# Extraordinary Response to Mitotane Monotherapy in Advanced Aggressive Adrenocortical Carcinoma

**Authors:** Maria Elena Aloini, Pina Lardo, Roberta Maggio, Iolanda Matarazzo, Alfredo Berruti, Antonio Stigliano

PMC · DOI: 10.1210/jcemcr/luaf174 · JCEM Case Reports · 2025-07-31

## TL;DR

A patient with advanced adrenal cancer showed a strong response to mitotane treatment, even at lower-than-usual drug levels.

## Contribution

Demonstrates mitotane monotherapy effectiveness in advanced ACC with plasma levels below the typical threshold.

## Key findings

- A 45% reduction in primary tumor and regression of lung metastases occurred after 4 months of mitotane.
- Effective response was observed at mitotane plasma levels of 5 mg/L, below the typical threshold of >14 mg/L.

## Abstract

Adrenocortical carcinoma (ACC) is an aggressive tumor; the 5-year overall survival rate for advanced disease is <15%. First-line therapy for advanced disease is mitotane, either as monotherapy or in combination with chemotherapy. Overall survival after these strategies is comparable when used in the appropriate subgroup of patients. Mitotane monotherapy is usually reserved for biologically low-risk tumors, with a reported partial response rate of 13% to 31%. Typically, responses are observed when mitotane plasma levels are >14 mg/L, but sometimes partial and complete responses have been reached with lower levels. No single clinical or pathological factor has been extensively validated to predict the response to mitotane monotherapy. We describe the case of a 45-year-old patient with metastatic, rapidly growing, unresectable ACC who had a remarkable response to mitotane monotherapy. After 4 months, a 45% reduction of the primary tumor and regression of lung metastases were observed, despite plasmatic mitotane levels of 5 mg/L. Mitotane may represent an effective therapy in selected cases of advanced ACC and despite plasma levels <14 mg/L.

## Linked entities

- **Chemicals:** mitotane (PubChem CID 4211)
- **Diseases:** adrenocortical carcinoma (MONDO:0006639), ACC (MONDO:0006639)

## Full-text entities

- **Genes:** S100A6 (S100 calcium binding protein A6) [NCBI Gene 6277] {aka 2A9, 5B10, CABP, CACY, PRA, S10A6}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, DST (dystonin) [NCBI Gene 667] {aka BP240, BPA, BPAG1, CATX-15, CATX15, CMYO29}
- **Diseases:** depression (MESH:D003866), anemia (MESH:D000740), hypercortisolism (MESH:D003480), lung metastases (MESH:D009362), Adrenal Tumors (MESH:D000310), hyperandrogenism (MESH:D017588), hypertriglyceridemia (MESH:D015228), weight loss (MESH:D015431), pulmonary embolism (MESH:D011655), M+ (MESH:C566367), tumor (MESH:D009369), edema (MESH:D004487), acute kidney injury (MESH:D058186), hypercholesterolemia (MESH:D006937), endocrine malignancy (MESH:D004700), lung nodules (MESH:D003074), anorexia (MESH:D000855), ACC (MESH:D018268), lymphadenopathy (MESH:D008206), Rare Disease (MESH:D035583), hypothyroidism (MESH:D007037)
- **Chemicals:** dexamethasone (MESH:D003907), gemcitabine (MESH:D000093542), cisplatin (MESH:D002945), capecitabine (MESH:D000069287), heparin (MESH:D006493), cortisol (MESH:D006854), metyrapone (MESH:D008797), testosterone (MESH:D013739), 17 hydroxyprogesterone (MESH:D019326), dehydroepiandrosterone sulphate (MESH:D019314), metanephrines (MESH:D008676), Cortisone acetate (MESH:D003348), doxorubicin (MESH:D004317), Mitotane (MESH:D008939), etoposide (MESH:D005047), streptozocin (MESH:D013311), creatinine (MESH:D003404), 17OHPG (-), Fluorodeoxyglucose (MESH:D019788), DHEAS (MESH:D003687)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12311424/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12311424/full.md

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Source: https://tomesphere.com/paper/PMC12311424