Hyperthermic intrathoracic chemotherapy explained

Hyperthermic intrathoracic chemotherapy
Synonym:HITOC
Specialty:oncology

Hyperthermic intrathoracic chemotherapy (HITOC) is part of a surgical strategy employed in the treatment of various pleural malignancies. The pleura in this situation could be considered to include the surface linings of the chest wall, lungs, mediastinum, and diaphragm. HITOC is the chest counterpart of HIPEC. Traditionally used in the treatment of malignant mesothelioma, a primary malignancy of the pleura, this modality has recently been evaluated in the treatment of secondary pleural malignancies (e.g. thymic tumors, secondary pleural carcinosis).

Metastases to the pleural surface from any primary tumor represents Stage IV disease which carries in general an extremely poor prognosis. In addition; in highly selected situations the pleura can be involved by local spread or “seeding” from thoracic tumors such as lung, esophageal, and thymic cancers.[1]

Secondary pleural malignancies include metastasis from distant primary tumors including breast, colon, ovarian, uterine and renal cell carcinoma among others; as well as certain sarcomas and pseudomyxoma peritonei.

Treatment options for such advanced diseases are limited to systemic chemotherapy, radiation, and supportive care measures. These may include management for shortness of breath due to recurrent, symptomatic malignant pleural effusions.

However, the surgical removal of large pleural deposits with infusion of hyperthermic chemotherapy may offer significant survival and symptomatic benefit for patients in this disease category.

The rationale for this approach is the simultaneous utilization of three different antineoplastic strategies: surgical resection, chemotherapy, and hyperthermia.

The goal of surgical cytoreduction is to remove all gross disease including tumors that are in resectable areas of the lung or other structures and any large pleural nodules. After complete resection of visible disease, the chest cavity is perfused with hyperthermic chemotherapy with the goal of treating microscopic or minimally visible disease. The chemotherapy bathes the inside of the chest in concentrations that are very effective against the cancer cells but without the level of toxicity that could occur if the chemotherapy was given through the blood stream.

The increased heat of the chemotherapy perfusion can itself injure the cancer cells and makes the chemotherapy more effective.

Diseases treated

There are other intra-abdominal malignancies that may cross the diaphragm and cause disease in the chest that could be potentially helped by HITOC. Some examples would include:

Notes and References

  1. Refaely. Y. Simansky, DA . Paley, M . Gottfried, M . Yellin, A . Resection and perfusion thermochemotherapy: a new approach for the treatment of thymic malignancies with pleural spread.. The Annals of Thoracic Surgery. August 2001. 72. 2. 366–70. 11515868. 10.1016/s0003-4975(01)02786-2. free.
  2. Markowiak. T. Neu, R . Ansari, MKA . Grosser, C . Klinkhammer-Schalke, M . Hofmann, HS . Ried, M . Surgical Cytoreduction and HITOC for Thymic Malignancies with Pleural Dissemination.. Thorac Cardiovasc Surg. November 2019. 69. 2. 157–164. 10.1055/s-0039-1700883. 31731316. 208060714. free.
  3. Ambrogi. MC. Korasidis, S . Pleural recurrence of thymoma: surgical resection followed by hyperthermic intrathoracic perfusion chemotherapy.. Eur J Cardiothorac Surg. Feb 2015. 25666471. 10.1093/ejcts/ezv039. 49. 1. 321–326. free.
  4. Ratto. GB . Civalleri, D . Esposito, M . Spessa, E . Alloisio, A . De Cian, F . Vannozzi, MO . Pleural space perfusion with cisplatin in the multimodality treatment of malignant mesothelioma: a feasibility and pharmacokinetic study.. The Journal of Thoracic and Cardiovascular Surgery. April 1999. 117. 4. 759–65. 10096972. 10.1016/s0022-5223(99)70297-7. free.
  5. Kodama. K. Doi, O . Tatsuta, M . Kuriyama, K . Tateishi, R . Development of postoperative intrathoracic chemo-thermotherapy for lung cancer with objective of improving local cure.. Cancer. Oct 1, 1989. 64. 7. 1422–8. 2476210. 10.1002/1097-0142(19891001)64:7<1422::aid-cncr2820640710>3.0.co;2-t.