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. 2022 Jun 30;5(6):e2219535. doi: 10.1001/jamanetworkopen.2022.19535

Table 2. Facility Characteristics and Patient Logistical Considerations in Pre–FDA Approval and Early Post–FDA Approval Eras.

Characteristic Facilities, No./total No. (%)
NSCLCa RCCb Melanomac
Pre–FDA approval Early post–FDA approval Pre–FDA approval Early post–FDA approval Pre–FDA approval Early post–FDA approval
Total facilities (any treatment), No.d 1259 1294 1255 1261 1031 1063
Facilities treating with immunotherapye 934/1259 (74.2) 1243/1294 (96.1) 441/1255 (35.1) 927/1261 (73.5) 253/1031 (24.5) 440/1063 (41.4)
Facility type
Community 153/934 (16.4) 263/1243 (21.1) 37/441 (8.4) 138/927 (14.9) 17/253 (6.7) 35/440 (8.0)
Comprehensive community program 373/934 (39.9) 476/1243 (38.3) 179/441 (40.6) 382/927 (41.2) 87/253 (34.4) 176/440 (40.0)
Academic 174/934 (18.6) 207/1243 (16.7) 126/441 (28.6) 192/927 (20.7) 71/253 (28.1) 113/440 (25.7)
Integrated network cancer program 232/934 (24.8) 296/1243 (23.8) 93/441 (21.1) 208/927 (22.4) 52/253 (20.6) 102/440 (23.2)
Unknownf 68/934 (7.3) 131/1243 (10.5) 36/441 (8.2) 77/927 (8.3) 59/253 (23.3) 67/440 (15.2)
Facility location
Northeast 178/934 (19.1) 243/1243 (19.5) 85/441 (19.3) 172/927 (18.6) 43/253 (17.0) 75/440 (17.0)
Midwest 271/934 (29.0) 347/1243 (27.9) 119/441 (27.0) 257/927 (27.7) 66/253 (26.1) 125/440 (28.4)
South 336/934 (36.0) 431/1243 (34.7) 155/441 (35.1) 324/927 (35.0) 79/253 (31.2) 143/440 (32.5)
West 147/934 (15.7) 221/1243 (17.8) 76/441 (17.2) 167/927 (18.0) 39/253 (15.4) 83/440 (18.9)
Unknownf 68/934 (7.2) 131/1243 (10.5) 36/441 (8.2) 77/927 (8.3) 59/253 (23.3) 67/440 (15.2)
Patients who received immunotherapy during era, No. 6271 23 908 1155 3890 504 1143
Residential classification of patient receiving immunotherapyg
Metropolitan 5010/6271 (80.0) 19 523/23 908 (81.7) 931/1155 (80.6) 3119/3890 (80.2) 427/504 (84.7) 923/1143 (80.8)
Urban 933/6271 (14.9) 3336/23 908 (14.0) 152/1155 (13.2) 573/3890 (14.7) 58/504 (11.5) 153/1143 (13.4)
Rural 149/6271 (2.4) 411/23 908 (1.7) 31/1155 (2.7) 83/3890 (2.1) 7/504 (1.4) 14/1143 (1.2)
Missing 179/6271 (2.9) 638/23 908 (2.7) 41/1155 (3.5) 115/3890 (3.0) 12/504 (2.4) 53/1143 (4.6)
Travel distance for patient receiving immunotherapy, milesg
0-20 4109/6271 (65.5) 14 733/23 908 (61.6) 580/1155 (50.2) 2016/3890 (51.8) 246/504 (48.8) 605/1143 (52.9)
>20-40 994/6271 (15.9) 3311/23 908 (13.8) 173/1155 (15.0) 601/3890 (15.4) 96/504 (19.0) 185/1143 (16.2)
>40-60 356/6271 (5.7) 1239/23 908 (5.2) 84/1155 (7.3) 258/3890 (6.6) 42/504 (8.3) 86/1143 (7.5)
>60 511/6271 (8.1) 1597/23 908 (6.7) 188/1155 (16.3) 450/3890 (11.6) 105/504 (20.8) 200/1143 (17.5)
Missing 301/6271 (4.8) 3028/23 908 (12.7) 130/1155 (11.3) 565/3890 (14.5) 15/504 (3.0) 67/1143 (5.9)

Abbreviations: FDA, Food and Drug Administration; NSCLC, non–small cell lung cancer; RCC, renal cell carcinoma.

a

For NSCLC, the pre–FDA approval era was 2011 to 2014, and the early post–FDA approval era was 2015 to 2017.

b

For RCC, the pre–FDA approval era was 2012 to 2015, and the early post–FDA approval era was 2016 to 2018.

c

For melanoma, the pre–FDA approval era was 2007 to 2010, and the early post–FDA approval era was 2011 to 2013.

d

Includes facilities that treated at least 1 patient with specified stage IV cancers with any treatment during the pre–FDA approval era.

e

Includes facilities that treated at least 1 patient with specified stage IV cancers with immunotherapy during the pre–FDA approval era. These data include the number and percentage of total facilities providing any treatment in the respective era.

f

Includes facilities that treated at least 1 patient aged 0 to 39 years. Facility type and location were suppressed for patients aged 0 to 39 years because of small sample sizes. Therefore, some hospitals were counted twice, and the total does not equal the total number of facilities providing treatment with immunotherapy.

g

Includes the number and percentage of patients who received immunotherapy in the respective era.