Variable | Primary adrenal insufficiency | ACTH-dependent Cushing’s syndrome | Hypoparathyroidism | Diabetes Insipidus |
---|---|---|---|---|
Reports No. | 6 | 1 | 1 | 3 |
Cases No. | 6 | 1 | 1 | 3 |
Gender | Male = 3; Female = 2; Not reported =1 | Female = 1 | Male = 1 | Male = 3 |
Age (years) | Median = 52; Mean + SD = 51.2 + 4.7 Range 43–56 | 53 | 73 | Median = 62; Mean + SD = 61.7 + 11.5 Range = 50–73 |
Pertinent medical history | PHx EndoD: NR = 6 FHx EndoD: NR = 6 HX AutoD: NR = 6 | PHx EndoD: NR FHx EndoD: NR Hx AutoD: NR | PHx EndoD: NR FHx EndoD: NR Hx AutoD: No | PHx EndoD: NR = 3 FHx EndoD: NR = 3 Hx AutoD: NR = 3 |
Type of cancer (all metastatic) | Melanoma = 3; RCC = 1; Lung adenoCa = 1; NSCLC = 1 | Melanoma | Melanoma | Prostate Ca = 1; Melanoma = 1; Merkel cell Ca = 1. |
Check point inhibitor(s) | Ipilimumab =2; Nivolumab =3; Pembrolizumab =1 | Ipilumumab + Nivolumab | Nivolumab +Ipilimumab | C1: Ipilimumab. C2: Ipilimumab C3: Avelumab |
ICI Drug D/C? | Yes = 1; Not reported = 5 | Yes = 1 at 12 wks. | Not reported =1 | |
Clinical presentation | Fatigue, weight loss, anorexia, nausea, vomiting, headache, etc | Anorexia, weakness | Paresthesia, weakness, etc | C1: Polydipsia, polyuria C2: Polydipsia, polyuria C3: Polydipsia, polyuria. |
Onset (weeks) after 1st dose | Median = 10 Mean + SD =14.92 + 14 Range = 1.5–36 | 14 wks | 6 wks | Median = 12; Mean + SD = 3 + 16; Range = 3–16 |
Biochemical tests | ↑ACTH in 5; ↓cortisol in 4; Synactin test +ve & + ve adrenal Ab in 1 without cortisol. In 1 cosyntropin stimulation test was negative and pt. had enlarged adrenal glands preceded by secondary adrenal \insufficiency. | 9wks: slight ↑ in cortisol; 12 wks: ↑ACTH, ↑cortisol, ↑[cortisol]u. Abnormal low dose dexamethasone suppression test. 16 wks: ↓ACTH, cortisol. 6wks: ↓TSH, ↑FT4, FT3. Then ↓TSH, FT4, FT3. ↓LH, estradiol. Normal PRL. | ↓Calcium, undetectable PTH, ↑ phosphate4, ↓vitamin D, magnesium 7wks: ↓TSH, ↑FT4, FT3, then ↓TSH, FT4, FT3. | C1: ↓ACTH, cortisol, TSH, FT4, FT3, LH & FSH. Normal glucose. C2: ↓ACTH, cortisol, TSH, FT4, FT3, LH & FSH. Normal glucose. Water deprivation test: partial diabetes insipidus C3: ↑[sodium],[osmolality]s, ↓[osmolality]u. Normal glucose |
Diagnosis | Primary adrenal insufficiency | Cushing’s disease, then 2o adrenal insufficiency. Thyroiditis, then hypothyroidism. 2o hypogonadism. | Primary hypoparathyroidism | Diabetes insipidus |
Imaging MRI/CT | MRI brain: 2 normal & 2 enlarged pituitary. Abd CT scan: atrophied adrenals; enlarged in 1 | MRI pituitary at 12 wks: enlarged | EKG: prolonged QT interval | MRI pituitary: Normal in all |
CTCAE grade reported | Severity not reported in all: | Not reported | Not reported; | Not reported in all. |
Therapy at onset at diagnosis | iv steroids in 4. Oral steroids in 2. Florinef in 2 | Wk5: LT4 Wk16: HCT & LT4. | iv calcium gluconate, then oral vitamin D & Ca carbonate. LT4. | C1: High dose steroidsC2: HCT, LT4 & desmopressin. C3: Desmopressin |
Outcome | 5 discharged on steroids. 1 NR. | HCT & LT4. | Calcium carbonate + calcitriol LT4. | C1: NR. C2: HCT, LT4 & desmopressin; C3: Desmopressin D/C |