In September of 1996, the Council completed a review of Senate Bill 1334 (of 1995) at the request of Senator Edwin G. Holl, Chairman of the Senate Banking and Insurance Committee. Senate Bill 1334 provided for reimbursement for patient care costs when an insured, enrollee or subscriber participates in a cancer clinical trial.
The Council report on Senate Bill 1334 (of 1995) stated, "the Pennsylvania Health Care Cost Containment Council concludes that it is unable to make a recommendation regarding the passage of Senate Bill 1334 in its current form, and that it is unlikely that a formal Mandated Benefits Review Panel could or would conclude any differently, now or in the future." In our report to the General Assembly, the Council found the following:
The bill currently under review, Senate Bill 1198, is very similar to Senate Bill 1334 (of 1995). While there are slight differences in the two bills, the intent appears to be the same.
The first difference between Senate Bill 1198 and Senate Bill 1334 (of 1995) is the addition of the word "routine" before the phrase "patient care costs." This addition may have been an attempt to tighten up the language surrounding the issue of what is considered to be "patient care costs."
Another difference is the addition of the word "approved" prior to the phrase "cancer clinical trials." In Senate Bill 1198, third-party reimbursement would apply only to "routine patient care costs" when an insured, enrollee or subscriber participates in "approved cancer clinical trials." This change may also be the result of the Council's analysis of Senate Bill 1334 (of 1995) and an attempt to further clarify language in the bill.
A third difference between the two bills is that Senate Bill 1198 broadens the scope of cancer clinical trials which are eligible for coverage. In Senate Bill 1334 (of 1995), eligible options were limited to those cancer clinical trials authorized by the National Institutes of Health or the U.S. Food and Drug Administration. Senate Bill 1198 would apply to cancer clinical trials authorized by those two agencies as well as trials authorized by the U.S. Department of Defense and the U.S. Department of Veterans Affairs.
The composition of the proposed Cancer Clinical Trials Review Board evolved slightly since the initial proposal in Senate Bill 1334 (of 1995). In Senate Bill 1198, the consumer representative on the Board would be a consumer of oncology services, whereas in Senate Bill 1334 (of 1995) this representative would merely be a health care consumer.
The final noticeable difference between the two bills does not impact the intent of the legislation. Senate Bill 1334 (of 1995) would have had a sunset date of June 30, 2003 and Senate Bill 1198 (of 1997) has a sunset date of June 30, 2005. This change does not have an impact on the actual length of the proposed legislation (which would be 8 years in both cases).