Trial Outcomes & Findings for Treatment Outcomes in Japanese RCC Patients Treated With Avelumab Plus Axitinib as First-line Therapy: Retrospective Study (J-DART2) (NCT NCT05650164)

NCT ID: NCT05650164

Last Updated: 2025-03-28

Results Overview

The age of participants at baseline was reported.

Recruitment status

COMPLETED

Target enrollment

171 participants

Primary outcome timeframe

At Baseline (prior to initial treatment with avelumab plus axitinib)

Results posted on

2025-03-28

Participant Flow

Participant milestones

Participant milestones
Measure
Participants With Metastatic Renal Cell Carcinoma
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Overall Study
STARTED
171
Overall Study
COMPLETED
171
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Treatment Outcomes in Japanese RCC Patients Treated With Avelumab Plus Axitinib as First-line Therapy: Retrospective Study (J-DART2)

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Age, Categorical
<=18 years
0 Participants
n=99 Participants
Age, Categorical
Between 18 and 65 years
112 Participants
n=99 Participants
Age, Categorical
>=65 years
58 Participants
n=99 Participants
Sex: Female, Male
Female
45 Participants
n=99 Participants
Sex: Female, Male
Male
125 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
170 Participants
n=99 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

The age of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Age of Participants at Baseline
71.0 years
Interval 33.0 to 87.0

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria. Here, number analyzed represents the number of participants evaluable for the outcome measure.

The height of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=169 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Height of Participants at Baseline
163.23 centimeters
Standard Deviation 8.60

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria. Here, number analyzed represents the number of participants evaluable for the outcome measure.

The body weight of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=169 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Body Weight of Participants at Baseline
63.117 kilograms
Standard Deviation 12.642

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria. Here, number analyzed represents the number of participants evaluable for the outcome measure.

The body mass index (BMI) of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=169 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Body Mass Index of Participants at Baseline
23.593 kilogram per square meter
Standard Deviation 3.798

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria. Here, number analyzed represents the number of participants evaluable for the outcome measure.

The C-reactive protein levels of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=167 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
C-Reactive Protein Levels of Participants at Baseline
1.575 milligrams per liter
Standard Deviation 3.001

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

The estimated Glomerular Filtration Rate (eGFR) is an index of kidney function. eGFR was calculated using factors such as serum creatinine level, age, sex, and in millimeter per minute per 1.73 square meter (ml/min/1.73 m\^2), and tabulated in three categories (\<60, ≥60, unknown). An eGFR \<60 indicates some degree of kidney impairment. And eGFR \> 60 is generally considered to be within the normal range.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Estimated Glomerular Filtration Rate of Participants at Baseline
Less than 60
124 Participants
Estimated Glomerular Filtration Rate of Participants at Baseline
More than or equal to 60
45 Participants
Estimated Glomerular Filtration Rate of Participants at Baseline
Unknown
1 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

The smoking history status of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Smoking History Status of Participants at Baseline
No (no past smoking)
67 Participants
Smoking History Status of Participants at Baseline
No (history of past smoking)
62 Participants
Smoking History Status of Participants at Baseline
Yes
26 Participants
Smoking History Status of Participants at Baseline
Unknown
15 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria. Here, number analyzed represents the number of participants evaluable for the outcome measure.

ECOG-PS assessed participant's performance status on a 5 point scale: 0= fully active/able to carry on all pre-disease activities without restriction; 1= restricted in physically strenuous activity, ambulatory/able to carry out light or sedentary work; 2= ambulatory (\>50% of waking hours), capable of all self-care, unable to carry out any work activities; 3= capable of only limited self-care, confined to bed/chair \>50% of waking hours; 4= completely disabled, cannot carry on any self-care, totally confined to bed/chair.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=169 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Eastern Cooperative Oncology Group (ECOG) Performance Scale Score Status of Participants at Baseline
0
132 Participants
Eastern Cooperative Oncology Group (ECOG) Performance Scale Score Status of Participants at Baseline
1
25 Participants
Eastern Cooperative Oncology Group (ECOG) Performance Scale Score Status of Participants at Baseline
2
5 Participants
Eastern Cooperative Oncology Group (ECOG) Performance Scale Score Status of Participants at Baseline
3
6 Participants
Eastern Cooperative Oncology Group (ECOG) Performance Scale Score Status of Participants at Baseline
4
1 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

The Number of participants with Metastatic Organs of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Metastatic Organs at Baseline
Bone
28 Participants
Number of Participants With Metastatic Organs at Baseline
Brain
3 Participants
Number of Participants With Metastatic Organs at Baseline
Regional lymph node
22 Participants
Number of Participants With Metastatic Organs at Baseline
Distant lymph node
19 Participants
Number of Participants With Metastatic Organs at Baseline
Other
45 Participants
Number of Participants With Metastatic Organs at Baseline
Lung
101 Participants
Number of Participants With Metastatic Organs at Baseline
Liver
13 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Efficacy Analysis Set is a subset of the FAS comprising patients whose index date is prior to April 30, 2022, to ensure a 6-month follow-up period.

TX: Primary tumor cannot be assessed, T0: No evidence of primary tumor, T1: Tumor ≤7 cm in greatest dimension, limited to the kidney, T1a: Tumor≤4cm in greatest dimension, limited to the kidney, T1b: Tumor\>4 cm but ≤7 cm in greatest dimension, limited to the kidney, T2: Tumor \>7 cm in greatest dimension, limited to the kidney, T2a: Tumor \>7 cm but ≤10 cm in greatest dimension, limited to the kidney, T2b: Tumor \>10 cm, limited to the kidney, T3: Tumor extends into major veins or perinephric tissues, but not into the ipsilateral adrenal gland and not beyond Gerota's fascia,T3a: Tumor extends into the renal vein or its segmental branches, or invades the pelvicalyceal system, or invades perirenal and, T3b: Tumor extends into the vena cava below the diaphragm, T3c: Tumor extends into the vena cava above the diaphragm or invades the wall of the vena cava, T4: Tumor invades beyond Gerota's fascia (including contiguous extension into the ipsilateral adrenal gland)

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=150 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Invasion Depth (T Factor) of Participants at Baseline
T1
1 Participants
Invasion Depth (T Factor) of Participants at Baseline
T3b
10 Participants
Invasion Depth (T Factor) of Participants at Baseline
TX
6 Participants
Invasion Depth (T Factor) of Participants at Baseline
T0
0 Participants
Invasion Depth (T Factor) of Participants at Baseline
T1a
26 Participants
Invasion Depth (T Factor) of Participants at Baseline
T1b
29 Participants
Invasion Depth (T Factor) of Participants at Baseline
T2
2 Participants
Invasion Depth (T Factor) of Participants at Baseline
T2a
6 Participants
Invasion Depth (T Factor) of Participants at Baseline
T2b
2 Participants
Invasion Depth (T Factor) of Participants at Baseline
T3
2 Participants
Invasion Depth (T Factor) of Participants at Baseline
T3a
43 Participants
Invasion Depth (T Factor) of Participants at Baseline
T3c
2 Participants
Invasion Depth (T Factor) of Participants at Baseline
T4
10 Participants
Invasion Depth (T Factor) of Participants at Baseline
Unknown
11 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Lymph node metastasis (N factor) of participants at baseline was reported. NX: Regional lymph nodes cannot be assessed, N0: No regional lymph node metastasis, N1: Metastasis in regional lymph node(s).

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Lymph Node Metastasis (N Factor) Status of Participants at Baseline
NX
7 Participants
Lymph Node Metastasis (N Factor) Status of Participants at Baseline
N0
127 Participants
Lymph Node Metastasis (N Factor) Status of Participants at Baseline
N1
30 Participants
Lymph Node Metastasis (N Factor) Status of Participants at Baseline
Unknown
6 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Distant metastasis (M factor) of participants at baseline was reported. M0: No distant metastasis, M1: Distant metastasis.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Distant Metastasis (M Factor) Status of Participants at Baseline
MX
0 Participants
Distant Metastasis (M Factor) Status of Participants at Baseline
M0
20 Participants
Distant Metastasis (M Factor) Status of Participants at Baseline
M1
150 Participants
Distant Metastasis (M Factor) Status of Participants at Baseline
Unknown
0 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Tumor histological type of participants at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Tumor Histological Type of Participants at Baseline
Clear cell renal cell carcinoma
154 Participants
Tumor Histological Type of Participants at Baseline
Papillary renal cell carcinoma
4 Participants
Tumor Histological Type of Participants at Baseline
Chromophobe renal cell carcinoma
2 Participants
Tumor Histological Type of Participants at Baseline
Other
4 Participants
Tumor Histological Type of Participants at Baseline
Unknown
6 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria. . Here "Number of Participants Analyzed" signifies those participants who were evaluated at the specified time point.

Number of Participants with Presence or Absence of Sarcomatoid Component at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=169 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Presence or Absence of Sarcomatoid Component in Participants at Baseline
Presence
11 Participants
Number of Participants With Presence or Absence of Sarcomatoid Component in Participants at Baseline
Absence
158 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

The four-tiered Fuhrman grading evaluates nuclear size, nuclear shape and presence of nucleolar prominence. Grade 1: small (=10 micrometer \[mcm\]) nuclear diameter, round/uniform nuclear shape and absent/inconspicuous nucleoli; Grade 2: large (=15 mcm) nuclear diameter, irregular outline nuclear shape and visible at \*400 magnification nucleoli; Grade 3: larger (=20 mcm) nuclear diameter, obvious irregular outline nuclear shape and visible and prominent at \*100 magnification nucleoli; Grade 4: grade 3 plus bizarre multilobed nuclei +/- spindle cells. Participants whose Fuhrman Grade were not known were reported against "Unknown'.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Fuhrman Grade Status of Participants at Baseline
Grade 1
57 Participants
Fuhrman Grade Status of Participants at Baseline
Grade 2
0 Participants
Fuhrman Grade Status of Participants at Baseline
Grade 3
33 Participants
Fuhrman Grade Status of Participants at Baseline
Grade 4
16 Participants
Fuhrman Grade Status of Participants at Baseline
Unknown
64 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Proteinuria is the presence of an excess of serum proteins in the urine, which may be an early sign of kidney disease. Here, negative (-)= \<15 milligrams per deciliter (mg/dL) (Normal), positive (±) =15-29 mg/dL (increased risk for kidney disease), (1+) = 30 mg/dL(Early stages of kidney disease), (2+)= 100 mg/dL (Underlying kidney disease), (3+)= 300 mg/dL (kidney dysfunction).

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Availability of Proteinuria in Participants at Baseline
minus (-)
92 Participants
Availability of Proteinuria in Participants at Baseline
plus minus (+-)
22 Participants
Availability of Proteinuria in Participants at Baseline
1+
17 Participants
Availability of Proteinuria in Participants at Baseline
2+
6 Participants
Availability of Proteinuria in Participants at Baseline
3+
6 Participants
Availability of Proteinuria in Participants at Baseline
Not measured
27 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Performance of nephrectomy at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Performance of Nephrectomy in Participants
No
45 Participants
Performance of Nephrectomy in Participants
Yes
125 Participants
Performance of Nephrectomy in Participants
Unknown
0 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of Participants with Presence or absence of clinically important comorbidities at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Presence or Absence of Clinically Important Comorbidities of Participants at Baseline
No
59 Participants
Number of Participants With Presence or Absence of Clinically Important Comorbidities of Participants at Baseline
Yes
111 Participants
Number of Participants With Presence or Absence of Clinically Important Comorbidities of Participants at Baseline
Unknown
0 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of participants with Presence or absence of clinically important concomitant drugs at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Presence or Absence of Clinically Important Concomitant Drugs in Participants at Baseline
Yes
95 Participants
Number of Participants With Presence or Absence of Clinically Important Concomitant Drugs in Participants at Baseline
No
75 Participants
Number of Participants With Presence or Absence of Clinically Important Concomitant Drugs in Participants at Baseline
Unknown
0 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of Participants with Initiation of Systemic Therapy within One Year of Diagnosis was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Initiation of Systemic Therapy Within One Year of Diagnosis
No
81 Participants
Number of Participants With Initiation of Systemic Therapy Within One Year of Diagnosis
Yes
89 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Karnofsky performance score was used to quantify participant's general well-being and activities of daily life and participants were classified based on their functional impairment. Karnofsky performance score ranges between 0 (death) to 100 (no evidence of disease). Higher score means higher ability to perform daily tasks.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Karnofsky Performance Status Less Than (<) 80 Percent (%) at Baseline
No
157 Participants
Number of Participants With Karnofsky Performance Status Less Than (<) 80 Percent (%) at Baseline
Yes
13 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of participants with Hemoglobin value below the lower normal limit at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Hemoglobin Value Below the Lower Normal Limit at Baseline
No
85 Participants
Number of Participants With Hemoglobin Value Below the Lower Normal Limit at Baseline
Yes
85 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of participants with Corrected calcium value above the upper normal limit at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Corrected Calcium Value Above the Upper Normal Limit in Participants at Baseline
No
150 Participants
Number of Participants With Corrected Calcium Value Above the Upper Normal Limit in Participants at Baseline
Yes
20 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of Participants with Neutrophil count above the upper normal limit at baseline was reported.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Neutrophil Count Above the Upper Normal Limit in Participants at Baseline
No
146 Participants
Number of Participants With Neutrophil Count Above the Upper Normal Limit in Participants at Baseline
Yes
24 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

IMDC criteria had 6 risk factors: Karnofsky Performance Status less than (\<) 80% (ability to perform ordinary tasks, 0 \[dead\] -100 \[normal\]); time from diagnosis to start of systemic therapy \<1 year; corrected serum calcium; neutrophils and platelets more than (\>) upper limit of normal (ULN); hemoglobin \<lower limit of normal (LLN). Present risk factors were added, and then participants were stratified as: Low risk (0 factor), Medium risk (1-2 factors), High risk (more than or equal to \[\>=\]3 factors).

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
International Metastatic RCC Database Consortium (IMDC) Risk Group in Participants at Baseline
Low risk
44 Participants
International Metastatic RCC Database Consortium (IMDC) Risk Group in Participants at Baseline
Medium risk
92 Participants
International Metastatic RCC Database Consortium (IMDC) Risk Group in Participants at Baseline
High risk
34 Participants

PRIMARY outcome

Timeframe: At Baseline (prior to initial treatment with avelumab plus axitinib)

Population: The Full Analysis Set comprised of participants who met the inclusion criteria and did not meet the exclusion criteria.

Number of risk factors in participants at baseline was reported

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=170 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Risk Factors in Participants at Baseline
0
44 Participants
Number of Risk Factors in Participants at Baseline
1
50 Participants
Number of Risk Factors in Participants at Baseline
2
42 Participants
Number of Risk Factors in Participants at Baseline
3
21 Participants
Number of Risk Factors in Participants at Baseline
4
12 Participants
Number of Risk Factors in Participants at Baseline
5
1 Participants
Number of Risk Factors in Participants at Baseline
6
0 Participants

SECONDARY outcome

Timeframe: From index date up to 31 Oct 2022, where index date was date of first prescription for avelumab plus axitinib between 20 December 2019 and 17 October 2022 (maximum observation period was of 34 months approximately)

Population: The efficacy analysis set is a subset of the FAS that includes patients whose index date is prior to 30 April 2022 to ensure a 6-months follow-up period.

rwPFS is defined as: The time from start of avelumab plus axitinib therapy to date of first disease progression (as clinically assessed by local investigator based on radiology, laboratory evidence, pathology, or other assessments) or death due to any cause, whichever occurred first.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=150 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Real-World Progression-Free Survival (Rw-PFS)
13.8 months
Interval 12.5 to 18.0

SECONDARY outcome

Timeframe: From index date up to 31 Oct 2022, where index date was date of first prescription for avelumab plus axitinib between 20 December 2019 and 17 October 2022 (maximum observation period was of 34 months approximately)

Population: The efficacy analysis set is a subset of the FAS that includes patients whose index date is prior to 30 April 2022 to ensure a 6-months follow-up period.

TTD is defined as the time from the start of treatment with avelumab plus axitinib to the end of treatment due to any cause except the effectiveness of the treatment.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=150 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Time to Treatment Discontinuation (TTD)
17.2 months
Interval 11.2 to 23.0

SECONDARY outcome

Timeframe: From index date up to 31 Oct 2022, where index date was date of first prescription for avelumab plus axitinib between 20 December 2019 and 17 October 2022 (maximum observation period was of 34 months approximately)

Population: The efficacy analysis set is a subset of the FAS that includes patients whose index date is prior to 30 April 2022 to ensure a 6-months follow-up period.

OS is defined as the time from the start of treatment with avelumab plus axitinib to the date of death due to any cause. If there are no clinical records of death, the date when the patient was last documented to be alive will be confirmed based on medical records. The data will be censored at the date of last contact.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=150 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Overall Survival (OS)
18.7 months
Interval 16.3 to 20.6

SECONDARY outcome

Timeframe: From index date up to 31 Oct 2022, where index date was date of first prescription for avelumab plus axitinib between 20 December 2019 and 17 October 2022 (maximum observation period was of 34 months approximately)

Population: The efficacy analysis set is a subset of the FAS that includes patients whose index date is prior to 30 April 2022 to ensure a 6-months follow-up period.

The ORR is defined as the proportion of participants with a documented BOR (complete response (CR) or partial response (PR)) by the investigator during treatment with avelumab plus axitinib as firstline therapy. The BOR is defined as the best tumor response recorded during the observation period. The definitions of tumor responses are as follows: Complete or PR as the best adjudication result (CR \> PR \> stable disease \[SD\] \> progressive disease \[PD\], not Evaluable \[NE\]) complies with the RECIST tumor assessment guidelines as closely as possible in clinical practice.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=150 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Percentage of Participants With Best Overall Response of CR or PR (Objective Response Rate)
53.3 percentage of participants
Interval 44.6 to 62.0

SECONDARY outcome

Timeframe: From index date up to 31 Oct 2022, where index date was date of first prescription for avelumab plus axitinib between 20 December 2019 and 17 October 2022 (maximum observation period was of 34 months approximately)

Population: The efficacy analysis set is a subset of the FAS that includes patients whose index date is prior to 30 April 2022 to ensure a 6-months follow-up period. Here "Number of Participants Analyzed" signifies those participants who were evaluated at the specified time point.

BOR is the best tumor response recorded during observation period.Tumor response are defined as follows:Complete or PR as the best adjudication result (CR \> PR \> stable disease \[SD\] \> progressive disease \[PD\],not Evaluable\[NE\]) in a method complied with RECIST version. 1.1tumor assessment as closely as possible in clinical practice by investigator's judgment.CR:Disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to \<10 mm. PR:Atleast 30% decrease in sum of diameters of target lesions,taking as reference the baseline sum diameters.SD:Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD,taking as reference the smallest sum diameters. PD:atleast a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study.In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5mm.

Outcome measures

Outcome measures
Measure
Participants With Metastatic Renal Cell Carcinoma
n=135 Participants
Participants with metastatic renal cell carcinoma who were treated using avelumab plus axitinib as a first-line therapy.
Number of Participants With Best Overall Response (BOR) for Primary Lesions
CR
12 Participants
Number of Participants With Best Overall Response (BOR) for Primary Lesions
PR
60 Participants
Number of Participants With Best Overall Response (BOR) for Primary Lesions
SD
48 Participants
Number of Participants With Best Overall Response (BOR) for Primary Lesions
PD
14 Participants
Number of Participants With Best Overall Response (BOR) for Primary Lesions
NE
1 Participants

Adverse Events

Participants With Metastatic Renal Cell Carcinoma

Serious events: 0 serious events
Other events: 0 other events
Deaths: 19 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Communication Center

Merck Healthcare KGaA, DarmstadtGermany, an affiliate of Merck KGaA,Darmstadt, Germany

Phone: +49-6151-72-5200

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place