTE: Tumors of any size on genitalia, hands, and feet may be eligible at the discretion of the treating surgical oncologist.
e. NOTE: Patients with tumors that arise in the setting of chronic inflammation (Marjolin's ulcer) such as chronic wounds and/or scars are excluded.
f. NOTE: Determination of surgical resectability must be made before enrollment by the treating surgical oncologist (or ENT surgeon or equivalent).
2. Male participants: A male participant must agree to use a contraception during the treatment period and for at least 120 days after the last dose of study treatment and refrain from donating sperm during this period.
3. Female participants:
A female participant is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies:
Not a woman of childbearing potential (WOCBP)
OR
A WOCBP who agrees to follow the contraceptive guidance during the treatment period and for at least 120 days after the last dose of study treatment.
4. The participant (or legally acceptable representative if applicable) provides written informed consent for the trial.
5. Have at least a single site of measurable disease based on RECIST 1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.
6. Willing to undergo pre-treatment biopsies.
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Minimum tissue requirements: core (16G or 18G, 6 cores; preferred), punch or excisional biopsy of a tumor lesion that has not been previously irradiated.
7. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.
a. ECOG evaluation should be performed at Screening and repeated on Cycle 1 Day 1.
8. Have adequate organ function, per protocol criteria
Exclusion Criteria:
Has received a live vaccine within 30 days prior to the first dose of study drug.
Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs).
Concurrent non-hematologic malignancy other than cSCC within 3 years of data of first planned dose of therapy except for tumors with a negligible risk of metastasis and/or death as defined below:
a. Adequately treated non-invasive malignancies including but not limited to melanoma in situ (MIS), BCC, CIS of cervix, or DCIS of breast may be enrolled.
b. Low-risk early stage prostate adenocarcinoma (T1-T2a N0 M0 and Gleason score ≤6 and PSA ≤10 ng/mL) for which the management plan is active surveillance, or prostate adenocarcinoma with biochemical-only recurrence with documented PSA doubling time of > 12 months for which the management plan is active surveillance may be enrolled.
c. Indolent hematologic malignancies for which the management plan is active surveillance including but not limited to CLL/indolent lymphoma may be enrolled.
i. Patients with high-risk hematologic malignancies (CML, ALL, AML, Hodgkin's or non- Hodgkin's lymphoma) are excluded even if the management plan is active surveillance.
Has known active CNS metastases and/or carcinomatous meningitis.
a. Note: Participants with previously treated brain metastases may participate provided they are radiologically stable, i.e. without evidence of progression for at least 4 weeks by repeat imaging (note that the repeat imaging should be performed during Screening), clinically stable and without requirement of steroid treatment for at least 14 days prior to first dose of study intervention.
Has a known history of Hepatitis B (defined as Hepatitis B surface antigen [HBsAg] reactive) and/or known active Hepatitis C virus (defined as anti-HCV reactive) infection.
a. Patients with treated Hepatitis B/C with no evidence of active infection may be enrolled.
Neoadjuvant Phase: 200 mg IV infusion, every 3 weeks (Day 1 of each 3-week cycle, 2 cycles) Adjuvant Phase: Day 1 of each 3-week cycle, 15 cycles
Drug: Pembrolizumab Injection
200 mg IV infusion
Also known as: Keytura
Pathologic Response
Percentage of patients with either pathologic complete response (pCR) or partial pathologic response (pPR) per Immune-Related Pathologic Response Criteria (immunotherapy-specific pathologic response criteria (irPRC) criteria. Per (irPRC), pCR = 0% residual viable tumor (RVT) remaining in post-therapy specimen (no signs of cancer) in tissue samples removed during surgery, and pPR = \>10% but ≤50% RVT remaining in post-therapy specimen in tissue samples removed during surgery.
Time frame: At time of surgery, up to 6 weeks post-baseline
Response Assessment Per Immune-Related Pathologic Response Criteria (irPRC)
Number of patients with pathologic complete response (pCR), partial pathologic response (pPR), pathologic non-response (pNR) per Immune-Related Pathologic Response Criteria ((irPRC) criteria. Per (irPRC), pCR = 0% residual viable tumor (RVT) (no signs of cancer), pPR = \>10% but ≤50% RVT, or pNR = \>50% RVT remaining in post-therapy specimen tissue samples removed during surgery.
Time frame: At time of surgery
Progression-free Survival (PFS)
The median length of time from initiation of study drug(s) until disease relapse (disease progression) as defined by RECIST v1.1, or death. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Time frame: Up to 60 months
1-year PRS
The proportion of patients whose disease does not progress/relapse (as defined by RECIST v1.1), or cease to breath at 1 year after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Time frame: Up to 12 months
6-month PFS
The proportion of patients whose disease does not progress/relapse (as defined by RECIST v1.1), or cease to breath at 6 months after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Time frame: Up to 6 months
2-year PFS
The proportion of patients whose disease does not progress (as defined by RECIST v1.1), or cease to breath at 2 years after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Time frame: Up to 24 months
3-year PFS
The proportion of patients whose disease does not progress/relapse (as defined by RECIST v1.1), or cease to breath at 3 years after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Time frame: Up to 36 months
Overall Survival (OS)
The median length of time from initiation of study treatment that patients remain alive.
Time frame: Up to 84 months
1-year OS
The proportion of patients alive at 1 year after the initiation of treatment.
Time frame: Up to 12 months
2-year OS
The proportion of patients alive at 2 years after the initiation of treatment.
Time frame: Up to 24 months
Pathologic Response
Number of patients with response per Immune-Related Pathologic Response Criteria (irPRC) criteria: major pathologic response (\<0 to ≤10% RVT); partial pathologic response (\<10 to ≤50% RVT).
Time frame: From start of treatment, up to 24 months
| Milestone | Pembrolizumab |
|---|---|
| Started | 30 |
| Completed | 30 |
| Not completed | 0 |
Percentage of patients with either pathologic complete response (pCR) or partial pathologic response (pPR) per Immune-Related Pathologic Response Criteria (immunotherapy-specific pathologic response criteria (irPRC) criteria. Per (irPRC), pCR = 0% residual viable tumor (RVT) remaining in post-therapy specimen (no signs of cancer) in tissue samples removed during surgery, and pPR = \>10% but ≤50% RVT remaining in post-therapy specimen in tissue samples removed during surgery.
| percentage of patients | Pembrolizumab |
|---|---|
| pCR | 63.0 (42.4 to 80.6) |
| pPR | 7.4 (0.9 to 24.3) |
The median length of time from initiation of study drug(s) until disease relapse (disease progression) as defined by RECIST v1.1, or death. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Results for this outcome have not been posted.
The proportion of patients whose disease does not progress/relapse (as defined by RECIST v1.1), or cease to breath at 1 year after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Results for this outcome have not been posted.
The proportion of patients whose disease does not progress/relapse (as defined by RECIST v1.1), or cease to breath at 6 months after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Results for this outcome have not been posted.
The proportion of patients whose disease does not progress (as defined by RECIST v1.1), or cease to breath at 2 years after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Results for this outcome have not been posted.
The proportion of patients whose disease does not progress/relapse (as defined by RECIST v1.1), or cease to breath at 3 years after the initiation of treatment. Progressive Disease (PD): ≥20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). The sum must also demonstrate an absolute increase of ≥5 mm. The appearance ≥1 new lesion(s) is considered progression.
Results for this outcome have not been posted.
The median length of time from initiation of study treatment that patients remain alive.
Results for this outcome have not been posted.
The proportion of patients alive at 1 year after the initiation of treatment.
Results for this outcome have not been posted.
The proportion of patients alive at 2 years after the initiation of treatment.
Results for this outcome have not been posted.
Number of patients with response per Immune-Related Pathologic Response Criteria (irPRC) criteria: major pathologic response (\<0 to ≤10% RVT); partial pathologic response (\<10 to ≤50% RVT).
Results for this outcome have not been posted.
Number of patients with pathologic complete response (pCR), partial pathologic response (pPR), pathologic non-response (pNR) per Immune-Related Pathologic Response Criteria ((irPRC) criteria. Per (irPRC), pCR = 0% residual viable tumor (RVT) (no signs of cancer), pPR = \>10% but ≤50% RVT, or pNR = \>50% RVT remaining in post-therapy specimen tissue samples removed during surgery.
| Participants | Pembrolizumab |
|---|---|
| pCR | 17 |
| pPR | 2 |
| pNR | 8 |
Collected over Adverse Events data collected for a total of approximately 45 months for the study population. Up to approximately 16 months after start of treatment for individuals.. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Pembrolizumab | 6/30 (20%) | 13/30 (43.3%) | 29/30 (96.7%) |
| Event | Pembrolizumab |
|---|---|
| Urinary tract infectionINFECTIONS AND INFESTATIONS | 2/30 |
| PneumothoraxRESPIRATORY, THORACIC AND MEDIASTINAL DISORDERS | 2/30 |
| Respiratory failureRESPIRATORY, THORACIC AND MEDIASTINAL DISORDERS | 2/30 |
| Cardiac arrestCARDIAC DISORDERS | 1/30 |
| Heart failureCARDIAC DISORDERS | 1/30 |
| Mobitz (type) II atrioventricular blockCARDIAC DISORDERS | 1/30 |
| Myocardial infarctionCARDIAC DISORDERS | 1/30 |
| MyocarditisCARDIAC DISORDERS | 1/30 |
| GI bleedGASTROINTESTINAL DISORDERS | 1/30 |
| PainGENERAL DISORDERS AND ADMINISTRATION SITE CONDITIONS | 1/30 |
| Event | Pembrolizumab |
|---|---|
| AnemiaBLOOD AND LYMPHATIC SYSTEM DISORDERS | 17/30 |
| Blood lactate dehydrogenase increasedINVESTIGATIONS | 15/30 |
| HyperglycemiaMETABOLISM AND NUTRITION DISORDERS | 15/30 |
| HyponatremiaMETABOLISM AND NUTRITION DISORDERS | 15/30 |
| FatigueGENERAL DISORDERS AND ADMINISTRATION SITE CONDITIONS | 12/30 |
| PainGENERAL DISORDERS AND ADMINISTRATION SITE CONDITIONS | 10/30 |
| Lymphocyte count decreasedINVESTIGATIONS | 9/30 |
| HypertensionVASCULAR DISORDERS | 9/30 |
| Aspartate aminotransferase increasedINVESTIGATIONS | 8/30 |
| Thyroid stimulating hormone increasedINVESTIGATIONS | 8/30 |
| Age, Continuous(years) | Pembrolizumab |
|---|---|
| Mean | 76.5 ± 9.18 |
| Sex: Female, Male(Participants) | Pembrolizumab |
|---|---|
| Female | 8 |
| Male | 22 |
| Ethnicity (NIH/OMB)(Participants) | Pembrolizumab |
|---|---|
| Hispanic or Latino | 1 |
| Not Hispanic or Latino | 27 |
| Unknown or Not Reported | 2 |
| Race (NIH/OMB)(Participants) | Pembrolizumab |
|---|---|
| American Indian or Alaska Native | 0 |
| Asian | 0 |
| Native Hawaiian or Other Pacific Islander | 0 |
| Black or African American | 0 |
| White | 30 |
| More than one race | 0 |
| Unknown or Not Reported | 0 |
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Diwakar Davar