Moffitt Onco Update

Pancoast (Superior Sulcus) Tumors of the Lung: Improved Results with a Coordinated Approach

June 28, 2014

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Lary A. Robinson, MD

One of the most distressing and vexing presentations of lung cancer is that of the superior sulcus tumor. In 1932 when Henry Pancoast, the first chairman of radiology at the University of Pennsylvania, described this tumor, he wrongly thought that it started from embryonic rests that invaded the lung. Later, it was determined that this cancer started in the upper lobe of either lung and involved the apex of the pleural cavity (the superior sulcus). The tumor causes severe, painful symptoms by invading the brachial plexus, ribs, vertebrae, subclavian vessels, and occasionally the stellate ganglion.

Pancoast Tumor Seen on MRI
Pancoast Tumor Seen on MRI

Presentation

Unfortunately, the presenting arm and shoulder pain and neurologic symptoms may be misleading, often delaying the diagnosis for months while mistaken benign orthopedic causes, such as cervical spine disease, are investigated. The characteristic Pancoast symptoms include some or all of the following: 1) dysesthesias, paresthesias and weakness in the arm and hand in the C-8, T-1 and T-2 distribution; 2) subclavian (vein or artery) impairment to the involved upper extremity; 3) pain in the shoulder, upper arm, scapula and/or shoulder; 4) Horner’s syndrome (ptosis, miosis, anhidrosis, and apparent enophthalmos due to the ptosis). The diagnosis requires symptoms plus a lung cancer located in the apex of chest (superior sulcus).

An estimated 3-5% of non-small cell carcinomas present with a symptomatic Pancoast tumor. With 17,860 new lung cancers in Florida yearly (2012 date), approximately 550 of these are Pancoast tumors and deserve evaluation for potential curative, multimodality therapy. Squamous cell carcinoma represents 52% of Pancoast cases, with the rest composed of 23% adenocarcinomas, 20% large cell carcinomas and 5% small cell carcinomas.

Evaluation

Lung masses with a Pancoast tumor presentation require the same initial evaluation as other lung masses (chest CT with contrast and PET scan). To assess the extent of chest wall involvement and to further stage the tumor, an MRI with contrast of the brachial plexus and thoracic inlet (which includes the upper thoracic vertebrae) is mandatory. Once a Pancoast tumor is suspected, a needle biopsy is required for a histologic diagnosis since induction therapy is recommended. If the tumor is deemed potentially resectable, then pulmonary function tests and possibly a cardiac evaluation are recommended.

Treatment 

Prior to 1950, this was a uniformly fatal tumor. In 1961, Shaw, Paulson and Kee described neoadjuvant radiotherapy followed by surgery for Pancoast tumors, and they had some long-term survivors. Forty years later in 2001, the phase II Intergroup Pancoast tumor trial added chemotherapy to the induction regimen (two cycles of induction cisplatin/etoposide chemotherapy with concurrent 4500 cGy radiotherapy followed by resection), reporting an excellent 41% five-year survival in the 83 of 111 patients who subsequently underwent surgery. This regimen has been adopted as the current standard of care.

However, there are a number of significant limitations of the concurrent preoperative chemoradiotherapy. In these debilitated patients, induction chemoradiotherapy causes significant morbidity, as indicated by the fact that only 75% of the patients in the Intergroup trial could tolerate treatment long enough to undergo surgery. In addition, the 4500 cGy preop radiation dose is not tumorcidal. Since the surgical incision directly crosses the radiation portal (radiated skin), there are potential wound problems. Finally and most importantly, if there are close or microscopically positive surgical margins, further radiotherapy after surgery is generally ineffective since this split-course radiation has proven unsuccessful. Additionally, postoperative chemotherapy in Pancoast tumor patients is poorly tolerated.

Which Patients Are Candidates For Triple Modality Therapy?

Most ECOG performance status 1 or 2 Pancoast tumor patients with adequate cardiopulmonary reserve will tolerate induction chemotherapy, surgery and postoperative radiotherapy with a very low expected morbidity and mortality. Patients with T3N0 or T3N1 as well as selected T4N0 or T4N1 tumors with no mediastinal lymph node involvement should be considered for treatment including surgery. If mediastinal N2 node involvement is suspected, we generally obtain histologic confirmation of tumor in the nodes by EBUS, EUS or mediastinoscopy before ruling out surgery. Contraindications to surgery for Pancoast tumors are definite N2 or N3 mediastinal lymph node metastases or extensive involvement of the brachial plexus, and these patients need chemoradiotherapy alone. Interestingly, we rarely encounter Pancoast tumors with nodal metastasis or unresectable chest wall involvement, probably because the pain from the tumor brings the patient to medical attention before there is unresectable spread.  

The key point is to have every patient evaluated by a Pancoast tumor experienced thoracic surgeon (and neurosurgeon) before ruling out surgery, and before starting induction therapy.

Moffitt’s Pancoast Tumor Program 

In order to avoid the drawbacks of induction chemoradiotherapy, the Thoracic Oncology Department has adopted a slightly different approach, also favored by several other major cancer centers. We use induction chemotherapy with a platinum doublet for three cycles. The tumor pain usually lessens or resolves within 7-10 days after beginning chemotherapy. A chest CT with contrast is repeated after chemotherapy to verify there has been no progression. Surgical resection is then performed 3-5 weeks after completing chemotherapy. Six weeks after surgery, patients start full-dose radiotherapy (6600 cGy) to the tumor bed; which is tumorcidal for close margins and any residual microscopic disease. This entire treatment regimen is well tolerated, as evidenced by virtually 100% of our current series of 105 Pancoast patients completing all therapy including surgery, with only a 1.9% operative mortality. 

In order to provide the most efficient and effective care, we have focused our approach for these difficult lung cancer patients by creating the Pancoast Tumor Program. The dedicated, multidisciplinary team is composed of thoracic surgery, neurosurgery, vascular surgery, and medical and radiation oncology specialists. We work closely with the patient’s referring medical oncologist to coordinate the timing of care, since almost all induction chemotherapy is administered by the patient’s personal oncologist close to home. Likewise, most postoperative radiation therapy can be delivered readily in the patient’s local area.

Pancoast tumors present a real challenge to the oncology community, particularly in the aging Florida population. Nevertheless, we feel that with a focused, coordinated effort, almost all patients can successfully undergo aggressive, multimodality therapy including surgery for this cancer at low risk, with a significant chance for longterm cure.

About Lary A. Robinson, MD

A thoracic surgeon and senior member in the Division of Thoracic Oncology at Moffitt Cancer Center, Dr. Robinson specializes in the aggressive surgical treatment for a wide variety of thoracic cancers. He obtained his M.D. degree at Washington University in St. Louis. His surgery residency and thoracic surgery fellowship were completed at the Duke University Medical Center. He is board certified in thoracic surgery, surgical critical care and general surgery. He is author or co-author of more than 100 papers and book chapters. He is also co-director of the Pancoast Tumor Program and co-director of the Center for Infection Research in Cancer at Moffitt. His research interests include elucidating the role of microorganisms in the pathogenesis of lung cancer and in sarcoidosis. He currently is accepting new patients at Moffitt Cancer Center. 



Adapted from Florida MD, December 2013